Deciphering the genetic interconnection between sarcopenia and osteoporosis: SCD1.

IF 2.4 3区 医学 Q3 ENDOCRINOLOGY & METABOLISM
Yan Lv, Yong-Jun Du, Jia-Mian Liu, Jian-Qing Liao, Cheng-Jie Ma, Rui Xu, Jun-Hua Fang, Lv Zhao, Shao-Quan Pu, Sheng Lu
{"title":"Deciphering the genetic interconnection between sarcopenia and osteoporosis: SCD1.","authors":"Yan Lv, Yong-Jun Du, Jia-Mian Liu, Jian-Qing Liao, Cheng-Jie Ma, Rui Xu, Jun-Hua Fang, Lv Zhao, Shao-Quan Pu, Sheng Lu","doi":"10.1007/s00774-025-01612-z","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Sarcopenia is closely related to osteoporosis, but the causal direction of these associations remains unclear. This study aims to explore these potential causal associations from the perspective of gene regulation.</p><p><strong>Materials and methods: </strong>Differentially expressed genes between sarcopenia and control, were identified as exposure factors, with osteoporosis serving as outcome variable, to identify key genes that had potential causal association with osteoporosis. Further analysis was conducted to investigate the causal links between key genes and sarcopenia-related characteristics. Moreover, enrichment analyses, ceRNA and Gene-Gene Interaction network were studied.</p><p><strong>Results: </strong>Only SCD1 demonstrated a potential causal association with osteoporosis (OR = 0.9970, P = 0.0217), acting as a protective factor against the disease. The potential causal links between SCD1 and sarcopenia-related characteristics are executed. SCD1 was identified as a risk factor for low hand grip strength (OR = 1.1397, P = 0.0290), while being pinpointed as a protective factor for appendicular lean mass (OR = 0.8777, P = 0.0147), usual walking pace (OR = 0.9834, P = 0.0290), whole body fat-free mass (OR = 0.9412, P = 0.0227), and trunk fat-free mass (OR = 0.9425, P = 0.0257). All analyses passed Steiger directional test, indicating a unidirectional causal association. Moreover, indicated that SCD1 was significantly associated with metabolic pathways related to lipid biosynthesis and regulation.</p><p><strong>Conclusion: </strong>SCD1 was identified as a protective factor for osteoporosis and a risk factor for sarcopenia. This research provides new insights for the study of sarcopenia and osteoporosis, and offers theoretical backing for the positive effects of exercise in the elderly.</p>","PeriodicalId":15116,"journal":{"name":"Journal of Bone and Mineral Metabolism","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2025-06-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Bone and Mineral Metabolism","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s00774-025-01612-z","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Sarcopenia is closely related to osteoporosis, but the causal direction of these associations remains unclear. This study aims to explore these potential causal associations from the perspective of gene regulation.

Materials and methods: Differentially expressed genes between sarcopenia and control, were identified as exposure factors, with osteoporosis serving as outcome variable, to identify key genes that had potential causal association with osteoporosis. Further analysis was conducted to investigate the causal links between key genes and sarcopenia-related characteristics. Moreover, enrichment analyses, ceRNA and Gene-Gene Interaction network were studied.

Results: Only SCD1 demonstrated a potential causal association with osteoporosis (OR = 0.9970, P = 0.0217), acting as a protective factor against the disease. The potential causal links between SCD1 and sarcopenia-related characteristics are executed. SCD1 was identified as a risk factor for low hand grip strength (OR = 1.1397, P = 0.0290), while being pinpointed as a protective factor for appendicular lean mass (OR = 0.8777, P = 0.0147), usual walking pace (OR = 0.9834, P = 0.0290), whole body fat-free mass (OR = 0.9412, P = 0.0227), and trunk fat-free mass (OR = 0.9425, P = 0.0257). All analyses passed Steiger directional test, indicating a unidirectional causal association. Moreover, indicated that SCD1 was significantly associated with metabolic pathways related to lipid biosynthesis and regulation.

Conclusion: SCD1 was identified as a protective factor for osteoporosis and a risk factor for sarcopenia. This research provides new insights for the study of sarcopenia and osteoporosis, and offers theoretical backing for the positive effects of exercise in the elderly.

解读骨骼肌减少症和骨质疏松症之间的遗传联系:SCD1。
前言:骨骼肌减少症与骨质疏松症密切相关,但这些关联的因果方向尚不清楚。本研究旨在从基因调控的角度探讨这些潜在的因果关系。材料与方法:以骨骼肌减少症与对照组差异表达基因为暴露因素,以骨质疏松症为结局变量,确定与骨质疏松症有潜在因果关系的关键基因。进一步分析了关键基因与肌少症相关特征之间的因果关系。此外,还对富集分析、ceRNA和基因-基因互作网络进行了研究。结果:只有SCD1与骨质疏松症有潜在的因果关系(OR = 0.9970, P = 0.0217),是预防骨质疏松症的保护因素。SCD1与肌少症相关特征之间存在潜在的因果关系。SCD1是低握力的危险因素(OR = 1.1397, P = 0.0290),是阑尾瘦质量(OR = 0.8777, P = 0.0147)、常步速(OR = 0.9834, P = 0.0290)、全身无脂质量(OR = 0.9412, P = 0.0227)、躯干无脂质量(OR = 0.9425, P = 0.0257)的保护因素。所有分析均通过Steiger方向检验,表明单向因果关系。此外,研究表明SCD1与脂质生物合成和调节相关的代谢途径显著相关。结论:SCD1是骨质疏松症的保护因子和肌肉减少症的危险因子。本研究为骨骼肌减少症和骨质疏松症的研究提供了新的见解,为老年人运动的积极作用提供了理论依据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Bone and Mineral Metabolism
Journal of Bone and Mineral Metabolism 医学-内分泌学与代谢
CiteScore
6.30
自引率
3.00%
发文量
89
审稿时长
6-12 weeks
期刊介绍: The Journal of Bone and Mineral Metabolism (JBMM) provides an international forum for researchers and clinicians to present and discuss topics relevant to bone, teeth, and mineral metabolism, as well as joint and musculoskeletal disorders. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. Acceptance is based on the originality, significance, and validity of the material presented. The journal is aimed at researchers and clinicians dedicated to improvements in research, development, and patient-care in the fields of bone and mineral metabolism.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信