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与年龄相关的肌肉减少症的遗传关联的初步研究。

Pilot Study on Genetic Associations With Age-Related Sarcopenia.

作者信息

Urzi Felicita, Pokorny Boštjan, Buzan Elena

机构信息

Faculty of Mathematics, Natural Sciences and Information Technologies, University of Primorska, Koper, Slovenia.

Environmental Protection College, Velenje, Slovenia.

出版信息

Front Genet. 2021 Jan 11;11:615238. doi: 10.3389/fgene.2020.615238. eCollection 2020.

Abstract

Despite strong evidence of an inheritable component of muscle phenotypes, little progress has been made in identifying the specific genetic factors involved in the development of sarcopenia. Even rarer are studies that focus on predicting the risk of sarcopenia based on a genetic risk score. In the present study, we tested the single and combined effect of seven candidate gene variants on the risk of sarcopenia. Single nucleotide polymorphisms in candidate genes were genotyped using the KASP assay. We examined 190 older adults that were classified as non-sarcopenic or sarcopenic according to the diagnostic criteria of the European Working Group on Sarcopenia in Older People. Sarcopenia was associated with Methylenetetrahydrofolate reductase, Alpha-actinin-3, and Nuclear respiratory factor 2 genotypes. The combined effect of all three polymorphisms explained 39% of the interindividual variation in sarcopenia risk. Our results suggest that the single and combined effect of Methylenetetrahydrofolate reductase, Alpha-actinin-3, and Nuclear respiratory factor 2 polymorphism is associated with sarcopenia risk in older adults. Nowadays, as the population is getting older and older, great efforts are being made to research the etiology, diagnosis and treatment of sarcopenia. At the same time, small progress has been made in understanding the genetic etiology of sarcopenia. Given the importance of research on this disease, further genetic studies are needed to better understand the genetic risk underlying sarcopenia. We believe that this small-scale study will help to demonstrate that there is still much to be discovered in this field.

摘要

尽管有强有力的证据表明肌肉表型存在可遗传成分,但在确定与肌肉减少症发展相关的具体遗传因素方面进展甚微。基于遗传风险评分来预测肌肉减少症风险的研究更为罕见。在本研究中,我们测试了7种候选基因变异对肌肉减少症风险的单一和联合影响。使用竞争性等位基因特异性PCR(KASP)分析对候选基因中的单核苷酸多态性进行基因分型。我们检查了190名老年人,根据欧洲老年人肌肉减少症工作组的诊断标准将其分类为非肌肉减少症或肌肉减少症患者。肌肉减少症与亚甲基四氢叶酸还原酶、α-辅肌动蛋白-3和核呼吸因子2的基因型有关。所有这三种多态性的联合作用解释了肌肉减少症风险个体间变异的39%。我们的结果表明,亚甲基四氢叶酸还原酶、α-辅肌动蛋白-3和核呼吸因子2多态性的单一和联合作用与老年人的肌肉减少症风险相关。如今,随着人口老龄化,人们正在大力研究肌肉减少症的病因、诊断和治疗。与此同时,在理解肌肉减少症的遗传病因方面取得了微小进展。鉴于对这种疾病研究的重要性,需要进一步的遗传学研究以更好地了解肌肉减少症背后的遗传风险。我们相信这项小规模研究将有助于证明在该领域仍有许多有待发现的地方。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/768b/7831746/c8fada2f1f8a/fgene-11-615238-g001.jpg

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