PMID- 38274236 OWN - NLM STAT- MEDLINE DCOM- 20240129 LR - 20240306 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 14 DP - 2023 TI - Combined effects of sodium-glucose cotransporter 2 inhibitor and angiotensin receptor-neprilysin inhibitor on renal function in cardiovascular disease patients with type 2 diabetes mellitus: a retrospective cohort study. PG - 1326611 LID - 10.3389/fendo.2023.1326611 [doi] LID - 1326611 AB - BACKGROUND: Angiotensin receptor/neprilysin inhibitor (ARNI) and sodium-glucose cotransporter 2 inhibitor (SGLT2i) have shown a significant protective role against cardiovascular diseases and type 2 diabetes mellitus (T2DM), and there is a growing proportion of patients who are undergoing combined therapy with the two drugs. However, the effect of this combination treatment on renal function has not yet been determined. METHODS: This study included 539 patients who were diagnosed with cardiovascular disease combined with T2DM. According to the use of SGLT2i and ARNI, patients were divided into the combination treatment group, SGLT2i group, ARNI group and control group. Primary outcomes were serum creatinine (Scr) and estimated glomerular filtration rate (eGFR) changes in the 6th month and 12th month. RESULTS: In the ARNI group, no significant changes in Scr or eGFR were observed during the follow-up period, while the above indicators showed a trend of deterioration in the other three groups. The univariate analysis results showed that at 6 months of follow-up, the renal function indicators of patients treated with ARNI (either alone or in combination) were better than those treated with SGLT2i alone. After 12 months of follow-up, the Scr results were the same as before, while the difference in eGFR between groups disappeared. After multivariate analysis, in terms of delaying the progression of Scr, the ARNI group was superior to the other groups at the end of follow-up. No significant difference in eGFR was observed between groups during follow-up. CONCLUSION: In patients with cardiovascular disease and T2DM, combination therapy with ARNI and SGLT2i did not show an advantage over monotherapy in delaying renal insufficiency progression, and renal function seems to be better preserved in patients treated with ARNI alone. CLINICAL TRIAL REGISTRATION: clinicaltrials.gov, identifier NCT05922852. CI - Copyright (c) 2024 Xu, Chen, Zhang and Zhu. FAU - Xu, Ling AU - Xu L AD - Department of Cardiology, Peking University Third Hospital, NHC Key, Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Peking University, Beijing, China. FAU - Chen, Bo AU - Chen B AD - Department of Cardiology, Peking University Third Hospital, NHC Key, Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Peking University, Beijing, China. FAU - Zhang, Hua AU - Zhang H AD - Research Center of Clinical Epidemiology, Peking University Third Hospital, Peking University, Beijing, China. FAU - Zhu, Dan AU - Zhu D AD - Department of Cardiology, Peking University Third Hospital, NHC Key, Laboratory of Cardiovascular Molecular Biology and Regulatory Peptides, Peking University, Beijing, China. LA - eng SI - ClinicalTrials.gov/NCT05922852 PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20240111 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 RN - EC 3.4.24.11 (Neprilysin) RN - 0 (Receptors, Angiotensin) RN - IY9XDZ35W2 (Glucose) RN - 9NEZ333N27 (Sodium) SB - IM MH - Humans MH - *Diabetes Mellitus, Type 2/complications/drug therapy MH - *Cardiovascular Diseases MH - Neprilysin MH - Retrospective Studies MH - Kidney MH - Receptors, Angiotensin/therapeutic use MH - Glucose/therapeutic use MH - Sodium PMC - PMC10808758 OTO - NOTNLM OT - ARNI OT - SGLT-2 inhibitor OT - cardiovascular disease OT - combination treatment OT - diabetes OT - renal function COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2024/01/26 06:43 MHDA- 2024/01/29 06:43 PMCR- 2023/01/01 CRDT- 2024/01/26 03:50 PHST- 2023/10/23 00:00 [received] PHST- 2023/12/20 00:00 [accepted] PHST- 2024/01/29 06:43 [medline] PHST- 2024/01/26 06:43 [pubmed] PHST- 2024/01/26 03:50 [entrez] PHST- 2023/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2023.1326611 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2024 Jan 11;14:1326611. doi: 10.3389/fendo.2023.1326611. eCollection 2023.