From the Univ. Bordeaux (L.G.), Inserm, Bordeaux Population Health Research Center, Team VINTAGE, UMR 1219; Inserm, CIC1401-EC, Bordeaux, France; Department of Epidemiology (A.Z.A.H., F.M., P.L.), Mailman School of Public Health, Columbia University, NY; Division of Medicine (T.E.), Miller School of Medicine, University of Miami, FL; Clinical Research Institute (M.E.), Department of Internal Medicine, American University of Beirut, Lebanon; and Departments of Psychiatry (E.V., K.Y.), Neurology, and Epidemiology and Biostatistics, University of California, San Francisco.
Neurology. 2024 Jul;103(1):e209510. doi: 10.1212/WNL.0000000000209510. Epub 2024 Jun 12.
The nature of associations between depressive symptoms and cognition early in the life course remains unclear, and racial differences in these associations are not well characterized. The aim of this study was to examine the relationship between trajectories of depressive symptom over 20 years, beginning in young adulthood, and cognitive functions in middle-age among Black and White adults.
We used prospective data from participants of the Coronary Artery Risk Development in Young Adults Study. Depressive symptoms were measured at 5 study visits between 1990 and 2010 using the Center for Epidemiologic Studies Depression scale. We used latent class group-based modeling to identify 4 trajectories: "persistently low," "persistently medium," "medium decreasing," and "high increasing" depressive symptoms. In 2015, cognitive function was measured using the Digit Symbol Substitution Test (DSST), Stroop test (reverse coded), and Rey Auditory-Verbal Learning Test (RAVLT).We excluded participants who missed the cognitive battery or had no depressive symptoms measurements, resulting in a total of 3,117 participants. All cognitive tests were standardized, and linear regression was used to relate depressive trajectories with 2015 cognitive functions.
The mean [SD] baseline age was 30.1 [3.6] years, and 57% were female. The associations between depressive symptoms and cognition significantly differed by race ( < 0.05). Among Black individuals, compared with having "persistently low," having "medium decreasing," "persistently medium," or "high increasing" depressive symptoms were associated with worse verbal memory, processing speed, and executive function scores (RAVLT persistently medium vs low: β = -0.30, 95% CI -0.48 to -0.12; and high increasing vs low: β = -0.49, 95% CI -0.70 to -0.27; DSST persistently medium vs low: β = -0.28, 95% CI -0.47 to -0.09; and high increasing vs low: β = -0.64, 95% CI -0.87 to -0.42; Stroop persistently medium vs low: β = -0.46, 95% CI -0.70 to -0.23; and high increasing vs low: β = -0.76, 95% CI -1.04 to -0.47). Associations were slightly weaker among White individuals, but we still found that having 'high increasing' depressive symptoms was associated with worse verbal memory and processing speed scores (high increasing vs low: β = -0.38, 95% CI -0.61 to -0.15; and β = -0.40, 95% CI -0.63 to -0.18, respectively).
Prolonged exposure to elevated depressive symptoms beginning in young adulthood may result in worse cognitive function over midlife. This association was stronger among Black adults.
抑郁症状与生命早期认知之间的关联性质尚不清楚,且这些关联在不同种族之间的差异也尚未得到很好的描述。本研究旨在探讨始于成年早期的 20 年间抑郁症状轨迹与黑人和白人成年人中年认知功能之间的关系。
我们使用了来自冠状动脉风险发展青年研究参与者的前瞻性数据。1990 年至 2010 年间,使用中心流行病学研究抑郁量表在 5 次研究访问中测量抑郁症状。我们使用潜在类别基于组的建模来确定 4 种轨迹:“持续低”、“持续中”、“中降”和“高增”抑郁症状。在 2015 年,使用数字符号替代测试(DSST)、斯特鲁普测试(反向编码)和 Rey 听觉言语学习测试(RAVLT)测量认知功能。我们排除了错过认知测试或没有抑郁症状测量的参与者,因此共有 3117 名参与者。所有认知测试均进行了标准化,线性回归用于将抑郁轨迹与 2015 年的认知功能联系起来。
平均[SD]基线年龄为 30.1[3.6]岁,57%为女性。抑郁症状与认知之间的关联在种族间差异显著(<0.05)。在黑人个体中,与“持续低”相比,“中降”、“持续中”或“高增”的抑郁症状与较差的言语记忆、加工速度和执行功能评分相关(RAVLT 持续中 vs 低:β=-0.30,95%CI-0.48 至-0.12;高增 vs 低:β=-0.49,95%CI-0.70 至-0.27;DSST 持续中 vs 低:β=-0.28,95%CI-0.47 至-0.09;高增 vs 低:β=-0.64,95%CI-0.87 至-0.42;斯特鲁普持续中 vs 低:β=-0.46,95%CI-0.70 至-0.23;高增 vs 低:β=-0.76,95%CI-1.04 至-0.47)。在白人个体中,关联稍弱,但我们仍然发现“高增”的抑郁症状与较差的言语记忆和加工速度评分相关(高增 vs 低:β=-0.38,95%CI-0.61 至-0.15;β=-0.40,95%CI-0.63 至-0.18)。
始于成年早期的长期暴露于升高的抑郁症状可能导致中年认知功能下降。这种关联在黑人成年人中更强。