Peking University Sixth Hospital, Peking University Institute of Mental Health, NHC Key Laboratory of Mental Health (Peking University), National Clinical Research Center for Mental Disorders (Peking University Sixth Hospital), Beijing, 100191, China.
Chinese Institute for Brain Research, Beijing, 102206, China.
BMC Med. 2024 Sep 13;22(1):392. doi: 10.1186/s12916-024-03614-6.
Air pollution, a reversible environmental factor, was significantly associated with the cognitive domains that are impaired in major depressive disorder (MDD), notably processing speed. Limited evidence explores the interactive effect of air pollution and the genetic risk of depression on cognition. This cross-sectional study aims to extend the research by specifically examining how this interaction influences depression-related cognitive impairment and resting-state brain function.
Eligible participants were 497 healthy adult volunteers (48.7% males, mean age 24.5) living in Beijing for at least 1 year and exposed to relatively high air pollution from the local community controlling for socioeconomic and genomic. Six months' ambient air pollution exposures were assessed based on residential addresses using monthly averages of fine particulate matter with a diameter of less than or equal to 2.5 μm (PM). A cross-sectional analysis was conducted using functional magnetic resonance imaging (fMRI) and cognitive performance assessments. The polygenic risk score (PRS) of MDD was used to estimate genetic susceptibility.
Using a general linear model and partial least square regression, we observed a negative association between resting-state local connectivity in precuneus and PRS-by-PM interactive effect (P = 0.028), indicating that PM exposure reduced the spontaneous activity in precuneus in individuals at high genetic risk for MDD. DNA methylation and gene expression of the SLC30A3 gene, responsible for maintaining zinc-glutamate homeostasis, was suggestively associated with this local connectivity. For the global functional connectivity, the polygenic risk for MDD augmented the neural impact of PM exposure, especially in the frontal-parietal and frontal-limbic regions of the default mode network (P < 0.05). In those genetically predisposed to MDD, increased PM exposure positively correlated with resting-state functional connectivity between the left angular gyrus and left cuneus gyrus. This connectivity was negatively associated with processing speed.
Our cross-sectional study suggests that air pollution may be associated with an increased likelihood of cognitive impairment in individuals genetically predisposed to depression, potentially through alterations in the resting-state function of the occipitoparietal and default mode network.
空气污染是一种可逆转的环境因素,与重度抑郁症(MDD)受损的认知领域显著相关,尤其是处理速度。有限的证据探讨了空气污染和抑郁遗传风险对认知的交互作用。本横断面研究旨在通过专门研究这种相互作用如何影响与抑郁相关的认知障碍和静息态大脑功能来扩展研究。
合格的参与者是 497 名居住在北京至少 1 年并暴露于当地社区相对较高空气污染的健康成年志愿者(48.7%为男性,平均年龄 24.5 岁),同时控制了社会经济和基因组。根据居住地址,使用直径小于或等于 2.5μm(PM)的细颗粒物的月平均值来评估 6 个月的环境空气污染暴露。使用功能磁共振成像(fMRI)和认知表现评估进行横断面分析。使用 MDD 的多基因风险评分(PRS)来估计遗传易感性。
使用一般线性模型和偏最小二乘回归,我们观察到静息状态下楔前叶的局部连通性与 PRS-PM 交互作用呈负相关(P=0.028),表明 PM 暴露降低了 MDD 遗传高风险个体楔前叶的自发活动。负责维持锌-谷氨酸稳态的 SLC30A3 基因的 DNA 甲基化和基因表达与这种局部连通性呈提示性相关。对于全局功能连通性,MDD 的多基因风险增强了 PM 暴露对神经的影响,特别是在默认模式网络的额顶叶和额-边缘区域(P<0.05)。在那些遗传易患 MDD 的人中,PM 暴露增加与左角回和左楔回之间静息状态功能连接呈正相关。这种连通性与处理速度呈负相关。
本横断面研究表明,空气污染可能与遗传易患抑郁症的个体认知障碍的可能性增加有关,这可能是通过改变顶枕和默认模式网络的静息状态功能。