4.4 Article

Sex-specific alteration in human muscle transcriptome with age

期刊

GEROSCIENCE
卷 45, 期 3, 页码 1303-1316

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SPRINGER
DOI: 10.1007/s11357-023-00795-5

关键词

Sarcopenia; Sex; Aging; Muscle

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Sarcopenia, a condition characterized by decreased muscle mass, altered muscle composition, and reduced muscle strength, disproportionately affects males and females with age. This study identified differentially regulated genes in aged skeletal muscle from males and females, with 269 genes showing at least a twofold expression difference. Gene Ontology analysis revealed distinct pathways involved in aged female and male skeletal muscle, suggesting the potential for sex-specific therapeutic targets to combat sarcopenia and promote healthy aging.
Sarcopenia is a medical condition that progressively develops with age and results in reduced skeletal muscle mass, alteration in muscle composition, and decreased muscle strength. Several clinical studies suggested that sarcopenia disproportionally affects males and females with age. Despite this knowledge, the molecular mechanism governing the pathophysiology is not well understood in a sex-specific manner. In this study, we utilized human gastrocnemius muscles from males and females to identify differentially regulated genes with age. We found 269 genes with at least a twofold expression difference in the aged muscle transcriptome. Among the female muscle samples, there were 239 differentially regulated genes, and the novel protein-coding genes include KIF20A, PIMREG, MTRNR2L6, TRPV6, EFNA2, RNF24, and SFN. In aged male skeletal muscle, there were 166 differentially regulated genes, and the novel-protein coding genes are CENPK, CDKN2A, BHLHA15, and EPHA. Gene Ontology (GO) enrichment revealed glucose catabolism, NAD metabolic processes, and muscle fiber transition pathways that are involved in aged female skeletal muscle, whereas replicative senescence, cytochrome C release, and muscle composition pathways are disrupted in aged male skeletal muscle. Targeting these novels, differentially regulated genes, and signaling pathways could serve as sex-specific therapeutic targets to combat the age-related onset of sarcopenia and promote healthy aging.

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