Chiang Pei-Chun, Hsieh Cheng-Yang, Sung Sheng-Feng
Division of Nephrology, Department of Internal Medicine, Ditmanson Medical Foundation Chia-Yi Christian Hospital, Chiayi City, Taiwan.
Department of Neurology, Tainan Sin Lau Hospital, Tainan, Taiwan; School of Pharmacy, Institute of Clinical Pharmacy and Pharmaceutical Sciences, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
J Stroke Cerebrovasc Dis. 2025 May;34(5):108276. doi: 10.1016/j.jstrokecerebrovasdis.2025.108276. Epub 2025 Mar 4.
Diabetes is a significant risk factor for both stroke and dementia. This study aimed to compare the risk of incident dementia between sodium-glucose cotransporter 2 (SGLT2) inhibitors and dipeptidyl peptidase-4 (DPP-4) inhibitors in diabetic patients with a history of ischemic stroke.
We conducted a propensity-matched retrospective cohort study using observational data from the TriNetX global federated health research network. Patients aged 18 years or older with type 2 diabetes (T2D) and a history of ischemic stroke, newly prescribed either an SGLT2 or DPP-4 inhibitor from July 1, 2013, to June 30, 2024, were included. Propensity score matching was employed to balance baseline characteristics between treatment groups. The primary outcome was incident dementia, with secondary outcomes including degenerative and vascular dementia.
After propensity score matching, each group consisted of 15901 patients. Over a mean follow-up of 2.52 years, SGLT2 inhibitor use was associated with lower risks of overall dementia (hazard ratio [HR] 0.66; 95% confidence interval [CI] 0.59-0.74), degenerative dementia (HR 0.68; 95% CI 0.60-0.76), and vascular dementia (HR 0.59, 95% CI 0.49-0.70) compared to DPP-4 inhibitor use. These findings remained consistent across various sensitivity and subgroup analyses.
In diabetic patients with a history of ischemic stroke, initiating SGLT2 inhibitors, compared to DPP-4 inhibitors, is associated with a lower risk of incident dementia. This association was observed for both degenerative and vascular dementias. These findings support the preferential use of SGLT2 inhibitors in this high-risk population, warranting further investigation through randomized clinical trials.
糖尿病是中风和痴呆的重要危险因素。本研究旨在比较钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂和二肽基肽酶-4(DPP-4)抑制剂在有缺血性中风病史的糖尿病患者中发生痴呆的风险。
我们使用来自TriNetX全球联合健康研究网络的观察数据进行了一项倾向匹配回顾性队列研究。纳入了年龄在18岁及以上、患有2型糖尿病(T2D)且有缺血性中风病史、在2013年7月1日至2024年6月30日期间新开具SGLT2或DPP-4抑制剂处方的患者。采用倾向评分匹配来平衡治疗组之间的基线特征。主要结局是发生痴呆,次要结局包括退行性和血管性痴呆。
倾向评分匹配后,每组有15901名患者。在平均2.52年的随访中,与使用DPP-抑制剂相比,使用SGLT2抑制剂与总体痴呆(风险比[HR]0.66;95%置信区间[CI]0.59 - 0.74)、退行性痴呆(HR 0.68;95%CI 0.60 - 0.76)和血管性痴呆(HR 0.59,95%CI 0.49 - 0.70)的风险较低相关。这些发现在各种敏感性和亚组分析中保持一致。
在有缺血性中风病史的糖尿病患者中,与DPP-4抑制剂相比,起始使用SGLT2抑制剂与发生痴呆的风险较低相关。在退行性和血管性痴呆中均观察到这种关联。这些发现支持在这一高危人群中优先使用SGLT2抑制剂,需要通过随机临床试验进行进一步研究。