Biological pathways underlying the relationship between childhood maltreatment and Multimorbidity: A two-step, multivariable Mendelian randomisation study

IF 7.6 2区 医学 Q1 IMMUNOLOGY Brain, Behavior, and Immunity Pub Date : 2025-05-01 Epub Date: 2025-02-01 DOI:10.1016/j.bbi.2025.01.024
Vilte Baltramonaityte , Ville Karhunen , Janine F. Felix , Brenda W.J.H. Penninx , Charlotte A.M. Cecil , Graeme Fairchild , Yuri Milaneschi , Esther Walton , on behalf of the EarlyCause Consortium
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Abstract

Childhood maltreatment has been associated with multimorbidity of depression, coronary artery disease and type 2 diabetes. However, the biological mechanisms underlying this association remain unclear. We employed two-step and multivariable Mendelian randomisation (MR) to understand the role of three potential biological mediating mechanisms – inflammation (92 proteins), metabolic processes (54 markers), and cortisol – in the link between childhood maltreatment liability and multimorbidity. Using summary statistics from large-scale genome-wide association studies of European ancestry for childhood maltreatment (N = 185,414) and multimorbidity (Neffective = 156,717), we tested for the presence of an indirect effect via each mediator individually. We found a potential role of metabolic pathways. Up to 11% of the effect of childhood maltreatment on multimorbidity was mediated by triglycerides (indirect effect [95% CI]: 0.018 [0.009–0.027]), 8% by glycated haemoglobin (indirect effect: 0.013 [0.003–0.023]), and up to 7% by high-density lipoprotein cholesterol (indirect effect: 0.011 [0.005–0.017]). We did not find evidence for mediation via any inflammatory protein or cortisol. Our findings shed light on the biological mechanisms linking childhood maltreatment liability to multimorbidity, highlighting the role of metabolic pathways. Future studies may explore underlying pathways via non-biological mediators (e.g., lifestyle factors) or via multiple mediators simultaneously.
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儿童虐待与多发病之间关系的生物学途径:一项两步、多变量孟德尔随机化研究。
儿童虐待与抑郁症、冠状动脉疾病和2型糖尿病的多重发病率有关。然而,这种关联背后的生物学机制尚不清楚。我们采用两步和多变量孟德尔随机化(MR)来了解三种潜在的生物介导机制——炎症(92种蛋白质)、代谢过程(54种标志物)和皮质醇——在儿童虐待倾向和多重发病率之间的联系中的作用。利用欧洲血统儿童虐待(N = 185,414)和多发病(Neffective = 156,717)的大规模全基因组关联研究的汇总统计数据,我们分别通过每种中介检验了间接影响的存在。我们发现了代谢途径的潜在作用。儿童期虐待对多重疾病的影响高达11. %是由甘油三酯介导的(间接效应[95 %CI]: 0.018[0.009-0.027]), 8. %是由糖化血红蛋白介导的(间接效应:0.013[0.003-0.023]),高达7. %是由高密度脂蛋白胆固醇介导的(间接效应:0.011[0.005-0.017])。我们没有发现任何炎症蛋白或皮质醇介导的证据。我们的研究结果揭示了将儿童虐待倾向与多种疾病联系起来的生物学机制,强调了代谢途径的作用。未来的研究可能会通过非生物介质(如生活方式因素)或同时通过多种介质探索潜在的途径。
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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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