Neuropsychopharmacology Research Group (DK, RW, KLL, NH, DG), Sunnybrook Research Institute, Toronto, Ontario, Canada; Department of Pharmacology and Toxicology (DK, RW, KLL), University of Toronto, Toronto, Ontario, Canada.
Neuropsychopharmacology Research Group (DK, RW, KLL, NH, DG), Sunnybrook Research Institute, Toronto, Ontario, Canada; Department of Pharmacology and Toxicology (DK, RW, KLL), University of Toronto, Toronto, Ontario, Canada.
Am J Geriatr Psychiatry. 2021 Sep;29(9):917-926. doi: 10.1016/j.jagp.2020.12.031. Epub 2021 Jan 6.
Our understanding of why older adults with depression are at increased risk of Alzheimer's disease (AD) remains incomplete. Most adults living with AD are women, and women have a near twofold lifetime risk of depression. We examined the risk of depression upon incident AD, and how sex influences this risk.
Using the National Alzheimer's Coordinating Center database, older adults (age 50+) with normal cognition, who visited memory clinics across the United States between September 2005 and December 2019, were followed until first diagnosis of AD or loss to follow up. Multivariable survival analyses were performed to determine if recent and/or remote depression were independent risk factors for AD, if this depression-related risk exists for each sex or was moderated by sex.
Six hundred and fifty-two of 10,739 enrolled participants developed AD over a median follow-up of 55.3 months. Recent depression (active within the last 2 years) was independently associated with increased risk of AD (hazard ratio [HR] = 2.0; 95%CI, 1.5-2.6) while a remote history of depression was not (HR = 1.0; 95%CI, 0.7-1.5). After stratification by sex, recent depression was an independent predictor in females (HR = 2.3; 95%CI, 1.7-3.1) but not in males (HR = 1.4; 95%CI, 0.8-2.6). No interaction between recent depression and sex was observed.
Only a recent history of depression was associated with higher risk of AD. This association was significant among women only, but was not moderated by sex. Future analyses should determine if these findings extend to other populations and may be explained by variable distribution of neurobiological or other modifiable risk factors between the sexes.
我们对于为什么老年抑郁症患者患阿尔茨海默病(AD)的风险增加仍了解不足。大多数患有 AD 的成年人是女性,而女性一生中患抑郁症的风险几乎是男性的两倍。我们研究了 AD 发病后抑郁的风险,以及性别如何影响这种风险。
利用国家阿尔茨海默病协调中心数据库,对在美国各地记忆诊所就诊的年龄在 50 岁及以上、认知正常的老年人进行随访,随访至首次诊断为 AD 或失访。采用多变量生存分析来确定近期和/或远期抑郁是否为 AD 的独立危险因素,这种与抑郁相关的风险是否存在于每一种性别中,或是否受性别影响。
在中位随访 55.3 个月期间,10739 名入组参与者中有 652 人发展为 AD。近期抑郁(在过去 2 年内活跃)与 AD 风险增加独立相关(风险比[HR] = 2.0;95%CI,1.5-2.6),而既往抑郁史则无此相关性(HR = 1.0;95%CI,0.7-1.5)。按性别分层后,近期抑郁是女性的独立预测因素(HR = 2.3;95%CI,1.7-3.1),但不是男性的独立预测因素(HR = 1.4;95%CI,0.8-2.6)。未观察到近期抑郁与性别之间的相互作用。
只有近期的抑郁史与 AD 风险增加相关。这种关联仅在女性中显著,但不受性别影响。未来的分析应确定这些发现是否适用于其他人群,以及这些发现是否可以通过性别之间神经生物学或其他可改变的风险因素的分布不同来解释。