Yaqing Gao, Cornelia van Duijn, Thomas J. Littlejohns , Najaf Amin
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引用次数: 0
Abstract
Background
High levels of neuroticism are associated with an increased risk of dementia, yet the underlying biological mechanisms remain poorly understood. Investigating the role of metabolites, the downstream products of metabolic processes, may offer valuable insights into this association.
Methods
In 215,624 dementia-free UK Biobank participants aged 40–69 years, we assessed neuroticism's associations with 249 nuclear magnetic resonance-measured metabolites using linear regression. Metabolites reaching Bonferroni-corrected significance were further tested for associations with incident all-cause dementia, Alzheimer's disease (AD) and vascular dementia (VaD) using Cox proportional-hazards regression, and with white matter hyperintensities volume using linear regression. Causality in significant observational relationships was evaluated through two-sample Mendelian randomization.
Results
Neuroticism was significantly associated with 119 out of 249 metabolites (Bonferroni-adjusted p < 0.05). Among these, five metabolites involved in fatty acid metabolism showed consistent directional associations with both neuroticism and incident all-cause dementia. Specifically, four metabolites, including docosahexaenoic acid (DHA), DHA% of total fatty acids, omega-3 % of total fatty acids, and degree of unsaturation, were associated with lower neuroticism levels and a decreased risk of incident dementia. Conversely, the omega-6/omega-3 ratio was positively associated with both neuroticism and dementia risk. Associations between these five metabolites and VaD were stronger than those with AD. Mendelian randomization analysis suggested that high levels of neuroticism reduce DHA levels, which, in turn, contribute to white matter pathology, a hallmark of VaD.
Conclusions
Neuroticism is associated with lower levels of omega-3 fatty acids, particularly DHA, which may increase dementia risk, primarily through cerebrovascular mechanisms.
背景:高水平的神经质与痴呆风险增加有关,但其潜在的生物学机制尚不清楚。研究代谢物(代谢过程的下游产物)的作用,可能为这种关联提供有价值的见解。方法:在215,624名年龄在40-69岁 岁无痴呆的英国生物银行参与者中,我们使用线性回归评估了神经质与249种核磁共振测量代谢物的关联。使用Cox比例风险回归进一步检测达到bonferroni校正显著性的代谢物与事件性全因痴呆、阿尔茨海默病(AD)和血管性痴呆(VaD)的相关性,并使用线性回归进一步检测与白质高强度的相关性。通过双样本孟德尔随机化评估显著观察关系的因果关系。结果:神经质与249种代谢物中的119种显著相关(Bonferroni-adjusted p )。结论:神经质与低水平的omega-3脂肪酸,特别是DHA相关,这可能增加痴呆的风险,主要是通过脑血管机制。
期刊介绍:
The Journal of Affective Disorders publishes papers concerned with affective disorders in the widest sense: depression, mania, mood spectrum, emotions and personality, anxiety and stress. It is interdisciplinary and aims to bring together different approaches for a diverse readership. Top quality papers will be accepted dealing with any aspect of affective disorders, including neuroimaging, cognitive neurosciences, genetics, molecular biology, experimental and clinical neurosciences, pharmacology, neuroimmunoendocrinology, intervention and treatment trials.