PMID- 35710921 OWN - NLM STAT- MEDLINE DCOM- 20220620 LR - 20220817 IS - 2045-2322 (Electronic) IS - 2045-2322 (Linking) VI - 12 IP - 1 DP - 2022 Jun 16 TI - Association of SGLT2 inhibitors with lower incidence of death in type 2 diabetes mellitus and causes of death analysis. PG - 10147 LID - 10.1038/s41598-022-13760-7 [doi] LID - 10147 AB - Sodium-glucose cotransporter 2 inhibitor (SGLT2i) potentially decrease all-cause and cardiovascular death, however, associations with non-cardiovascular death remain unclear. Therefore, we investigated SGLT2i associations with death and the cause of death. We used the Taiwanese National Health Institutes Research database linked to the National Register of Deaths (NRD). Incident type 2 diabetes mellitus (T2DM) patients and propensity score matched T2DM SGLT2i and Dipeptidyl peptidase 4 inhibitor (DPP4i) users were investigated. The index year was the SGLT2i or DPP4i prescription date from May 2016. Patients were followed-up until death or December 2018. Deaths verified by the NRD and grouped accordingly. Multiple Cox proportional hazards models were used. In total, 261,211 patients were included in the population; 47% of the patients were female and the average age was 62 years. The overall incidence of all-cause death was 8.67/1000 patient-years for SGLT2i and 12.41 for DPP4i users during follow-up. After adjusting for potential risk factors in the propensity score matched population, SGLT2i users were associated with lower risks of all-cause death, cardiovascular death, cancer death, and non-cancer, non-vascular death compared with DPP4i-users. For specific death causes, significantly lower death risks from heart disease, cerebrovascular disease, and accidents were associated with SGLT2i-use. SGLT2i benefits for T2DM patients were not different across subgroups. Compared with DPP4i-use, SGLT2i-use for T2DM was associated with lower disease and death risk. CI - (c) 2022. The Author(s). FAU - Chung, Mu-Chi AU - Chung MC AD - Division of Nephrology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan. AD - Ph.D. Program in Translational Medicine, National Chung Hsing University, Taichung, Taiwan. AD - Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, Taiwan. AD - Department of Biotechnology, Asia University, Taichung, Taiwan. FAU - Hsu, Hui-Tsung AU - Hsu HT AD - Department of Public Health, College of Public Health, China Medical University, No. 100, Sec. 1, Jingmao Rd., Beitun Dist., Taichung City, 406040, Taiwan. FAU - Chang, Chao-Hsiang AU - Chang CH AD - Department of Urology, China Medical University and Hospital, Taichung, Taiwan. FAU - Hung, Peir-Haur AU - Hung PH AD - Department of Internal Medicine, Ditmanson Medical Foundation Chiayi Christian Hospital, Chiayi, Taiwan. AD - Department of Applied Life Science and Health, Chia-Nan University of Pharmacy and Science, Tainan, Taiwan. FAU - Hsiao, Po-Jen AU - Hsiao PJ AD - Department of Urology, China Medical University and Hospital, Taichung, Taiwan. FAU - Wu, Laing-You AU - Wu LY AD - Department of Public Health, College of Public Health, China Medical University, No. 100, Sec. 1, Jingmao Rd., Beitun Dist., Taichung City, 406040, Taiwan. FAU - Wu, Ming-Ju AU - Wu MJ AD - Division of Nephrology, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan. FAU - Shieh, Jeng-Jer AU - Shieh JJ AD - Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, Taiwan. AD - Institute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan. AD - Department of Education and Research, Taichung Veterans General Hospital, Taichung, Taiwan. FAU - Chung, Chi-Jung AU - Chung CJ AD - Department of Public Health, College of Public Health, China Medical University, No. 100, Sec. 1, Jingmao Rd., Beitun Dist., Taichung City, 406040, Taiwan. cjchung@mail.cmu.edu.tw. AD - Department of Medical Research, China Medical University Hospital, Taichung, Taiwan. cjchung@mail.cmu.edu.tw. LA - eng PT - Journal Article PT - Research Support, Non-U.S. Gov't DEP - 20220616 PL - England TA - Sci Rep JT - Scientific reports JID - 101563288 RN - 0 (Dipeptidyl-Peptidase IV Inhibitors) RN - 0 (Hypoglycemic Agents) RN - 0 (Sodium-Glucose Transporter 2 Inhibitors) SB - IM MH - Cause of Death MH - *Diabetes Mellitus, Type 2/complications MH - *Dipeptidyl-Peptidase IV Inhibitors/pharmacology MH - Female MH - Humans MH - Hypoglycemic Agents/adverse effects MH - Incidence MH - Male MH - Middle Aged MH - *Sodium-Glucose Transporter 2 Inhibitors/pharmacology PMC - PMC9203810 COIS- The authors declare no competing interests. EDAT- 2022/06/18 06:00 MHDA- 2022/06/22 06:00 PMCR- 2022/06/16 CRDT- 2022/06/17 00:20 PHST- 2022/03/25 00:00 [received] PHST- 2022/05/27 00:00 [accepted] PHST- 2022/06/17 00:20 [entrez] PHST- 2022/06/18 06:00 [pubmed] PHST- 2022/06/22 06:00 [medline] PHST- 2022/06/16 00:00 [pmc-release] AID - 10.1038/s41598-022-13760-7 [pii] AID - 13760 [pii] AID - 10.1038/s41598-022-13760-7 [doi] PST - epublish SO - Sci Rep. 2022 Jun 16;12(1):10147. doi: 10.1038/s41598-022-13760-7.