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The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study
by
Yu, Qinyang
, Li, Ji
, Mao, Rui
in
Acne
/ Atopic dermatitis
/ Causality
/ Confounding (Statistics)
/ Dermatitis
/ Eczema
/ Genes
/ Genome-wide association studies
/ Genomes
/ Genotype & phenotype
/ Gut microbiota
/ Immunology
/ Inflammation
/ Intestinal microflora
/ Microbiomes
/ Microbiota
/ Pleiotropy
/ Probiotics
/ Psoriasis
/ Rosacea
/ Skin diseases
/ two-sample mendelian randomization
/ Variables
/ Vitiligo
2023
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The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study
by
Yu, Qinyang
, Li, Ji
, Mao, Rui
in
Acne
/ Atopic dermatitis
/ Causality
/ Confounding (Statistics)
/ Dermatitis
/ Eczema
/ Genes
/ Genome-wide association studies
/ Genomes
/ Genotype & phenotype
/ Gut microbiota
/ Immunology
/ Inflammation
/ Intestinal microflora
/ Microbiomes
/ Microbiota
/ Pleiotropy
/ Probiotics
/ Psoriasis
/ Rosacea
/ Skin diseases
/ two-sample mendelian randomization
/ Variables
/ Vitiligo
2023
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While trying to remove the title from your shelf something went wrong :( Kindly try again later!
Do you wish to request the book?
The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study
by
Yu, Qinyang
, Li, Ji
, Mao, Rui
in
Acne
/ Atopic dermatitis
/ Causality
/ Confounding (Statistics)
/ Dermatitis
/ Eczema
/ Genes
/ Genome-wide association studies
/ Genomes
/ Genotype & phenotype
/ Gut microbiota
/ Immunology
/ Inflammation
/ Intestinal microflora
/ Microbiomes
/ Microbiota
/ Pleiotropy
/ Probiotics
/ Psoriasis
/ Rosacea
/ Skin diseases
/ two-sample mendelian randomization
/ Variables
/ Vitiligo
2023
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The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study
Journal Article
The causal relationship between gut microbiota and inflammatory dermatoses: a Mendelian randomization study
2023
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Overview
BackgroundObservational studies have shown that gut microbiota is closely associated with inflammatory dermatoses such as psoriasis, rosacea, and atopic dermatitis (AD). However, the causal relationship between gut microbiota and inflammatory dermatosis remains unclear.MethodsBased on Maximum Likelihood (ML), MR-Egger regression, Inverse Variance Weighted (IVW), MR Pleiotropy RESidual Sum and Outlier (MR-PRESSO), Weighted Mode, and Weighted Median Estimator (WME) methods, we performed a bidirectional two-sample Mendelian randomization (MR) analysis to explore the causal relationship between gut microbiota and inflammatory dermatosis. The genome-wide association study (GWAS) summary data of gut microbiota came from the MiBioGen consortium, while the GWAS summary data of inflammatory dermatosis (including psoriasis, AD, rosacea, vitiligo, acne, and eczema) came from the FinnGen consortium and IEU Open GWAS project. Cochran’s IVW Q test tested the heterogeneity among instrumental variables (IVs). The horizontal pleiotropy was tested by MR-Egger regression intercept analysis and MR-PRESSO analysis.ResultsEventually, the results indicated that 5, 16, 17, 11, 15, and 12 gut microbiota had significant causal effects on psoriasis, rosacea, AD, vitiligo, acne, and eczema, respectively, including 42 protective and 34 risk causal relationships. Especially, Lactobacilli and Bifidobacteria at the Family and Genus Level, as common probiotics, were identified as protective factors for the corresponding inflammatory dermatoses. The results of reverse MR analysis suggested a bidirectional causal effect between AD and genus Eubacterium brachy group, vitiligo and genus Ruminococcaceae UCG004. The causal relationship between gut microbiota and psoriasis, rosacea, acne, and eczema is unidirectional. There was no significant heterogeneity among these IVs. In conclusion, this bidirectional two-sample MR study identified 76 causal relationships between the gut microbiome and six inflammatory dermatoses, which may be helpful for the clinical prevention and treatment of inflammatory dermatoses.
Publisher
Frontiers Media SA,Frontiers Media S.A
Subject
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