West China Biomedical Big Data Center, West China Hospital, Sichuan University, Chengdu, China.
Center of Public Health Sciences, Faculty of Medicine, University of Iceland, Reykjavík, Iceland.
JAMA Neurol. 2020 Jun 1;77(6):700-709. doi: 10.1001/jamaneurol.2020.0117.
Posttraumatic stress disorder (PTSD) has been associated with increased risk for dementia. Less is known, however, about other stress-related disorders and their associations with neurodegenerative diseases.
To examine the association between stress-related disorders and risk for neurodegenerative diseases.
DESIGN, SETTING, AND PARTICIPANTS: This population-matched and sibling cohort study was conducted in Sweden using data from nationwide health registers, including the Swedish National Patient Register. Individuals who received their first diagnosis of stress-related disorders between January 1, 1987, and December 31, 2008, were identified. Individuals who had a history of neurodegenerative diseases, had conflicting or missing information, had no data on family links, or were aged 40 years or younger at the end of the study were excluded. Individuals with stress-related disorders were compared with the general population in a matched cohort design; they were also compared with their siblings in a sibling cohort. Follow-up commenced from the age of 40 years or 5 years after the diagnosis of stress-related disorders, whichever came later, until the first diagnosis of a neurodegenerative disease, death, emigration, or the end of follow-up (December 31, 2013), whichever occurred first. Data analyses were performed from November 2018 to April 2019.
Diagnosis of stress-related disorders (PTSD, acute stress reaction, adjustment disorder, and other stress reactions).
Neurodegenerative diseases were identified through the National Patient Register and classified as primary or vascular. Alzheimer disease, Parkinson disease, and amyotrophic lateral sclerosis were evaluated separately. Cox proportional hazards regression models were used to estimate hazard ratios (HRs) with 95% CIs after controlling for multiple confounders.
The population-matched cohort included 61 748 exposed individuals and 595 335 matched unexposed individuals. A total of 44 839 exposed individuals and their 78 482 unaffected full siblings were included in the sibling cohort analysis. The median (interquartile range) age at the start of follow-up was 47 (41-56) years, and 24 323 (39.4%) of the exposed individuals were male. The median (interquartile range) follow-up was 4.7 (2.1-9.8) years. Compared with unexposed individuals, individuals with a stress-related disorder were at an increased risk of neurodegenerative diseases (HR, 1.57; 95% CI, 1.43-1.73). The risk increase was greater for vascular neurodegenerative diseases (HR, 1.80; 95% CI, 1.40-2.31) than for primary neurodegenerative diseases (HR, 1.31; 95% CI, 1.15-1.48). A statistically significant association was found for Alzheimer disease (HR, 1.36; 95% CI, 1.12-1.67) but not Parkinson disease (HR, 1.20; 95% CI, 0.98-1.47) or amyotrophic lateral sclerosis (HR, 1.20; 95% CI, 0.74-1.96). Results from the sibling cohort corroborated results from the population-matched cohort.
This study showed an association between stress-related disorders and an increased risk of neurodegenerative diseases. The relative strength of this association for vascular neurodegenerative diseases suggests a potential cerebrovascular pathway.
创伤后应激障碍(PTSD)与痴呆风险增加有关。然而,人们对其他应激相关障碍及其与神经退行性疾病的关系了解较少。
研究应激相关障碍与神经退行性疾病风险之间的关系。
设计、地点和参与者:本研究采用瑞典全国健康登记处的数据,包括瑞典国家患者登记处,进行了一项人群匹配和同胞队列研究。确定了在 1987 年 1 月 1 日至 2008 年 12 月 31 日期间首次诊断为应激相关障碍的个体。排除了有神经退行性疾病病史、信息冲突或缺失、没有家庭关系数据或在研究结束时年龄在 40 岁或以下的个体。应激相关障碍患者与一般人群进行匹配队列设计比较;他们还与同胞进行了同胞队列比较。随访从 40 岁或诊断应激相关障碍后 5 年开始,以较晚者为准,直到首次诊断出神经退行性疾病、死亡、移民或随访结束(2013 年 12 月 31 日),以先发生者为准。数据分析于 2018 年 11 月至 2019 年 4 月进行。
诊断为应激相关障碍(创伤后应激障碍、急性应激反应、适应障碍和其他应激反应)。
通过国家患者登记处确定神经退行性疾病,并分为原发性或血管性。分别评估阿尔茨海默病、帕金森病和肌萎缩侧索硬化症。使用 Cox 比例风险回归模型,在控制多种混杂因素后,估计风险比(HR)及其 95%置信区间。
人群匹配队列纳入了 61748 名暴露个体和 595335 名匹配未暴露个体。共有 44839 名暴露个体及其 78482 名未受影响的全同胞纳入了同胞队列分析。随访开始时的中位(四分位间距)年龄为 47(41-56)岁,24323 名(39.4%)暴露个体为男性。中位(四分位间距)随访时间为 4.7(2.1-9.8)年。与未暴露个体相比,应激相关障碍患者发生神经退行性疾病的风险增加(HR,1.57;95%CI,1.43-1.73)。血管性神经退行性疾病的风险增加(HR,1.80;95%CI,1.40-2.31)大于原发性神经退行性疾病(HR,1.31;95%CI,1.15-1.48)。发现阿尔茨海默病(HR,1.36;95%CI,1.12-1.67)存在统计学显著关联,但帕金森病(HR,1.20;95%CI,0.98-1.47)和肌萎缩侧索硬化症(HR,1.20;95%CI,0.74-1.96)没有关联。同胞队列的结果与人群匹配队列的结果一致。
本研究表明应激相关障碍与神经退行性疾病风险增加之间存在关联。这种关联对血管性神经退行性疾病的相对强度表明存在潜在的脑血管途径。