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array:24 [ "pii" => "S2254887418300791" "issn" => "22548874" "doi" => "10.1016/j.rceng.2018.03.015" "estado" => "S300" "fechaPublicacion" => "2018-10-01" "aid" => "1508" "copyright" => "Elsevier España, S.L.U. and Sociedad Española de Medicina Interna (SEMI)" "copyrightAnyo" => "2018" "documento" => "article" "crossmark" => 1 "subdocumento" => "ssu" "cita" => "Rev Clin Esp. 2018;218:372-81" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 1 "PDF" => 1 ] "Traduccion" => array:1 [ "es" => array:19 [ "pii" => "S0014256518301188" "issn" => "00142565" "doi" => "10.1016/j.rce.2018.03.020" "estado" => "S300" "fechaPublicacion" => "2018-10-01" "aid" => "1508" "copyright" => "Elsevier España, S.L.U. and Sociedad Española de Medicina Interna (SEMI)" "documento" => "article" "crossmark" => 1 "subdocumento" => "ssu" "cita" => "Rev Clin Esp. 2018;218:372-81" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 196 "formatos" => array:2 [ "HTML" => 151 "PDF" => 45 ] ] "es" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Revisión</span>" "titulo" => "Diabetes tipo 2 infantojuvenil" "tienePdf" => "es" "tieneTextoCompleto" => "es" "tieneResumen" => array:2 [ 0 => "es" 1 => "en" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "372" "paginaFinal" => "381" ] ] "titulosAlternativos" => array:1 [ "en" => array:1 [ "titulo" => "Infant-juvenile type 2 diabetes" ] ] "contieneResumen" => array:2 [ "es" => true "en" => true ] "contieneTextoCompleto" => array:1 [ "es" => true ] "contienePdf" => array:1 [ "es" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figura 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1886 "Ancho" => 2513 "Tamanyo" => 137698 ] ] "descripcion" => array:1 [ "es" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Diagrama de flujo para la clasificación de la diabetes mellitus en niños y adolescentes.</p> <p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">DM1: diabetes mellitus tipo 1; DM2: diabetes mellitus tipo 2; MODY: <span class="elsevierStyleItalic">Maturity onset of diabetes mellitus in youth</span>.</p> <p id="spar0025" class="elsevierStyleSimplePara elsevierViewall">Fuente: Reinehr<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">14</span></a>.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "M.L. 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"apellidos" => "Varela Aguilar" ] ] ] ] ] "idiomaDefecto" => "es" "Traduccion" => array:1 [ "en" => array:9 [ "pii" => "S2254887418300791" "doi" => "10.1016/j.rceng.2018.03.015" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2254887418300791?idApp=WRCEE" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0014256518301188?idApp=WRCEE" "url" => "/00142565/0000021800000007/v1_201809090435/S0014256518301188/v1_201809090435/es/main.assets" ] ] "itemSiguiente" => array:18 [ "pii" => "S2254887418300808" "issn" => "22548874" "doi" => "10.1016/j.rceng.2018.03.016" "estado" => "S300" "fechaPublicacion" => "2018-10-01" "aid" => "1492" "copyright" => "Elsevier España, S.L.U. and Sociedad Española de Medicina Interna (SEMI)" "documento" => "article" "crossmark" => 1 "subdocumento" => "sco" "cita" => "Rev Clin Esp. 2018;218:382-3" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 1 "PDF" => 1 ] "en" => array:11 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Medicine in Images</span>" "titulo" => "Tarlov cyst and involuntary movements" "tienePdf" => "en" "tieneTextoCompleto" => "en" "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "382" "paginaFinal" => "383" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Quistes de Tarlov y movimientos involuntarios" ] ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:6 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 2774 "Ancho" => 2500 "Tamanyo" => 317185 ] ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "E. Casas, S. Arnaiz, E. Cubo" "autores" => array:3 [ 0 => array:2 [ "nombre" => "E." "apellidos" => "Casas" ] 1 => array:2 [ "nombre" => "S." "apellidos" => "Arnaiz" ] 2 => array:2 [ "nombre" => "E." "apellidos" => "Cubo" ] ] ] ] ] "idiomaDefecto" => "en" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2254887418300808?idApp=WRCEE" "url" => "/22548874/0000021800000007/v1_201810011013/S2254887418300808/v1_201810011013/en/main.assets" ] "itemAnterior" => array:19 [ "pii" => "S2254887418300894" "issn" => "22548874" "doi" => "10.1016/j.rceng.2018.04.003" "estado" => "S300" "fechaPublicacion" => "2018-10-01" "aid" => "1514" "copyright" => "Elsevier España, S.L.U. and Sociedad Española de Medicina Interna (SEMI)" "documento" => "article" "crossmark" => 1 "subdocumento" => "fla" "cita" => "Rev Clin Esp. 2018;218:358-71" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:2 [ "total" => 1 "PDF" => 1 ] "en" => array:13 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Special article</span>" "titulo" => "Delphi-RAND consensus of the Spanish Society of Internal Medicine on the controversies in anticoagulant therapy and prophylaxis in medical diseases. INTROMBIN Project (Uncertainty in thromboprophylaxis in internal medicine)" "tienePdf" => "en" "tieneTextoCompleto" => "en" "tieneResumen" => array:2 [ 0 => "en" 1 => "es" ] "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "358" "paginaFinal" => "371" ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Consenso Delphi-RAND de la Sociedad Española de Medicina Interna sobre controversias en terapia y profilaxis anticoagulante en enfermedades médicas. Proyecto INTROMBIN (INcertidumbre en TROMBoprofilaxis en Medicina INterna)" ] ] "contieneResumen" => array:2 [ "en" => true "es" => true ] "contieneTextoCompleto" => array:1 [ "en" => true ] "contienePdf" => array:1 [ "en" => true ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0010" "etiqueta" => "Figure 2" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr2.jpeg" "Alto" => 649 "Ancho" => 1335 "Tamanyo" => 36759 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0020" class="elsevierStyleSimplePara elsevierViewall">Type of hospital in which those surveyed worked.</p>" ] ] ] "autores" => array:1 [ 0 => array:2 [ "autoresLista" => "F. Ruiz-Ruiz, F.J. Medrano, M.A. Navarro-Puerto, P. Rodríguez-Torres, A. Romero-Alonso, J.M. Santos-Lozano, C. Alonso-Ortiz del Rio, J.M. Varela-Aguilar, E.J. Calderón, I. Marín-León" "autores" => array:11 [ 0 => array:2 [ "nombre" => "F." "apellidos" => "Ruiz-Ruiz" ] 1 => array:2 [ "nombre" => "F.J." "apellidos" => "Medrano" ] 2 => array:2 [ "nombre" => "M.A." "apellidos" => "Navarro-Puerto" ] 3 => array:2 [ "nombre" => "P." "apellidos" => "Rodríguez-Torres" ] 4 => array:2 [ "nombre" => "A." "apellidos" => "Romero-Alonso" ] 5 => array:2 [ "nombre" => "J.M." "apellidos" => "Santos-Lozano" ] 6 => array:2 [ "nombre" => "C." "apellidos" => "Alonso-Ortiz del Rio" ] 7 => array:2 [ "nombre" => "J.M." "apellidos" => "Varela-Aguilar" ] 8 => array:2 [ "nombre" => "E.J." "apellidos" => "Calderón" ] 9 => array:2 [ "nombre" => "I." "apellidos" => "Marín-León" ] 10 => array:1 [ "colaborador" => "on behalf of the members of the INTROMBIN working group" ] ] ] ] ] "idiomaDefecto" => "en" "Traduccion" => array:1 [ "es" => array:9 [ "pii" => "S0014256518301449" "doi" => "10.1016/j.rce.2018.04.006" "estado" => "S300" "subdocumento" => "" "abierto" => array:3 [ "ES" => false "ES2" => false "LATM" => false ] "gratuito" => false "lecturas" => array:1 [ "total" => 0 ] "idiomaDefecto" => "es" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S0014256518301449?idApp=WRCEE" ] ] "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2254887418300894?idApp=WRCEE" "url" => "/22548874/0000021800000007/v1_201810011013/S2254887418300894/v1_201810011013/en/main.assets" ] "en" => array:21 [ "idiomaDefecto" => true "cabecera" => "<span class="elsevierStyleTextfn">Review</span>" "titulo" => "Infant-juvenile type 2 diabetes" "tieneTextoCompleto" => true "paginas" => array:1 [ 0 => array:2 [ "paginaInicial" => "372" "paginaFinal" => "381" ] ] "autores" => array:1 [ 0 => array:4 [ "autoresLista" => "M.L. Calero Bernal, J.M. Varela Aguilar" "autores" => array:2 [ 0 => array:4 [ "nombre" => "M.L." "apellidos" => "Calero Bernal" "email" => array:1 [ 0 => "mirota96@hotmail.com" ] "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">a</span>" "identificador" => "aff0005" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">*</span>" "identificador" => "cor0005" ] ] ] 1 => array:3 [ "nombre" => "J.M." "apellidos" => "Varela Aguilar" "referencia" => array:3 [ 0 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">b</span>" "identificador" => "aff0010" ] 1 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">c</span>" "identificador" => "aff0015" ] 2 => array:2 [ "etiqueta" => "<span class="elsevierStyleSup">d</span>" "identificador" => "aff0020" ] ] ] ] "afiliaciones" => array:4 [ 0 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital San Juan de Dios del Aljarafe, Bormujos, Sevilla, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Grupo de trabajo de Diabetes y Obesidad de SEMI, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital Virgen del Rocío, Sevilla, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "CIBER de Epidemiología y Salud Pública, Sevilla, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Diabetes tipo 2 infantojuvenil" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1886 "Ancho" => 2517 "Tamanyo" => 149482 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Flow diagram for the classification of diabetes mellitus in children and adolescents.</p> <p id="spar0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Abbreviations</span>: DM1: type 1 diabetes mellitus; DM2: type 2 diabetes mellitus; MODY: maturity onset of diabetes mellitus in youth.</p> <p id="spar0025" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Source</span>: Reinehr.<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">14</span></a></p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Background</span><p id="par0005" class="elsevierStylePara elsevierViewall">Until recently, diabetes mellitus in childhood and adolescence was synonymous with diabetes mellitus type 1 (DM1). However, this concept has changed in recent years with the onset of type 2 diabetes mellitus (DM2) in this population group. DM2 has ceased being a rare disease in the pediatric population. It is currently estimated that between 15% and 45% of new cases of diabetes in childhood and adolescence correspond to DM2,<a class="elsevierStyleCrossRefs" href="#bib0400"><span class="elsevierStyleSup">1,2</span></a> disproportionately affecting certain ethnic and racial minorities and disadvantaged societal environments.<a class="elsevierStyleCrossRef" href="#bib0410"><span class="elsevierStyleSup">3</span></a> In a study conducted in the United States between 2002 and 2012, the relative annual increase in the incidence rate was 1.8% for DM1 and 4.8% for DM2.<a class="elsevierStyleCrossRef" href="#bib0415"><span class="elsevierStyleSup">4</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">The epidemic of DM2 in childhood is the result of a variety of factors, the most important of which is the increase in pediatric obesity rates, which started in the 1960s, although it appears to be reaching a plateau.<a class="elsevierStyleCrossRef" href="#bib0420"><span class="elsevierStyleSup">5</span></a> Another determinant is that DM2 in young patients occurs in complex cultural and psychosocial environments, which makes it difficult to implement lifestyle changes and ensure compliance with medical recommendations. These complexities also hinder the success and completion of research programs and clinical trials,<a class="elsevierStyleCrossRef" href="#bib0425"><span class="elsevierStyleSup">6</span></a> leaving large gaps in our understanding of the treatment pathophysiology and optimization.</p><p id="par0015" class="elsevierStylePara elsevierViewall">In this review, we highlight the most relevant epidemiological, pathophysiological, clinical and therapeutic aspects of DM2 in children and adolescents.</p></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Epidemiology</span><p id="par0020" class="elsevierStylePara elsevierViewall">Over the past 20 years, we have witnessed a true epidemic of DM2 in children and adolescents.<a class="elsevierStyleCrossRefs" href="#bib0430"><span class="elsevierStyleSup">7–9</span></a> At the beginning of the 1990s, DM2 represented 3% of cases of pediatric diabetes in the US.<a class="elsevierStyleCrossRef" href="#bib0445"><span class="elsevierStyleSup">10</span></a> By 2003, however, DM2 represented 20% of cases of pediatric diabetes, and, depending on the geographical area, almost 50% of cases of diabetes among adolescents aged 15–19 years.<a class="elsevierStyleCrossRef" href="#bib0450"><span class="elsevierStyleSup">11</span></a> This increase in DM2 has been confirmed both in developed and developing countries and parallels the increased prevalence of obesity in childhood and adolescence.<a class="elsevierStyleCrossRefs" href="#bib0455"><span class="elsevierStyleSup">12,13</span></a></p><p id="par0025" class="elsevierStylePara elsevierViewall">The prevalence of DM2 in children and adolescents is estimated at 12/100,000 in the US and 2.5/100,000 in Europe.<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">14</span></a> Screening studies on adolescents with obesity 12 years of age or older have observed a DM2 prevalence of 0.4–1%. Another relevant issue is that most cases of DM2 in the young occur in ethnic subgroups such as African Americans, Hispanics, Asian Americans and Native Americans (22.3/1000 in children 10–14 years of age).<a class="elsevierStyleCrossRef" href="#bib0470"><span class="elsevierStyleSup">15</span></a></p><p id="par0030" class="elsevierStylePara elsevierViewall">Obesity is the main risk factor for developing DM2. As with adults, central obesity increases insulin resistance and promotes the development of DM2. Excess weight and obesity in children 2–19 years of age is classified according to the percentile of the body mass index (BMI, kg/m<span class="elsevierStyleSup">2</span>) by age and sex as follows: low weight (BMI<span class="elsevierStyleHsp" style=""></span><<span class="elsevierStyleHsp" style=""></span>5 percentile), normal (BMI within 5–85 percentile), excess weight (BMI within 85–95 percentile), obesity (BMI<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>95 percentile) and severe obesity (BMI<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>120% of the 95 percentile or BMI<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>99 percentile).</p><p id="par0035" class="elsevierStylePara elsevierViewall">The increase in excess weight and obesity rates in school-age children has been occurring worldwide in recent decades, reaching 34% and 10%, respectively, in America.<a class="elsevierStyleCrossRef" href="#bib0475"><span class="elsevierStyleSup">16</span></a> A third of adolescents with DM2 had not been previously diagnosed, and these patients had more obesity (BMI, 35.7<span class="elsevierStyleHsp" style=""></span>kg/m<span class="elsevierStyleSup">2</span>) than those who did know the diagnosis of DM2 (BMI, 29.1<span class="elsevierStyleHsp" style=""></span>kg/m<span class="elsevierStyleSup">2</span>).<a class="elsevierStyleCrossRef" href="#bib0480"><span class="elsevierStyleSup">17</span></a></p><p id="par0040" class="elsevierStylePara elsevierViewall">According to the cutoffs of the International Obesity Task Force, the highest excess weight and obesity rates in Europe among 7 to 11-year-old children are in Malta (35%) and Spain (34%).<a class="elsevierStyleCrossRef" href="#bib0485"><span class="elsevierStyleSup">18</span></a></p><p id="par0045" class="elsevierStylePara elsevierViewall">In Spain, obesity has grown exponentially in recent decades. According to data from the 2012 National Survey of Health in Spain, the prevalence of excess weight and obesity among 2–17 year olds is currently 27.6%, with the autonomous community of the Canary Islands in first place with 34.5%.<a class="elsevierStyleCrossRef" href="#bib0490"><span class="elsevierStyleSup">19</span></a></p><p id="par0050" class="elsevierStylePara elsevierViewall">Pediatric obesity is intimately tied to changes in eating habits, physical activity, physical inactivity, socioeconomic level and length of sleep. A study conducted with Spanish schoolchildren showed that BMI was inversely proportional to how often they performed physical activity.<a class="elsevierStyleCrossRef" href="#bib0495"><span class="elsevierStyleSup">20</span></a> Likewise, the study observed an increase in BMI in the schoolchildren who spent more than 2<span class="elsevierStyleHsp" style=""></span>h a day watching television and in those who slept less than 8<span class="elsevierStyleHsp" style=""></span>h daily. Other factors that influenced BMI were of a financial and educational nature in the family environment, such that families with higher incomes and education levels had a lower rate of excess weight and obesity.<a class="elsevierStyleCrossRef" href="#bib0500"><span class="elsevierStyleSup">21</span></a> It has also been reported that adverse experiences during childhood, such as threats to the child's physical, family or social safety and childhood violence and abuse and school bullying were associated with an increased risk of DM2 in adulthood.<a class="elsevierStyleCrossRef" href="#bib0505"><span class="elsevierStyleSup">22</span></a></p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Pathophysiology</span><p id="par0055" class="elsevierStylePara elsevierViewall">DM2 is a complex metabolic disorder in which various societal, behavioral and environmental risk factors act on a foundation of genetic susceptibility. The disease has a strong hereditary component (probably polygenic), which is responsible for the differences in the prevalence of DM2 in different racial groups.<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">23</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">DM2 is characterized not only by hyperglycemia and insulin resistance but also by a relative reduction in insulin secretion. Both characteristics are influenced by genetic and environmental factors. Insulin resistance explains the clinical association of DM2 with obesity. Patients have a combination of differing degrees of insulin resistance and reduced insulin concentrations. Hyperglycemia by itself can change the function of pancreatic beta cells and exacerbate insulin resistance, resulting in a vicious cycle that worsens the metabolic condition. Adolescents and adults typically have lost 80% of the function of pancreatic beta cells before the diagnosis of DM2.<a class="elsevierStyleCrossRef" href="#bib0400"><span class="elsevierStyleSup">1</span></a></p><p id="par0065" class="elsevierStylePara elsevierViewall">The progression of a normal blood glucose condition to that of impaired glucose tolerance (IGT) is associated with a worsening of insulin resistance. IGT is an intermediate stage in the natural history of DM2 and is a predictor of the risk of developing DM and cardiovascular diseases.<a class="elsevierStyleCrossRefs" href="#bib0515"><span class="elsevierStyleSup">24,25</span></a> Likewise, it has been proposed that hyperglycemia can worsen both insulin resistance and insulin secretion, facilitating the transition of IGT to diabetes.<a class="elsevierStyleCrossRef" href="#bib0520"><span class="elsevierStyleSup">25</span></a> However, a high rate of spontaneous conversion to normal glucose tolerance has been observed in children and adolescents with IGT within 3–5 years.<a class="elsevierStyleCrossRefs" href="#bib0520"><span class="elsevierStyleSup">25–27</span></a></p><p id="par0070" class="elsevierStylePara elsevierViewall">Puberty appears to play an important role in the development of DM2 in children.<a class="elsevierStyleCrossRef" href="#bib0510"><span class="elsevierStyleSup">23</span></a> It has been postulated that an increase in growth hormone secretion could be responsible for insulin resistance during this period of development.<a class="elsevierStyleCrossRef" href="#bib0535"><span class="elsevierStyleSup">28</span></a> This hypothesis could explain why the presentation of DM2 in children coincides with the mean age of puberty.<a class="elsevierStyleCrossRefs" href="#bib0520"><span class="elsevierStyleSup">25–29</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">The adverse effect of obesity on glucose metabolism is already apparent in childhood. Children with obesity have hyperinsulinemia and an approximately 40% lower insulin-stimulated glucose metabolization (assessed by blood glucose under fasting conditions and 2<span class="elsevierStyleHsp" style=""></span>h after eating) than children who have no obesity.<a class="elsevierStyleCrossRef" href="#bib0545"><span class="elsevierStyleSup">30</span></a> The inverse relationship between insulin sensitivity and abdominal fat distribution is stronger for visceral fat than for subcutaneous fat.<a class="elsevierStyleCrossRefs" href="#bib0545"><span class="elsevierStyleSup">30,31</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">The adipose tissue that increases with obesity synthesizes and secretes metabolites and signaling proteins such as leptin, adiponectin and tumor necrosis factor alpha.<a class="elsevierStyleCrossRef" href="#bib0555"><span class="elsevierStyleSup">32</span></a> These factors change insulin secretion and sensitivity and can even cause insulin resistance in experimental and clinical conditions.<a class="elsevierStyleCrossRef" href="#bib0560"><span class="elsevierStyleSup">33</span></a></p><p id="par0085" class="elsevierStylePara elsevierViewall">The racial differences in insulin sensitivity are well-established. African-American children 7–11 years of age have significantly higher insulin concentrations than white children of the same age.<a class="elsevierStyleCrossRefs" href="#bib0565"><span class="elsevierStyleSup">34,35</span></a> These data suggest that certain ethnic groups have a genetic predisposition to insulin resistance, which can increase their risk of developing DM2. These racial differences have also been observed in Europe, where Swedish children with obesity have higher glucose concentrations under fasting conditions than German children with obesity.<a class="elsevierStyleCrossRef" href="#bib0570"><span class="elsevierStyleSup">35</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">It has also been observed that a low pancreatic reserve and a high glycated hemoglobin (HbA1c) level are independent predictors for the loss of glycemic control in patients undergoing drug treatment.<a class="elsevierStyleCrossRefs" href="#bib0575"><span class="elsevierStyleSup">36,37</span></a> The deterioration in pancreatic beta cell function is also observed in adults with DM2, although it is not as accelerated as in the young.<a class="elsevierStyleCrossRefs" href="#bib0585"><span class="elsevierStyleSup">38–41</span></a></p></span><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Clinical presentation</span><p id="par0095" class="elsevierStylePara elsevierViewall">DM2 in the young occurs predominantly in the female sex. The mean age at diagnosis is 13.5 years, although DM2 almost always starts at the age of 10 years, unlike DM1, which starts before the age of 10 years in 50% of cases.<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">29</span></a> In most cases, DM2 is associated with obesity as the main determinant.<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">29</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">The clinical presentation in children can be diverse and varies from asymptomatic hyperglycemia to ketoacidosis (6% of cases in patients between 10–19 years of age).<a class="elsevierStyleCrossRef" href="#bib0605"><span class="elsevierStyleSup">42</span></a> Unlike the onset of DM1, the cardinal symptoms of DM2 are unclear. Thus, children with DM2 usually present glycosuria without ketonuria, mild or nonexistent polyuria, polydipsia and little or no weight loss. Although it is uncommon, children with DM2 are at risk of presenting nonketotic hyperosmolar hyperglycemic decompensation, which is associated with high mortality.<a class="elsevierStyleCrossRef" href="#bib0610"><span class="elsevierStyleSup">43</span></a> Differing clinical characteristics, depending on the patients’ ethnicity and race, have also been observed, with a predominance of DM1 in whites and DM2 in at-risk ethnic groups<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">29</span></a> (African Americans, American Hispanics, Asians and Native Americans). The differential characteristics between the two types of diabetes are shown in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>.<a class="elsevierStyleCrossRef" href="#bib0615"><span class="elsevierStyleSup">44</span></a></p><elsevierMultimedia ident="tbl0005"></elsevierMultimedia><p id="par0105" class="elsevierStylePara elsevierViewall">One of the characteristics of adult-onset DM2 is the lack of beta cell antibodies. However, a number of studies have observed the presence of these antibodies in almost 30% of children and adolescents with DM2 in Europe.<a class="elsevierStyleCrossRef" href="#bib0620"><span class="elsevierStyleSup">45</span></a> This group of adolescents does not usually require insulin therapy, at least during the first year. It has been postulated that this clinical form is an early presentation of latent autoimmune diabetes mellitus in adulthood.<a class="elsevierStyleCrossRef" href="#bib0625"><span class="elsevierStyleSup">46</span></a> In adolescents, the term “latent autoimmune diabetes mellitus in youth” has been proposed.<a class="elsevierStyleCrossRef" href="#bib0630"><span class="elsevierStyleSup">47</span></a></p><p id="par0110" class="elsevierStylePara elsevierViewall">Maturity-onset diabetes of the young (MODY) is a form of maturity diabetes that occurs in children. MODY is an uncommon form of diabetes in children that includes several forms caused by monogenic defects in beta cell function (the most common of which are the hepatocyte nuclear factor 4 alpha gene mutation and the glucokinase gene mutation). Patients with MODY have dominant genetic traits, do not have obesity and have low insulin concentrations under fasting conditions. These genetic anomalies are believed to be rare and require molecular diagnostic techniques. Recent studies have suggested that the clinical presentation spectrum of MODY is broad and ranges from asymptomatic hyperglycemia to severe acute onset.<a class="elsevierStyleCrossRef" href="#bib0635"><span class="elsevierStyleSup">48</span></a> This variety of diabetes has been reported in all races and ethnicities. The main characteristics of MODY are listed in <a class="elsevierStyleCrossRef" href="#tbl0005">Table 1</a>.</p><p id="par0115" class="elsevierStylePara elsevierViewall">Diabetes mellitus can be classified reliably, in most patients, based on the clinical presentation and progression.<a class="elsevierStyleCrossRef" href="#bib0515"><span class="elsevierStyleSup">24</span></a> In the unusual situation in which a more precise classification is needed, other specific measurements might be required, such as insulin and peptide <span class="elsevierStyleSmallCaps">C</span> concentrations under fasting conditions and, occasionally, beta cell antibody levels.<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">14</span></a> The diagnostic criteria for DM in children and adolescents does not differ from those established by the American Diabetes Association (ADA) for adults.<a class="elsevierStyleCrossRef" href="#bib0640"><span class="elsevierStyleSup">49</span></a><a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a> shows a flow diagram for classifying DM in children and adolescents.</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Diabetes screening in childhood</span><p id="par0120" class="elsevierStylePara elsevierViewall">Most white European children and adolescents with DM2 and a third of children in the US were asymptomatic at the time of diagnosis.<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">29</span></a> Accordingly, DM2 screening studies appear to be necessary, given that hyperglycemia can go unnoticed and contribute to long-term microvascular and macrovascular damage. A DM2 screening for the entire young population is currently not cost effective; it is therefore only advisable to study patients at greater risk. Due to the close direct relationship with obesity, the ADA recommends DM2 screening for children and adolescents with excess weight at the onset of puberty who also have other risk factors (<a class="elsevierStyleCrossRef" href="#tbl0010">Table 2</a>).<a class="elsevierStyleCrossRef" href="#bib0640"><span class="elsevierStyleSup">49</span></a> The screening test of choice is measuring fasting plasma glucose and the oral glucose overload test (OGTT). However, these recommendations have a number of drawbacks. Fasting plasma glucose is a comfortable, simple and inexpensive procedure but failed in a quarter of patients in a European study.<a class="elsevierStyleCrossRef" href="#bib0540"><span class="elsevierStyleSup">29</span></a> The OGTT can be a better screening method but costs more, is more labor intense and at times has little reproducibility.<a class="elsevierStyleCrossRef" href="#bib0645"><span class="elsevierStyleSup">50</span></a> We also do not know if the cutoffs for OGTT established for adulthood are applicable for childhood. With regard to the use of HbA1c for diagnosing DM2, the ADA continues to recommend it despite its limitations for children and adolescents due to its low sensitivity and high cost.<a class="elsevierStyleCrossRefs" href="#bib0650"><span class="elsevierStyleSup">51–53</span></a></p><elsevierMultimedia ident="tbl0010"></elsevierMultimedia></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Treatment</span><p id="par0125" class="elsevierStylePara elsevierViewall">The American Academy of Pediatrics has published guidelines on treating DM2 in children and adolescents.<a class="elsevierStyleCrossRef" href="#bib0665"><span class="elsevierStyleSup">54</span></a> Most of these recommendations have been extrapolated from experience with adults.<a class="elsevierStyleCrossRef" href="#bib0670"><span class="elsevierStyleSup">55</span></a> The 3 main treatment objectives are lifestyle changes, blood glucose normalization and control of associated comorbidities.<a class="elsevierStyleCrossRef" href="#bib0515"><span class="elsevierStyleSup">24</span></a> The final treatment objective is to decrease the risk of acute and chronic complications.</p><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Nondrug therapy: lifestyle changes</span><p id="par0130" class="elsevierStylePara elsevierViewall">Weight control is essential to achieving the therapeutic objectives. The dietary recommendations consist of eliminating soft drinks and juices with high sugar content, increasing the intake of fruits and vegetables, controlling portion sizes, changing the family eating behaviors and eliminating unhealthy food from the home.<a class="elsevierStyleCrossRef" href="#bib0675"><span class="elsevierStyleSup">56</span></a></p><p id="par0135" class="elsevierStylePara elsevierViewall">Regular exercise, even without caloric restriction and without weight loss, is associated with a reduction in insulin resistance in the young with excess weight or obesity, regardless of whether they previously had DM2.<a class="elsevierStyleCrossRefs" href="#bib0680"><span class="elsevierStyleSup">57–59</span></a> The current recommendations for children's physical activity include 60<span class="elsevierStyleHsp" style=""></span>min a day of moderate-vigorous activity, which can be performed all at once or divided into sessions.<a class="elsevierStyleCrossRef" href="#bib0695"><span class="elsevierStyleSup">60</span></a></p><p id="par0140" class="elsevierStylePara elsevierViewall">Despite the efforts, the results achieved with lifestyle changes are very limited. In one study, only 17% of the patients managed to reduce their BMI 1 year after implementing a diet program plus exercise, and only 23% managed to withdraw the medication after more than 2 years.<a class="elsevierStyleCrossRef" href="#bib0700"><span class="elsevierStyleSup">61</span></a> Another study observed that less than 10% of young individuals with DM2 reached their blood glucose objectives exclusively with lifestyle changes.<a class="elsevierStyleCrossRefs" href="#bib0705"><span class="elsevierStyleSup">62,63</span></a></p><p id="par0145" class="elsevierStylePara elsevierViewall">Although observational studies on young individuals with DM2<a class="elsevierStyleCrossRef" href="#bib0715"><span class="elsevierStyleSup">64</span></a> have suggested that higher activity levels are associated with improved blood glucose control, the only large-scale therapeutic trial to assess the effects of lifestyle changes in 699 young individuals with DM2 did not support this assumption.<a class="elsevierStyleCrossRef" href="#bib0565"><span class="elsevierStyleSup">34</span></a> The study showed that, after 24 months, the intense lifestyle changes (200–300<span class="elsevierStyleHsp" style=""></span>min of moderate-to-intense exercise per week and a daily intake of 1200–1500 calories), compared with metformin in monotherapy did not improve the long-term blood glucose control. Other cardiovascular risk factors, such as dyslipidemia and inflammatory markers, also did not improve with lifestyle changes compared with monotherapy with metformin.<a class="elsevierStyleCrossRef" href="#bib0720"><span class="elsevierStyleSup">65</span></a> These poor results could be related to the follow-up loss rates,<a class="elsevierStyleCrossRefs" href="#bib0725"><span class="elsevierStyleSup">66,67</span></a> factors related to the socioeconomic status and high rates of depression.<a class="elsevierStyleCrossRef" href="#bib0735"><span class="elsevierStyleSup">68</span></a></p></span></span><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Pharmacotherapy</span><p id="par0150" class="elsevierStylePara elsevierViewall">Pharmacotherapy is indicated if the treatment objective (HbA1c <7.5% and blood glucose under fasting conditions <130<span class="elsevierStyleHsp" style=""></span>mg/dL) is not achieved through nutritional education and exercise. There are many available drugs for treating diabetes, although only metformin and insulin have been approved by regulatory agencies for use in patients younger than 18 years.<a class="elsevierStyleCrossRef" href="#bib0515"><span class="elsevierStyleSup">24</span></a> Most pediatric diabetologists use oral agents as the first therapeutic approach because they facilitate therapeutic compliance.</p><p id="par0155" class="elsevierStylePara elsevierViewall">Metformin, a biguanide, is unquestionably the most appropriate starting point for the pharmacotherapy of DM2 in children, as it is for adults.<a class="elsevierStyleCrossRef" href="#bib0740"><span class="elsevierStyleSup">69</span></a> The drug reduces hepatic glucose production and increases hepatic and muscle sensitivity to insulin without a direct effect on beta cell function. Metformin has the advantage of slightly reducing weight, improving the lipid profile without increasing the risk of hypoglycemia and is easy to use and inexpensive. The initial dose is 500<span class="elsevierStyleHsp" style=""></span>mg/d and is increased progressively to 1000<span class="elsevierStyleHsp" style=""></span>g/12<span class="elsevierStyleHsp" style=""></span>h within 4 weeks, unless there are adverse gastrointestinal effects. The drug's most common adverse effects are gastrointestinal abnormalities (bloating and diarrhea) and, although it has a good safety profile, should not be administered in cases of hypoxemia, severe infection, severe liver or kidney disease or alcohol abuse, due to the risk of lactic acidosis. Metformin should be used with caution and its dosage adjusted if the patient has impaired renal function. If monotherapy with metformin is ineffective after 3–6 months, combining another drug should be considered.</p><p id="par0160" class="elsevierStylePara elsevierViewall">The efficacy of metformin in adolescents has been tested in 2 clinical trials.<a class="elsevierStyleCrossRefs" href="#bib0565"><span class="elsevierStyleSup">34,70</span></a> In the Treatment Options for type 2 Diabetes in Adolescents and Youth (TODAY) trial,<a class="elsevierStyleCrossRef" href="#bib0565"><span class="elsevierStyleSup">34</span></a> children and adolescents were distributed to the 3 treatment arms (metformin, metformin plus rosiglitazone and metformin plus lifestyle changes). The results suggest that in standard clinical practice a large portion of young patients with DM2 could require combined therapy with insulin a few years after the diagnosis. In this study,<a class="elsevierStyleCrossRef" href="#bib0565"><span class="elsevierStyleSup">34</span></a> monotherapy with metformin was associated with adequate blood glucose control in approximately half of the patients with DM2. The marketing of rosiglitazone was restricted by the Food and Drug Administration in 2010 after a slight increase in cardiovascular risk was observed. Another study that compared metformin versus placebo observed a 1–2% reduction in HbA1c after 4 weeks of therapy, with a similar tolerance to that reported in adults.<a class="elsevierStyleCrossRef" href="#bib0745"><span class="elsevierStyleSup">70</span></a></p><p id="par0165" class="elsevierStylePara elsevierViewall">The use of insulin is preferred for patients with ketosis or intense hyperglycemia and who have mixed characteristics of DM1 and DM2. The new guidelines recommend insulin therapy when the plasma glucose concentrations are ≥250<span class="elsevierStyleHsp" style=""></span>mg/dL or HbA1c levels are >9, with monitoring every 3 months to adjust the dosage or withdraw it if the control is optimal.<a class="elsevierStyleCrossRef" href="#bib0750"><span class="elsevierStyleSup">71</span></a></p><p id="par0170" class="elsevierStylePara elsevierViewall">There is no specific contraindication for insulin therapy in children, and the most appropriate administration regimen for each patient's lifestyle should be selected. The most common adverse effects are weight gain and hypoglycemia. NPH insulin once a day or basal insulin (glargine, detemir or degludec) at an initial dose of 0.25–0.5<span class="elsevierStyleHsp" style=""></span>units/kg is often effective for metabolic control.<a class="elsevierStyleCrossRef" href="#bib0755"><span class="elsevierStyleSup">72</span></a></p><p id="par0175" class="elsevierStylePara elsevierViewall">Although studies have been conducted on the use of other hypoglycemic agents (thiazolidinediones, sulfonylureas, meglitinides, alpha-glucosidase inhibitors, dipeptidyl peptidase-4 inhibitors, glucagon-like peptide-1 analogs and amylin analogs) in this population group, their use has still not been approved.<a class="elsevierStyleCrossRef" href="#bib0760"><span class="elsevierStyleSup">73</span></a></p><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Surgical treatment</span><p id="par0180" class="elsevierStylePara elsevierViewall">Bariatric surgery can be a useful therapeutic option, although the experience with adolescents with DM2 is very limited. In a retrospective series of 11 postpubertal adolescents with DM2 who underwent gastric bypass with jejunal Roux-en-Y anastomosis, significant improvements were achieved in BMI, blood glucose control, serum lipid concentrations and blood pressure compared with 67 adolescents who underwent medical treatment for 1 year.<a class="elsevierStyleCrossRef" href="#bib0765"><span class="elsevierStyleSup">74</span></a> In particular, 10 of the 11 patients treated surgically had remission of the diabetes without the need for medication. The recommended selection criteria for bariatric surgery in the young are as follows: BMI >35, advanced puberty development (Tanner stage IV or V) and skeletal maturity.<a class="elsevierStyleCrossRef" href="#bib0770"><span class="elsevierStyleSup">75</span></a></p><p id="par0185" class="elsevierStylePara elsevierViewall">Other techniques such as tubular gastrectomy and gastric band surgery have also been put into practice, but there is little experience with children and adolescents, and more studies are needed to offer concrete recommendations.<a class="elsevierStyleCrossRef" href="#bib0775"><span class="elsevierStyleSup">76</span></a></p></span></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Comorbidities</span><p id="par0190" class="elsevierStylePara elsevierViewall">The comorbidities that accompany DM2 in the young are very common and need to be properly approached to prevent the development of vascular complications.</p><p id="par0195" class="elsevierStylePara elsevierViewall">The SEARCH study observed that 92% of the adolescents with DM2 met the criteria of metabolic syndrome by presenting 2 risk factors for cardiovascular disease, as well as DM, compared with 14% of the patients with DM1.<a class="elsevierStyleCrossRef" href="#bib0780"><span class="elsevierStyleSup">77</span></a> In addition to obesity, the presence of other comorbidities such as arterial hypertension, dyslipidemia, retinopathy, nephropathy and depression should be ruled out. The recommendations for their screening and treatment are shown in <a class="elsevierStyleCrossRef" href="#tbl0015">Table 3</a>.<a class="elsevierStyleCrossRef" href="#bib0785"><span class="elsevierStyleSup">78</span></a></p><elsevierMultimedia ident="tbl0015"></elsevierMultimedia><p id="par0200" class="elsevierStylePara elsevierViewall">In a study conducted in the US that included children and adolescents with DM1 or DM2 with a mean disease duration of 7.9 years, the patients with DM2 had a higher prevalence (adjusted for age) of diabetic nephropathy, retinopathy, peripheral neuropathy, arterial stiffness and hypertension than those with DM1.<a class="elsevierStyleCrossRef" href="#bib0790"><span class="elsevierStyleSup">79</span></a></p><p id="par0205" class="elsevierStylePara elsevierViewall">We therefore need to pay attention to preventing excess weight and obesity in this population group through public education in healthy life habits and early detection in consultations.</p></span><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">Conflicts of interest</span><p id="par0210" class="elsevierStylePara elsevierViewall">The authors declare that they have no conflicts of interest.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:14 [ 0 => array:3 [ "identificador" => "xres1087560" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1031522" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres1087559" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec1031523" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Background" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Epidemiology" ] 6 => array:2 [ "identificador" => "sec0015" "titulo" => "Pathophysiology" ] 7 => array:2 [ "identificador" => "sec0020" "titulo" => "Clinical presentation" ] 8 => array:2 [ "identificador" => "sec0025" "titulo" => "Diabetes screening in childhood" ] 9 => array:3 [ "identificador" => "sec0030" "titulo" => "Treatment" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0035" "titulo" => "Nondrug therapy: lifestyle changes" ] ] ] 10 => array:3 [ "identificador" => "sec0040" "titulo" => "Pharmacotherapy" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0045" "titulo" => "Surgical treatment" ] ] ] 11 => array:2 [ "identificador" => "sec0050" "titulo" => "Comorbidities" ] 12 => array:2 [ "identificador" => "sec0055" "titulo" => "Conflicts of interest" ] 13 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2017-12-10" "fechaAceptado" => "2018-03-22" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1031522" "palabras" => array:6 [ 0 => "Type 2 diabetes mellitus" 1 => "Obesity" 2 => "Childhood" 3 => "Adolescence" 4 => "Comorbidities" 5 => "Treatment" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec1031523" "palabras" => array:6 [ 0 => "Diabetes mellitus tipo 2" 1 => "Obesidad" 2 => "Infancia" 3 => "Adolescencia" 4 => "Comorbilidades" 5 => "Tratamiento" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">In recent years, we have witnessed an increase in the number of cases of type 2 diabetes mellitus (DM2) in children and adolescents, which has paralleled the increase in the worldwide prevalence of obesity. Although screening the general population does not appear to be cost-effective, special attention should be paid to children with excess weight, obesity or other factors that predispose them to a state of insulin resistance. When faced with the diagnosis of childhood DM2, the presence of comorbidities (such as hypertension, dyslipidemia and microalbuminuria) should be assessed, and appropriate treatment and follow-up should be administered to prevent the onset of complications, given that the DM2 in this population group will last longer than that started in adulthood.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">En los últimos años asistimos a un aumento en el número de casos de diabetes mellitus tipo 2 (DM2) en niños y adolescentes, que ocurre de forma paralela al aumento de la prevalencia de obesidad en todo el mundo. A pesar de que un cribado de la población general no parece coste-efectivo, debería prestarse especial atención a los niños con sobrepeso, obesidad u otros factores que predispongan a un estado de resistencia a la insulina. Ante el diagnóstico de DM2 en la infancia debe evaluarse la presencia de comorbilidades, como la hipertensión, la dislipidemia y la microalbuminuria, así como llevar a cabo un adecuado tratamiento y seguimiento para evitar la aparición de complicaciones, pues en este grupo de población la duración de la DM2 será mayor que en la iniciada en el adulto.</p></span>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0020">Please cite this article as: Calero Bernal ML, Varela Aguilar JM. Diabetes tipo 2 infantojuvenil. Rev Clin Esp. 2018;218:372–381.</p>" ] ] "apendice" => array:1 [ 0 => array:1 [ "seccion" => array:1 [ 0 => array:4 [ "apendice" => "<p id="par0220" class="elsevierStylePara elsevierViewall">The following are the supplementary data to this article:<elsevierMultimedia ident="upi0005"></elsevierMultimedia></p>" "etiqueta" => "Appendix A" "titulo" => "Supplementary data" "identificador" => "sec0065" ] ] ] ] "multimedia" => array:5 [ 0 => array:7 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 1886 "Ancho" => 2517 "Tamanyo" => 149482 ] ] "descripcion" => array:1 [ "en" => "<p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">Flow diagram for the classification of diabetes mellitus in children and adolescents.</p> <p id="spar0020" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Abbreviations</span>: DM1: type 1 diabetes mellitus; DM2: type 2 diabetes mellitus; MODY: maturity onset of diabetes mellitus in youth.</p> <p id="spar0025" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Source</span>: Reinehr.<a class="elsevierStyleCrossRef" href="#bib0465"><span class="elsevierStyleSup">14</span></a></p>" ] ] 1 => array:8 [ "identificador" => "tbl0005" "etiqueta" => "Table 1" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at1" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0035" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Abbreviations</span>: anti-GAD: glutamic acid decarboxylase antibodies; DM1: type 1 diabetes mellitus; DM2: type 2 diabetes mellitus; ICA: islet cell autoantigen; MODY: maturity onset of diabetes mellitus in youth; ODD: oral diabetes drugs; PCOS: polycystic ovary syndrome.</p><p id="spar0040" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Source</span>: Alberti et al.<a class="elsevierStyleCrossRef" href="#bib0615"><span class="elsevierStyleSup">44</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="" valign="top" scope="col" style="border-bottom: 2px solid black"> \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">DM1 \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">DM2 \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">MODY \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Age at onset \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Preschool-Adolescent \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">>10 years \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top"><25 years \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Sex \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Female<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>male \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Female<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>male \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Female<span class="elsevierStyleHsp" style=""></span>=<span class="elsevierStyleHsp" style=""></span>male \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Ethnic group \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">White \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">At-risk ethnic groups \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">All races/ethnicities \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Obesity \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Uncommon (20–25%) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Frequent (>80%) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Uncommon \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Onset \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Acute-symptomatic \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Insidious-asymptomatic \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">From asymptomatic hyperglycemia to acute severe presentation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Symptoms \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Weight loss<br>Polyuria<br>Polydipsia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Variable<br>Family history of DM2 \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Family history of diabetes in more than 2 generations \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Ketosis \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Frequent (30–40%) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Typically absent (Hispanics and African Americans) \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Low risk \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Peptide C \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">↓ ↓ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Normal or ↑ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Normal \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Antibodies \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">ICA+<br>Anti-GAD+<br>ICA 512+ \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">ICA−<br>Anti-GAD−<br>ICA 512− \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Absent \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Treatment \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Insulin \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">ODD \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Depending on the genetic defect: diet, sulfonylureas or insulin \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Associated diseases \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Autoimmune (thyroid, adrenal, vitiligo), celiac disease \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">PCOS, acanthosis nigricans \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Low birth weight, agenesis or severe pancreatic hypoplasia, nephropathy, acanthosis nigricans \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1858446.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0030" class="elsevierStyleSimplePara elsevierViewall">Differential characteristics of type 1 and type 2 diabetes mellitus in adolescence.</p>" ] ] 2 => array:8 [ "identificador" => "tbl0010" "etiqueta" => "Table 2" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at2" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Criteria \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleItalic">Excess weight defined as</span> … \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>BMI<span class="elsevierStyleHsp" style=""></span>≥<span class="elsevierStyleHsp" style=""></span>85 percentile for sex and age \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Weight<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>120% of ideal for height \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Weight/height<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>85 percentile 85 \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleItalic">Two or more of the following risk factors:</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Family history of DM2 in first or second-degree relatives \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>At-risk ethnic group (Native American, African, Latino, Asian, Pacific Islander) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Signs of insulin resistance or conditions associated with insulin resistance (acanthosis nigricans, AHT, dyslipidemia, polycystic ovaries or low birth weight) \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleHsp" style=""></span>Maternal history of diabetes or gestational diabetes during child's gestation \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleVsp" style="height:0.5px"></span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleItalic">Age of onset: at 10 years or at the onset of puberty, whichever comes first</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top"><span class="elsevierStyleItalic">Frequency: every 3 years</span> \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1858444.png" ] ] ] "notaPie" => array:1 [ 0 => array:3 [ "identificador" => "tblfn0005" "etiqueta" => "a" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Individuals<span class="elsevierStyleHsp" style=""></span>≤<span class="elsevierStyleHsp" style=""></span>18<span class="elsevierStyleHsp" style=""></span>years of age.</p> <p class="elsevierStyleNotepara" id="npar0010"><span class="elsevierStyleItalic">Abbreviations</span>: AHT: arterial hypertension; BMI: body mass index; DM2: type 2 diabetes mellitus.</p> <p class="elsevierStyleNotepara" id="npar0015"><span class="elsevierStyleItalic">Source</span>: Standards of Medical Care in diabetes 2017.<a class="elsevierStyleCrossRef" href="#bib0640"><span class="elsevierStyleSup">49</span></a></p>" ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0045" class="elsevierStyleSimplePara elsevierViewall">Screening for type 2 diabetes mellitus and prediabetes in asymptomatic children.<a class="elsevierStyleCrossRef" href="#tblfn0005"><span class="elsevierStyleSup">a</span></a></p>" ] ] 3 => array:8 [ "identificador" => "tbl0015" "etiqueta" => "Table 3" "tipo" => "MULTIMEDIATABLA" "mostrarFloat" => true "mostrarDisplay" => false "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at3" "detalle" => "Table " "rol" => "short" ] ] "tabla" => array:2 [ "leyenda" => "<p id="spar0065" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Abbreviations</span>: ACEI: angiotensin-converting enzyme inhibitors; ARB-II: angiotensin-receptor blockers; BP: blood pressure; HDL: high density lipoprotein; LDL: low density lipoprotein.</p><p id="spar0070" class="elsevierStyleSimplePara elsevierViewall"><span class="elsevierStyleItalic">Source</span>: Kao and Sabin.<a class="elsevierStyleCrossRef" href="#bib0785"><span class="elsevierStyleSup">78</span></a></p>" "tablatextoimagen" => array:1 [ 0 => array:2 [ "tabla" => array:1 [ 0 => """ <table border="0" frame="\n \t\t\t\t\tvoid\n \t\t\t\t" class=""><thead title="thead"><tr title="table-row"><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Comorbidity \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Prevalence \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Screening \t\t\t\t\t\t\n \t\t\t\t</th><th class="td" title="table-head " align="left" valign="top" scope="col" style="border-bottom: 2px solid black">Therapeutic recommendation \t\t\t\t\t\t\n \t\t\t\t</th></tr></thead><tbody title="tbody"><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Hypertension \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Affects up to 36% of the young within 1.3 years of the diagnosis; up to 66% in a number of cross-sectional studies. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">At the time of the diagnosis and at every subsequent visit. Use the appropriate cuff size and adjust the readings according to age, sex and height. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Lifestyle modifications: Treatment with ACEI if the lifestyle modification is not successful after 6 months.<br>ARB-II if ACEI is not tolerated. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Dyslipidemia \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Hypertriglyceridemia in 60–65%.<br>Reduction in HDL-cholesterol in 73%. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">At the time of diagnosis. If monitoring every 2 years is normal.<br>If more frequent follow-up is abnormal. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Evaluation and change in diet. If failure after 6 months, consider…<br>Treatment with statins if LDL<span class="elsevierStyleHsp" style=""></span>>130<span class="elsevierStyleHsp" style=""></span>mg/dL.<br>Therapy with fibrates if triglycerides<span class="elsevierStyleHsp" style=""></span>><span class="elsevierStyleHsp" style=""></span>800–1000<span class="elsevierStyleHsp" style=""></span>mg/dL and if patient is >10 years of age due to risk of acute pancreatitis. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Retinopathy \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">9.3% at the time of diagnosis.<br>12.7% have proliferative retinopathy at 35 years.<br>23.7% go blind at a mean age of 32 years. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Examination with pupil dilation by ophthalmologist at the time of the diagnosis. Annual examination if the examination results are normal and more often if abnormal. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Consult an ophthalmologist if there is evidence of retinopathy. Laser therapy might be required if there is proliferative retinopathy, clinically significant macular edema or severe nonproliferative retinopathy. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Kidney disease \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Frequently present in the diagnosis.<br>14–22% in cross-sectional studies. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Microalbuminuria in urine sample: 30–299<span class="elsevierStyleHsp" style=""></span>mg/g.<br>Proteinuria in 24-h urine: 20–199<span class="elsevierStyleHsp" style=""></span>μg/min.<br>Can be increased by tobacco use, exercise and menstruation.<br>Rule out orthostatic proteinuria. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">If condition persists (>2 samples), start with ACEI, even with normal BP.<br>The objective is to normalize proteinuria.<br>Treat the hypertension. \t\t\t\t\t\t\n \t\t\t\t</td></tr><tr title="table-row"><td class="td-with-role" title="table-entry ; entry_with_role_rowhead " align="left" valign="top">Depression \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Up to 14.7%; more common in women. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Detect symptoms of depression at the time of the diagnosis and periodically, especially in those with deficient blood glucose control and/or frequent visits to the emergency department. \t\t\t\t\t\t\n \t\t\t\t</td><td class="td" title="table-entry " align="left" valign="top">Consult with a mental health specialist. \t\t\t\t\t\t\n \t\t\t\t</td></tr></tbody></table> """ ] "imagenFichero" => array:1 [ 0 => "xTab1858445.png" ] ] ] ] "descripcion" => array:1 [ "en" => "<p id="spar0060" class="elsevierStyleSimplePara elsevierViewall">Comorbidity management guidelines for children with type 2 diabetes mellitus.</p>" ] ] 4 => array:5 [ "identificador" => "upi0005" "tipo" => "MULTIMEDIAECOMPONENTE" "mostrarFloat" => false "mostrarDisplay" => true "Ecomponente" => array:2 [ "fichero" => "mmc1.docx" "ficheroTamanyo" => 31768 ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0015" "bibliografiaReferencia" => array:79 [ 0 => array:3 [ "identificador" => "bib0400" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "Beta-cell function across the spectrum of glucose tolerance in obese youth" "autores" => array:1 [ 0 => array:2 [ "etal" => false "autores" => array:6 [ 0 => "R. 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