Murabito Joanne M, Rong Jian, Lunetta Kathryn L, Huan Tianxiao, Lin Honghuang, Zhao Qiang, Freedman Jane E, Tanriverdi Kahraman, Levy Daniel, Larson Martin G
The Framingham Heart Study, Framingham, MA, USA.
Department of Medicine, Section of General Internal Medicine, Boston University School of Medicine, Boston, MA, USA.
Aging Cell. 2017 Aug;16(4):888-894. doi: 10.1111/acel.12622. Epub 2017 Jun 8.
MicroRNAs (miRNAs) regulate gene expression with emerging data suggesting miRNAs play a role in skeletal muscle biology. We sought to examine the association of miRNAs with grip strength in a community-based sample. Framingham Heart Study Offspring and Generation 3 participants (n = 5668 54% women, mean age 55 years, range 24, 90 years) underwent grip strength measurement and miRNA profiling using whole blood from fasting morning samples. Linear mixed-effects regression modeling of grip strength (kg) versus continuous miRNA 'Cq' values and versus binary miRNA expression was performed. We conducted an integrative miRNA-mRNA coexpression analysis and examined the enrichment of biologic pathways for the top miRNAs associated with grip strength. Grip strength was lower in women than in men and declined with age with a mean 44.7 (10.0) kg in men and 26.5 (6.3) kg in women. Among 299 miRNAs interrogated for association with grip strength, 93 (31%) had FDR q value < 0.05, 54 (18%) had an FDR q value < 0.01, and 15 (5%) had FDR q value < 0.001. For almost all miRNA-grip strength associations, increasing miRNA concentration is associated with increasing grip strength. miR-20a-5p (FDR q 1.8 × 10 ) had the most significant association and several among the top 15 miRNAs had links to skeletal muscle including miR-126-3p, miR-30a-5p, and miR-30d-5p. The top associated biologic pathways included metabolism, chemokine signaling, and ubiquitin-mediated proteolysis. Our comprehensive assessment in a community-based sample of miRNAs in blood associated with grip strength provides a framework to further our understanding of the biology of muscle strength.
微小RNA(miRNA)可调节基因表达,新出现的数据表明miRNA在骨骼肌生物学中发挥作用。我们试图在一个基于社区的样本中研究miRNA与握力之间的关联。弗雷明汉心脏研究后代及第三代参与者(n = 5668,54%为女性,平均年龄55岁,范围24至90岁)接受了握力测量,并使用空腹早晨样本的全血进行了miRNA分析。对握力(千克)与连续的miRNA“Cq”值以及与二元miRNA表达进行了线性混合效应回归建模。我们进行了miRNA-mRNA共表达综合分析,并检查了与握力相关的顶级miRNA的生物途径富集情况。女性的握力低于男性,且随年龄下降,男性平均为44.7(10.0)千克,女性为26.5(6.3)千克。在检测的299种与握力相关的miRNA中,93种(31%)的错误发现率(FDR)q值<0.05,54种(18%)的FDR q值<0.01,15种(5%)的FDR q值<0.001。对于几乎所有的miRNA-握力关联,miRNA浓度增加与握力增加相关。miR-20a-5p(FDR q 1.8×10)具有最显著的关联,前15种miRNA中的几种与骨骼肌有关,包括miR-126-3p、miR-30a-5p和miR-30d-5p。最相关的生物途径包括代谢、趋化因子信号传导和泛素介导的蛋白水解。我们在一个基于社区的血液miRNA样本中对与握力相关的情况进行的综合评估,为进一步了解肌肉力量生物学提供了一个框架。