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DOI 10.3389/fmicb.2024.1434521

Медицинская библиотека · Frontiers in microbiology · 2024

Genetic insights into the gut microbiota and risk of psoriasis: a bidirectional mendelian randomization study.

Qian Minyu, Shi Jianxin, Zhang Zhuoya, Bi Dezhao, Tan Cheng

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Аннотация

BACKGROUND

Growing evidence indicates a potential association between the gut microbiome and psoriasis. Nevertheless, the precise nature of these associations and whether they constitute causal relationships remain unclear.

METHODS

A rigorous bidirectional two-sample Mendelian randomization study was undertaken to establish a putative causal link between gut microbiota and psoriasis. We drew upon publicly available datasets containing summary statistics from GWAS to accomplish this. Utilizing various analytical techniques, including inverse variance weighting, MR-Egger, weighted median, weighted model, and MR-PRESSO, we sought to validate the putative causal association between gut microbiota and psoriasis. A reverse Mendelian randomization analysis was conducted to further investigate the relationship.

RESULTS

After conducting a forward Mendelian randomization analysis, a causal relationship was established between 19 gut microbiota and psoriasis. Furthermore, the reverse MR study revealed causality between psoriasis and 13 gut microbiota. Notably, no substantial heterogeneity of instrumental variables or horizontal pleiotropy was observed.

CONCLUSION

This research suggests a potential genetic association and causal nexus between gut microorganisms and psoriasis, indicating potential implications for the clinical management and therapy of psoriasis. Additional observational studies with a larger population sample size and animal model experiments are imperative to fully elucidate this association's underlying mechanisms.

Для цитирования: Qian Minyu, Shi Jianxin, Zhang Zhuoya, Bi Dezhao, Tan Cheng. Genetic insights into the gut microbiota and risk of psoriasis: a bidirectional mendelian randomization study.. Frontiers in microbiology. 2024. DOI: 10.3389/fmicb.2024.1434521.
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