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SGLT2 inhibitors in T2D and associated comorbidities - differentiating within the class.
Schernthaner, Guntram; Drexel, Heinz; Moshkovich, Evgeny; Zilaitiene, Birute; Martinka, Emil; Czupryniak, Leszek; Várkonyi, Tamás; Janez, Andrej; Ducena, Kristine; Lalic, Katarina; Tankova, Tsvetalina; Prázný, Martin; Smircic Duvnjak, Lea; Sukhareva, Olga; Sourij, Harald.
  • Schernthaner G; Department of Medicine I, Rudolfstitung Hospital, Vienna, Austria. guntram.schernthaner@meduniwien.ac.at.
  • Drexel H; VIVIT-Institute, Academic Teaching Hospital Feldkirch, Feldkirch, Austria. heinz.drexel@extern.insel.ch.
  • Moshkovich E; Vorarlberg Institute for Vascular Investigation and Treatment (VIVIT), Feldkirch, Austria. heinz.drexel@extern.insel.ch.
  • Zilaitiene B; Division of Angiology, Swiss Cardiovascular Center, University Hospital of Berne, Bern, Switzerland. heinz.drexel@extern.insel.ch.
  • Martinka E; Private University of the Principality of Liechtenstein, Triesen, Liechtenstein. heinz.drexel@extern.insel.ch.
  • Czupryniak L; Drexel University College of Medicine, Philadelphia, PA, USA. heinz.drexel@extern.insel.ch.
  • Várkonyi T; Unit of Endocrinology and Metabolism, Sapir Medical Center, Kfar-Saba, Israel.
  • Janez A; Institute of Endocrinology, Lithuanian University of Health Sciences, Kaunas, Lithuania.
  • Ducena K; National Institute of Endocrinology and Diabetology, Lubochna, Slovakia.
  • Lalic K; Department of Diabetology and Internal Medicine, Warsaw Medical University, Warsaw, Poland.
  • Tankova T; 1st Dept of Internal Medicine, University of Szeged, Szeged, Hungary.
  • Prázný M; Department of Endocrinology, Diabetes and Metabolic Diseases, University Medical Centre, Ljubljana, Slovenia.
  • Smircic Duvnjak L; Division of Endocrinology, Faculty of Internal Medicine, University of Latvia, Riga, Latvia.
  • Sukhareva O; Clinic for Endocrinology, Diabetes and Metabolic Diseases, Clinical Centre of Serbia, Faculty of Medicine, University of Belgrade, Beograd, Serbia.
  • Sourij H; Clinical Centre of Endocrinology, Medical University - Sofia, Sofia, Bulgaria.
BMC Endocr Disord ; 19(1): 64, 2019 Jun 17.
Article en En | MEDLINE | ID: mdl-31208401
ABSTRACT

BACKGROUND:

For patients with type 2 diabetes (T2D), cardiovascular disease (CVD) is the single most common cause of mortality. In 2008 and 2012, the Federal Drug Administration (FDA) and the European Medicines Agency (EMA) respectively mandated cardiovascular outcomes trials (CVOTs) on all new anti-diabetic agents, as prospective trials statistically powered to rule out excess cardiovascular risk in patients with T2D. Unexpectedly, some of these CVOTs have demonstrated not only cardiovascular safety, but also cardioprotective effects, as was first shown for the SGLT2 inhibitor empagliflozin in EMPA-REG OUTCOME. EXPERT OPINION To debate newly available CVOT data and to put them into context, we convened as a group of medical experts from the Central and Eastern European Region. Here we describe our discussions, focusing on the conclusions we can draw from EMPA-REG OUTCOME and other SGLT2 inhibitor CVOTs, including when considered alongside real-world evidence.

CONCLUSION:

CVOTs investigating SGLT2 inhibitors have suggested benefits beyond glucose lowering that have been confirmed in real-world evidence studies.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Enfermedades Cardiovasculares / Diabetes Mellitus Tipo 2 / Inhibidores del Cotransportador de Sodio-Glucosa 2 Tipo de estudio: Etiology_studies / Incidence_studies / Prognostic_studies / Risk_factors_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article