Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study

Abstract Febrile seizures (FS) is the most common type of convulsion in infants and preschool children. This study aimed to investigate the associations between gut microbiota abundance, plasma metabolites, circulating cytokines, and FS. Summary statistics of 211 gut microbiota traits, 1,400 plasma...

Full description

Saved in:
Bibliographic Details
Main Authors: Chenyue Zhao, Huiqin Xue, Min Guo, Hao Yue, Xintong Chen, Jingbo Gao
Format: Article
Language:English
Published: Nature Portfolio 2025-04-01
Series:Scientific Reports
Subjects:
Online Access:https://doi.org/10.1038/s41598-025-97759-w
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1849699799565074432
author Chenyue Zhao
Huiqin Xue
Min Guo
Hao Yue
Xintong Chen
Jingbo Gao
author_facet Chenyue Zhao
Huiqin Xue
Min Guo
Hao Yue
Xintong Chen
Jingbo Gao
author_sort Chenyue Zhao
collection DOAJ
description Abstract Febrile seizures (FS) is the most common type of convulsion in infants and preschool children. This study aimed to investigate the associations between gut microbiota abundance, plasma metabolites, circulating cytokines, and FS. Summary statistics of 211 gut microbiota traits, 1,400 plasma metabolite traits, 91 circulating cytokine traits, and FS were obtained from publicly available genome-wide association studies. Two-sample Mendelian randomization (MR) analysis and causality was inferred using Inverse variance-weighted (IVW), Weighted median, MR-Egger, simple mode-based estimate and weighted mode-based estimate 5 methods. Several sensitivity analyses were also used to ensure the robustness of the results. Furthermore, mediation analysis was used to determine the pathway from gut microbiota to FS mediated by plasma metabolites and circulating cytokines. MR revealed the associations of 1 gut microbiota (phylum Verrucomicrobia), 4 circulating cytokines and 50 plasma metabolites on FS. Based on the known pathogenic metabolites, we observed that the tryptophan, androgen, and sphingolipids pathways are associated with FS. Mediation analysis revealed 1 strongly documented plasma metabolite (Ascorbic acid 2-sulfate) as a mediator linking “gut microbiota to plasma metabolite to FS”. Sensitivity analysis was represented no heterogeneity or pleiotropy in this study.Our study provides some causal evidence concerning the effects of the gut microbiota, circulating cytokines, and plasma metabolites on FS, which needs to be verified in randomized controlled trials. These biomarkers provide new insights into the underlying mechanisms of FS and contribute to its prevention, diagnosis, and treatment.
format Article
id doaj-art-4e196f8baa864eb08a7e88e57f683c16
institution DOAJ
issn 2045-2322
language English
publishDate 2025-04-01
publisher Nature Portfolio
record_format Article
series Scientific Reports
spelling doaj-art-4e196f8baa864eb08a7e88e57f683c162025-08-20T03:18:30ZengNature PortfolioScientific Reports2045-23222025-04-011511910.1038/s41598-025-97759-wEvaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization studyChenyue Zhao0Huiqin Xue1Min Guo2Hao Yue3Xintong Chen4Jingbo Gao5Department of Cytogenetic Laboratory, Children’s Hospital of Shanxi, Women Health Center of ShanxiDepartment of Cytogenetic Laboratory, Children’s Hospital of Shanxi, Women Health Center of ShanxiDepartment of Pediatric Medicine, Shanxi Medical UniversityDepartment of Pediatric Medicine, Shanxi Medical UniversityDepartment of Pediatric Medicine, Shanxi Medical UniversityDepartment of Cytogenetic Laboratory, Children’s Hospital of Shanxi, Women Health Center of ShanxiAbstract Febrile seizures (FS) is the most common type of convulsion in infants and preschool children. This study aimed to investigate the associations between gut microbiota abundance, plasma metabolites, circulating cytokines, and FS. Summary statistics of 211 gut microbiota traits, 1,400 plasma metabolite traits, 91 circulating cytokine traits, and FS were obtained from publicly available genome-wide association studies. Two-sample Mendelian randomization (MR) analysis and causality was inferred using Inverse variance-weighted (IVW), Weighted median, MR-Egger, simple mode-based estimate and weighted mode-based estimate 5 methods. Several sensitivity analyses were also used to ensure the robustness of the results. Furthermore, mediation analysis was used to determine the pathway from gut microbiota to FS mediated by plasma metabolites and circulating cytokines. MR revealed the associations of 1 gut microbiota (phylum Verrucomicrobia), 4 circulating cytokines and 50 plasma metabolites on FS. Based on the known pathogenic metabolites, we observed that the tryptophan, androgen, and sphingolipids pathways are associated with FS. Mediation analysis revealed 1 strongly documented plasma metabolite (Ascorbic acid 2-sulfate) as a mediator linking “gut microbiota to plasma metabolite to FS”. Sensitivity analysis was represented no heterogeneity or pleiotropy in this study.Our study provides some causal evidence concerning the effects of the gut microbiota, circulating cytokines, and plasma metabolites on FS, which needs to be verified in randomized controlled trials. These biomarkers provide new insights into the underlying mechanisms of FS and contribute to its prevention, diagnosis, and treatment.https://doi.org/10.1038/s41598-025-97759-wFebrile seizuresGut microbiotaCirculating cytokinesPlasma metabolitesMendelian randomizationMediation analysis
spellingShingle Chenyue Zhao
Huiqin Xue
Min Guo
Hao Yue
Xintong Chen
Jingbo Gao
Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
Scientific Reports
Febrile seizures
Gut microbiota
Circulating cytokines
Plasma metabolites
Mendelian randomization
Mediation analysis
title Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
title_full Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
title_fullStr Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
title_full_unstemmed Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
title_short Evaluating the impact of gut microbiota, circulating cytokines and plasma metabolites on febrile seizure risk in Mendelian randomization study
title_sort evaluating the impact of gut microbiota circulating cytokines and plasma metabolites on febrile seizure risk in mendelian randomization study
topic Febrile seizures
Gut microbiota
Circulating cytokines
Plasma metabolites
Mendelian randomization
Mediation analysis
url https://doi.org/10.1038/s41598-025-97759-w
work_keys_str_mv AT chenyuezhao evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy
AT huiqinxue evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy
AT minguo evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy
AT haoyue evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy
AT xintongchen evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy
AT jingbogao evaluatingtheimpactofgutmicrobiotacirculatingcytokinesandplasmametabolitesonfebrileseizureriskinmendelianrandomizationstudy