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Trimethylamine N-oxide and risk of inflammatory bowel disease: A Mendelian randomization study

A previous study suggested that inflammatory bowel disease (IBD) patients have low plasma levels of trimethylamine N-oxide (TMAO). In the present study, we examined this hypothesis using Mendelian randomization analysis. We used summary statistics data for single-nucleotide polymorphisms associated...

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Detalles Bibliográficos
Autores principales: Banno, Yukika, Nomura, Miho, Hara, Risako, Asami, Momoko, Tanaka, Kotone, Mukai, Yuuka, Tomata, Yasutake
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10470767/
https://www.ncbi.nlm.nih.gov/pubmed/37653747
http://dx.doi.org/10.1097/MD.0000000000034758
Descripción
Sumario:A previous study suggested that inflammatory bowel disease (IBD) patients have low plasma levels of trimethylamine N-oxide (TMAO). In the present study, we examined this hypothesis using Mendelian randomization analysis. We used summary statistics data for single-nucleotide polymorphisms associated with plasma levels of TMAO, and the corresponding data for IBD from a genome-wide association meta-analysis of 59,957 individuals (25,042 diagnosed IBD cases, 34,915 controls). The association between genetically predicted plasma TMAO levels and IBD showed odds ratios (95% confidence interval [CI]) per 1 interquartile range increment (per 2.4 μmol/L) in TMAO levels were 0.91 (0.81–1.01, P = .084) for IBD, 0.88 (0.76–1.02, P = .089) for ulcerative colitis, 0.91 (0.79–1.05, P = .210) for Crohn disease. There was no evidence for pleiotropy based on the Mendelian randomization-Egger regression analyses (P-intercept = 0.669 for IBD). Further investigations would be needed to understand the causal relationship between TMAO and IBD.