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      Exploring the mortality and cardiovascular outcomes with SGLT-2 inhibitors in patients with T2DM at dialysis commencement: a health global federated network analysis

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          Abstract

          Background

          Sodium-glucose cotransporter 2 inhibitors (SGLT-2is) have demonstrated associations with lowering cardiovascular outcomes in patients with type 2 diabetes mellitus (T2DM). However, the impact of SGLT-2is on individuals at dialysis commencement remains unclear. The aim of this real-world study is to study the association between SGLT-2is and outcomes in patients with T2DM at dialysis commencement.

          Methods

          This is a retrospective cohort study of electronic health records (EHRs) of patients with T2DM from TriNetX Research Network database between January 1, 2012, and January 1, 2024. New-users using intention to treatment design was employed and propensity score matching was utilized to select the cohort. Clinical outcomes included major adverse cardiac events (MACE) and all-cause mortality. Safety outcomes using ICD-10 codes, ketoacidosis, urinary tract infection (UTI) or genital infection, dehydration, bone fracture, below-knee amputation, hypoglycemia, and achieving dialysis-free status at 90 days and 90-day readmission.

          Results

          Of 49,762 patients with T2DM who initiated dialysis for evaluation, a mere 1.57% of patients utilized SGLT-2is within 3 months after dialysis. 771 SGLT-2i users (age 63.3 ± 12.3 years, male 65.1%) were matched with 771 non-users (age 63.1 ± 12.9 years, male 65.8%). After a median follow-up of 2.0 (IQR 0.3–3.9) years, SGLT-2i users were associated with a lower risk of MACE (adjusted Hazard Ratio [aHR] = 0.52, p value < 0.001), all-cause mortality (aHR = 0.49, p < 0.001). SGLT-2i users were more likely to become dialysis-free 90 days after the index date (aHR = 0.49, p < 0.001). No significant differences were observed in the incidence of ketoacidosis, UTI or genital infection, hypoglycemia, dehydration, bone fractures, below-knee amputations, or 90-day readmissions.

          Conclusions

          Our findings indicated a lower incidence of all-cause mortality and MACE after long-term follow-up, along with a higher likelihood of achieving dialysis-free status at 90 days in SGLT-2i users. Importantly, they underscored the potential cardiovascular protection and safety of SGLT-2is use in T2DM patients at the onset of dialysis.

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12933-024-02424-7.

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          Most cited references49

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          World Medical Association Declaration of Helsinki: ethical principles for medical research involving human subjects.

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            Empagliflozin, Cardiovascular Outcomes, and Mortality in Type 2 Diabetes.

            The effects of empagliflozin, an inhibitor of sodium-glucose cotransporter 2, in addition to standard care, on cardiovascular morbidity and mortality in patients with type 2 diabetes at high cardiovascular risk are not known.
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              IDF Diabetes Atlas: Global, regional and country-level diabetes prevalence estimates for 2021 and projections for 2045

              To provide global, regional, and country-level estimates of diabetes prevalence and health expenditures for 2021 and projections for 2045.
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                Author and article information

                Contributors
                q91421028@ntu.edu.tw
                Journal
                Cardiovasc Diabetol
                Cardiovasc Diabetol
                Cardiovascular Diabetology
                BioMed Central (London )
                1475-2840
                3 September 2024
                3 September 2024
                2024
                : 23
                : 327
                Affiliations
                [1 ]College of Medicine, Taipei Medical University, ( https://ror.org/05031qk94) Taipei, Taiwan
                [2 ]Department of Internal Medicine, National Taiwan University Hospital, ( https://ror.org/03nteze27) 7 Chung-Shan South Road, Taipei, 100 Taiwan
                [3 ]Division of Nephrology, Department of Internal Medicine, Chi-Mei Medical Center, ( https://ror.org/02y2htg06) Tainan, Taiwan
                [4 ]Department of Health and Nutrition, Chia Nan University of Pharmacy and Science, ( https://ror.org/02834m470) Tainan, Taiwan
                [5 ]GRID grid.416911.a, ISNI 0000 0004 0639 1727, Division of Nephrology, Department of Internal Medicine, , Taoyuan General Hospital, Ministry of Healthy and Welfare, ; Taoyuan, Taiwan
                [6 ]Department of Biomedical Engineering, Chung Yuan Christian University, ( https://ror.org/02w8ws377) Chungli, Taiwan
                [7 ]Primary Aldosteronism Center of Internal Medicine, National Taiwan University Hospital, ( https://ror.org/03nteze27) Taipei, Taiwan
                [8 ]National Taiwan University Hospital Study Group of Acute Renal Failure (NSARF), Consortium for Acute Kidney Injury and Renal Diseases, ( https://ror.org/03nteze27) Taipei, Taiwan
                [9 ]Department of Internal Medicine, National Taiwan University Hospital, ( https://ror.org/03nteze27) Room 1555, B4, Clinical Research Building, 7 Chung-Shan South Road, Taipei, 100 Taiwan
                Article
                2424
                10.1186/s12933-024-02424-7
                11373240
                39227933
                da05de1f-5273-484b-a7d1-fa821c9605f7
                © The Author(s) 2024

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 June 2024
                : 27 August 2024
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2024

                Endocrinology & Diabetes
                type 2 diabetes mellitus,dialysis initiation,major adverse cardiovascular events,propensity score matching,sodium-glucose cotransporter 2 inhibitors

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