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精神分裂症常见变异对婴儿脑容量的影响:发展中的人类连接组计划中 207 名足月新生儿的横断面研究。

Effect of schizophrenia common variants on infant brain volumes: cross-sectional study in 207 term neonates in developing Human Connectome Project.

机构信息

Centre for the Developing Brain, Perinatal Imaging and Health Department, King's College London, London, UK.

Translational Bioinformatics Platform, NIHR Biomedical Research Centre, Guy's and St. Thomas' NHS Foundation Trust and King's College London, London, UK.

出版信息

Transl Psychiatry. 2023 Apr 10;13(1):121. doi: 10.1038/s41398-023-02413-6.

DOI:10.1038/s41398-023-02413-6
PMID:37037832
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10085987/
Abstract

Increasing lines of evidence suggest deviations from the normal early developmental trajectory could give rise to the onset of schizophrenia during adolescence and young adulthood, but few studies have investigated brain imaging changes associated with schizophrenia common variants in neonates. This study compared the brain volumes of both grey and white matter regions with schizophrenia polygenic risk scores (PRS) for 207 healthy term-born infants of European ancestry. Linear regression was used to estimate the relationship between PRS and brain volumes, with gestational age at birth, postmenstrual age at scan, ancestral principal components, sex and intracranial volumes as covariates. The schizophrenia PRS were negatively associated with the grey (β = -0.08, p = 4.2 × 10) and white (β = -0.13, p = 9.4 × 10) matter superior temporal gyrus volumes, white frontal lobe volume (β = -0.09, p = 1.5 × 10) and the total white matter volume (β = -0.062, p = 1.66 × 10). This result also remained robust when incorporating individuals of Asian ancestry. Explorative functional analysis of the schizophrenia risk variants associated with the right frontal lobe white matter volume found enrichment in neurodevelopmental pathways. This preliminary result suggests possible involvement of schizophrenia risk genes in early brain growth, and potential early life structural alterations long before the average age of onset of the disease.

摘要

越来越多的证据表明,正常早期发育轨迹的偏差可能导致青少年和成年早期精神分裂症的发作,但很少有研究调查与精神分裂症常见变异体相关的新生儿脑成像变化。本研究比较了 207 名欧洲血统健康足月出生婴儿的灰质和白质区域的脑容量与精神分裂症多基因风险评分(PRS)。线性回归用于估计 PRS 与脑容量之间的关系,出生时的胎龄、扫描时的月经龄、祖先主成分、性别和颅内体积作为协变量。精神分裂症 PRS 与灰质(β=-0.08,p=4.2×10)和白质(β=-0.13,p=9.4×10)颞上回体积、白质额区体积(β=-0.09,p=1.5×10)和总白质体积(β=-0.062,p=1.66×10)呈负相关。当纳入亚洲血统个体时,该结果仍然稳健。对与右侧额叶白质体积相关的精神分裂症风险变异体进行探索性功能分析,发现神经发育途径富集。这一初步结果表明,精神分裂症风险基因可能参与早期大脑生长,并在疾病平均发病年龄之前很久就可能导致早期生活结构改变。

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