Background
Sarcopenia is associated with adverse health outcomes and incurs a substantial health care cost [
1‐
3]. Defined as the loss of skeletal muscle mass and function, sarcopenia is common in both men and women over the age of 65 across a range of healthcare settings [
4]. For example, among community dwelling older people in the UK, prevalence rates for sarcopenia have been estimated at 4.6 % for men and 7.9 % for women [
5]. Sarcopenia has been defined based on lean mass indices i.e., total lean mass, appendicular lean mass and muscle function i.e., grip strength or physical performance. Notable diagnostic algorithms include The European Working Group on Sarcopenia in Older People (EWGSOP) [
6], The Foundation for the National Health Institutes of Health (FNIH) Sarcopenia Project [
7], and the Asian Working Group for Sarcopenia (AWGS) [
8], the latter definition to account for ethnic variations in muscle mass and muscle function.
There is considerable interest in understanding the mechanisms driving sarcopenia and there have been a number of small studies investigating morphological changes in skeletal muscle with increasing age. For example, it has been reported that between the sixth and ninth decades, myofibre size and number decrease in both men and women [
9]. In addition there is type I and type II myofibre atrophy, as well as other changes in muscle morphology including the appearance of hybrid fibres, the presence of hypertrophied fibres and fibre type grouping [
10‐
12]. Although not completely understood, several factors contribute to these morphological changes including, inflammation, denervation, oxidative stress, imbalance in protein synthesis and reduced satellite cell number and or function [
13].
Studies of muscle morphology have rarely been population based and how these morphological changes relate to altered skeletal muscle mass, function and sarcopenia is unclear. The objective of this study was therefore to determine the relationship between muscle morphology and sarcopenia as defined using the European Working Group Sarcopenia in Older People (EWGSOP) criteria in a population based study of community dwelling older men.
Discussion
We have investigated the association between skeletal muscle morphology and sarcopenia defined by the EWGSOP criteria in a population based study of community dwelling older men. In this study, there was a suggestion that the six HSS men with sarcopenia had lower average SC density and SC/fibre ratio in comparison with those without sarcopenia but the relationship was not significant at the 5 % level.
Satellite cells (SC) are undifferentiated stem cells responsible for myofibre maintenance and are central to the growth and repair of muscle and have the ability to enter the cell cycle, proliferate and self-renew [
20,
21]. SC number fluctuate in younger and older adults in response to both intrinsic and extrinsic regulatory cues [
22]. For example, physical activity [
23] as well as with drug treatment [
24]. The niche surrounding the SC is also a critical regulator of function and is governed by growth factors, signalling molecules as well as innervation [
22,
25].
In support of our results, satellite cell content of fibres has been reported to decrease in the muscles of older humans. For example, Verdijk et al. showed that in older humans, SC content, specifically in type II myofibres, were lower when compared to younger controls [
22]. In a study by Kadi et al. SC per fibre ratio was significantly lower in healthy older men and women compared to their younger counterparts [
26]. In the later study, no inference was made on whether there was a fibre specific reduction as was reported by Verdijk et al. Therefore it appears that a reduction in satellite cells may mediate the observed muscle atrophy, specifically of type II fibres, with age. However, a detailed morphological study conducted by Purves-Smith et al. suggested that in very old individuals who may have severe muscle atrophy, both myofibre types show atrophic changes [
12].
The exact reasons for a decrease in SC content or a decline in SC function with age are unknown. Contributing factors include alterations in the surrounding environment including denervation and oxidative damage [
27] as well as decrease in activity of crucial myogenic regulatory factors coupled with an increase in negative regulators of muscle growth [
28,
29]. For example, myostatin appears to suppress certain myogenic regulatory factors crucial for proliferation and differentiation and therefore has been postulated to impair function as well as self-renewal of satellite cells [
30]. Taken together, it appears that loss of SC or reduced SC function diminishes the ability of ageing muscle to both hypertrophy in response to stimulus or repair and self-renew in response to injury thereby contributing to sarcopenia [
27]. However, a recent study in older mice who were SC deplete suggested that neither force generation nor single fibre cross sectional area was affected by a reduction in SC number [
31]. Clearly, further studies are needed in both male and female ageing cohorts to investigate the role of SC in sarcopenia.
We observed a non-significant trend (
p > 0.05) for men with sarcopenia to have, on average, smaller slow and fast fibre areas and lower capillary to fibre ratios. Whereas myofibre morphology measurements in relation to exercise, immobilisation and ageing have been described in a number of studies [
9], this is one of the first studies to describe muscle morphology in relation to sarcopenia in community dwelling older men. Muscle mass and cross sectional area (CSA) are functions of myofibre size and number [
32] and we speculate that smaller fibres seen in our study are associated with the decrease in total lean mass in men who were sarcopenic. The results of a longitudinal study by Frontera et al. [
33] which revealed age related reductions in muscle cross sectional area as well as capillary to fibre ratio in men is in partial support of our cross sectional findings.
Our study had several limitations. First, the sample size was modest which will have limited statistical power. Second, the immunohistochemical methodology used to quantify the morphology parameters was open to observer error although consistent and rigorous methods were applied throughout the study in order to limit this possibility. Also, we did not evaluate SC content per specific fibre type or other indices of muscle capillarity [
34]. Finally, the parameters measured may not accurately reflect the morphological changes occurring in muscle. Longitudinal studies would be helpful to more fully characterise the morphological changes that occur over time in the muscle of people with sarcopenia.
However, our study has a number of strengths. First, we have shown that it is feasible to obtain tissue from community dwelling older men in the context of an epidemiological birth cohort. The advantage of this is that morphological data can be combined with the extensive phenotypic data that has already been collected. Second, the immunohistochemical methodologies employed were based on tested protocols and can be applied to future large scale studies. For example, whereas SC have typically been studied through electron microscopy and immunofluorescence [
35], few studies have employed simple immunohistochemistry techniques to quantify satellite cells in healthy individuals [
26]. Our study shows that quantification of several morphological variables is possible using these methods. However, measurements of specific fibre type/SC content as well as other indices of capillarisation will need to be considered when applied to future studies.
Conclusions
Our results suggest that men with sarcopenia may have decreased satellite cell content and perhaps also smaller fibres and lower capillary to fibre ratios in comparison with men without sarcopenia. We can only speculate, given the sample size and cross sectional nature of the study, that the morphological results seen not only have an effect on muscle mass but also on muscle quality [
31]. These morphological changes impact on muscle performance in men with sarcopenia, who by definition have grip strengths of less than 30 kg, walking speed less than 0.8 m per second and low muscle mass [
5].
The importance of this work is that the identification of morphological changes in older people with sarcopenia has the potential to identify cellular and molecular targets for therapeutic intervention. Methodological findings from this study now need to be applied to large scale studies that also include women.
Competing interests
The authors declare that they have no competing interests.
Authors’ contributions
HPP, HES, AAS, CC, MW, PJS, GC participated in the conception, design and conduct of the study. LW and HES conducted statistical analyses. HPP drafted the first version of the manuscript. All authors read and approved the final manuscript.