Department of Psychiatry, China Medical University Hospital, China Medical University, Taichung, Taiwan.
Translational Medicine Program, National Taiwan University and Academia Sinica, Taipei, Taiwan.
J Clin Psychiatry. 2017 Feb;78(2):e139-e145. doi: 10.4088/JCP.15m10304.
Current evidence for the association between use of lithium and risk of dementia is mixed. The objective of this study was to assess the risk of Alzheimer's disease associated with use of lithium.
A population-based, nested case-control study was conducted using data from the National Health Insurance Research Database in 2002 covering 24.5 million beneficiaries of the Taiwan National Health Insurance Program from January 1, 1997, to December 31, 2009. A total of 2,548,625 older people were included in the study cohort. We analyzed 63,347 cases of Alzheimer's disease (ICD-9-CM codes 290.0-290.3, and 331.0) and 2 controls per case matched by age, sex, and index date (the date of the first AD claim). Conditional logistic regression was performed, adjusting for health care utilization, use of other common mood stabilizers (valproic acid and carbamazepine), hypothyroidism, type 2 diabetes, hypertension, hyperlipidemia, chronic kidney disease, epilepsy, schizophrenia, and bipolar disorder.
We identified 63,347 cases with Alzheimer's disease and 126,694 controls. The adjusted odds ratio (aOR) of Alzheimer's disease risk with lithium use was 1.79 (95% confidence interval [CI], 1.34-2.38) in the general population. However, when we restricted the analyses to patients with bipolar disorder to minimize potential confounding by indication, lithium was not associated with Alzheimer's disease risk (aOR = 1.36; 95% CI, 0.89-2.09), and there were no apparent trends of greater risk with increasing duration or dose.
These findings do not support an increased or decreased risk of lithium use with Alzheimer's disease when taking into account potential confounding by indication. Further investigations of the effect of lithium with dementia need to consider the influence of confounding by indication.
目前关于锂的使用与痴呆风险之间关联的证据存在差异。本研究旨在评估锂的使用与阿尔茨海默病风险的相关性。
采用基于人群的巢式病例对照研究,数据来源于 2002 年台湾全民健康保险研究数据库,涵盖了 1997 年 1 月 1 日至 2009 年 12 月 31 日期间全民健康保险计划的 2450 万受益人的数据。共有 254.8625 名老年人纳入研究队列。我们分析了 63347 例阿尔茨海默病(ICD-9-CM 代码 290.0-290.3 和 331.0)病例和每个病例匹配的 2 名对照,匹配因素包括年龄、性别和索引日期(首次 AD 索赔日期)。采用条件逻辑回归,调整了医疗保健利用、其他常见心境稳定剂(丙戊酸和卡马西平)的使用、甲状腺功能减退症、2 型糖尿病、高血压、高血脂、慢性肾脏病、癫痫、精神分裂症和双相情感障碍。
我们确定了 63347 例阿尔茨海默病病例和 126694 例对照。在一般人群中,锂的使用与阿尔茨海默病风险的调整后比值比(aOR)为 1.79(95%置信区间[CI],1.34-2.38)。然而,当我们将分析仅限于双相情感障碍患者,以尽量减少潜在的混杂因素,锂与阿尔茨海默病风险无关(aOR=1.36;95%CI,0.89-2.09),并且没有明显的风险随使用时间或剂量增加而增加的趋势。
这些发现不支持锂的使用与阿尔茨海默病风险增加或降低之间的关联,在考虑到潜在的混杂因素时。需要进一步研究锂与痴呆的影响,需要考虑混杂因素的影响。