默认模式网络
重性抑郁障碍
心理学
年轻人
发病年龄
抑郁症状
神经科学
听力学
功能磁共振成像
医学
内科学
扁桃形结构
发展心理学
认知
疾病
作者
Yicheng Long,Xuemei Li,Hengyi Cao,Manqi Zhang,Bing Lü,Yang Huang,Mengqi Liu,Ming Xu,Zhening Liu,Chao‐Gan Yan,Jing Sui,Xuan Ouyang,Xinyu Zhou
标识
DOI:10.1017/s0033291723002234
摘要
Abstract Background The age-related heterogeneity in major depressive disorder (MDD) has received significant attention. However, the neural mechanisms underlying such heterogeneity still need further investigation. This study aimed to explore the common and distinct functional brain abnormalities across different age groups of MDD patients from a large-sample, multicenter analysis. Methods The analyzed sample consisted of a total of 1238 individuals including 617 MDD patients (108 adolescents, 12–17 years old; 411 early-middle adults, 18–54 years old; and 98 late adults, > = 55 years old) and 621 demographically matched healthy controls (60 adolescents, 449 early-middle adults, and 112 late adults). MDD-related abnormalities in brain functional connectivity (FC) patterns were investigated in each age group separately and using the whole pooled sample, respectively. Results We found shared FC reductions among the sensorimotor, visual, and auditory networks across all three age groups of MDD patients. Furthermore, adolescent patients uniquely exhibited increased sensorimotor-subcortical FC; early-middle adult patients uniquely exhibited decreased visual-subcortical FC; and late adult patients uniquely exhibited wide FC reductions within the subcortical, default-mode, cingulo-opercular, and attention networks. Analysis of covariance models using the whole pooled sample further revealed: (1) significant main effects of age group on FCs within most brain networks, suggesting that they are decreased with aging; and (2) a significant age group × MDD diagnosis interaction on FC within the default-mode network, which may be reflective of an accelerated aging-related decline in default-mode FCs. Conclusions To summarize, these findings may deepen our understanding of the age-related biological and clinical heterogeneity in MDD.
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