Jia-Ai Yeh , Shu-Man Lin , Yu-Chang Liu , Ji-Ze Hsu , Amy Huaishiuan Huang , Kashif M. Munir , Carol Chiung-Hui Peng , Ching-Hui Loh , Huei-Kai Huang
{"title":"SGLT2抑制剂和GLP-1受体激动剂与2型糖尿病患者帕金森病风险的关联:一项倾向评分匹配的队列研究和荟萃分析","authors":"Jia-Ai Yeh , Shu-Man Lin , Yu-Chang Liu , Ji-Ze Hsu , Amy Huaishiuan Huang , Kashif M. Munir , Carol Chiung-Hui Peng , Ching-Hui Loh , Huei-Kai Huang","doi":"10.1016/j.diabres.2025.112914","DOIUrl":null,"url":null,"abstract":"<div><h3>Aims</h3><div>This study aimed to investigate the association between sodium-glucose cotransporter 2 inhibitors (SGLT2is), glucagon-like peptide-1 receptor agonists (GLP-1RAs), and the risk of Parkinson’s disease (PD) in patients with type 2 diabetes (T2D).</div></div><div><h3>Methods</h3><div>We conducted a real-world cohort study using the TriNetX U.S. Research Network. Adults aged ≥ 50 years with T2D initiating SGLT2is, GLP-1RAs, or dipeptidyl peptidase-4 inhibitors (DPP4is) between 2015 and 2022 were included. A landmark analysis using a new-user, active-comparator design with propensity score matching was applied. The primary outcome was incident PD. A meta-analysis incorporating additional real-world studies was also performed.</div></div><div><h3>Results</h3><div>In total, 93,872, 110,366, and 95,838 patients were included in the SGLT2i vs. DPP4i, GLP-1RA vs. DPP4i, and SGLT2i vs. GLP-1RA comparisons, respectively. SGLT2i users had a significantly lower risk of PD compared with both DPP4i users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003) and GLP-1RA users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003). No significant difference was observed between GLP-1RA and DPP4i users (HR = 0.97, 95 % CI: 0.85–1.10, p = 0.656). The meta-analysis further supported the reduced PD risk associated with SGLT2i use.</div></div><div><h3>Conclusions</h3><div>SGLT2i use was associated with a significantly lower risk of PD compared with both DPP4i and GLP-1RA use in patients with T2D.</div></div>","PeriodicalId":11249,"journal":{"name":"Diabetes research and clinical practice","volume":"229 ","pages":"Article 112914"},"PeriodicalIF":7.4000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Association of SGLT2 inhibitors and GLP-1 receptor agonists with the risk of Parkinson’s disease in patients with type 2 diabetes: A propensity score–matched cohort study with meta-analysis\",\"authors\":\"Jia-Ai Yeh , Shu-Man Lin , Yu-Chang Liu , Ji-Ze Hsu , Amy Huaishiuan Huang , Kashif M. Munir , Carol Chiung-Hui Peng , Ching-Hui Loh , Huei-Kai Huang\",\"doi\":\"10.1016/j.diabres.2025.112914\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Aims</h3><div>This study aimed to investigate the association between sodium-glucose cotransporter 2 inhibitors (SGLT2is), glucagon-like peptide-1 receptor agonists (GLP-1RAs), and the risk of Parkinson’s disease (PD) in patients with type 2 diabetes (T2D).</div></div><div><h3>Methods</h3><div>We conducted a real-world cohort study using the TriNetX U.S. Research Network. Adults aged ≥ 50 years with T2D initiating SGLT2is, GLP-1RAs, or dipeptidyl peptidase-4 inhibitors (DPP4is) between 2015 and 2022 were included. A landmark analysis using a new-user, active-comparator design with propensity score matching was applied. The primary outcome was incident PD. A meta-analysis incorporating additional real-world studies was also performed.</div></div><div><h3>Results</h3><div>In total, 93,872, 110,366, and 95,838 patients were included in the SGLT2i vs. DPP4i, GLP-1RA vs. DPP4i, and SGLT2i vs. GLP-1RA comparisons, respectively. SGLT2i users had a significantly lower risk of PD compared with both DPP4i users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003) and GLP-1RA users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003). No significant difference was observed between GLP-1RA and DPP4i users (HR = 0.97, 95 % CI: 0.85–1.10, p = 0.656). The meta-analysis further supported the reduced PD risk associated with SGLT2i use.</div></div><div><h3>Conclusions</h3><div>SGLT2i use was associated with a significantly lower risk of PD compared with both DPP4i and GLP-1RA use in patients with T2D.</div></div>\",\"PeriodicalId\":11249,\"journal\":{\"name\":\"Diabetes research and clinical practice\",\"volume\":\"229 \",\"pages\":\"Article 112914\"},\"PeriodicalIF\":7.4000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diabetes research and clinical practice\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0168822725009283\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetes research and clinical practice","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168822725009283","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
Association of SGLT2 inhibitors and GLP-1 receptor agonists with the risk of Parkinson’s disease in patients with type 2 diabetes: A propensity score–matched cohort study with meta-analysis
Aims
This study aimed to investigate the association between sodium-glucose cotransporter 2 inhibitors (SGLT2is), glucagon-like peptide-1 receptor agonists (GLP-1RAs), and the risk of Parkinson’s disease (PD) in patients with type 2 diabetes (T2D).
Methods
We conducted a real-world cohort study using the TriNetX U.S. Research Network. Adults aged ≥ 50 years with T2D initiating SGLT2is, GLP-1RAs, or dipeptidyl peptidase-4 inhibitors (DPP4is) between 2015 and 2022 were included. A landmark analysis using a new-user, active-comparator design with propensity score matching was applied. The primary outcome was incident PD. A meta-analysis incorporating additional real-world studies was also performed.
Results
In total, 93,872, 110,366, and 95,838 patients were included in the SGLT2i vs. DPP4i, GLP-1RA vs. DPP4i, and SGLT2i vs. GLP-1RA comparisons, respectively. SGLT2i users had a significantly lower risk of PD compared with both DPP4i users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003) and GLP-1RA users (HR = 0.80, 95 % CI: 0.69–0.93, p = 0.003). No significant difference was observed between GLP-1RA and DPP4i users (HR = 0.97, 95 % CI: 0.85–1.10, p = 0.656). The meta-analysis further supported the reduced PD risk associated with SGLT2i use.
Conclusions
SGLT2i use was associated with a significantly lower risk of PD compared with both DPP4i and GLP-1RA use in patients with T2D.
期刊介绍:
Diabetes Research and Clinical Practice is an international journal for health-care providers and clinically oriented researchers that publishes high-quality original research articles and expert reviews in diabetes and related areas. The role of the journal is to provide a venue for dissemination of knowledge and discussion of topics related to diabetes clinical research and patient care. Topics of focus include translational science, genetics, immunology, nutrition, psychosocial research, epidemiology, prevention, socio-economic research, complications, new treatments, technologies and therapy.