Cortical thickness and low-grade inflammation moderate the association between depressive symptoms and cognitive function in early widowhood: A preliminary study

IF 8.8 2区 医学 Q1 IMMUNOLOGY
E. Lydia Wu-Chung , Kristen M. Kennedy , Luis D. Medina , Paul E. Schulz , Frederick L. Oswald , Cobi J. Heijnen , Stephanie L. Leal , Bryan T. Denny , Christopher P. Fagundes
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引用次数: 0

Abstract

Spousal bereavement is a major life stressor that significantly increases the risk of dementia. However, it remains unclear how the bereavement experience accelerates cognitive aging. In the broader neurocognitive aging literature, depression and cognitive function are closely linked, such that depression is sometimes accompanied by cognitive impairments. Individual differences in depression-related cognitive function may depend on low-grade inflammation and cortical atrophy, two phenomena implicated in cognitive dysfunction and dementia risk. No study to date has examined how psychobiological health relates to cognition in early widowhood. Among recently bereaved spouses, we examined (1) whether depressive symptom severity accounted for variations in cognitive performance and (2) whether the association between depressive symptoms and cognitive function depended on one’s biological profile. In a sample of 68 bereaved spouses, depressive symptom severity, cortical thickness in 8 a priori regions, serum proinflammatory composite (IL-6, sIL-6R, TNF-⍺, sTNFRI, and sTNFRII), and a battery of cognitive tests were evaluated at 6 months post-loss. Using multiple linear regression to test hypotheses, we observed a significant negative association between depressive symptoms and performance on global cognitive function, cognitive inhibition, visuospatial processing, and working memory. The interaction between depressive symptoms and the cortical signature composite on global cognition was statistically significant: Depressive symptoms were negatively associated with global cognitive function, only for widow(er)s with average and less than average cortical gray matter. The interaction between depressive symptoms and low-grade inflammation on cognitive inhibition was also statistically significant: Depressive symptoms were negatively associated with cognitive inhibition only for those with average and higher than average levels of the serum inflammatory composite. This suggests that widow(er)s experiencing higher levels of depressive symptoms were more likely to have poorer cognitive function, especially if they presented with a more adverse biological profile (i.e., higher cytokine levels and less cortical gray matter than average); in contrast, for widow(er)s with less adverse biological profiles, there was no evidence for an association between depressive symptoms and cognitive function. This exploratory study identifies psychobiological correlates of cognitive function in early widowhood, offering insight into risk factors for abnormal cognitive aging after profound interpersonal loss.
皮层厚度和轻度炎症调节早期丧偶抑郁症状和认知功能之间的关系:一项初步研究
配偶丧亲是一个主要的生活压力源,会显著增加患痴呆症的风险。然而,尚不清楚丧亲经历如何加速认知衰老。在更广泛的神经认知衰老文献中,抑郁症和认知功能密切相关,因此抑郁症有时伴随着认知障碍。抑郁症相关认知功能的个体差异可能取决于低度炎症和皮质萎缩,这两种现象与认知功能障碍和痴呆风险有关。迄今为止,还没有研究调查过心理生物学健康与早期丧偶认知之间的关系。在最近失去亲人的配偶中,我们研究了(1)抑郁症状的严重程度是否与认知表现的变化有关;(2)抑郁症状和认知功能之间的联系是否取决于一个人的生物学特征。在68名丧偶配偶的样本中,在丧偶后6 个月评估8个先天区域的抑郁症状严重程度、血清促炎复合物(IL-6、sIL-6R、TNF- 、sTNFRI和sTNFRII)和一系列认知测试。使用多元线性回归检验假设,我们观察到抑郁症状与整体认知功能、认知抑制、视觉空间加工和工作记忆的表现之间存在显著的负相关。抑郁症状与整体认知的皮质特征复合物之间的相互作用具有统计学意义:抑郁症状与整体认知功能呈负相关,仅适用于皮质灰质平均和低于平均水平的寡妇(er)。抑郁症状和低度炎症对认知抑制的相互作用也具有统计学意义:仅在血清炎症复合物水平平均和高于平均水平的患者中,抑郁症状与认知抑制呈负相关。这表明,经历较高程度抑郁症状的寡妇(鳏夫)更有可能具有较差的认知功能,特别是如果他们表现出更不利的生物学特征(即,细胞因子水平较高,皮层灰质低于平均水平);相反,对于生理状况较差的寡妇,没有证据表明抑郁症状与认知功能之间存在关联。本探索性研究确定了早期丧偶认知功能的心理生物学相关性,为深刻的人际丧失后异常认知衰老的危险因素提供了见解。
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来源期刊
CiteScore
29.60
自引率
2.00%
发文量
290
审稿时长
28 days
期刊介绍: Established in 1987, Brain, Behavior, and Immunity proudly serves as the official journal of the Psychoneuroimmunology Research Society (PNIRS). This pioneering journal is dedicated to publishing peer-reviewed basic, experimental, and clinical studies that explore the intricate interactions among behavioral, neural, endocrine, and immune systems in both humans and animals. As an international and interdisciplinary platform, Brain, Behavior, and Immunity focuses on original research spanning neuroscience, immunology, integrative physiology, behavioral biology, psychiatry, psychology, and clinical medicine. The journal is inclusive of research conducted at various levels, including molecular, cellular, social, and whole organism perspectives. With a commitment to efficiency, the journal facilitates online submission and review, ensuring timely publication of experimental results. Manuscripts typically undergo peer review and are returned to authors within 30 days of submission. It's worth noting that Brain, Behavior, and Immunity, published eight times a year, does not impose submission fees or page charges, fostering an open and accessible platform for scientific discourse.
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