Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study

Abstract Background The aim of this study was to analyze the bi‐directional causal relationship between lipid profile and characteristics related to muscle atrophy by using a bi‐directional Mendelian randomization (MR) analysis. Methods The appendicular lean mass (ALM), whole body fat‐free mass (WBF...

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Main Authors: Kun Chen, Peng Gao, Xiaoxiang Fang, Kexing Tang, Pan Ouyang, Zongchao Li, Liangjun Li, Zhenhan Deng
Format: Article
Language:English
Published: Wiley 2025-01-01
Series:Animal Models and Experimental Medicine
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Online Access:https://doi.org/10.1002/ame2.12373
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author Kun Chen
Peng Gao
Xiaoxiang Fang
Kexing Tang
Pan Ouyang
Zongchao Li
Liangjun Li
Zhenhan Deng
author_facet Kun Chen
Peng Gao
Xiaoxiang Fang
Kexing Tang
Pan Ouyang
Zongchao Li
Liangjun Li
Zhenhan Deng
author_sort Kun Chen
collection DOAJ
description Abstract Background The aim of this study was to analyze the bi‐directional causal relationship between lipid profile and characteristics related to muscle atrophy by using a bi‐directional Mendelian randomization (MR) analysis. Methods The appendicular lean mass (ALM), whole body fat‐free mass (WBFFM) and trunk fat‐free mass (TFFM) were used as genome‐wide association study (GWAS) data for evaluating muscle mass; the usual walking pace (UWP) and low grip strength (LGS) were used as GWAS data for evaluating muscle strength; and the triglycerides (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL), low density lipoprotein cholesterol (LDL), apolipoprotein A‐1 (Apo A‐1), and apolipoprotein B (Apo B) were used as GWAS data for evaluating lipid profile. For specific investigations, we mainly employed inverse variance weighting for causal estimation and MR‐Egger for pleiotropy analysis. Results MR results showed that the lipid profile predicted by genetic variants was negatively correlated with muscle mass, positively correlated with UWP, and was not causally correlated with LGS. On the other hand, the muscle mass predicted by genetic variants was negatively correlated with lipid profile, the UWP predicted by genetic variants was mainly positively correlated with lipid profile, while the LGS predicted by genetic variants had no relevant causal relationship with lipid profile. Conclusions Findings of this MR analysis suggest that hyperlipidemia may affect muscle mass and lead to muscle atrophy, but has no significant effect on muscle strength. On the other hand, increased muscle mass may reduce the incidence of dyslipidemia.
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spelling doaj-art-0aea5549e818470b859df41b2c80966c2025-02-06T03:52:56ZengWileyAnimal Models and Experimental Medicine2576-20952025-01-018115416110.1002/ame2.12373Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization studyKun Chen0Peng Gao1Xiaoxiang Fang2Kexing Tang3Pan Ouyang4Zongchao Li5Liangjun Li6Zhenhan Deng7Department of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedics, The Affiliated Changsha Central Hospital Hengyang Medical School, University of South China Changsha Hunan ChinaDepartment of Orthopaedic Surgery The First Affiliated Hospital of Wenzhou Medical University Wenzhou Zhejiang ChinaAbstract Background The aim of this study was to analyze the bi‐directional causal relationship between lipid profile and characteristics related to muscle atrophy by using a bi‐directional Mendelian randomization (MR) analysis. Methods The appendicular lean mass (ALM), whole body fat‐free mass (WBFFM) and trunk fat‐free mass (TFFM) were used as genome‐wide association study (GWAS) data for evaluating muscle mass; the usual walking pace (UWP) and low grip strength (LGS) were used as GWAS data for evaluating muscle strength; and the triglycerides (TG), total cholesterol (TC), high density lipoprotein cholesterol (HDL), low density lipoprotein cholesterol (LDL), apolipoprotein A‐1 (Apo A‐1), and apolipoprotein B (Apo B) were used as GWAS data for evaluating lipid profile. For specific investigations, we mainly employed inverse variance weighting for causal estimation and MR‐Egger for pleiotropy analysis. Results MR results showed that the lipid profile predicted by genetic variants was negatively correlated with muscle mass, positively correlated with UWP, and was not causally correlated with LGS. On the other hand, the muscle mass predicted by genetic variants was negatively correlated with lipid profile, the UWP predicted by genetic variants was mainly positively correlated with lipid profile, while the LGS predicted by genetic variants had no relevant causal relationship with lipid profile. Conclusions Findings of this MR analysis suggest that hyperlipidemia may affect muscle mass and lead to muscle atrophy, but has no significant effect on muscle strength. On the other hand, increased muscle mass may reduce the incidence of dyslipidemia.https://doi.org/10.1002/ame2.12373lipid profileMendelian randomizationmuscle atrophy
spellingShingle Kun Chen
Peng Gao
Xiaoxiang Fang
Kexing Tang
Pan Ouyang
Zongchao Li
Liangjun Li
Zhenhan Deng
Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
Animal Models and Experimental Medicine
lipid profile
Mendelian randomization
muscle atrophy
title Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
title_full Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
title_fullStr Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
title_full_unstemmed Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
title_short Causal relationship between lipid profile and muscle atrophy: A bi‐directional Mendelian randomization study
title_sort causal relationship between lipid profile and muscle atrophy a bi directional mendelian randomization study
topic lipid profile
Mendelian randomization
muscle atrophy
url https://doi.org/10.1002/ame2.12373
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