A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases

BackgroundThere is increasing evidence pointing to a close relationship between sarcopenia and inflammatory bowel disease. However, it remains unclear whether or in which direction causal relationships exist, because these associations could be confounded.MethodsWe conducted a two-sample bidirection...

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Main Authors: Xin Jiao, Wen-yu Wu, Shao-feng Zhan, Jian-bo Liu, Xian-jin Zhang
Format: Article
Language:English
Published: Frontiers Media S.A. 2023-11-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2023.1240811/full
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author Xin Jiao
Xin Jiao
Wen-yu Wu
Wen-yu Wu
Shao-feng Zhan
Jian-bo Liu
Xian-jin Zhang
author_facet Xin Jiao
Xin Jiao
Wen-yu Wu
Wen-yu Wu
Shao-feng Zhan
Jian-bo Liu
Xian-jin Zhang
author_sort Xin Jiao
collection DOAJ
description BackgroundThere is increasing evidence pointing to a close relationship between sarcopenia and inflammatory bowel disease. However, it remains unclear whether or in which direction causal relationships exist, because these associations could be confounded.MethodsWe conducted a two-sample bidirectional mendelian randomization analysis using data from European genome-wide association studies of the appendicular lean mass(n = 450,243), walking pace(n = 459,915), grip strength (left hand, n = 461,026; right hand, n = 461,089), inflammatory bowel disease (25,042 patients and 34,915 controls), ulcerative colitis (12,366 patients and 33,609 controls), and Crohn’s disease (12,194 patients and 28,072 controls) to investigate the causal relationship between sarcopenia-related traits and inflammatory bowel disease and its subtypes on each other. The inverse-variance weighted method was used as the primary analysis method to assess the causality, and a comprehensive sensitivity test was conducted.ResultsGenetically predicted appendicular lean mass was significantly associated with inflammatory bowel disease (OR = 0.916, 95%CI: 0.853–0.984, P = 0.017), ulcerative colitis (OR =0.888, 95%CI: 0.813–0.971, P = 0.009), and Crohn’s disease (OR = 0.905, 95%CI: 0.820–0.999, P = 0.049). Similar results also revealed that the usual walking pace was causally associated with Crohn’s disease (OR = 0.467, 95%CI: 0.239–0.914, P = 0.026). Reverse mendelian randomization analysis results found that genetic susceptibility to inflammatory bowel disease, and Crohn’s disease were associated with lower appendicular lean mass. A series of sensitivity analyses ensured the reliability of the present research results.ConclusionThe mendelian randomization study supports a bidirectional causality between inflammatory bowel disease, Crohn’s disease and appendicular lean mass, but no such bidirectional causal relationship was found in ulcerative colitis. In addition, genetically predicted usual walking pace may reduce the risk of Crohn’s disease. These findings have clinical implications for sarcopenia and inflammatory bowel disease management.
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spelling doaj.art-3ab290c1f8f84dbda9bf78ef6d7c3ea22023-11-09T16:05:06ZengFrontiers Media S.A.Frontiers in Immunology1664-32242023-11-011410.3389/fimmu.2023.12408111240811A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseasesXin Jiao0Xin Jiao1Wen-yu Wu2Wen-yu Wu3Shao-feng Zhan4Jian-bo Liu5Xian-jin Zhang6The First Clinical Medical College of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Clinical Medical College of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaThe First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, ChinaBackgroundThere is increasing evidence pointing to a close relationship between sarcopenia and inflammatory bowel disease. However, it remains unclear whether or in which direction causal relationships exist, because these associations could be confounded.MethodsWe conducted a two-sample bidirectional mendelian randomization analysis using data from European genome-wide association studies of the appendicular lean mass(n = 450,243), walking pace(n = 459,915), grip strength (left hand, n = 461,026; right hand, n = 461,089), inflammatory bowel disease (25,042 patients and 34,915 controls), ulcerative colitis (12,366 patients and 33,609 controls), and Crohn’s disease (12,194 patients and 28,072 controls) to investigate the causal relationship between sarcopenia-related traits and inflammatory bowel disease and its subtypes on each other. The inverse-variance weighted method was used as the primary analysis method to assess the causality, and a comprehensive sensitivity test was conducted.ResultsGenetically predicted appendicular lean mass was significantly associated with inflammatory bowel disease (OR = 0.916, 95%CI: 0.853–0.984, P = 0.017), ulcerative colitis (OR =0.888, 95%CI: 0.813–0.971, P = 0.009), and Crohn’s disease (OR = 0.905, 95%CI: 0.820–0.999, P = 0.049). Similar results also revealed that the usual walking pace was causally associated with Crohn’s disease (OR = 0.467, 95%CI: 0.239–0.914, P = 0.026). Reverse mendelian randomization analysis results found that genetic susceptibility to inflammatory bowel disease, and Crohn’s disease were associated with lower appendicular lean mass. A series of sensitivity analyses ensured the reliability of the present research results.ConclusionThe mendelian randomization study supports a bidirectional causality between inflammatory bowel disease, Crohn’s disease and appendicular lean mass, but no such bidirectional causal relationship was found in ulcerative colitis. In addition, genetically predicted usual walking pace may reduce the risk of Crohn’s disease. These findings have clinical implications for sarcopenia and inflammatory bowel disease management.https://www.frontiersin.org/articles/10.3389/fimmu.2023.1240811/fullsarcopeniainflammatory bowel diseaseCrohn’s diseaseulcerative colitisMendelian randomizationcausal relationship
spellingShingle Xin Jiao
Xin Jiao
Wen-yu Wu
Wen-yu Wu
Shao-feng Zhan
Jian-bo Liu
Xian-jin Zhang
A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
Frontiers in Immunology
sarcopenia
inflammatory bowel disease
Crohn’s disease
ulcerative colitis
Mendelian randomization
causal relationship
title A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
title_full A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
title_fullStr A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
title_full_unstemmed A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
title_short A bidirectional Mendelian randomization study of sarcopenia-related traits and inflammatory bowel diseases
title_sort bidirectional mendelian randomization study of sarcopenia related traits and inflammatory bowel diseases
topic sarcopenia
inflammatory bowel disease
Crohn’s disease
ulcerative colitis
Mendelian randomization
causal relationship
url https://www.frontiersin.org/articles/10.3389/fimmu.2023.1240811/full
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