Department of Clinical Epidemiology, Aarhus University and Aarhus University Hospital, Aarhus, Denmark.
Department of Neurology, Hospital of the University of Pennsylvania, Philadelphia.
JAMA Neurol. 2023 Sep 1;80(9):949-958. doi: 10.1001/jamaneurol.2023.2309.
Late-life depressive symptoms are associated with subsequent dementia diagnosis and may be an early symptom or response to preclinical disease. Evaluating associations with early- and middle-life depression will help clarify whether depression influences dementia risk.
To examine associations of early-, middle-, and late-life depression with incident dementia.
DESIGN, SETTING, AND PARTICIPANTS: This was a nationwide, population-based, cohort study conducted from April 2020 to March 2023. Participants included Danish citizens from the general population with depression diagnoses who were matched by sex and birth year to individuals with no depression diagnosis. Participants were followed up from 1977 to 2018. Excluded from analyses were individuals followed for less than 1 year, those younger than 18 years, or those with baseline dementia.
Depression was defined using diagnostic codes from the International Classification of Diseases (ICD) within the Danish National Patient Registry (DNPR) and Danish Psychiatric Central Research Register (DPCRR).
Incident dementia was defined using ICD diagnostic codes within the DPCRR and DNPR. Cox proportional hazards regression was used to examine associations between depression and dementia adjusting for education, income, cardiovascular disease, chronic obstructive pulmonary disease, diabetes, anxiety disorders, stress disorders, substance use disorders, and bipolar disorder. Analyses were stratified by age at depression diagnosis, years since index date, and sex.
There were 246 499 individuals (median [IQR] age, 50.8 [34.7-70.7] years; 159 421 women [64.7%]) with diagnosed depression and 1 190 302 individuals (median [IQR] age, 50.4 [34.6-70.0] years; 768 876 women [64.6%]) without depression. Approximately two-thirds of those diagnosed with depression were diagnosed before the age of 60 years (684 974 [67.7%]). The hazard of dementia among those diagnosed with depression was 2.41 times that of the comparison cohort (95% CI, 2.35-2.47). This association persisted when the time elapsed from the index date was longer than 20 to 39 years (hazard ratio [HR], 1.79; 95% CI, 1.58-2.04) and among those diagnosed with depression in early, middle, or late life (18-44 years: HR, 3.08; 95% CI, 2.64-3.58; 45-59 years: HR, 2.95; 95% CI, 2.75-3.17; ≥60 years: HR, 2.31; 95% CI, 2.25-2.38). The overall HR was greater for men (HR, 2.98; 95% CI, 2.84-3.12) than for women (HR, 2.21; 95% CI, 2.15-2.27).
Results suggest that the risk of dementia was more than doubled for both men and women with diagnosed depression. The persistent association between dementia and depression diagnosed in early and middle life suggests that depression may increase dementia risk.
晚年抑郁症状与随后的痴呆诊断有关,可能是疾病前阶段的早期症状或反应。评估早、中年期抑郁与痴呆的关联有助于阐明抑郁是否会影响痴呆风险。
检查早、中、晚年期抑郁与痴呆发病的关联。
设计、地点和参与者:这是一项全国性的、基于人群的队列研究,于 2020 年 4 月至 2023 年 3 月进行。参与者包括丹麦普通人群中患有抑郁诊断的公民,他们通过性别和出生年份与没有抑郁诊断的个体相匹配。参与者从 1977 年至 2018 年被跟踪。未纳入分析的是随访时间少于 1 年、年龄小于 18 岁或基线时患有痴呆的个体。
抑郁使用丹麦国家患者登记处(DNPR)和丹麦精神病学中央研究登记处(DPCRR)中的国际疾病分类(ICD)诊断代码来定义。
使用 DPCRR 和 DNPR 中的 ICD 诊断代码定义痴呆发病。使用 Cox 比例风险回归检查抑郁与痴呆之间的关联,调整了教育、收入、心血管疾病、慢性阻塞性肺疾病、糖尿病、焦虑障碍、应激障碍、物质使用障碍和双相情感障碍。分析按抑郁诊断时的年龄、距索引日期的年数和性别进行分层。
共有 246499 名(中位数[IQR]年龄,50.8 [34.7-70.7]岁;159421 名女性[64.7%])被诊断患有抑郁症和 1190302 名(中位数[IQR]年龄,50.4 [34.6-70.0]岁;768876 名女性[64.6%])未患抑郁症的个体。大约三分之二的抑郁症患者是在 60 岁之前被诊断出来的(684974 人[67.7%])。与对照组相比,被诊断患有抑郁症的个体痴呆的风险高出 2.41 倍(95%CI,2.35-2.47)。当从索引日期开始的时间超过 20 至 39 年时(风险比[HR],1.79;95%CI,1.58-2.04),这种关联仍然存在,并且在早、中、晚生命期间被诊断为抑郁症的个体中也存在(18-44 岁:HR,3.08;95%CI,2.64-3.58;45-59 岁:HR,2.95;95%CI,2.75-3.17;≥60 岁:HR,2.31;95%CI,2.25-2.38)。男性(HR,2.98;95%CI,2.84-3.12)的总体 HR 大于女性(HR,2.21;95%CI,2.15-2.27)。
结果表明,患有抑郁症的男性和女性痴呆的风险增加了一倍以上。痴呆与早期和中年期诊断的抑郁症之间持续存在的关联表明,抑郁症可能会增加痴呆的风险。