Department of Internal Medicine, Gangneung Asan Hospital, University of Ulsan College of Medicine, Gangneung, Republic of Korea.
Department of Internal Medicine, Inje University Ilsan Paik Hospital, Inje University College of Medicine, Goyang, Republic of Korea.
J Alzheimers Dis. 2021;81(3):1263-1272. doi: 10.3233/JAD-201535.
There are few reports that evaluated the association between various types of dementia and dual oral therapy with antihyperglycemic medication.
The goal of this study was to investigate the association between treatment of dual antihyperglycemic medication and dementia subclass in type 2 diabetes mellitus using the Korean National Health Insurance System.
This study included 701,193 individuals with diabetes prescribed dual oral therapy between 2009 and 2012 from the Korean National Health Insurance Service Database, which were tracked until 2017. All-cause, Alzheimer's (AD) and vascular dementia (VaD) were investigated by dual oral therapy. Adjustments were made for age, sex, income, diabetes duration, hypertension, dyslipidemia, smoking, drinking, exercise, body mass index, glucose level, and estimated glomerular filtration rate.
Dual therapy with metformin (Met) + dipeptidyl peptidase-4 inhibitor (DPP-4i), Met + thiazolidinedione (TZD), and sulfonylurea (SU) + thiazolidinediones (TZD) were significantly associated with all-cause dementia (HR = 0.904, 0.804, and 0.962, respectively) and VaD (HR = 0.865, 0.725, and 0.911, respectively), compared with Met + SU. Met + DPP-4i and Met + TZD were associated with significantly lower risk of AD (HR = 0.922 and 0.812), compared with Met + SU. Dual therapy with TZD was associated with a significantly lower risk of all-cause dementia, AD, and VaD than nonusers of TZD (HR = 0.918, 0.925 and 0.859, respectively).
Adding TZD or DPP-4i instead of SU as second-line anti-diabetic treatment may be considered for delaying or preventing dementia. Also, TZD users relative to TZD non-users on dual oral therapy were significantly associated with lower risk of various types of dementia.
目前鲜有研究评估不同类型痴呆与双口服降糖药物治疗之间的关联。
本研究旨在利用韩国国民健康保险系统评估 2 型糖尿病患者接受双口服降糖药物治疗与痴呆亚类之间的关联。
本研究纳入了 2009 年至 2012 年期间在韩国国民健康保险服务数据库中接受双口服药物治疗的 701193 例糖尿病患者,对其进行了为期 7 年的随访。通过双口服药物治疗,调查全因、阿尔茨海默病(AD)和血管性痴呆(VaD)的发生情况。调整了年龄、性别、收入、糖尿病病程、高血压、血脂异常、吸烟、饮酒、运动、体重指数、血糖水平和估算肾小球滤过率等因素。
与 Met+SU 相比,Met+DPP-4i、Met+TZD 和 SU+TZD 与全因痴呆(HR=0.904、0.804 和 0.962)和 VaD(HR=0.865、0.725 和 0.911)的发生显著相关。与 Met+SU 相比,Met+DPP-4i 和 Met+TZD 与 AD 的发生风险显著降低(HR=0.922 和 0.812)。与 TZD 非使用者相比,TZD 使用者的全因痴呆、AD 和 VaD 风险显著降低(HR=0.918、0.925 和 0.859)。
与 SU 相比,将 TZD 或 DPP-4i 作为二线降糖治疗药物添加到治疗方案中可能有助于延缓或预防痴呆的发生。此外,与 TZD 非使用者相比,TZD 使用者在接受双口服药物治疗时,各种类型痴呆的风险显著降低。