» Articles » PMID: 39372270

Unveiling Genetic Links Between Gut Microbiota and Asthma: a Mendelian Randomization

Overview
Journal Front Microbiol
Specialty Microbiology
Date 2024 Oct 7
PMID 39372270
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Multiple studies suggest a potential connection between the gut microbiome and asthma. Our objective is to use advanced genetic and metagenomic techniques to elucidate the causal relationships and underlying mechanisms between gut microbiota and asthma.

Methods: The study utilized comprehensive Linkage Disequilibrium Score Regression (LDSC) and Mendelian randomization (MR) analyses to examine the relationship between 119 gut microbiota genera and asthma, using publicly accessible genome-wide association studies (GWAS). The meta-analysis synthesized summary effect estimates obtained from LDSC, forward MR, and reverse MR. The MiBioGen collaboration, involving 18,340 individuals, identified genetic variations associated with gut bacteria. Asthma data were collected from the UK Biobank, FinnGen, and GERA, encompassing a total of 82,060 cases and 641,049 controls.

Results: LDSC analysis revealed significant negative genetic correlations between asthma and (Rg = -0.55, = 7.66 × 10) and (Rg = -0.35, = 3.61 × 10). Forward MR analysis suggested associations between (OR = 0.92, = 0.01), (OR = 0.95, = 0.025), (OR = 0.98, = 0.047), and reduced asthma risk. Conversely, (OR = 1.10, = 0.035) and (OR = 1.07, = 0.039) were associated with increased risk. Reverse MR analysis indicated significant associations between genetically predicted asthma and (Beta = -0.08, = 9.25 × 10), (Beta = -0.05, = 1.26 × 10), and (Beta = 0.06, = 0.015, Rg_ = 0.043).

Conclusion: The findings underscore significant genetic correlations and causal relationships between specific gut microbiota and asthma. These insights highlight the potential of gut microbiota as both markers and modulators of asthma risk, offering new avenues for targeted therapeutic strategies.

References
1.
Bowden J, Davey Smith G, Haycock P, Burgess S . Consistent Estimation in Mendelian Randomization with Some Invalid Instruments Using a Weighted Median Estimator. Genet Epidemiol. 2016; 40(4):304-14. PMC: 4849733. DOI: 10.1002/gepi.21965. View

2.
Kurilshikov A, Medina-Gomez C, Bacigalupe R, Radjabzadeh D, Wang J, Demirkan A . Large-scale association analyses identify host factors influencing human gut microbiome composition. Nat Genet. 2021; 53(2):156-165. PMC: 8515199. DOI: 10.1038/s41588-020-00763-1. View

3.
Sayin S, Wahlstrom A, Felin J, Jantti S, Marschall H, Bamberg K . Gut microbiota regulates bile acid metabolism by reducing the levels of tauro-beta-muricholic acid, a naturally occurring FXR antagonist. Cell Metab. 2013; 17(2):225-35. DOI: 10.1016/j.cmet.2013.01.003. View

4.
Burgess S, Thompson S . Interpreting findings from Mendelian randomization using the MR-Egger method. Eur J Epidemiol. 2017; 32(5):377-389. PMC: 5506233. DOI: 10.1007/s10654-017-0255-x. View

5.
Zheng Y, Dang E . Novel mechanistic insights underlying fungal allergic inflammation. PLoS Pathog. 2023; 19(9):e1011623. PMC: 10499257. DOI: 10.1371/journal.ppat.1011623. View