The Interaction Effects of Age, Sex, APOE and Common Health Risk Factors on Human Brain Functions

Tengfei Li, Jie Chen, Bingxin Zhao, Hui Chen, Changzheng Yuan, Gwenn A. Garden, Kelly S. Giovanello, Guorong Wu, Hongtu Zhu
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Abstract

Recent studies have shed light on the complex nonlinear changes in brain functions across the lifespan, demonstrating the variability in the individual cognitive and neural development during aging. This variability is influenced by factors such as sex, age, genetics, and modifiable health risk factors (MHRFs), which collectively shape unique patterns of brain functional connectivities (FCs) across different regions. However, their joint effects and underlying mechanisms remain unclear. We conduct a comprehensive analysis to jointly examine the association of common risk factors with brain functional measures, using data from 36,630 UK Biobank participants aged 44-81. Participants were assessed for age, sex, Apolipoprotein E (APOE) genotypes, ten common MHRFs, and brain FCs measured via resting-state functional magnetic resonance imaging. Using the fine-grained HCP-MMP parcellation and Ji-12 network atlases, we identified 91 associations with network functional connectivity (NFC) and 102 associations with network edge strength (NES) measures. Hypertension, BMI, and education emerged as the top three influential factors across networks. Notably, a negative interaction between sex and APOE4 genotype was observed, with male APOE4 carriers showing greater reductions in NFC between the cingulo-opercular (CON) and posterior multimodal (PMN) networks. Additionally, a negative age-BMI interaction on NES between the visual and dorsal attention (DAN) networks suggested that higher BMI accelerates the decline in visual-DAN connectivity. A positive age-hypertension interaction between the frontoparietal (FPN) and default mode (DMN) networks indicated a more rapid decrease in functional segregation associated with hypertension. We also identified sex-education interactions, showing more pronounced positive effects on CON-FPN networks in females and PMN-DMN networks in males. Further interactions involving sex and other MHRFs, such as smoking, alcohol consumption, diabetes, and BMI, revealed that smoking, alcohol, and BMI had more detrimental effects in males, while diabetes had a more pronounced negative impact in females within specific networks. These findings underscore the necessity of jointly considering sex, age, genetic factors, and MHRFs to accurately delineate the multifactorial alterations in the FCs during brain aging.
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年龄、性别、APOE 和常见健康风险因素对人类大脑功能的交互影响
最近的研究揭示了大脑功能在整个生命周期中的复杂非线性变化,显示了衰老过程中个体认知和神经发展的差异性。这种变异性受到性别、年龄、遗传和可改变的健康风险因素(MHRFs)等因素的影响,这些因素共同塑造了不同区域大脑功能连接性(FCs)的独特模式。然而,它们的共同作用和内在机制仍不清楚。我们利用英国生物库(UK Biobank)中 36,630 名 44-81 岁参与者的数据进行了一项综合分析,以共同研究常见风险因素与大脑功能测量之间的关联。我们对参与者的年龄、性别、载脂蛋白 E (APOE) 基因型、十种常见的 MHRFs 以及通过静息态功能磁共振成像测量的脑功能指数进行了评估。利用细粒度的 HCP-MMP 剖析和 Ji-12 网络图,我们确定了 91 项与网络功能连通性(NFC)相关的研究和 102 项与网络边缘强度(NES)相关的研究。高血压、体重指数(BMI)和教育程度是影响网络的三大因素。值得注意的是,性别与 APOE4 基因型之间存在负交互作用,男性 APOE4 基因型携带者在椎体-小脑(CON)和后部多模态(PMN)网络之间的 NFC 降低幅度更大。此外,年龄-体重指数对视觉和背侧注意力(DAN)网络之间的 NES 的负交互作用表明,体重指数越高,视觉-DAN 连接性的下降越快。额顶(FPN)和默认模式(DMN)网络之间存在年龄-高血压的正向交互作用,这表明与高血压有关的功能分离下降得更快。我们还发现了性别与教育的相互作用,女性的 CON-FPN 网络和男性的 PMN-DMN 网络受到了更明显的积极影响。性别与吸烟、饮酒、糖尿病和体重指数等其他 MHRF 的进一步交互作用显示,吸烟、饮酒和体重指数对男性的不利影响更大,而在特定网络中,糖尿病对女性的负面影响更明显。这些发现强调,有必要联合考虑性别、年龄、遗传因素和MHRFs,以准确界定大脑衰老过程中FC的多因素改变。
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