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代谢组学特征可预测 10 年内肌肉力量的纵向下降

Metabolomic signatures for the longitudinal reduction of muscle strength over 10 years.

机构信息

Division of Biomedical Sciences (Genetics), Faculty of Medicine, Memorial University of Newfoundland, St. John's, Canada.

Menzies Research Institute, University of Tasmania, Hobart, Australia.

出版信息

Skelet Muscle. 2022 Feb 7;12(1):4. doi: 10.1186/s13395-022-00286-9.

Abstract

BACKGROUND

Skeletal muscles are essential components of the neuromuscular skeletal system that have an integral role in the structure and function of the synovial joints which are often affected by osteoarthritis (OA). The aim of this study was to identify the baseline metabolomic signatures for the longitudinal reduction of muscle strength over 10 years in the well-established community-based Tasmanian Older Adult Cohort (TASOAC).

METHODS

Study participants were 50-79 year old individuals from the TASOAC. Hand grip, knee extension, and leg strength were measured at baseline, 2.6-, 5-, and 10-year follow-up points. Fasting serum samples were collected at 2.6-year follow-up point, and metabolomic profiling was performed using the TMIC Prime Metabolomics Profiling Assay. Generalized linear mixed effects model was used to identify metabolites that were associated with the reduction in muscle strength over 10 years after controlling for age, sex, and BMI. Significance level was defined at α=0.0004 after correction of multiple testing of 129 metabolites with Bonferroni method. Further, a genome-wide association study (GWAS) analysis was performed to explore if genetic factors account for the association between the identified metabolomic markers and the longitudinal reduction of muscle strength over 10 years.

RESULTS

A total of 409 older adults (50% of them females) were included. The mean age was 60.93±6.50 years, and mean BMI was 27.12±4.18 kg/m at baseline. Muscle strength declined by 0.09 psi, 0.02 kg, and 2.57 kg per year for hand grip, knee extension, and leg strength, respectively. Among the 143 metabolites measured, 129 passed the quality checks and were included in the analysis. We found that the elevated blood level of asymmetric dimethylarginine (ADMA) was associated with the reduction in hand grip (p=0.0003) and knee extension strength (p=0.008) over 10 years. GWAS analysis found that a SNP rs1125718 adjacent to WISP1gene was associated with ADMA levels (p=4.39*10). Further, we found that the increased serum concentration of uric acid was significantly associated with the decline in leg strength over 10 years (p=0.0001).

CONCLUSION

Our results demonstrated that elevated serum ADMA and uric acid at baseline were associated with age-dependent muscle strength reduction. They might be novel targets to prevent muscle strength loss over time.

摘要

背景

骨骼肌是神经肌肉骨骼系统的重要组成部分,对滑膜关节的结构和功能具有整体作用,而滑膜关节常受骨关节炎(OA)的影响。本研究的目的是确定基线代谢组学特征,以预测在既定的塔斯马尼亚老年人群队列(TASOAC)中,肌肉力量在 10 年内的纵向下降。

方法

研究对象为 TASOAC 中 50-79 岁的个体。在基线、2.6、5 和 10 年随访点测量握力、膝关节伸展和腿部力量。在 2.6 年随访时采集空腹血清样本,并使用 TMIC Prime 代谢组学分析试剂盒进行代谢组学分析。使用广义线性混合效应模型,在控制年龄、性别和 BMI 后,确定与 10 年内肌肉力量下降相关的代谢物。在使用 Bonferroni 方法对 129 种代谢物进行多次检验校正后,将显著性水平定义为α=0.0004。此外,还进行了全基因组关联研究(GWAS)分析,以探讨遗传因素是否解释了所确定的代谢标志物与肌肉力量在 10 年内的纵向下降之间的关联。

结果

共纳入 409 名老年人(其中 50%为女性)。平均年龄为 60.93±6.50 岁,基线时平均 BMI 为 27.12±4.18kg/m。握力、膝关节伸展和腿部力量每年分别下降 0.09psi、0.02kg 和 2.57kg。在测量的 143 种代谢物中,有 129 种通过了质量检查并纳入了分析。我们发现,不对称二甲基精氨酸(ADMA)的血液水平升高与握力(p=0.0003)和膝关节伸展力量(p=0.008)在 10 年内的下降有关。GWAS 分析发现,位于 WISP1 基因附近的 SNP rs1125718 与 ADMA 水平相关(p=4.39*10)。此外,我们发现,血清尿酸浓度升高与 10 年内腿部力量下降显著相关(p=0.0001)。

结论

我们的研究结果表明,基线时血清 ADMA 和尿酸升高与年龄相关的肌肉力量下降有关。它们可能是预防肌肉力量随时间下降的新靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5eab/8819943/d02bef913373/13395_2022_286_Fig1_HTML.jpg

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