Causal Relationship Between Gut Microbiota, Metabolites, and Sarcopenia: A Mendelian Randomization Study.

Xiangyu Zhang, Guang Yang, Shide Jiang, Bingzhou Ji, Wenqing Xie, Hengzhen Li, Jianfeng Sun, Yusheng Li
{"title":"Causal Relationship Between Gut Microbiota, Metabolites, and Sarcopenia: A Mendelian Randomization Study.","authors":"Xiangyu Zhang, Guang Yang, Shide Jiang, Bingzhou Ji, Wenqing Xie, Hengzhen Li, Jianfeng Sun, Yusheng Li","doi":"10.1093/gerona/glae173","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Gut microbiota imbalance and sarcopenia are frequently observed in older adults. Gut microbiota and their metabolites are considered risk factors contributing to the heightened risk of sarcopenia, but whether these associations are causal remains unclear.</p><p><strong>Methods: </strong>We conducted linkage disequilibrium score regression and 2-sample Mendelian randomization (MR) methods with single-nucleotide polymorphisms sourced from large-scale genome-wide association studies as instrumental variables to examine the causal associations linking gut microbiota with their metabolites to the sarcopenia. Following the MR analysis, subsequent sensitivity analyses were conducted to reinforce the robustness and credibility of the obtained results.</p><p><strong>Results: </strong>MR analysis yielded compelling evidence demonstrating the correlation between genetically predicted gut microbiota and metabolites and the risk of sarcopenia. The abundance of Porphyromonadaceae, Rikenellaceae, Terrisporobacter, and Victivallis was found to be associated with walking pace. Our study also found suggestive associations of 12 intestinal bacteria with appendicular lean mass, and of Streptococcaceae, Intestinibacter, Paraprevotella, Ruminococcaceae UCG009, and Sutterella with grip strength. Specifically, we identified 21 gut microbiota-derived metabolites that may be associated with the risk of sarcopenia.</p><p><strong>Conclusions: </strong>Utilizing a 2-sample MR approach, our study elucidates the causal interplay among gut microbiota, gut microbiota-derived metabolites, and the occurrence of sarcopenia. These findings suggest that gut microbiota and metabolites may represent a potential underlying risk factor for sarcopenia, and offer the promise of novel therapeutic focal points.</p>","PeriodicalId":94243,"journal":{"name":"The journals of gerontology. Series A, Biological sciences and medical sciences","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11329623/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The journals of gerontology. Series A, Biological sciences and medical sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1093/gerona/glae173","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Gut microbiota imbalance and sarcopenia are frequently observed in older adults. Gut microbiota and their metabolites are considered risk factors contributing to the heightened risk of sarcopenia, but whether these associations are causal remains unclear.

Methods: We conducted linkage disequilibrium score regression and 2-sample Mendelian randomization (MR) methods with single-nucleotide polymorphisms sourced from large-scale genome-wide association studies as instrumental variables to examine the causal associations linking gut microbiota with their metabolites to the sarcopenia. Following the MR analysis, subsequent sensitivity analyses were conducted to reinforce the robustness and credibility of the obtained results.

Results: MR analysis yielded compelling evidence demonstrating the correlation between genetically predicted gut microbiota and metabolites and the risk of sarcopenia. The abundance of Porphyromonadaceae, Rikenellaceae, Terrisporobacter, and Victivallis was found to be associated with walking pace. Our study also found suggestive associations of 12 intestinal bacteria with appendicular lean mass, and of Streptococcaceae, Intestinibacter, Paraprevotella, Ruminococcaceae UCG009, and Sutterella with grip strength. Specifically, we identified 21 gut microbiota-derived metabolites that may be associated with the risk of sarcopenia.

Conclusions: Utilizing a 2-sample MR approach, our study elucidates the causal interplay among gut microbiota, gut microbiota-derived metabolites, and the occurrence of sarcopenia. These findings suggest that gut microbiota and metabolites may represent a potential underlying risk factor for sarcopenia, and offer the promise of novel therapeutic focal points.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
肠道微生物群、代谢物与 "肌肉疏松症 "之间的因果关系:孟德尔随机化研究。
背景:在老年人群中经常观察到肠道微生物群失衡和肌肉疏松症。肠道微生物群及其代谢产物被认为是导致肌少症风险增加的风险因素,但这些关联是否是因果关系仍不清楚:我们以大规模全基因组关联研究中的 SNPs 为工具变量,采用关联不平衡得分回归和双样本孟德尔随机方法,研究肠道微生物群及其代谢物与肌肉疏松症之间的因果关系。在进行了MR分析后,又进行了敏感性分析,以加强所得结果的稳健性和可信度:磁共振分析得出了令人信服的证据,证明了基因预测的肠道微生物群和代谢物与肌肉疏松症风险之间的相关性。研究发现,卟啉单胞菌科(Porphyromonadaceae)、Rikenellaceae、Terrisporobacter 和 Victivallis 的丰度与 WP 相关。我们的研究还发现,12 种肠道细菌与 ALM 相关,链球菌科、肠杆菌科、副链球菌科、反刍球菌科 UCG009 和 Sutterella 与 GS 相关。具体来说,我们发现了 21 种肠道微生物群衍生代谢物可能与肌少症风险有关:我们的研究利用双样本磁共振方法,阐明了肠道微生物群、肠道微生物群衍生代谢物与肌少症发生之间的因果关系。这些发现表明,肠道微生物群和代谢物可能是导致肌肉疏松症的潜在风险因素,并有望成为新的治疗重点。
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 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Disentangling Anemia in Frailty: Exploring the Role of Inflammation. Inflammatory Indices and Their Associations with Postoperative Delirium. Metabolic signature of insulin resistance and risk of Alzheimer's disease. Higher-order disease interactions in multimorbidity measurement: marginal benefit over additive disease summation. Sex Differences in the Association Between 24-hour Rest-Activity Rhythms and Frailty Among U.S. Older Adults: Findings from NHANES 2011-2014.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1