Shih Hsin-I, Lin Che-Chen, Tu Yi-Fang, Chang Chia-Ming, Hsu Hsiang-Chin, Chi Chih-Hsien, Kao Chia-Hung
From the Department of Emergency Medicine, National Cheng Kung University Hospital (H-IS, H-CH); Department of Emergency Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan (H-IS, C-HC); Department of Pediatrics, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan (Y-FT); Management Office for Health Data, China Medical University Hospital, Taichung (C-CL); Department of Internal Medicine, Division of Geriatrics and Gerontology, National Cheng Kung University Hospital (C-MC); Institute of Gerontology, College of Medicine, National Cheng Kung University, Tainan (C-MC); Graduate Institute of Clinical Medical Science and School of Medicine, College of Medicine, China Medical University (C-HK); and Department of Nuclear Medicine and PET Center, China Medical University Hospital, Taichung, Taiwan (C-HK).
Medicine (Baltimore). 2015 May;94(17):e809. doi: 10.1097/MD.0000000000000809.
We evaluate the effects of zolpidem use to develop dementia or Alzheimer disease from the Taiwan National Health Insurance Research Database (NHIRD).A retrospective population-based nested case-control study. Newly diagnosed dementia patients 65 years and older and controls were sampled. A total of 8406 dementia and 16,812 control subjects were enrolled from Taiwan NHIRD during 2006 to 2010. The relationships between zolpidem use and dementia were measured using odds and adjusted odds ratios. The relationship between the average cumulative doses for zolpidem and dementia was also analyzed.Zolpidem alone or with other underlying diseases, such as hypertension, diabetes, and stroke, was significantly associated with dementia after controlling for potential confounders, such as age, sex, coronary artery disease, diabetes, anti-hypertension drugs, stroke, anticholesterol statin drugs, depression, anxiety, benzodiazepine, anti-psychotic, and anti-depressant agents' use (Adjusted OR = 1.33, 95% CI 1.24-1.41). Zolpidem use also has significant dose-response effects for most of the types of dementia. In patient with Alzheimer diseases, the effects of zolpidem among patients with Alzheimer's disease remained obscure. The adjusted OR for patients whose cumulative exposure doses were between 170 and 819 mg/year (adjusted OR: 1.65, 95% CI 1.08-2.51, P = 0.0199) was significant; however, the effects for lower and higher cumulative dose were not significant.Zolpidem used might be associated with increased risk for dementia in elderly population. Increased accumulative dose might have higher risk to develop dementia, especially in patients with underlying diseases such as hypertension, diabetes, and stroke.
我们利用台湾国民健康保险研究数据库(NHIRD)评估使用唑吡坦与罹患痴呆症或阿尔茨海默病之间的关系。一项基于人群的回顾性巢式病例对照研究。选取65岁及以上新诊断的痴呆症患者及对照。2006年至2010年期间,从台湾NHIRD中纳入了8406例痴呆症患者和16812例对照。使用比值比和调整后的比值比来衡量唑吡坦使用与痴呆症之间的关系。还分析了唑吡坦的平均累积剂量与痴呆症之间的关系。在控制了年龄、性别、冠状动脉疾病、糖尿病、抗高血压药物、中风、抗胆固醇他汀类药物、抑郁症、焦虑症、苯二氮䓬类药物、抗精神病药物和抗抑郁药物使用等潜在混杂因素后,单独使用唑吡坦或与高血压、糖尿病和中风等其他基础疾病合并使用,均与痴呆症显著相关(调整后的OR = 1.33,95% CI 1.24 - 1.41)。唑吡坦的使用对大多数类型的痴呆症也具有显著的剂量反应效应。在阿尔茨海默病患者中,唑吡坦的影响仍不明确。累积暴露剂量在170至819毫克/年之间的患者调整后的OR(调整后的OR:1.65,95% CI 1.08 - 2.51,P = 0.0199)具有显著性;然而,较低和较高累积剂量的影响并不显著。使用唑吡坦可能与老年人群患痴呆症的风险增加有关。累积剂量增加可能患痴呆症的风险更高,尤其是在患有高血压、糖尿病和中风等基础疾病的患者中。