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Effect of preceding drug therapy on the renal and cardiovascular outcomes of combined sodium-glucose cotransporter-2 inhibitor and glucagon-like peptide-1 receptor agonist treatment in patients with type 2 diabetes and chronic kidney disease.
Tsukamoto, Shunichiro; Kobayashi, Kazuo; Toyoda, Masao; Tone, Atsuhito; Kawanami, Daiji; Suzuki, Daisuke; Tsuriya, Daisuke; Machimura, Hideo; Shimura, Hidetoshi; Wakui, Hiromichi; Takeda, Hiroshi; Yokomizo, Hisashi; Takeshita, Kei; Chin, Keiichi; Kanasaki, Keizo; Miyauchi, Masaaki; Saburi, Masuo; Morita, Miwa; Yomota, Miwako; Kimura, Moritsugu; Hatori, Nobuo; Nakajima, Shinichi; Ito, Shun; Murata, Takashi; Matsushita, Takaya; Furuki, Takayuki; Hashimoto, Takuya; Umezono, Tomoya; Muta, Yoshimi; Takashi, Yuichi; Tamura, Kouichi.
  • Tsukamoto S; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Kobayashi K; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Toyoda M; Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Tone A; Department of Internal Medicine, Diabetes Center, Okayama Saiseikai General Hospital, Okayama, Japan.
  • Kawanami D; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
  • Suzuki D; Suzuki Diabetes Clinic, Atsugi, Japan.
  • Tsuriya D; Division of Endocrinology and Metabolism, 2nd Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Machimura H; Machimura Internal Medicine Clinic, Hiratuska, Japan.
  • Shimura H; Shimura Clinic, Sagamihara, Japan.
  • Wakui H; Department of Medical Science and Cardiorenal Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Takeda H; Takeda Clinic, Isehara, 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, Hamamatsu, Japan.
  • Chin K; Hakuai Clinic, Sagamihara, Japan.
  • Kanasaki K; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Izumo, Japan.
  • Miyauchi M; Miyauchi Diabetes Clinic, Hadano, Japan.
  • Saburi M; Department of Diabetology, Endocrinology and Metabolism, Tokyo Medical University Hachioji Medical Center, Hachioji, Japan.
  • Morita M; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Izumo, Japan.
  • Yomota M; Department of Internal Medicine 1, Endocrinology and Metabolism, Shimane University Faculty of Medicine, Izumo, Japan.
  • Kimura M; Division of Nephrology, Endocrinology and Metabolism, Department of Internal Medicine, Tokai University School of Medicine, Isehara, Japan.
  • Hatori N; Kobayashi Hospital, Odawara, Japan.
  • Nakajima S; Sagami Junkanki Clinic, Sagamihara, Japan.
  • Ito S; Department of Internal Medicine, Sagamihara Red Cross Hospital, Sagamihara, 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, Hachioji, Japan.
  • Hashimoto T; Hadano Station South Gate Clinic, Hadano, Japan.
  • Umezono T; Division of Endocrinology and Metabolism, 2nd Department of Internal Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.
  • Muta Y; Umezono Internal Medicine Clinic, Atsugi, Japan.
  • Takashi Y; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
  • Tamura K; Department of Endocrinology and Diabetes, Fukuoka University School of Medicine, Fukuoka, Japan.
Diabetes Obes Metab ; 26(8): 3248-3260, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38764356
ABSTRACT

AIM:

To conduct a post hoc subgroup analysis of patients with type 2 diabetes (T2D) from the RECAP study, who were treated with sodium-glucose cotransporter-2 (SGLT2) inhibitor and glucagon-like peptide 1 receptor agonist (GLP-1RA) combination therapy, focusing only on those patients who had chronic kidney disease (CKD), to examine whether the composite renal outcome differed between those who received SGLT2 inhibitor treatment first and those who received a GLP-1RA first.

METHODS:

We included 438 patients with CKD (GLP-1RA-first group, n = 223; SGLT2 inhibitor-first group, n = 215) from the 643 T2D patients in the RECAP study. The incidence of the composite renal outcome, defined as progression to macroalbuminuria and/or a ≥50% decrease in estimated glomerular filtration rate (eGFR), was analysed using a propensity score (PS)-matched model. Furthermore, we calculated the win ratio for these composite renal outcomes, which were weighted in the following order (1) both a ≥50% decrease in eGFR and progression to macroalbuminuria; (2) a decrease in eGFR of ≥50% only; and (3) progression to macroalbuminuria only.

RESULTS:

Using the PS-matched model, 132 patients from each group were paired. The incidence of renal composite outcomes did not differ between the two groups (GLP-1RA-first group, 10%; SGLT2 inhibitor-first group, 17%; odds ratio 1.80; 95% confidence interval [CI] 0.85 to 4.26; p = 0.12). The win ratio of the GLP-1RA-first group versus the SGLT2 inhibitor-first group was 1.83 (95% CI 1.71 to 1.95; p < 0.001).

CONCLUSION:

Although the renal composite outcome did not differ between the two groups, the win ratio of the GLP-1RA-first group versus the SGLT2 inhibitor-first group was significant. These results suggest that, in GLP-1RA and SGLT2 inhibitor combination therapy, the addition of an SGLT2 inhibitor to baseline GLP-1RA treatment may lead to more favourable renal outcomes.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Nefropatías Diabéticas / Quimioterapia Combinada / Insuficiencia Renal Crónica / Receptor del Péptido 1 Similar al Glucagón / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Tasa de Filtración Glomerular Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Diabetes Mellitus Tipo 2 / Nefropatías Diabéticas / Quimioterapia Combinada / Insuficiencia Renal Crónica / Receptor del Péptido 1 Similar al Glucagón / Inhibidores del Cotransportador de Sodio-Glucosa 2 / Tasa de Filtración Glomerular Límite: Aged / Female / Humans / Male / Middle aged Idioma: En Año: 2024 Tipo del documento: Article