Division of Geriatric Psychiatry, Sunnybrook Health Sciences Centre and University of Toronto, Toronto, Ontario, Canada.
Sunnybrook Research Institute and Department of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.
Am J Geriatr Psychiatry. 2018 Aug;26(8):819-827. doi: 10.1016/j.jagp.2018.05.002. Epub 2018 May 9.
Older adults with depression are at increased risk of Alzheimer dementia, but predictors of increased risk remain incompletely understood. We aim to identify characteristics of older adults with depression most at risk of progressing to Alzheimer dementia. Identification of high-risk subgroups could facilitate future interventional strategies to reduce risk of Alzheimer dementia in older adults with depression.
Using data from the National Alzheimer's Coordinating Center, 1,965 participants with clinically defined depression and mild cognitive impairment at baseline were followed until development of Alzheimer dementia or loss to follow-up.
Seven hundred and eighty (39.7%) developed Alzheimer dementia over a median follow-up duration of 27 months. In survival analyses, age (hazard ratio [HR] 1.04, 95% 1.03-1.05), baseline Mini-Mental State Exam (HR 0.85, 95% confidence interval 0.83-0.87), amnestic subtype of mild cognitive impairment (HR 1.66, 95% 1.30-2.12), presence of APOE4 allele (HR 1.99, 1.69-2.36), and presence of active depression within the last two years (HR 1.44, 95% confidence interval 1.16-1.79) were all independently associated with increased risk of Alzheimer dementia. Six hundred and fifty-six (41.7%) participants with mild cognitive impairment and active depression within the last two years developed Alzheimer dementia compared to 120 (31.6%) of those with a more remote history of depression.
Older adults with depression and mild cognitive impairment demonstrated a high rate of progression to Alzheimer dementia over a relatively short duration of follow-up. Individuals with a combination of mild cognitive impairment and recently active depression are a particularly high-risk subgroup.
患有抑郁症的老年人患阿尔茨海默病痴呆的风险增加,但风险增加的预测因素仍不完全清楚。我们的目的是确定患有抑郁症的老年人中最有可能发展为阿尔茨海默病痴呆的特征。确定高风险亚组可以促进未来针对抑郁症老年人的干预策略,以降低他们患阿尔茨海默病痴呆的风险。
使用来自国家阿尔茨海默病协调中心的数据,在基线时患有临床定义的抑郁症和轻度认知障碍的 1965 名参与者被随访,直到发展为阿尔茨海默病痴呆或失访。
780 人(39.7%)在中位数为 27 个月的随访期间发展为阿尔茨海默病痴呆。在生存分析中,年龄(风险比 [HR] 1.04,95%置信区间 1.03-1.05)、基线简易精神状态检查(HR 0.85,95%置信区间 0.83-0.87)、遗忘型轻度认知障碍亚型(HR 1.66,95%置信区间 1.30-2.12)、APOE4 等位基因(HR 1.99,1.69-2.36)和过去两年内存在活跃性抑郁症(HR 1.44,95%置信区间 1.16-1.79)均与阿尔茨海默病痴呆风险增加独立相关。在过去两年内有轻度认知障碍和活跃性抑郁症的 656 名参与者与仅有较遥远抑郁症病史的 120 名参与者相比,发展为阿尔茨海默病痴呆的比例更高(656/656[100%] vs 120/120[100%])。
患有抑郁症和轻度认知障碍的老年人在相对较短的随访期间有很高的进展为阿尔茨海默病痴呆的风险。患有轻度认知障碍和近期活跃性抑郁症的个体是一个特别高风险的亚组。