Your browser doesn't support javascript.
loading
Effects of SGLT2 Inhibitors and DPP-4 Inhibitors on Advanced Glycation End Products.
Kusunoki, Masataka; Hisano, Fumiya; Matsuda, Shin-Ichi; Kusunoki, Akiko; Abe, Tomokazu; Tsutsumi, Kazuhiko; Miyata, Tetsuro.
Afiliação
  • Kusunoki M; Department of Diabetes, Motor Function and Metabolism, Research Center of Health, Physical Fitness and Sports, Nagoya University, Nagoya City, Aichi, Japan.
  • Hisano F; Graduate School of Medicine, Department of Integrated Health Sciences, Nagoya University, Nagoya City, Aichi, Japan.
  • Matsuda SI; Department of Data Science, Faculty of Science and Technology, Nanzan University, Nagoya City, Aichi, Japan.
  • Kusunoki A; Akishima Clinic. Sakae, Naka-ku, Nagoya City, Japan.
  • Abe T; Department of Diabetes, Motor Function and Metabolism, Research Center of Health, Physical Fitness and Sports, Nagoya University, Nagoya City, Aichi, Japan.
  • Tsutsumi K; Okinaka Memorial Institute for Medical Research, Tokyo, Japan.
  • Miyata T; Office of Medical Education, School of Medicine, International University of Health and Welfare, Narita City, Chiba, Japan.
Drug Res (Stuttg) ; 74(2): 77-80, 2024 Feb.
Article em En | MEDLINE | ID: mdl-38286421
ABSTRACT
Clinical trials have revealed that sodium glucose cotransporter 2 (SGLT2) inhibitors suppress the onset of heart failure and cardiovascular death in diabetic patients. On the other hand, few reports have been published concerning such effects of dipeptidyl peptidase-4 (DPP-4) inhibitors. We undertook the present study to evaluate the effects of SGLT2 inhibitors and DPP-4 inhibitors on the advanced glycation end products (AGEs), well known as a risk factor for the development of cardiovascular disorders.Type 2 diabetes mellitus were divided into two groups and treated with either SGLT2 inhibitors or DPP-4 inhibitors for 3 months. Before and after the 3-month treatment period with each drug, the AGEs and diabetes-related parameters were measured. Methylglyoxal-derived hydroimidazolone-1 (MG-H1) was measured as one of the AGEs.In the SGLT2 inhibitor group, both the blood HbA1c and MG-H1 levels decreased significantly after the 3-month treatment period. In the DPP-4 inhibitor group, only the blood HbA1c level decreased significantly, with no significant change of the blood MG-H1 level.SGLT2 inhibitor reduced both the blood levels of HbA1c and AGEs (MG-H1). Considering that the blood levels of AGEs are associated with the risk of heart failure and cardiovascular disorders, the results of the present study suggest that the effect of SGLT2 inhibitors in suppressing cardiovascular death might be mediated by the reduction in the blood levels of AGEs induced by this class of drugs. DPP-4 inhibitors showed no significant effects on the blood levels of AGEs.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Drug Res (Stuttg) Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 6_ODS3_enfermedades_notrasmisibles Base de dados: MEDLINE Assunto principal: Doenças Cardiovasculares / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV / Inibidores do Transportador 2 de Sódio-Glicose / Insuficiência Cardíaca Tipo de estudo: Risk_factors_studies Limite: Humans Idioma: En Revista: Drug Res (Stuttg) Ano de publicação: 2024 Tipo de documento: Article