Han Dandan, Zhao Shaohua
Medical Imaging Center, Xuchang Central Hospital Affiliated to Henan University of Science and Technology, Xuchang, P. R. China.
Department of Plastic Surgery, Xuchang Central Hospital Affiliated to Henan University of Science and Technology, Xuchang, P. R. China.
Brain Behav. 2025 May;15(5):e70560. doi: 10.1002/brb3.70560.
Asthma is a common chronic respiratory disease, and its potential association with the central nervous system has garnered increasing attention in recent years. While observational studies suggest that asthma may affect hippocampal structure and function through mechanisms such as chronic inflammation and hypoxia, its causal relationship remains unclear.
In this study, we employed a two-sample Mendelian randomization (MR) analysis, utilizing large-scale genome-wide association study (GWAS) data to systematically investigate the potential causal relationship between asthma and hippocampal volume. Data from a GWAS of asthma involving 155,386 individuals of European ancestry and GWAS imaging-derived phenotypes (IDPs) of hippocampal volume from 33,219 European individuals were analyzed.
The results revealed a significant negative correlation between asthma and multiple hippocampal IDPs (P < 0.05), indicating that asthma may contribute to reduced hippocampal volume. We identified 19 independent SNPs significantly associated with asthma (P < 5×10⁻⁸), of which 16 SNPs were retained after clumping (r < 0.001) and harmonization. Sensitivity analyses revealed no heterogeneity or horizontal pleiotropy, and reverse MR analysis did not support a causal effect of hippocampal volume on asthma.
Our study provides genetic evidence for a causal relationship between asthma and changes in hippocampal volume, highlighting the need for closer monitoring and intervention in the neurocognitive health of asthma patients in clinical practice. Future studies should explore the causal relationship between asthma and brain structural changes across different racial groups and asthma subtypes, as well as the underlying biological mechanisms.
哮喘是一种常见的慢性呼吸道疾病,近年来其与中枢神经系统的潜在关联受到越来越多的关注。虽然观察性研究表明哮喘可能通过慢性炎症和缺氧等机制影响海马体结构和功能,但其因果关系仍不明确。
在本研究中,我们采用两样本孟德尔随机化(MR)分析,利用大规模全基因组关联研究(GWAS)数据系统地研究哮喘与海马体体积之间的潜在因果关系。分析了来自一项涉及155,386名欧洲血统个体的哮喘GWAS数据以及来自33,219名欧洲个体的海马体体积GWAS影像衍生表型(IDP)数据。
结果显示哮喘与多个海马体IDP之间存在显著负相关(P < 0.05),表明哮喘可能导致海马体体积减小。我们鉴定出19个与哮喘显著相关的独立单核苷酸多态性(SNP)(P < 5×10⁻⁸),其中16个SNP在连锁不平衡聚类(r < 0.001)和数据协调后得以保留。敏感性分析显示不存在异质性或水平多效性,反向MR分析不支持海马体体积对哮喘的因果效应。
我们的研究为哮喘与海马体体积变化之间的因果关系提供了遗传学证据,强调在临床实践中需要对哮喘患者的神经认知健康进行更密切的监测和干预。未来的研究应探讨哮喘与不同种族群体和哮喘亚型的脑结构变化之间的因果关系,以及潜在的生物学机制。