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Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study

BACKGROUND: With the advancement of world population aging, age-related osteoporosis (OP) and sarcopenia (SP) impose enormous clinical and economic burden on society. Evidence from accumulating studies indicates that they mutually influence one another. However, an observational study may be affecte...

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Autores principales: Liu, Chao, Liu, Ningyuan, Xia, Yu, Zhao, Ziyue, Xiao, Tao, Li, Hui
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515352/
https://www.ncbi.nlm.nih.gov/pubmed/36187130
http://dx.doi.org/10.3389/fendo.2022.975647
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author Liu, Chao
Liu, Ningyuan
Xia, Yu
Zhao, Ziyue
Xiao, Tao
Li, Hui
author_facet Liu, Chao
Liu, Ningyuan
Xia, Yu
Zhao, Ziyue
Xiao, Tao
Li, Hui
author_sort Liu, Chao
collection PubMed
description BACKGROUND: With the advancement of world population aging, age-related osteoporosis (OP) and sarcopenia (SP) impose enormous clinical and economic burden on society. Evidence from accumulating studies indicates that they mutually influence one another. However, an observational study may be affected by potential confounders. Meanwhile, a Mendelian randomization (MR) study can overcome these confounders to assess causality. OBJECTIVES: The aim of this study was to evaluate the causality between OP and SP, informing new strategies for prevention, diagnosis, and treatment of osteosarcopenia. METHODS: Instrumental variables (IVs) at the genome‐wide significance level were obtained from published summary statistics, and the inverse variance weighted method and several other MR methods were conducted to evaluate the bi-directional causality between SP and OP. Myopia was analyzed as a negative control outcome to test the validity of IVs. RESULTS: Femoral neck bone mineral density (FN BMD), lumbar spine BMD (LS BMD), and forearm BMD (FA BMD) had a direct causal effect on appendicular lean mass (ALM) [FA BMD-related analysis: odds ratio (OR) = 1.028, 95% confidence interval (CI) = (1.008,1.049), p = 0.006; FN BMD-related analysis: OR (95% CI) = 1.131 (1.092,1.170), p = 3.18E-12; LS BMD-related analysis: OR (95% CI) = 1.080 (1.062,1.098), p = 2.86E-19]. ALM had a significant causal effect on LS BMD [OR (95% CI) = (1.033,1.147), p = 0.001]. There was no evidence for causal association between BMD and low grip strength. CONCLUSIONS: OP and SP might mutually have a significant causal effect on each other. Our results supported the idea that the patient with severe OP was more susceptible to lose ALM and severe ALM loss might reduce LS BMD.
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spelling pubmed-95153522022-09-29 Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study Liu, Chao Liu, Ningyuan Xia, Yu Zhao, Ziyue Xiao, Tao Li, Hui Front Endocrinol (Lausanne) Endocrinology BACKGROUND: With the advancement of world population aging, age-related osteoporosis (OP) and sarcopenia (SP) impose enormous clinical and economic burden on society. Evidence from accumulating studies indicates that they mutually influence one another. However, an observational study may be affected by potential confounders. Meanwhile, a Mendelian randomization (MR) study can overcome these confounders to assess causality. OBJECTIVES: The aim of this study was to evaluate the causality between OP and SP, informing new strategies for prevention, diagnosis, and treatment of osteosarcopenia. METHODS: Instrumental variables (IVs) at the genome‐wide significance level were obtained from published summary statistics, and the inverse variance weighted method and several other MR methods were conducted to evaluate the bi-directional causality between SP and OP. Myopia was analyzed as a negative control outcome to test the validity of IVs. RESULTS: Femoral neck bone mineral density (FN BMD), lumbar spine BMD (LS BMD), and forearm BMD (FA BMD) had a direct causal effect on appendicular lean mass (ALM) [FA BMD-related analysis: odds ratio (OR) = 1.028, 95% confidence interval (CI) = (1.008,1.049), p = 0.006; FN BMD-related analysis: OR (95% CI) = 1.131 (1.092,1.170), p = 3.18E-12; LS BMD-related analysis: OR (95% CI) = 1.080 (1.062,1.098), p = 2.86E-19]. ALM had a significant causal effect on LS BMD [OR (95% CI) = (1.033,1.147), p = 0.001]. There was no evidence for causal association between BMD and low grip strength. CONCLUSIONS: OP and SP might mutually have a significant causal effect on each other. Our results supported the idea that the patient with severe OP was more susceptible to lose ALM and severe ALM loss might reduce LS BMD. Frontiers Media S.A. 2022-09-14 /pmc/articles/PMC9515352/ /pubmed/36187130 http://dx.doi.org/10.3389/fendo.2022.975647 Text en Copyright © 2022 Liu, Liu, Xia, Zhao, Xiao and Li https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Liu, Chao
Liu, Ningyuan
Xia, Yu
Zhao, Ziyue
Xiao, Tao
Li, Hui
Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title_full Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title_fullStr Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title_full_unstemmed Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title_short Osteoporosis and sarcopenia-related traits: A bi-directional Mendelian randomization study
title_sort osteoporosis and sarcopenia-related traits: a bi-directional mendelian randomization study
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9515352/
https://www.ncbi.nlm.nih.gov/pubmed/36187130
http://dx.doi.org/10.3389/fendo.2022.975647
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