University of California, San Francisco, California, CA, USA.
University of Pennsylvania, Philadelphia, PA, USA; Neuroimage Analytics Laboratory (NAL) and the Biggs Institute Neuroimaging Core (BINC), Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases, University of Texas Health Science Center San Antonio (UTHSCSA), San Antonio, TX, USA.
J Affect Disord. 2023 Jan 1;320:436-441. doi: 10.1016/j.jad.2022.09.164. Epub 2022 Oct 3.
Evidence suggests that depression may be a risk factor for dementia in older adults, but the link between depressive symptoms and brain health earlier in life is less understood. Our aim was to investigate the association between long-term depressive symptoms in young to mid-adulthood and a measure of brain age derived from structural MRI.
From the Coronary Artery Risk Development in Young Adults study, we identified 649 participants (age 23-36 at baseline) with brain MRI and cognitive testing. Long-term depressive symptoms were measured with the Center for Epidemiological Studies Depression scale (CESD) six times across 25 years and analyzed as time-weighted averages (TWA). Brain age was derived using previously validated high dimensional neuroimaging pattern analysis, quantifying individual differences in age-related atrophy. Elevated depressive symptoms were defined as CES-D ≥16. Linear regression was used to test the association between TWA depressive symptoms, brain aging, and cognition.
Each standard deviation (5-points) increment in TWA depression symptoms over 25 years was associated with one-year greater brain age (β: 1.14, 95 % confidence interval [CI]: 0.57 to 1.71). Participants with elevated TWA depressive symptoms had on average a 3-year greater brain age (β: 2.75, 95 % CI: 0.43 to 5.08). Moreover, elevated depressive symptoms were associated with higher odds of poor cognitive function in midlife (OR: 3.30, 95 % CI: 1.37 to 7.97).
Brain age was assessed at one time, limiting our ability to evaluate the temporality of depressive symptoms and brain aging.
Elevated depressive symptoms in early adulthood may have implications for brain health as early as in midlife.
有证据表明,抑郁可能是老年人痴呆的一个风险因素,但在生命早期,抑郁症状与大脑健康之间的联系还不太清楚。我们的目的是研究中青年时期长期的抑郁症状与从结构 MRI 得出的大脑年龄之间的关系。
我们从冠状动脉风险发展在年轻人研究中,确定了 649 名参与者(基线时年龄在 23-36 岁)具有脑 MRI 和认知测试。使用中心流行病学研究抑郁量表(CESD)在 25 年内六次测量长期抑郁症状,并作为时间加权平均值(TWA)进行分析。大脑年龄是使用以前验证过的高维神经影像学模式分析得出的,量化了与年龄相关的萎缩的个体差异。升高的抑郁症状定义为 CES-D≥16。线性回归用于测试 TWA 抑郁症状、大脑老化和认知之间的关系。
在 25 年内,TWA 抑郁症状每增加一个标准差(5 分),大脑年龄就会增加一年(β:1.14,95%置信区间[CI]:0.57 至 1.71)。TWA 抑郁症状升高的参与者平均大脑年龄大 3 岁(β:2.75,95%CI:0.43 至 5.08)。此外,升高的抑郁症状与中年认知功能较差的几率较高相关(OR:3.30,95%CI:1.37 至 7.97)。
大脑年龄仅在一次评估,限制了我们评估抑郁症状和大脑老化之间的时间关系的能力。
在成年早期,升高的抑郁症状可能会对中年的大脑健康产生影响。