Risk of New-onset Stroke in Patients with Type 2 Diabetes with Chronic Kidney Disease on Sodium-glucose Co-transporter-2 Inhibitor Users

被引:3
作者
Jong, Gwo-Ping [1 ,2 ]
Lin, Tsung-Kun [3 ,4 ]
Liao, Pei-Lun [5 ]
Huang, Jing-Yang [2 ,5 ]
Yang, Tsung-Yuan [1 ,2 ]
Pan, Lung-Fa [6 ,7 ]
机构
[1] Chung Shan Med Univ Hosp, Dept Internal Med, Div Cardiol, Taichung, Taiwan
[2] Chung Shan Med Univ, Inst Med, Coll Med, Taichung, Taiwan
[3] Taoyuan Armed Forces Gen Hosp, Dept Pharm, Taoyuan, Taiwan
[4] Natl Def Med Ctr, Sch Pharm, Taipei, Taiwan
[5] Chung Shan Med Univ Hosp, Dept Med Res, Taichung, Taiwan
[6] Taichung Armed Forces Gen Hosp, Dept Cardiol, Taichung, Taiwan
[7] Cent Taiwan Univ Sci & Technol, Dept Med Imaging & Radiol Sci, Taichung, Taiwan
关键词
New-onset stroke; SGLT2; inhibitor; Type; 2; DM; Chronic kidney disease; SGLT2; INHIBITION; DAPAGLIFLOZIN; INFLAMMATION; MORTALITY; MELLITUS;
D O I
10.1007/s12975-023-01174-0
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Clinical studies have investigated the effects of using sodium-glucose co-transporter-2 (SGLT2) inhibitors on the development of new-onset stroke (NOS) in patients with type 2 diabetes (T2D) and chronic kidney disease (CKD), but the findings are inconsistent. This study aimed to examine the association between the use of SGLT2 inhibitors and NOS risk in patients with T2D and CKD. We conducted a nationwide retrospective cohort study using data from the Taiwan Health Insurance Review and Assessment Service database for the years 2004 to 2019. The primary outcome was the risk of incident stroke, which was estimated using hazard ratios (HRs) and 95% confidence intervals (CIs). We used multiple Cox regression modeling to analyze the association between SGLT2 inhibitor use and the risk of stroke in patients with T2D and CKD. In a cohort of 113,710 patients with T2D and CKD who were using SGLT2 inhibitors and 227,420 patients with T2D and CKD who were not using SGLT2 inhibitors, after applying a 1:2 sex- and age-matching strategy, 2,842 and 7,169 NOS events were recorded, respectively. The event rate per 10,000 person-months was 10.60 (95% CI 10.21 to 11.03) for SGLT2 inhibitor users and 13.71 (13.39-14.03) for non-SGLT2 inhibitor users. After adjusting for the index year, sex, age, comorbidities, and concurrent medication, there was a decreased risk of NOS for SGLT2 inhibitor users (adjusted HR 0.80; 95% CI 0.77-0.84) compared with non-SGLT2 inhibitor users. The sensitivity test for the propensity score 1:1-matched analyses showed similar results (adjusted HR 0.80; 95% CI 0.76-0.84). The type of SGLT2 inhibitor subgroup analysis for incident stroke showed consistent results. We concluded that the use of SGLT2 inhibitors in patients with T2D and CKD was associated with significantly low rates of NOS. The significantly low rates of NOS in patients with T2D and CKD were greater among females and less than 50 years patients.
引用
收藏
页码:1098 / 1107
页数:10
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