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      Kidney outcomes with SGLT2is for type 2 diabetes patients: does background treatment with metformin or RASis matter?

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          Abstract

          Introduction

          There is a lack of real-world evidence regarding the impact of concomitant metformin and renin-angiotensin system inhibitors (RASis) on sodium-glucose cotransporter-2 inhibitor (SGLT2i)-associated kidney outcomes. This study was aimed to investigate whether SGLT2i-associated kidney outcomes were modified by the concomitant use of metformin or RASis in patients with type 2 diabetes.

          Methods

          SGLT2i users were identified from three electronic health record databases during May 2016 and December 2017 and categorized into those with and without concomitant use of metformin or RASis. Propensity score matching was performed to minimize baseline differences between groups. Study outcomes were mean estimated glomerular filtration rate (eGFR) change and time to 30%, 40%, and 50% eGFR reductions. A meta-analysis was performed to combine the estimates across databases.

          Results

          After matching, there were 6,625 and 3,260 SGLT2i users with and without metformin, and 6,654 and 2,746 SGLT2i users with and without RASis, respectively. The eGFR dip was similar in SGLT2i users with and without metformin therapy, but was greater in SGLT2i users with RASis compared to those without RASis. Neither metformin nor RASi use had a significant effect on SGLT2i-associated eGFR reductions, as evidenced by the hazard ratios (95% CIs) of 30% eGFR reductions for SGLT2is with versus without metformin/RASis, namely 1.02 (0.87–1.20)/1.09 (0.92–1.31). Such findings were also observed in the outcomes of 40% and 50% eGFR reductions.

          Conclusion

          Using metformin or RASis did not modify SGLT2i-associated kidney outcomes in type 2 diabetes.

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          Most cited references28

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          Meta-analysis in clinical trials

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            Canagliflozin and Cardiovascular and Renal Events in Type 2 Diabetes

            Background Canagliflozin is a sodium-glucose cotransporter 2 inhibitor that reduces glycemia as well as blood pressure, body weight, and albuminuria in people with diabetes. We report the effects of treatment with canagliflozin on cardiovascular, renal, and safety outcomes. Methods The CANVAS Program integrated data from two trials involving a total of 10,142 participants with type 2 diabetes and high cardiovascular risk. Participants in each trial were randomly assigned to receive canagliflozin or placebo and were followed for a mean of 188.2 weeks. The primary outcome was a composite of death from cardiovascular causes, nonfatal myocardial infarction, or nonfatal stroke. Results The mean age of the participants was 63.3 years, 35.8% were women, the mean duration of diabetes was 13.5 years, and 65.6% had a history of cardiovascular disease. The rate of the primary outcome was lower with canagliflozin than with placebo (occurring in 26.9 vs. 31.5 participants per 1000 patient-years; hazard ratio, 0.86; 95% confidence interval [CI], 0.75 to 0.97; P<0.001 for noninferiority; P=0.02 for superiority). Although on the basis of the prespecified hypothesis testing sequence the renal outcomes are not viewed as statistically significant, the results showed a possible benefit of canagliflozin with respect to the progression of albuminuria (hazard ratio, 0.73; 95% CI, 0.67 to 0.79) and the composite outcome of a sustained 40% reduction in the estimated glomerular filtration rate, the need for renal-replacement therapy, or death from renal causes (hazard ratio, 0.60; 95% CI, 0.47 to 0.77). Adverse reactions were consistent with the previously reported risks associated with canagliflozin except for an increased risk of amputation (6.3 vs. 3.4 participants per 1000 patient-years; hazard ratio, 1.97; 95% CI, 1.41 to 2.75); amputations were primarily at the level of the toe or metatarsal. Conclusions In two trials involving patients with type 2 diabetes and an elevated risk of cardiovascular disease, patients treated with canagliflozin had a lower risk of cardiovascular events than those who received placebo but a greater risk of amputation, primarily at the level of the toe or metatarsal. (Funded by Janssen Research and Development; CANVAS and CANVAS-R ClinicalTrials.gov numbers, NCT01032629 and NCT01989754 , respectively.).
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              Canagliflozin and Renal Outcomes in Type 2 Diabetes and Nephropathy

              Type 2 diabetes mellitus is the leading cause of kidney failure worldwide, but few effective long-term treatments are available. In cardiovascular trials of inhibitors of sodium-glucose cotransporter 2 (SGLT2), exploratory results have suggested that such drugs may improve renal outcomes in patients with type 2 diabetes.
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                Author and article information

                Contributors
                URI : https://loop.frontiersin.org/people/2571538Role:
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                Role:
                Role:
                URI : https://loop.frontiersin.org/people/1569538Role:
                URI : https://loop.frontiersin.org/people/241400Role:
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                URI : https://loop.frontiersin.org/people/1729895Role:
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                Journal
                Front Endocrinol (Lausanne)
                Front Endocrinol (Lausanne)
                Front. Endocrinol.
                Frontiers in Endocrinology
                Frontiers Media S.A.
                1664-2392
                27 June 2024
                2024
                : 15
                : 1329945
                Affiliations
                [1] 1 Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University , Tainan, Taiwan
                [2] 2 Department of Pharmacy, College of Medicine, National Cheng Kung University , Tainan, Taiwan
                [3] 3 School of Pharmacy, College of Medicine, National Taiwan University , Taipei, Taiwan
                [4] 4 Department of Pharmacy, Kaohsiung Chang Gung Memorial Hospital , Kaohsiung, Taiwan
                [5] 5 College of Pharmacy, Kaohsiung Medical University , Kaohsiung, Taiwan
                [6] 6 Graduate Institute of Clinical Pharmacy, College of Medicine, National Taiwan University , Taipei, Taiwan
                [7] 7 Department of Pharmacy, National Taiwan University Hospital , Taipei, Taiwan
                [8] 8 College of Medicine, National Taiwan University , Taipei, Taiwan
                [9] 9 Department of Internal Medicine, National Taiwan University Hospital , Taipei, Taiwan
                Author notes

                Edited by: Soraya Puglisi, University of Turin, Italy

                Reviewed by: Karoline Schousboe, Odense University Hospital, Denmark

                Aditya Yashwant Sarode, Columbia University, United States

                Hotimah Masdan Salim, Nahdlatul Ulama University of Surabaya, Indonesia

                Sara Urru, University of Padua, Italy

                *Correspondence: Huang-Tz Ou, huangtz@ 123456mail.ncku.edu.tw ; Fang-Ju Lin, fjilin@ 123456ntu.edu.tw

                †These authors have contributed equally to this work and share first authorship

                ‡These authors have contributed equally to this work

                Article
                10.3389/fendo.2024.1329945
                11236716
                38994012
                a8750433-4f6c-4409-a09b-6ec7451ce9f8
                Copyright © 2024 Chong, Chang, Lin, Hsu, Wang, Wang, Huang, Lin and Ou

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 November 2023
                : 10 June 2024
                Page count
                Figures: 3, Tables: 1, Equations: 0, References: 28, Pages: 10, Words: 5449
                Funding
                The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This study was partially supported by grants from the Ministry of Science and Technology in Taiwan (grant MOST 109-2320-B-006 -047-MY3, recipient: H-TO; grant MOST 110-2320-B-002-027, recipient: F-JL; grant MOST 111-2636-B-002 -019, recipient: C-CW).
                Categories
                Endocrinology
                Original Research
                Custom metadata
                Adrenal Endocrinology

                Endocrinology & Diabetes
                sodium-glucose cotransporter-2 inhibitors,metformin,renin-angiotensin system inhibitors,estimated glomerular filtration rate,kidney function

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