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Influence of the combination of SGLT2 inhibitors and GLP-1 receptor agonists on eGFR decline in type 2 diabetes: post-hoc analysis of RECAP study.
Muta, Yoshimi; Kobayashi, Kazuo; Toyoda, Masao; Tone, Atsuhito; Suzuki, Daisuke; Tsuriya, Daisuke; Machimura, Hideo; Shimura, Hidetoshi; Takeda, Hiroshi; Yokomizo, Hisashi; Takeshita, Kei; Chin, Keiichi; Kanasaki, Keizo; Tamura, Kouichi; Miyauchi, Masaaki; Saburi, Masuo; Morita, Miwa; Yomota, Miwako; Kimura, Moritsugu; Hatori, Nobuo; Nakajima, Shinichi; Ito, Shun; Tsukamoto, Shunichiro; Murata, Takashi; Matsushita, Takaya; Furuki, Takayuki; Hashimoto, Takuya; Umezono, Tomoya; Takashi, Yuichi; Kawanami, Daiji.
Afiliação
  • Muta Y; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
  • Kobayashi K; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Toyoda M; Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Kanagawa, Japan.
  • Tone A; Department of Internal Medicine, Diabetes Center, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Suzuki D; Suzuki Diabetes Clinic, Kanagawa, Japan.
  • Tsuriya D; Division of Endocrinology and Metabolism, 2nd Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Machimura H; Machimura Internal Medicine Clinic, Kanagawa, Japan.
  • Shimura H; Shimura Clinic, Kanagawa, Japan.
  • Takeda H; Takeda Clinic, Kanagawa, Japan.
  • Yokomizo H; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
  • Takeshita K; Division of Endocrinology and Metabolism, 2nd Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Chin K; Hakuai Clinic, Kanagawa, Japan.
  • Kanasaki K; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Shimane, Japan.
  • Tamura K; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Miyauchi M; Miyauchi Diabetes Clinic, Kanagawa, Japan.
  • Saburi M; Department of Diabetology, Endocrinology and Metabolism, Tokyo Medical University Hachioji Medical Center, Tokyo, Japan.
  • Morita M; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Shimane, Japan.
  • Yomota M; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Shimane, Japan.
  • Kimura M; Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Kanagawa, Japan.
  • Hatori N; Kobayashi Hospital, Kanagawa, Japan.
  • Nakajima S; Sagami Junkanki Clinic, Kanagawa, Japan.
  • Ito S; Department of Internal Medicine, Sagamihara Red Cross Hospital, Kanagawa, Japan.
  • Tsukamoto S; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Murata T; Department of Clinical Nutrition, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
  • Matsushita T; Diabetes Center, National Hospital Organization Kyoto Medical Center, Kyoto, Japan.
  • Furuki T; Department of Diabetology, Endocrinology and Metabolism, Tokyo Medical University Hachioji Medical Center, Tokyo, Japan.
  • Hashimoto T; Hadano Station South Gate Clinic, Kanagawa, Japan.
  • Umezono T; Division of Endocrinology and Metabolism, 2nd Department of Internal Medicine, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Takashi Y; Umezono Internal Medicine Clinic, Kanagawa, Japan.
  • Kawanami D; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
Front Pharmacol ; 15: 1358573, 2024.
Article em En | MEDLINE | ID: mdl-38601470
ABSTRACT
Accumulating evidence has demonstrated that both SGLT2 inhibitors (SGLT2i) and GLP-1 receptor agonists (GLP1Ra) have protective effects in patients with diabetic kidney disease. Combination therapy with SGLT2i and GLP1Ra is commonly used in patients with type 2 diabetes (T2D). We previously reported that in combination therapy of SGLT2i and GLP1Ra, the effect on the renal composite outcome did not differ according to the preceding drug. However, it remains unclear how the initiation of combination therapy is associated with the renal function depending on the preceding drug. In this post hoc analysis, we analyzed a total of 643 T2D patients (GLP1Ra-preceding group, n = 331; SGLT2i-preceding group, n = 312) and investigated the differences in annual eGFR decline. Multiple imputation and propensity score matching were performed to compare the annual eGFR decline. The reduction in annual eGFR decline in the SGLT2i-preceding group (pre -3.5 ± 9.4 mL/min/1.73 m2/year, post -0.4 ± 6.3 mL/min/1.73 m2/year, p < 0.001), was significantly smaller after the initiation of GLP1Ra, whereas the GLP1Ra-preceding group tended to slow the eGFR decline but not to a statistically significant extent (pre -2.0 ± 10.9 mL/min/1.73 m2/year, post -1.8 ± 5.4 mL/min/1.73 m2/year, p = 0.83) after the initiation of SGLT2i. After the addition of GLP1Ra to SGLT2i-treated patients, slower annual eGFR decline was observed. Our data raise the possibility that the renal benefits-especially annual eGFR decline-of combination therapy with SGLT2i and GLP1Ra may be affected by the preceding drug.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Front Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão

Texto completo: 1 Base de dados: MEDLINE Idioma: En Revista: Front Pharmacol Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Japão