Special article
Medical treatment of type 2 diabetes mellitus: Recommendations of the Diabetes, Obesity and Nutrition Group of the Spanish Society of Internal Medicine
Tratamiento médico de la diabetes mellitus tipo 2: recomendaciones del Grupo de Diabetes, Obesidad y Nutrición de la Sociedad Española de Medicina Interna
F.J. Carrasco-Sáncheza,
, J.M. Fernández-Rodríguezb, J. Enac, R. Gómez-Huelgasd, J. Carretero-Gómeze, on behalf of the Diabetes, Obesity and Nutrition Group of the Spanish Society of Internal Medicine
Corresponding author
a Área de Insuficiencia Cardíaca, Diabetes y Riesgo Vascular. Unidad de Gestión Clínica de Medicina Interna y Cuidados Paliativos, Hospital Universitario Juan Ramón Jiménez, Huelva, Spain
b Servicio de Medicina Interna, Hospital Carmen y Severo Ochoa, Cangas de Narcea, Asturias, Spain
c Servicio de Medicina Interna, Hospital Marina Baixa, Alicante, Spain
d Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, Servicio de Medicina Interna, Hospital Regional Universitario de Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain
e Servicio de Medicina Interna, Hospital de Zafra, Badajoz, Spain
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Unidad de Gestión Clínica de Medicina Interna y Cuidados Paliativos, Hospital Universitario Juan Ramón Jiménez, Huelva, Spain" "etiqueta" => "a" "identificador" => "aff0005" ] 1 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital Carmen y Severo Ochoa, Cangas de Narcea, Asturias, Spain" "etiqueta" => "b" "identificador" => "aff0010" ] 2 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital Marina Baixa, Alicante, Spain" "etiqueta" => "c" "identificador" => "aff0015" ] 3 => array:3 [ "entidad" => "Centro de Investigación Biomédica en Red de Fisiopatología de la Obesidad y Nutrición (CIBEROBN), Instituto de Salud Carlos III, Servicio de Medicina Interna, Hospital Regional Universitario de Málaga, Instituto de Investigación Biomédica de Málaga (IBIMA), Universidad de Málaga, Málaga, Spain" "etiqueta" => "d" "identificador" => "aff0020" ] 4 => array:3 [ "entidad" => "Servicio de Medicina Interna, Hospital de Zafra, Badajoz, Spain" "etiqueta" => "e" "identificador" => "aff0025" ] ] "correspondencia" => array:1 [ 0 => array:3 [ "identificador" => "cor0005" "etiqueta" => "⁎" "correspondencia" => "Corresponding author." ] ] ] ] "titulosAlternativos" => array:1 [ "es" => array:1 [ "titulo" => "Tratamiento médico de la diabetes mellitus tipo 2: recomendaciones del Grupo de Diabetes, Obesidad y Nutrición de la Sociedad Española de Medicina Interna" ] ] "resumenGrafico" => array:2 [ "original" => 0 "multimedia" => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 5305 "Ancho" => 3167 "Tamanyo" => 1751946 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Recommendations for type 2 diabetes mellitus treatment according to the clinical condition.</p>" ] ] ] "textoCompleto" => "<span class="elsevierStyleSections"><span id="sec0005" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0025">Introduction</span><p id="par0005" class="elsevierStylePara elsevierViewall">Internal medicine departments in Spain were responsible for 705,000 hospital discharges per year, which represents 19% of all discharges, during the period from 2013 to 2016.<a class="elsevierStyleCrossRef" href="#bib0005"><span class="elsevierStyleSup">1</span></a> It has been estimated that approximately 30%–35% of all patients hospitalized in internal medicine departments have diabetes mellitus as a secondary diagnosis.<a class="elsevierStyleCrossRefs" href="#bib0010"><span class="elsevierStyleSup">2,3</span></a></p><p id="par0010" class="elsevierStylePara elsevierViewall">In the Spanish population, the prevalence of diabetes is 13.8% and carbohydrate metabolism abnormalities, including prediabetic states, is 30%.<a class="elsevierStyleCrossRef" href="#bib0020"><span class="elsevierStyleSup">4</span></a> This population is elderly, has a high rate of comorbidities, and frequently presents with kidney failure and established cardiovascular disease (CVD).<a class="elsevierStyleCrossRefs" href="#bib0015"><span class="elsevierStyleSup">3,5</span></a></p><p id="par0015" class="elsevierStylePara elsevierViewall">In order to provide guidelines on the choice of antidiabetic agents, the Diabetes, Obesity, and Nutrition Working Group of the Spanish Society of Internal Medicine has developed recommendations based on a critical review of the most up-to-date literature. These guidelines are not intended to substitute clinical judgment; they must be applied with excellent clinical care, making the necessary adjustments to treatment according to individual preferences, comorbidities, and other patient-related factors.</p><p id="par0020" class="elsevierStylePara elsevierViewall">The main objective is the creation of a brief, practical document that encompasses recommendations for the pharmacological treatment of type 2 diabetes mellitus (DM2) which balances simplicity and scientific rigor in order to facilitate decision-making regarding treatment (<a class="elsevierStyleCrossRef" href="#fig0005">Fig. 1</a>).</p><elsevierMultimedia ident="fig0005"></elsevierMultimedia></span><span id="sec0010" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0030">Materials and methods</span><p id="par0025" class="elsevierStylePara elsevierViewall">The document consists of two parts: the first includes recommendations based on patients’ most frequent clinical conditions: established CVD, heart failure (HF), diabetic nephropathy (DN), obesity and overweight, patients over 75 years of age, those at high risk of hypoglycemic episodes, and time since onset of diabetes greater than 10 years. The second part consists of recommendations based on the therapeutic target for glycosylated hemoglobin (HbA<span class="elsevierStyleInf">1c</span>) that we wish to reach.</p><p id="par0030" class="elsevierStylePara elsevierViewall">Based on the January 2019 recommendations from the American Diabetes Association,<a class="elsevierStyleCrossRef" href="#bib0030"><span class="elsevierStyleSup">6</span></a> we conducted a literature search on PubMed and selected randomized clinical trials on cardiovascular (CV) safety, systematic reviews, and meta-analyses published in 2019 to support the changes made to the aforementioned recommendations. The keywords used were “type 2 diabetes” combined with “cardiovascular disease,” “heart failure,” “diabetic nephropathy,” “obesity,” “elderly,” “hypoglycemia,” “GLP1 receptor agonist,” “SGLT2 inhibitor,” “DPP4 inhibitor,” and “insulin.” The bibliography shows the main works that support recommendations prior to 2019.</p><p id="par0035" class="elsevierStylePara elsevierViewall">To evaluate the level of evidence, American Diabetes Association standards were used with the following classification: A (clear evidence from randomized, controlled trials), B (evidence from observational studies), C (evidence from uncontrolled studies), and E (expert consensus or clinical experience).<a class="elsevierStyleCrossRef" href="#bib0035"><span class="elsevierStyleSup">7</span></a> The corresponding letter appears in parentheses at the end of the main recommendations.</p><p id="par0040" class="elsevierStylePara elsevierViewall">Once the algorithm was built and the initial explanations drafted, the original text was debated in successive revisions by a committee of experts who are members of the Diabetes, Obesity, and Nutrition Working Group of the Spanish Society of Internal Medicine until a final consensus on its content was reached.</p></span><span id="sec0015" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0035">Results and recommendations</span><p id="par0045" class="elsevierStylePara elsevierViewall">Metformin continues to be the first pillar of antidiabetic treatment and must be recommended so long as there is no intolerance or contraindication. This recommendation is supported by the fact that 75 %–80 % of patients included in the different CV safety studies were administered metformin in combination with the antidiabetic drugs that were studied (A).</p><span id="sec0020" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0040">Cardiovascular disease/high cardiovascular risk</span><p id="par0050" class="elsevierStylePara elsevierViewall">Metformin is considered a safe drug from a CV point of view (C).<a class="elsevierStyleCrossRef" href="#bib0040"><span class="elsevierStyleSup">8</span></a> Glucagon-like peptide-1 receptor agonists (GLP-1ras) and sodium-glucose cotransporter-2 inhibitors (SGLT-2is) are the drugs of choice in patients with established CVD and/or multiple CV risk factors, as they have been demonstrated to lead to a reduction in CV events (A) versus a placebo.</p><p id="par0055" class="elsevierStylePara elsevierViewall">In the LEADER study, liraglutide decreased the main composite outcome variable of major adverse CV events (MACE): non-fatal stroke, non-fatal heart attack, and CV mortality (hazard ratio [HR] 0.87; 95% confidence interval [95%CI]: 0.78−0.97; <span class="elsevierStyleItalic">p</span> = .01). On the ungrouped analysis, the relative risk reduction (RRR) was 22% (<span class="elsevierStyleItalic">p</span> = .007) for CV mortality and 15% (<span class="elsevierStyleItalic">p</span> = .02) for total mortality.<a class="elsevierStyleCrossRef" href="#bib0045"><span class="elsevierStyleSup">9</span></a> In the SUSTAIN-6 study, semaglutide also decreased MACE (HR 0.74; 95%CI: 0.58−0.95; <span class="elsevierStyleItalic">p</span> = .02), with a RRR of 39% (<span class="elsevierStyleItalic">p</span> = .04) for stroke.<a class="elsevierStyleCrossRef" href="#bib0050"><span class="elsevierStyleSup">10</span></a> In the REWIND study, the reduction in MACE (HR 0.88; 95%CI: 0.79−0.99; <span class="elsevierStyleItalic">p</span> = .026) for dulaglutide was also as a result of a RRR of 24% (<span class="elsevierStyleItalic">p</span> = .017) for stroke. The rest of the events analyzed were not statistically significant.<a class="elsevierStyleCrossRef" href="#bib0055"><span class="elsevierStyleSup">11</span></a></p><p id="par0060" class="elsevierStylePara elsevierViewall">With respect to the characteristics of the study population, in the LEADER and SUSTAIN-6 studies, 81% and 83% of patients, respectively, had established CVD whereas in the REWIND study, 69% of patients did not have established CVD.</p><p id="par0065" class="elsevierStylePara elsevierViewall">In regard to SGLT-2i, in the EMPA-REG-OUTCOME study, empagliflozin also demonstrated a reduction in MACE (HR 0.86; 95%CI: 0.74−0.99; <span class="elsevierStyleItalic">p</span> = .04). The disaggregated analysis showed a RRR of 38% (<span class="elsevierStyleItalic">p</span> < .001) in CV mortality and 32% (<span class="elsevierStyleItalic">p</span> < .001) in total mortality.<a class="elsevierStyleCrossRef" href="#bib0060"><span class="elsevierStyleSup">12</span></a> In the CANVAS study, canagliflozin also decreased MACE (HR 0.86; 95%CI: 0.75−0.97; <span class="elsevierStyleItalic">p</span> = .02), though a disaggregated analysis of its components did not reach statistical significance.<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> However, in the DECLARE study, dapagliflozin was not statistically significant with respect to superiority in the reduction of MACE.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a> The populations in these studies differed: 100% of patients in the EMPA-REG-OUTCOME study and 65.5% in the CANVAS study presented with established CVD whereas only 40% of patients in the DECLARE study with dapagliflozin did.</p><p id="par0070" class="elsevierStylePara elsevierViewall">In the PROactive study, pioglitazone showed a RRR in MACE of 16% (<span class="elsevierStyleItalic">p</span> = .027) as a secondary objective.<a class="elsevierStyleCrossRef" href="#bib0075"><span class="elsevierStyleSup">15</span></a> In the prediabetic population, treatment with pioglitazone was associated with a RRR of 24% (<span class="elsevierStyleItalic">p</span> = .007) of the combined variable of stroke and/or heart attack (A).<a class="elsevierStyleCrossRef" href="#bib0080"><span class="elsevierStyleSup">16</span></a></p><p id="par0075" class="elsevierStylePara elsevierViewall">Dipeptidyl peptidase-4 inhibitors (DPP4i) demonstrated noninferiority with respect to standard antidiabetic treatment (A). Although vildagliptin did not have a CV safety study, a meta-analysis supports its neutrality (B).<a class="elsevierStyleCrossRef" href="#bib0085"><span class="elsevierStyleSup">17</span></a> In the CAROLINA study, linagliptin showed neutrality versus glimepiride in incidence of MACE, although a greater number of hypoglycemic events were observed in the sulfonylurea group (A).<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a></p><p id="par0080" class="elsevierStylePara elsevierViewall">With respect to basal insulin, insulin glargine showed CV safety in the ORIGIN study<a class="elsevierStyleCrossRef" href="#bib0095"><span class="elsevierStyleSup">19</span></a> and degludec, compared to insulin glargine in the DEVOTE study, showed noninferiority (A).<a class="elsevierStyleCrossRef" href="#bib0100"><span class="elsevierStyleSup">20</span></a></p></span><span id="sec0025" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0045">Heart failure</span><p id="par0085" class="elsevierStylePara elsevierViewall">SGLT-2is are the drugs of choice in patients with HF or who are at risk of developing it (A). In the aforementioned CV safety studies, empagliflozin (HR 0.65; 95%CI: 0.50−0.85; <span class="elsevierStyleItalic">p</span> = .002), canagliflozin (HR 0.67; 95%CI: 0.52−0.87; <span class="elsevierStyleItalic">p</span> < .001), and dapagliflozin (HR 0.73; 95%CI: 0.61−0.88; <span class="elsevierStyleItalic">p</span> = .0005) have demonstrated a significant decrease in hospitalizations due to HF.<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12–14</span></a> In the DAPA-HF study, dapagliflozin managed to reduce the primary composite outcome of CV death, hospitalizations due to HF, and/or emergency department visits due to HF in patients with a reduced ejection fraction (<40%) regardless of the presence of diabetes (HR 0.74; 95%CI: 0.65−0.85; <span class="elsevierStyleItalic">p</span> = .00001).<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a></p><p id="par0090" class="elsevierStylePara elsevierViewall">GLP-1ras behave in a neutral manner with respect to hospitalizations due to HF, with the exception of albiglutide, which reduced them (HR 0.71; 95%CI: 0.53−0.94; <span class="elsevierStyleItalic">p</span> < .0001) (A).<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a></p><p id="par0095" class="elsevierStylePara elsevierViewall">DPP-4is were also neutral, with the exception of saxagliptin, which was associated with an increase in hospital admissions due to HF (HR 1.27; 95%CI: 1.07–1.51; <span class="elsevierStyleItalic">p</span> = .007).<a class="elsevierStyleCrossRef" href="#bib0115"><span class="elsevierStyleSup">23</span></a> In the CAROLINA study, linagliptin also showed neutrality versus glimepiride in hospitalizations due to HF (A).<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a></p><p id="par0100" class="elsevierStylePara elsevierViewall">Basal insulin analogs were also demonstrated to be neutral with respect to HF in the aforementioned CV safety studies (A). Pioglitazone is contraindicated in these patients because it is associated with an increase in hospitalizations due to HF as a result of an increase in hydrosaline retention (A).</p></span><span id="sec0030" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0050">Diabetic nephropathy</span><p id="par0105" class="elsevierStylePara elsevierViewall">SGLT-2is reduce the risk of needing dialysis or kidney transplant as well as death due to renal causes (HR 0.67; 95%CI: 0.52−0.86; <span class="elsevierStyleItalic">p</span> = .0019), progression to end-stage kidney disease (HR 0.65; 95%CI: 0.53−0.81; <span class="elsevierStyleItalic">p</span> < .0001), and acute kidney injury (HR 0.75; 95%CI: 0.66−0.85; <span class="elsevierStyleItalic">p</span> < .0001), with benefits that are consistent across all studies (A). In an analysis by glomerular filtration rate (GFR) subgroups, the nephroprotective effects are sustained, even with a GFR of 30–45 mL/min/1.73 m<span class="elsevierStyleSup">2</span> (C). Kidney protection is independent of the presence of microalbuminuria and the use of renin-angiotensin system blockers.<a class="elsevierStyleCrossRef" href="#bib0120"><span class="elsevierStyleSup">24</span></a> Among the studies on SGLT-2is, only the CREDENCE<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> study with canagliflozin 100 mg included a majority of patients with GFR < 60 mL/min/1.73 m<span class="elsevierStyleSup">2</span> (60%). These patients were a minority in the DECLARE-TIMI 58 (8%), CANVAS (20%), and EMPA-REG OUTCOME studies (26%).</p><p id="par0110" class="elsevierStylePara elsevierViewall">The GLP-1ras liraglutide (HR 0.78; 95%CI: 0.67−0.92; <span class="elsevierStyleItalic">p</span> = .003), semaglutide (HR 0.64; 95%CI: 0.46−0.88; <span class="elsevierStyleItalic">p</span> = .006), and dulaglutide (HR 0.85; 95%CI: 0.77−0.93; <span class="elsevierStyleItalic">p</span> = .0004) reduced renal events (GFR deterioration, macroalbuminuria, and death due to renal causes). These benefits are mainly due to a reduction in macroalbuminuria (A).<a class="elsevierStyleCrossRef" href="#bib0110"><span class="elsevierStyleSup">22</span></a></p><p id="par0115" class="elsevierStylePara elsevierViewall">The remaining antidiabetic agents have not shown benefits in the prevention of kidney function deterioration. Metformin requires a dose reduction with GFR < 45 mL/min and DPP-4is, except for linagliptin, require dose adjustment depending on GFR. The use of pioglitazone is not recommended due to the risk of hydrosaline retention (A).</p><p id="par0120" class="elsevierStylePara elsevierViewall">Metformin, sulfonylureas, and SGLT-2is are contraindicated for GFR <30 mL/min/1.73 m<span class="elsevierStyleSup">2</span>. Liraglutide, semaglutide, and dulaglutide can be used with GFRs of up to 15 mL/min/1.73 m<span class="elsevierStyleSup">2</span> as their beneficial CV and renal effects persist (A). Basal insulin requires a 25% reduction for GFRs of 15−30 mL/min/1.73 m<span class="elsevierStyleSup">2</span> and 50% for GFRs <15 mL/min/1.73 m<span class="elsevierStyleSup">2</span>. Although it can be used in patients with advanced DN, repaglinide can increase the risk of hypoglycemia.</p></span></span><span id="sec0035" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0055">Obesity and overweight</span><p id="par0125" class="elsevierStylePara elsevierViewall">Obesity and overweight are related to an increase in CV events, HF, and overall mortality.<a class="elsevierStyleCrossRef" href="#bib0130"><span class="elsevierStyleSup">26</span></a> GLP-1ras are the drugs of choice. The weight loss obtained using different drugs is not equal; greater to lesser weight loss is achieved using semaglutide, liraglutide, dulaglutide, exenatide, and lixisenatide, in that order (A).</p><p id="par0130" class="elsevierStylePara elsevierViewall">SGLT-2is are also associated with a decrease in body weight, though of a lesser intensity and durability (A). The combined use of GLP-1ras and SGLT-2is is recommended to optimize weight loss objectives (E).</p><p id="par0135" class="elsevierStylePara elsevierViewall">Pioglitazone, sulfonylureas, and insulin are associated with an increase in body weight.<a class="elsevierStyleCrossRef" href="#bib0135"><span class="elsevierStyleSup">27</span></a> DPP-4is behave in a neutral manner (A). The role of antidiabetic drugs in the treatment of non-alcoholic fatty liver disease is currently under study; patients in treatment with GLP-1ras and/or SGLT-2is may benefit.<a class="elsevierStyleCrossRef" href="#bib0140"><span class="elsevierStyleSup">28</span></a></p><span id="sec0040" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0060">Patients older than 75 years of age</span><p id="par0140" class="elsevierStylePara elsevierViewall">Elderly patients are more vulnerable to the deleterious effects of hypoglycemia and other side effects. Therefore, laxer glucose control objectives must be proposed. However, there is evidence of CV, renal, and HF benefits in elderly patients.</p><p id="par0145" class="elsevierStylePara elsevierViewall">In the EMPA-REG OUTCOME study, the reduction in events in individuals older than 75 years was even greater than among the total population, both in terms of CV mortality (HR 0.55; 95%CI: 0.32−0.94), hospitalizations due to HF (HR 0.45; 95%CI: 0.22−0.89), and renal events (HR 0.54; 95%CI: 0.37−0.79).<a class="elsevierStyleCrossRef" href="#bib0145"><span class="elsevierStyleSup">29</span></a> In the CANVAS study, patients older than 65 years of age also had beneficial outcomes in terms of MACE (HR 0.80; 95%CI: 0.67−0.95).<a class="elsevierStyleCrossRef" href="#bib0065"><span class="elsevierStyleSup">13</span></a> In a combined analysis of patients older than 75 years of age, canagliflozin demonstrated efficacy and safety with an equal incidence of side effects as younger subjects.<a class="elsevierStyleCrossRef" href="#bib0150"><span class="elsevierStyleSup">30</span></a> GLP-1ras also maintained their beneficial effects in elderly patients (C).<a class="elsevierStyleCrossRef" href="#bib0155"><span class="elsevierStyleSup">31</span></a></p><p id="par0150" class="elsevierStylePara elsevierViewall">In addition, in the DAPA-HF study, patients older than 75 years of age were those who most benefited in terms of a reduction in hospitalizations due to HF and/or CV mortality (HR 0.68; 95%CI: 0.53−0.88; <span class="elsevierStyleItalic">p</span> = .003) with fewer side effects than the placebo, especially volume depletion and kidney injury (C).<a class="elsevierStyleCrossRef" href="#bib0160"><span class="elsevierStyleSup">32</span></a></p><p id="par0155" class="elsevierStylePara elsevierViewall">In the care of elderly patients with DM2, a clinical evaluation must be performed and a functional, cognitive, and social approach should be taken. It is recommended to limit the intensity of antidiabetic treatment in patients with functional or cognitive decline and/or those with a poor prognosis for life. In these cases, the most important aspect is to avoid severe symptomatic hyperglycemia and, most of all, hypoglycemia, by using drugs that have shown low risk of triggering them and, in the event insulin is needed, prioritizing safer ones. For more details, refer to the consensus on treatment of DM2 among the elderly by the Spanish Society of Internal Medicine.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a></p></span></span><span id="sec0045" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0065">Hypoglycemia</span><p id="par0160" class="elsevierStylePara elsevierViewall">Non-insulin-dependent drugs are to be prioritized due to their low risk of hypoglycemia (metformin, GLP-1ra, SGLT-2is, and DPP-4is) (E). Both insulin glargine U300 and degludec have a lower incidence of hypoglycemic episodes than glargine U100 (A).<a class="elsevierStyleCrossRefs" href="#bib0100"><span class="elsevierStyleSup">20,34</span></a></p></span><span id="sec0050" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0070">Diabetes with onset more than 10 years ago</span><p id="par0165" class="elsevierStylePara elsevierViewall">Both SGLT-2is<a class="elsevierStyleCrossRefs" href="#bib0060"><span class="elsevierStyleSup">12–14</span></a> and GLP-1ras<a class="elsevierStyleCrossRefs" href="#bib0045"><span class="elsevierStyleSup">9–11</span></a> have demonstrated beneficial effects in CV safety studies in patients with DM2 with disease onset more than 10 years ago, in contrast to what has been observed with sulfonylureas, metformin, and insulin (A).<a class="elsevierStyleCrossRefs" href="#bib0175"><span class="elsevierStyleSup">35–38</span></a></p><span id="sec0055" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0075">HbA<span class="elsevierStyleInf">1c</span>-dependent approach</span><p id="par0170" class="elsevierStylePara elsevierViewall">Metformin continues to be the foundation of antidiabetic treatment. The document recommends the number of drugs that should be used depending on initial HbA<span class="elsevierStyleInf">1c</span> levels and/or the level we can propose reaching based on the established therapeutic objective (E).</p><p id="par0175" class="elsevierStylePara elsevierViewall">GLP-1ras and/or SGLT-2is are recommended as a second option after metformin, thanks to the aforementioned CV and renal benefits (A). The algorithm recommends different antidiabetic drugs for metabolic control in an established order. Basal insulin can be used in all situations that require it if metabolic control is required, especially if low insulin reserves, glucose levels > 300 mg/dl, cardinal symptoms, or HbA1c >10% with symptoms of hyperglycemia are observed as well as when there is a contraindication or intolerance to other therapies (E).</p><p id="par0180" class="elsevierStylePara elsevierViewall">Even patients with long-duration diabetes (> 10 years) can use GLP-1ras and/or SGLT-2is so long as they are asymptomatic (A).</p></span></span><span id="sec0060" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0080">Discussion</span><p id="par0185" class="elsevierStylePara elsevierViewall">This document presents the recommendations of the Diabetes, Obesity, and Nutrition Working Group of the Spanish Society of Internal Medicine for decision-making on the pharmacological treatment of DM2. Although it is mainly aimed at internists, it may also be of use to other attending physicians who care for patients with DM2. The high prevalence and exponentially increasing incidence of DM2 mean that any physician may be faced with patients with DM2 in daily clinical practice.</p><p id="par0190" class="elsevierStylePara elsevierViewall">The first part of the algorithm must be read horizontally and vertically. That is, first, the patients’ clinical condition or conditions must be selected (horizontal) and then, the drug it is advisable to use in each situation must be evaluated (vertical). The physician must always evaluate drugs’ contraindications, the need to adjust the dose, and if the indication is approved on the technical datasheet. Furthermore, he or she must also avoid therapeutic inertia. This document makes some recommendations that are currently outside of indications on the technical datasheet, but the existence of solid evidence means that said indications may be revised in the short-term.</p><p id="par0195" class="elsevierStylePara elsevierViewall">With respect to the recommendations to reduce CV events, our document does not include differences in the use of GLP-1ra among patients with or without established CVD, unlike other consensus documents. Although the REWIND study with dulaglutide only had 31% of patients with established CVD and, consequently, the evidence on primary prevention seems to be more consistent than with other GLP-1ras, the differences in criteria in the definition of established CVD make it difficult to establish firm recommendations. The SUSTAIN-6 (83% with CVD) and LEADER (81% with CVD) studies also included presence of vascular stenosis greater than 50% in the coronary, carotid, or peripheral arteries; moderate kidney disease; and HF with functional class II-III as established CVD. On the contrary, these patients were not considered as having established CVD in the REWIND study. Therefore, the percentage of patients in secondary prevention could have been lower in the LEADER and SUSTAIN-6 studies if the same criteria were used as in the REWIND study.<a class="elsevierStyleCrossRef" href="#bib0195"><span class="elsevierStyleSup">39</span></a></p><p id="par0200" class="elsevierStylePara elsevierViewall">Although the overall perception of SGLT-2is shows a class effect in the reduction of CV events, in the DECLARE study, dapagliflozin did not achieve a reduction in MACE in the total population, although it was observed in patients with a prior history of acute myocardial infarction.<a class="elsevierStyleCrossRef" href="#bib0200"><span class="elsevierStyleSup">40</span></a> One of the explanations could lie in the lower number of patients with prior CVD and advanced DN included in the DECLARE-TIMI study compared to other studies with SGLT-2i.<a class="elsevierStyleCrossRef" href="#bib0070"><span class="elsevierStyleSup">14</span></a></p><p id="par0205" class="elsevierStylePara elsevierViewall">Taking into account their mechanisms of action, SGLT-2is could have a cardiorenal benefit through hemodynamic mechanisms whereas GLP-1ras could exercise antiarteriosclerotic action and as such, they would fit in more along the entire continuum of CV risk.</p><p id="par0210" class="elsevierStylePara elsevierViewall">With respect to the reduction in hospitalizations due to HF, SGLT-2is showed a class effect. However, the percentage of patients with prior HF in the initial studies was small; thus, the evidence on the prevention of incident HF is more robust.<a class="elsevierStyleCrossRef" href="#bib0205"><span class="elsevierStyleSup">41</span></a> To date, the only specific study on SGLT-2is in a population with HF is the DAPA-HF study, in which dapagliflozin showed a decrease in hospitalizations and/or CV mortality in patients with HF and reduced ejection fraction (< 40%), regardless of presence of diabetes.<a class="elsevierStyleCrossRef" href="#bib0105"><span class="elsevierStyleSup">21</span></a></p><p id="par0215" class="elsevierStylePara elsevierViewall">Despite the neutrality results on the CAROLINA study,<a class="elsevierStyleCrossRef" href="#bib0090"><span class="elsevierStyleSup">18</span></a> the increase in hypoglycemic events in the glimepiride arm advises against the use of sulfonylureas in patients with established CVD or high CV risk, given that numerous clinical trials and observational studies have linked the use of these antidiabetic drugs with an increase in CV risk.<a class="elsevierStyleCrossRef" href="#bib0210"><span class="elsevierStyleSup">42</span></a></p><p id="par0220" class="elsevierStylePara elsevierViewall">With respect to renal effects, the current indications on the SGLT-2i technical datasheet allow for initiating treatment in patients with GFR >60 mL/min/1.73 m<span class="elsevierStyleSup">2</span> and maintains it, with a dose reduction, for GFRs of as low as 45 mL/min/1.73 m<span class="elsevierStyleSup">2</span>. However, the protective renal and CV effects of SGLT-2is are independent of the degree of GFR and are maintained in lower GFR levels. The greatest amount of evidence to date has been provided by the CREDENCE study<a class="elsevierStyleCrossRef" href="#bib0125"><span class="elsevierStyleSup">25</span></a> with canagliflozin 100 mg, which included patients with GFRs of up to 30 mL/min/1.73 m<span class="elsevierStyleSup">2</span>, although these findings are not yet reflected in the technical datasheet. These results reveal an important aspect of renal and CV protection of patients with moderate-severe DN.</p><p id="par0225" class="elsevierStylePara elsevierViewall">Although in addition to CV and renal benefits, GLP1-ras have been demonstrated to reduce body weight both in patients with obesity and overweight, its funding is only authorized for patients with a body mass index ≥30 kg/m<span class="elsevierStyleSup">2</span>.</p><p id="par0230" class="elsevierStylePara elsevierViewall">In the care of elderly patients with DM2, a clinical evaluation must be performed and functional, cognitive, and social approach should be taken. Patients who, regardless of their age, maintain an adequate functional level should benefit from the same treatments and glycemic control objectives as younger subjects; chronological age is not in and of itself a limitation to treatment.</p><p id="par0235" class="elsevierStylePara elsevierViewall">The intensity of antidiabetic treatment should be limited in patients with functional or cognitive deterioration and/or those with a poor prognosis for life. In these cases, the most important aspect is to avoid severe symptomatic hyperglycemia and, most of all, hypoglycemia, using drugs that have shown low risk of triggering them and prioritizing those that are safer in patients who receive insulin.<a class="elsevierStyleCrossRef" href="#bib0165"><span class="elsevierStyleSup">33</span></a></p><p id="par0240" class="elsevierStylePara elsevierViewall">Classically, patients with long-duration DM2 have received insulin. However, new families of treatments provide a possible alternative for receiving therapies with CV and renal benefits.</p><p id="par0245" class="elsevierStylePara elsevierViewall">With respect to the metabolic approach, it is very important to set an HbA<span class="elsevierStyleInf">1c</span> target that is patient-facing. It is advisable to keep in mind that lifestyle measures and metformin continue to be the pillars of the therapeutic approach. The algorithm helps predict the need to use one, two, or three drugs to reach the objectives. Although classically, insulin was recommended in patients with HbA1c >10% at the time of diagnosis, GLP1-ras and/or SGLT-2is in combination with metformin in many cases allow for proper metabolic control without the need to use insulin or, at least, the use of insulin in a transitory manner. In patients with cardinal symptoms and/or onset of decompensated hyperglycemia, SGLT-2is must not be used due to risk of euglycemic diabetic ketoacidosis.</p><p id="par0250" class="elsevierStylePara elsevierViewall">Identifying insulinopenic patients who require insulin substitution therapy is of utmost importance, as metabolic failure is predicted if we start other therapies. However, insulin therapy in a basal-bolus regimen and the intensification of rapid-acting insulin with multiple doses is not the intention of this consensus.</p><p id="par0255" class="elsevierStylePara elsevierViewall">The goal of this document is to increase the proper prescription of antidiabetic drugs in order to improve prognosis and reduce complications in patients with DM2 in any area of the healthcare system.</p><p id="par0260" class="elsevierStylePara elsevierViewall">The main strength of this document is its simplicity, clarity, and brevity, all of which make it a highly useful tool in clinical practice. On the other hand, its main limitation is the fact that, due to the aforementioned reasons, it cannot provide a response to very specific and/or special clinical circumstances, as it lacks the depth to do so. However, the balance between simplicity and scientific rigor favor its applicability and acceptance of the consensus among the scientific and healthcare community in our setting.</p></span><span id="sec0065" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0085">Funding</span><p id="par0265" class="elsevierStylePara elsevierViewall">No funding was received for this study.</p></span><span id="sec0070" class="elsevierStyleSection elsevierViewall"><span class="elsevierStyleSectionTitle" id="sect0090">Conflicts of interest</span><p id="par0270" class="elsevierStylePara elsevierViewall">The authors declare no conflicts of interest in the creation of and consensus on the recommendations.</p></span></span>" "textoCompletoSecciones" => array:1 [ "secciones" => array:14 [ 0 => array:3 [ "identificador" => "xres1454556" "titulo" => "Abstract" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0005" ] ] ] 1 => array:2 [ "identificador" => "xpalclavsec1326354" "titulo" => "Keywords" ] 2 => array:3 [ "identificador" => "xres1454557" "titulo" => "Resumen" "secciones" => array:1 [ 0 => array:1 [ "identificador" => "abst0010" ] ] ] 3 => array:2 [ "identificador" => "xpalclavsec1326353" "titulo" => "Palabras clave" ] 4 => array:2 [ "identificador" => "sec0005" "titulo" => "Introduction" ] 5 => array:2 [ "identificador" => "sec0010" "titulo" => "Materials and methods" ] 6 => array:3 [ "identificador" => "sec0015" "titulo" => "Results and recommendations" "secciones" => array:3 [ 0 => array:2 [ "identificador" => "sec0020" "titulo" => "Cardiovascular disease/high cardiovascular risk" ] 1 => array:2 [ "identificador" => "sec0025" "titulo" => "Heart failure" ] 2 => array:2 [ "identificador" => "sec0030" "titulo" => "Diabetic nephropathy" ] ] ] 7 => array:3 [ "identificador" => "sec0035" "titulo" => "Obesity and overweight" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0040" "titulo" => "Patients older than 75 years of age" ] ] ] 8 => array:2 [ "identificador" => "sec0045" "titulo" => "Hypoglycemia" ] 9 => array:3 [ "identificador" => "sec0050" "titulo" => "Diabetes with onset more than 10 years ago" "secciones" => array:1 [ 0 => array:2 [ "identificador" => "sec0055" "titulo" => "HbA-dependent approach" ] ] ] 10 => array:2 [ "identificador" => "sec0060" "titulo" => "Discussion" ] 11 => array:2 [ "identificador" => "sec0065" "titulo" => "Funding" ] 12 => array:2 [ "identificador" => "sec0070" "titulo" => "Conflicts of interest" ] 13 => array:1 [ "titulo" => "References" ] ] ] "pdfFichero" => "main.pdf" "tienePdf" => true "fechaRecibido" => "2020-03-01" "fechaAceptado" => "2020-06-05" "PalabrasClave" => array:2 [ "en" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Keywords" "identificador" => "xpalclavsec1326354" "palabras" => array:8 [ 0 => "Type 2 diabetes" 1 => "Treatment" 2 => "Cardiovascular disease" 3 => "Heart failure" 4 => "Obesity" 5 => "Hypoglycemia" 6 => "Chronic renal disease" 7 => "Elderly" ] ] ] "es" => array:1 [ 0 => array:4 [ "clase" => "keyword" "titulo" => "Palabras clave" "identificador" => "xpalclavsec1326353" "palabras" => array:8 [ 0 => "Diabetes mellitus tipo 2" 1 => "Tratamiento" 2 => "Enfermedad cardiovascular" 3 => "Insuficiencia cardíaca" 4 => "Obesidad" 5 => "Hipoglucemia" 6 => "Enfermedad renal crónica" 7 => "Anciano" ] ] ] ] "tieneResumen" => true "resumen" => array:2 [ "en" => array:2 [ "titulo" => "Abstract" "resumen" => "<span id="abst0005" class="elsevierStyleSection elsevierViewall"><p id="spar0010" class="elsevierStyleSimplePara elsevierViewall">Type 2 diabetes is a big health concern due to its high prevalence and morbi-mortality. Medical treatment has a growing complexity which is focus on patients’ clinical situations. This article contains a consensus statement about recommendations on medical treatment of type-2 diabetes from the Working Group of Diabetes, Obesity and Nutrition of Spanish Society of Internal Medicine. The aim of this consensus is to facilitate therapeutic decision-making to improve the diabetes patients care. The document prioritizes treatments with cardiovascular, especially heart failure, and real benefits.</p></span>" ] "es" => array:2 [ "titulo" => "Resumen" "resumen" => "<span id="abst0010" class="elsevierStyleSection elsevierViewall"><p id="spar0015" class="elsevierStyleSimplePara elsevierViewall">La diabetes tipo 2 constituye un problema de salud de elevada prevalencia y morbimortalidad. El tratamiento médico tiene una complejidad creciente en relación con las diversas situaciones clínicas del paciente. Este articulo recoge un documento de consenso de las recomendaciones para el tratamiento médico de la diabetes tipo 2 del Grupo de Diabetes, Obesidad y Nutrición de la Sociedad Española de Medicina Interna. El objetivo principal de este articulo es facilitar la toma de decisiones terapéuticas para mejorar la atención de los pacientes con diabetes. El documento prioriza los tratamientos con beneficios cardiovasculares, especialmente la insuficiencia cardíaca, y renales.</p></span>" ] ] "NotaPie" => array:1 [ 0 => array:2 [ "etiqueta" => "☆" "nota" => "<p class="elsevierStyleNotepara" id="npar0005">Please cite this article as: Carrasco-Sánchez FJ, Fernández-Rodríguez JM, Ena J, Gómez-Huelgas R, Carretero-Gómez J. Tratamiento médico de la diabetes mellitus tipo 2: recomendaciones del Grupo de Diabetes, Obesidad y Nutrición de la Sociedad Española de Medicina Interna. Rev Clin Esp. 2021;221:101–108.</p>" ] ] "apendice" => array:1 [ 0 => array:1 [ "seccion" => array:1 [ 0 => array:4 [ "apendice" => "<p id="par0275" class="elsevierStylePara elsevierViewall">Fernández-Rodríguez JM, Carretero-Gómez J, Carrasco-Sánchez FJ, Ena J, Gómez-Huelgas R, León D, Miramontes P, Casado PP, García de Lucas D, Pérez-Soto I, Pérez-Belmonte L, and Formiga F.</p>" "etiqueta" => "Appendix A" "titulo" => "Appendix. Members of the committee of experts" "identificador" => "sec0075" ] ] ] ] "multimedia" => array:1 [ 0 => array:8 [ "identificador" => "fig0005" "etiqueta" => "Figure 1" "tipo" => "MULTIMEDIAFIGURA" "mostrarFloat" => true "mostrarDisplay" => false "figura" => array:1 [ 0 => array:4 [ "imagen" => "gr1.jpeg" "Alto" => 5305 "Ancho" => 3167 "Tamanyo" => 1751946 ] ] "detalles" => array:1 [ 0 => array:3 [ "identificador" => "at0005" "detalle" => "Figure " "rol" => "short" ] ] "descripcion" => array:1 [ "en" => "<p id="spar0005" class="elsevierStyleSimplePara elsevierViewall">Recommendations for type 2 diabetes mellitus treatment according to the clinical condition.</p>" ] ] ] "bibliografia" => array:2 [ "titulo" => "References" "seccion" => array:1 [ 0 => array:2 [ "identificador" => "bibs0005" "bibliografiaReferencia" => array:42 [ 0 => array:3 [ "identificador" => "bib0005" "etiqueta" => "1" "referencia" => array:1 [ 0 => array:2 [ "contribucion" => array:1 [ 0 => array:2 [ "titulo" => "RECALMIN. 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Das" ] ] ] ] ] "host" => array:1 [ 0 => array:2 [ "doi" => "10.1111/dom.12821" "Revista" => array:7 [ "tituloSerie" => "Diabetes Obes Metab." "fecha" => "2017" "volumen" => "19" "numero" => "3" "paginaInicial" => "329" "paginaFinal" => "335" "link" => array:1 [ 0 => array:2 [ "url" => "https://www.ncbi.nlm.nih.gov/pubmed/27862902" "web" => "Medline" ] ] ] ] ] ] ] ] ] ] ] ] ] "idiomaDefecto" => "en" "url" => "/22548874/0000022100000002/v1_202101270650/S2254887420301557/v1_202101270650/en/main.assets" "Apartado" => array:4 [ "identificador" => "3982" "tipo" => "SECCION" "en" => array:2 [ "titulo" => "Special Article" "idiomaDefecto" => true ] "idiomaDefecto" => "en" ] "PDF" => "https://static.elsevier.es/multimedia/22548874/0000022100000002/v1_202101270650/S2254887420301557/v1_202101270650/en/main.pdf?idApp=WRCEE&text.app=https://revclinesp.es/" "EPUB" => "https://multimedia.elsevier.es/PublicationsMultimediaV1/item/epub/S2254887420301557?idApp=WRCEE" ]
| Year/Month | Html | Total | |
|---|---|---|---|
| 2024 November | 1 | 0 | 1 |
| 2024 October | 29 | 1 | 30 |
| 2024 September | 20 | 0 | 20 |
| 2024 August | 26 | 0 | 26 |
| 2024 July | 26 | 0 | 26 |
| 2024 June | 12 | 0 | 12 |
| 2024 May | 21 | 0 | 21 |
| 2024 April | 19 | 0 | 19 |
| 2024 March | 13 | 0 | 13 |
| 2024 February | 5 | 0 | 5 |
| 2024 January | 7 | 0 | 7 |
| 2023 December | 15 | 0 | 15 |
| 2023 November | 19 | 0 | 19 |
| 2023 October | 12 | 0 | 12 |
| 2023 September | 17 | 1 | 18 |
| 2023 August | 11 | 0 | 11 |
| 2023 July | 17 | 0 | 17 |
| 2023 June | 16 | 0 | 16 |
| 2023 May | 13 | 4 | 17 |
| 2023 April | 11 | 0 | 11 |
| 2023 March | 13 | 3 | 16 |
| 2023 February | 8 | 0 | 8 |
| 2023 January | 16 | 0 | 16 |
| 2022 December | 17 | 0 | 17 |
| 2022 November | 14 | 0 | 14 |
| 2022 October | 15 | 2 | 17 |
| 2022 September | 10 | 0 | 10 |
| 2022 August | 12 | 2 | 14 |
| 2022 July | 19 | 2 | 21 |
| 2022 June | 13 | 0 | 13 |
| 2022 May | 20 | 2 | 22 |
| 2022 April | 15 | 2 | 17 |
| 2022 March | 23 | 2 | 25 |
| 2022 February | 14 | 2 | 16 |
| 2022 January | 19 | 0 | 19 |
| 2021 December | 10 | 0 | 10 |
| 2021 November | 5 | 0 | 5 |
| 2021 October | 0 | 1 | 1 |
| 2021 April | 2 | 2 | 4 |
| 2021 March | 2 | 4 | 6 |
| 2021 February | 16 | 4 | 20 |
| 2021 January | 8 | 2 | 10 |
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