Wang Jigan, Dou Hui-Hong, Liang Qiong-You
Maternal and Child Health Hospital of Guangxi Zhuang Autonomous Region, Nanning, People's Republic of China.
Department of Pediatrics, Guangxi Clinical Research Center for Pediatric Diseases, Nanning, People's Republic of China.
R Soc Open Sci. 2025 May 21;12(5):250158. doi: 10.1098/rsos.250158. eCollection 2025 May.
This study explored the causal relationships between gut microbiota, blood metabolites and autism spectrum disorder (ASD) in children and assessed whether metabolites mediate the relationship between microbiota and ASD. Using Mendelian randomization (MR), causal links between gut microbiota, blood metabolites and ASD were analysed, alongside reverse MR to examine reverse causality. A two-step MR mediation analysis was used to assess metabolite mediation. The study identified 15 gut microbiota types significantly associated with ASD, with Marinilabiliaceae showing the strongest positive link (odds ratio (OR) = 5.206, 95% confidence interval (CI) = 1.2783-21.2017, = 0.0213) and Poseidoniaceae the strongest negative association (OR = 0.1466, 95% CI = 0.0306-0.7035, = 0.0164). Among 52 blood metabolites, 4-methylcatechol sulphate was positively associated with ASD risk (OR = 1.6776, 95% CI = 1.0482-2.6849, = 0.0311), while the glucose-to-maltose ratio showed a negative relationship (OR = 0.6358). No significant reverse causal effects of ASD on microbiota or metabolites were found. Nine metabolites mediated the relationship between microbiota and ASD, with 1-methyl-5-imidazoleacetate showing the strongest negative mediation effect (mediating effect = -0.0862, mediation proportion = 12.30%). This study reveals complex causal pathways involving microbiota and metabolites in ASD, suggesting metabolites may mediate the microbiota-ASD relationship, offering insights into ASD mechanisms and potential interventions.
本研究探讨了儿童肠道微生物群、血液代谢物与自闭症谱系障碍(ASD)之间的因果关系,并评估了代谢物是否介导了微生物群与ASD之间的关系。使用孟德尔随机化(MR)分析肠道微生物群、血液代谢物与ASD之间的因果联系,同时进行反向MR以检验反向因果关系。采用两步MR中介分析来评估代谢物的中介作用。该研究确定了15种与ASD显著相关的肠道微生物群类型,其中海栖嗜盐菌科显示出最强的正相关(优势比(OR)=5.206,95%置信区间(CI)=1.2783 - 21.2017,P = 0.0213),而波塞冬菌科显示出最强的负相关(OR = 0.1466,95% CI = 0.0306 - 0.7035,P = 0.0164)。在52种血液代谢物中,硫酸4 - 甲基邻苯二酚与ASD风险呈正相关(OR = 1.6776,95% CI = 1.0482 - 2.6849,P = 0.0311),而葡萄糖与麦芽糖的比值呈负相关(OR = 0.6358)。未发现ASD对微生物群或代谢物有显著的反向因果效应。9种代谢物介导了微生物群与ASD之间的关系,其中1 - 甲基 - 5 - 咪唑乙酸显示出最强的负中介效应(中介效应=-0.0862,中介比例=12.30%)。本研究揭示了ASD中涉及微生物群和代谢物的复杂因果途径,表明代谢物可能介导微生物群与ASD之间的关系,为ASD的机制和潜在干预提供了见解。