Kaup Allison R, Byers Amy L, Falvey Cherie, Simonsick Eleanor M, Satterfield Suzanne, Ayonayon Hilsa N, Smagula Stephen F, Rubin Susan M, Yaffe Kristine
Research Service, San Francisco Veterans Affairs Medical Center, San Francisco, California2Department of Psychiatry, University of California, San Francisco.
Department of Psychiatry, University of California, San Francisco.
JAMA Psychiatry. 2016 May 1;73(5):525-31. doi: 10.1001/jamapsychiatry.2016.0004.
Depression has been identified as a risk factor for dementia. However, most studies have measured depressive symptoms at only one time point, and older adults may show different patterns of depressive symptoms over time.
To investigate the association between trajectories of depressive symptoms and risk of dementia in older adults.
DESIGN, SETTING, AND PARTICIPANTS: This was a prospective cohort investigation of black and white community-dwelling older adults in the Health, Aging, and Body Composition study. Participants were enrolled between May 1997 and June 1998 and followed up through 2001-2002. The dates of this analysis were September 2014 to December 2015. The setting was community research centers in Memphis, Tennessee, and Pittsburgh, Pennsylvania. Trajectories of depressive symptoms were assessed from baseline to year 5. Symptoms were measured with the Center for Epidemiologic Studies Depression Scale Short Form, and trajectories were calculated using latent class growth curve analysis.
Incident dementia through year 11, determined by dementia medication use, hospital records, or significant cognitive decline (≥1.5 SD race-specific decline on the Modified Mini-Mental State Examination). We examined the association between depressive symptom trajectories and dementia incidence using Cox proportional hazards regression models adjusted for demographics, health factors that differed between groups, and cognition during the depressive symptom assessment period (baseline to year 5).
The analytic cohort included 2488 black and white older adults with repeated depressive symptom assessments from baseline to year 5 who were free of dementia throughout that period. Their mean (SD) age at baseline was 74.0 (2.8) years, and 53.1% (n = 1322) were female. The following 3 depressive symptom trajectories were identified: consistently minimal symptoms (62.0% [n = 1542] of participants), moderate and increasing symptoms (32.2% [n = 801] of participants), and high and increasing symptoms (5.8% [n = 145] of participants). Compared with the consistently minimal trajectory, having a high and increasing depressive symptom trajectory was associated with significantly increased risk of dementia (fully adjusted hazard ratio, 1.94; 95% CI, 1.30-2.90), while the moderate and increasing trajectory was not associated with risk of dementia after full adjustment. Sensitivity analyses indicated that the high and increasing trajectory was associated with dementia incidence, while depressive symptoms at individual time points were not.
Older adults with a longitudinal pattern of high and increasing depressive symptoms are at high risk for dementia. Individuals' trajectory of depressive symptoms may inform dementia risk more accurately than one-time assessment of depressive symptoms.
抑郁症已被确定为痴呆症的一个风险因素。然而,大多数研究仅在一个时间点测量抑郁症状,而老年人的抑郁症状可能随时间呈现不同模式。
调查老年人抑郁症状轨迹与痴呆症风险之间的关联。
设计、背景和参与者:这是一项对健康、衰老和身体成分研究中社区居住的黑人和白人老年人进行的前瞻性队列研究。参与者于1997年5月至1998年6月入组,并随访至2001 - 2002年。本分析的日期为2014年9月至2015年12月。研究地点是田纳西州孟菲斯市和宾夕法尼亚州匹兹堡市的社区研究中心。从基线到第5年评估抑郁症状轨迹。使用流行病学研究中心抑郁量表简表测量症状,并使用潜在类别增长曲线分析计算轨迹。
到第11年的新发痴呆症,通过痴呆症药物使用、医院记录或显著认知衰退(改良简易精神状态检查中种族特异性下降≥1.5标准差)确定。我们使用Cox比例风险回归模型检查抑郁症状轨迹与痴呆症发病率之间的关联,该模型针对人口统计学、组间不同的健康因素以及抑郁症状评估期(基线到第5年)的认知情况进行了调整。
分析队列包括2488名黑人和白人老年人,他们从基线到第5年进行了多次抑郁症状评估,且在此期间均无痴呆症。他们在基线时的平均(标准差)年龄为74.0(2.8)岁,53.1%(n = 1322)为女性。确定了以下3种抑郁症状轨迹:始终症状轻微(62.0% [n = 1542] 的参与者)、症状中度且逐渐增加(32.2% [n = 801] 的参与者)以及症状严重且逐渐增加(5.8% [n = 145] 的参与者)。与始终症状轻微的轨迹相比,抑郁症状严重且逐渐增加的轨迹与痴呆症风险显著增加相关(完全调整后的风险比为1.94;95%置信区间为1.30 - 2.90),而症状中度且逐渐增加的轨迹在完全调整后与痴呆症风险无关。敏感性分析表明,症状严重且逐渐增加的轨迹与痴呆症发病率相关,而单个时间点的抑郁症状则不然。
抑郁症状呈纵向严重且逐渐增加模式的老年人患痴呆症的风险很高。个体的抑郁症状轨迹可能比一次性评估抑郁症状更准确地反映痴呆症风险。