A review of epigenetics and its association with ageing of muscle and bone. (November 2022)

• Record Type: Journal Article
• Authors: Fuggle, N.R.; Laskou, F.; Harvey, N.C.; Dennison, E.M.
• Is Part Of: Maturitas. Volume 165(2022)
• Page Start: 12
• Page End: 17
• Publication Date: 2022-11
• Subjects: Epigenetics -- Muscle -- Bone -- Ageing -- Review; Climacteric -- Periodicals; Menopause -- Periodicals; Climacteric -- Periodicals; Geriatrics -- Periodicals; Menopause -- Periodicals; Middle Aged -- Periodicals; Climatère -- Périodiques; Ménopause -- Périodiques; Climacterium; Climacteric; Menopause; Electronic journals; Periodicals; 612.66
• DOI: 10.1016/j.maturitas.2022.06.014
• Languages: English
• ISSNs: 0378-5122

Abstract

Highlights: Ageing is a biological process of a gradual decline in physiological capabilities. With ageing there are distinct epigenetic changes; different types of epigenetic mechanisms exist that may affect rates of musculoskeletal ageing. This review provides a comprehensive overview of the key role of epigenetic mechanisms in relation to musculoskeletal ageing. Abstract: Ageing is defined as the 'increasing frailty of an organism with time that reduces the ability of that organism to deal with stress'. It has been suggested that epigenetics may underlie the observation that some individuals appear to age faster than others. Epigenetics is the study of changes which occur in an organism due to changes in expression of the genetic code rather than changes to the genetic code itself; that is, epigenetic mechanisms impact upon the function of DNA without changing the DNA sequence. It is important to recognise that epigenetic changes, in contrast to genetic changes, can vary according to different cell types and therefore can demonstrate significant tissue-specificity. There are different types of epigenetic mechanisms: histone modification, non-coding RNAs and DNA methylation. Epigenetic clocks have been developed using statistical techniques to identify the optimal combination of CpG sites (from methylation arrays) to correlate with chronological age. This review considers how epigenetic factors may affect rates of ageing of muscle and bone and provides an overview of current understanding in this area. We discuss studies using first-generation epigenetic clocks, as well as the second-generation iterations, which appear to show stronger associations with the ageing muscle phenotype. We also review epigenome-wide association studies that have been performed in various tissues examining relationships with osteoporosis and fracture. It is hoped that an understanding of this area will lead to interventions that might prevent or reduce rates of musculoskeletal ageing in later life.