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Incorporating SGLT2i and GLP-1RA for Cardiovascular and Kidney Disease Risk Reduction: Call for Action to the Cardiology Community.
Nelson, Adam J; Pagidipati, Neha J; Aroda, Vanita R; Cavender, Matthew A; Green, Jennifer B; Lopes, Renato D; Al-Khalidi, Hussein; Gaynor, Tanya; Kaltenbach, Lisa A; Kirk, Julienne K; Lingvay, Ildiko; Magwire, Melissa L; O'Brien, Emily C; Pak, Jonathan; Pop-Busui, Rodica; Richardson, Caroline R; Reed, Monica; Senyucel, Cagri; Webb, Laura; McGuire, Darren K; Granger, Christopher B.
Afiliação
  • Nelson AJ; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Pagidipati NJ; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Aroda VR; Brigham and Women's Hospital, Boston, MA (V.R.A.).
  • Cavender MA; University of North Carolina, Chapel Hill (M.A.C.).
  • Green JB; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Lopes RD; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Al-Khalidi H; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Gaynor T; Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, CT (T.G., J.P.).
  • Kaltenbach LA; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Kirk JK; Wake Forest School of Medicine, Winston-Salem, NC (J.K.K.).
  • Lingvay I; University of Texas Southwestern Medical Center, Dallas (I.L., D.K.).
  • Magwire ML; St Luke's Health System, Kansas City, MO (M.L.M.).
  • O'Brien EC; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Pak J; Boehringer Ingelheim Pharmaceuticals Inc, Ridgefield, CT (T.G., J.P.).
  • Pop-Busui R; University of Michigan, Ann Arbor (R.P.-B.).
  • Richardson CR; University of Michigan Medical School, Ann Arbor (C.R.R.).
  • Reed M; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • Senyucel C; Eli Lilly and Company, Indianapolis, IN (C.S.).
  • Webb L; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
  • McGuire DK; Parkland Health and Hospital System, Dallas, TX (D.K.M.).
  • Granger CB; Duke Clinical Research Institute, Durham, NC (A.J.N., N.J.P., J.B.G., R.D.L., H.A., L.A.K., E.C.O., M.R., L.W., C.B.G.).
Circulation ; 144(1): 74-84, 2021 07 06.
Article em En | MEDLINE | ID: mdl-34228476
Multiple sodium glucose cotransporter-2 inhibitors (SGLT-2i) and glucagon-like peptide-1 receptor agonists (GLP-1RA) have been shown to impart significant cardiovascular and kidney benefits, but are underused in clinical practice. Both SGLT-2i and GLP-1RA were first studied as glucose-lowering drugs, which may have impeded uptake by cardiologists in the wake of proven cardiovascular efficacy. Their significant effect on cardiovascular and kidney outcomes, which are largely independent of glucose-lowering effects, must drive a broader use of these drugs. Cardiologists are 3 times more likely than endocrinologists to see patients with both type 2 diabetes and cardiovascular disease, thus they are ideally positioned to share responsibility for SGLT-2i and GLP-1RA treatment with primary care providers. In order to increase adoption, SGLT-2i and GLP-1RA must be reframed as primarily cardiovascular and kidney disease risk-reducing agents with a side effect of glucose-lowering. Coordinated and multifaceted interventions engaging clinicians, patients, payers, professional societies, and health systems must be implemented to incentivize the adoption of these medications as part of routine cardiovascular and kidney care. Greater use of SGLT-2i and GLP-1RA will improve outcomes for patients with type 2 diabetes at high risk for cardiovascular and kidney disease.
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Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Cardiologia / Doenças Cardiovasculares / Comportamento de Redução do Risco / Receptor do Peptídeo Semelhante ao Glucagon 1 / Inibidores do Transportador 2 de Sódio-Glicose / Nefropatias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 / 2_ODS3 Base de dados: MEDLINE Assunto principal: Cardiologia / Doenças Cardiovasculares / Comportamento de Redução do Risco / Receptor do Peptídeo Semelhante ao Glucagon 1 / Inibidores do Transportador 2 de Sódio-Glicose / Nefropatias Tipo de estudo: Etiology_studies / Risk_factors_studies Limite: Humans Idioma: En Revista: Circulation Ano de publicação: 2021 Tipo de documento: Article