From the Department of Psychiatry (J.H., K.Y.K., E.K.), Institute of Behavioral Science in Medicine, and Division of Geriatrics (K.J.K.), Department of Internal Medicine, and Department of Preventive Medicine (C.M.N.), and Graduate School of Medical Science (E.K.), Brain Korea 21 FOUR Project for Medical Science, Yonsei University College of Medicine, Seoul, Republic of Korea; Cancer Big Data Center (D.-W.C.), National Cancer Control Institute, National Cancer Center, Gyeonggi-do, Republic of Korea; and Department of Psychiatry (K.Y.K.), Seoul Metropolitan Government-Seoul National University Boramae Medical Center, Seoul, Republic of Korea.
Neurology. 2023 Apr 25;100(17):e1799-e1811. doi: 10.1212/WNL.0000000000207069. Epub 2023 Feb 15.
Previous studies have reported the protective effect of pioglitazone on dementia in patients with type 2 diabetes mellitus (DM). Recent studies have shown that pioglitazone also lowers the risk of primary and recurrent stroke. Understanding the characteristics of patients particularly associated with the benefits of pioglitazone would facilitate its personalized use by specifying subpopulations during routine clinical care. The aim of this study was to examine the effects of pioglitazone use on dementia in consideration of stroke occurrence.
Using nationwide longitudinal data of patients with DM from the Korean National Health Insurance Service DM cohort (2002-2017), we investigated the association of pioglitazone use with incident dementia in patients with new-onset type 2 DM. The heterogeneity of the treatment effect was examined using exploratory analyses. Using a multistate model, we assessed the extent to which incident stroke affects the association between pioglitazone use and dementia.
Pioglitazone use was associated with a reduced risk of dementia, compared with nonuse (adjusted hazard ratio [aHR] = 0.84, 95% CI 0.75-0.95); the risk reduction in dementia was greater among patients with a history of ischemic heart disease or stroke before DM onset (aHR = 0.46, 95% CI 0.24-0.90; aHR = 0.57, 95% CI 0.38-0.86, respectively). The incidence of stroke was also reduced by pioglitazone use (aHR = 0.81, 95% CI 0.66-1.00). However, when the stroke developed during the observation period of pioglitazone use, such lowered risk of dementia was not observed (aHR = 1.27, 95% CI 0.80-2.04).
Pioglitazone use is associated with a lower risk of dementia in patients with DM, particularly in those with a history of stroke or ischemic heart disease, suggesting the possibility of applying a personalized approach when choosing pioglitazone to suppress dementia in patients with DM.
先前的研究报告了吡格列酮对 2 型糖尿病(DM)患者痴呆的保护作用。最近的研究表明,吡格列酮也降低了原发性和复发性中风的风险。了解与吡格列酮益处特别相关的患者特征将有助于在常规临床护理中通过指定亚群来促进其个体化使用。本研究旨在检查在考虑中风发生的情况下,吡格列酮的使用对痴呆的影响。
使用来自韩国国家健康保险服务糖尿病队列(2002-2017 年)的患者的全国性纵向 DM 患者数据,我们调查了新诊断 2 型 DM 患者中吡格列酮使用与新发痴呆之间的关联。使用探索性分析检查了治疗效果的异质性。使用多状态模型,我们评估了中风对吡格列酮使用与痴呆之间关联的影响程度。
与未使用者相比,吡格列酮使用者痴呆的风险降低(调整后的危险比[aHR] = 0.84,95%CI 0.75-0.95);在 DM 发病前有缺血性心脏病或中风病史的患者中,痴呆的风险降低更为显著(aHR = 0.46,95%CI 0.24-0.90;aHR = 0.57,95%CI 0.38-0.86)。吡格列酮的使用也降低了中风的发生率(aHR = 0.81,95%CI 0.66-1.00)。然而,当在吡格列酮使用期间发生中风时,并未观察到痴呆风险降低(aHR = 1.27,95%CI 0.80-2.04)。
在 DM 患者中,吡格列酮的使用与痴呆风险降低相关,特别是在有中风或缺血性心脏病病史的患者中,这表明在选择吡格列酮来抑制 DM 患者的痴呆时,可以采用个性化方法。