SYSTEMATIC REVIEW article
Sec. Exercise Physiology
Volume 12 - 2021 | https://doi.org/10.3389/fphys.2021.706189
A Systematic Review of the Association Between Muscular Fitness and Telomere Length Across the Adult Lifespan
- 1CIPER, Faculty of Human Kinetics, University of Lisbon, Lisbon, Portugal
- 2ISAMB, University of Lisbon, Lisbon, Portugal
- 3Faculty of Human Kinetics, University of Lisbon, Lisbon, Portugal
- 4Departamento de Educação Física e Desporto, Universidade da Madeira, Funchal, Portugal
- 5Interactive Technologies Institute, LARSyS, Funchal, Portugal
- 6Laboratorio de Ciencias de la Actividad Física, el Deporte y la Salud, Facultad de Ciencias Medicas, Universidad de Santiago de Chile, Santiago, Chile
- 7University of Coimbra, Research Unit for Sport and Physical Activity (CIDAF) Faculty of Sport Sciences and Physical Education, Coimbra, Portugal
- 8Center for the Interdisciplinary Study of Gerontology and Vulnerability, University of Geneva, Geneva, Switzerland
- 9Swiss National Centre of Competence in Research LIVES—Overcoming Vulnerability: Life Course Perspectives, Lausanne and Geneva, Switzerland
- 10Department of Psychology, University of Geneva, Geneva, Switzerland
This study aimed to systematically review the association between telomere length (TL) and muscular fitness. In October 2020, an articles search was applied to PubMed, Scopus, and Web of Science. Eligibility criteria included: cross-sectional, prospective, and experimental study design; outcomes included TL; results expressed the relationship between muscular fitness and TL; studies published in English, Portuguese, or Spanish. Nine studies were included in the review. Results from the four prospective studies are mixed. In one study, the changes in TL were associated with grip strength. Another study concluded that longer mid-life TL was associated with increased grip strength later in life. However, in the other two studies, the association between TL and sarcopenia was not strong. Nevertheless, longer TL was associated with a slower decline in grip strength in older people. From the four cross-sectional studies, three indicated that TL was associated with muscular fitness. On the other hand, in a study with powerlifters, TL remained within the range of values found in subjects with no history of regular strength training, supporting the notion that muscular fitness was not associated with TL. The cross-sectional and prospective studies showed that the relationship between TL and muscular fitness is not conclusive. It seems that there is a positive association between TL and muscular fitness in middle-aged and older adults. However, among younger adults, this relationship was not observed.
Chromosome ends are protected by tandem repeats of hexanucleotide units named telomeres (Lu et al., 2013). Telomeres are critical in regulating cellular replicative capacity (Codd et al., 2013). The functional status of telomeres depends on the telomeric nucleoprotein structure's stability and length (Wang et al., 2018). The telomeres shorten each time a cell divides because of the inability of the DNA polymerase to replicate the ends of the linear molecules completely. Telomere length (TL) shortening is associated with cellular senescence (Liu et al., 2019), oxidative stress (Mundstock et al., 2015a), increased inflammatory process (Arsenis et al., 2017), tobacco smoking, alcohol consumption, and physical activity (Mather et al., 2010; Codd et al., 2013; Lin et al., 2019). Also, psychological disorders and low social-economic levels can accelerate the TL shortening process (Zhang et al., 2014). However, TL shortening is not an irreversible process because of telomerase, an enzyme capable of extending telomeres. Thus, it seems likely that TL is subject to different regulations in body systems to maintain tissue integrity (Kadi et al., 2008). TL in skeletal muscle can be considered more dynamic structures under the influence of the environment, such as physical activity, exercise, and physical fitness (Kadi and Ponsot, 2010).
Physical activity and physical fitness appear to play an essential role in the TL shortening process (Soares-Miranda et al., 2015; Tucker, 2017). Several potential mechanisms are involved, including changes in telomerase activity, oxidative stress, inflammation, and decreased skeletal muscle satellite cell content (Arsenis et al., 2017). Oxidative stress is improved by physical activity (Polidori et al., 2000). However, practice time could induce anti-oxidant activity and improve inflammatory balance (Simioni et al., 2018). Moreover, resistance and aerobic training have been shown to increase the number of satellite cells, which may be necessary for regulating skeletal muscle TL (Kadi and Ponsot, 2010).
Studies systematically reviewing the effect of physical activity on TL concluded that physical activity seems to positively affect TL (Mundstock et al., 2015b; Arsenis et al., 2017; Lin et al., 2019). However, there is not enough evidence to fully elucidate the underlying mechanisms in detail from these studies. Another systematic review focused on the association between cardiorespiratory fitness and TL, and the evidence was also not sufficient to entirely understand this complex issue (Marques et al., 2020). Thus, the role of physical activity in combating the typical age-induced decrements in TL remains without a clear definition. Given the importance of TL, there is a need to understand better the potential association with another important component of health-related physical fitness, such as muscular fitness. Thus, this study systematically reviewed the evidence regarding the association between TL and muscular fitness in adults. Given the exposed mechanisms of TL, it is hypothesized that greater TL is associated with better muscular fitness.
Inclusion Criteria and Search Strategy
The review was performed following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines (Moher et al., 2009). Articles on the relationship between muscular fitness and TL published in peer-reviewed journals until the 31st of October 2020 served as a basis for this review. Eligibility criteria included the following: (a) cross-sectional, prospective, and experimental study design (study design criterion); (b) outcomes included TL (outcome measure criterion); (c) muscular fitness and TL (relationship criterion); (d) young, adults, and older adults (participants criterion); (e) articles published in English, Portuguese, or Spanish (language criterion); (f) articles were left out if they did not meet inclusion criteria or did not have findings associated to the inclusion criteria (exclusion criteria).
In October 2020, the article search was conducted in PubMed, Scopus, and Web of Science. Articles that assessed the relationship between muscular fitness and TL were included. The search was performed using the following terms: telomer* AND fitness OR muscle* OR muscular. The research team defined search terms, and the same terms were used in each database to identify articles for review. Two reviewers worked individually and screened titles and abstracts to identify articles that met the inclusion criteria. Duplicate entries were removed. Articles meeting the inclusion criteria were retrieved for a full read. Two authors reviewed the full text of potential studies, and decisions to include or exclude articles in the review were made by consensus. However, a third reviewer served as a judge to solve eventual disagreements.
The PRISMA statement (Moher et al., 2009) was used for data extraction. From each article, it was extracted the authors' name, year of publication, study design, sample characteristics, country, method of TL evaluation, methods of muscular fitness evaluation, study quality, and main results. The extraction was carried out by one author, and coding was verified by two other authors.
Study Quality and Risk of Bias
The methodological quality of the articles was assessed by two researchers independently using the Physiotherapy Evidence Database (PEDro) scale. Agreement between reviewers was assessed using k statistics (k = 0.96) for full-text screening and rating of relevance and risk of bias. A third reviewer solved eventual disagreements about the risk of bias and made the final decision. The methodological quality of the included articles was assessed with a total score ranging from zero (lowest) to 11 (highest quality).
Synthesis of Results
The review analyzed the relationship between muscular fitness and TL. Substantial heterogeneity existed across the reviewed studies for several study parameters. These parameters included: participant characteristics, tissue or fluid used to analyse telomeres, method of TL evaluation, and methods of muscular fitness evaluation. The details for each study, including design, measures, sample size and participant characteristics, and study quality and results, are presented consistently.
The search in the databases brought forth 312 records, and one record was identified through other sources. After excluding the 146 duplicates, 167 were selected for the title and abstract reading. Of these 167 articles, 24 records were discarded because not being research studies, seven were abstracts or letters to the editors, and 113 did not contain an assessment of muscular fitness and TL. From the 23 remained records, after reading the full text, 14 were discarded because five did not have a focus on muscular fitness and nine were studies with animals. Therefore, nine studies were finally included in the systematic review. The flow diagram is presented in Figure 1.
Table 1 presents the characteristics of the final set of studies. Nine studies were included in the review, totalling 20,269 adults, from six countries (China, Finland, South Korea, Sweden, United Kingdom, and the United States of America). Among the studies, four were cross-sectional, observational comparative studies, four were prospective studies, and one was a cross-sectional and a prospective observational study. The methods to assess TL were polymerase chain reaction (PCR) (6/9), Southern blot (2/9), and G-spin TM Genomic (1/9). The most frequent method used to evaluate muscular fitness was through maximal isometric grip strength (kg) measured by a hand dynamometer (7/9). Other measures of muscular fitness were the gait speed test (1/9) and powerlifting national completion performance (1/9).
The main results from each study on the relationship between muscular fitness and TL are also presented in Table 1. The four prospective studies are mixed (Baylis et al., 2014; Woo et al., 2014; Williams et al., 2017). One observed that changes in TL over 10-years of follow-up were significantly associated with grip strength, and faster TL attrition was associated with lower grip strength (Baylis et al., 2014). Another study concluded that longer mid-life blood leukocyte TL was associated with increased grip strength later in life (Chang et al., 2020). However, in the other two prospective studies, the observed inverse association between TL and sarcopenia was not strong (Woo et al., 2014). Although longer LT was associated with higher aerobic fitness and trunk muscle endurance, it was not associated with grip strength in young adulthood (Williams et al., 2017). Nevertheless, longer TL was associated with a slower decline in grip strength in older persons (Woo et al., 2014). From the four cross-sectional studies, three indicated that leukocyte TL was associated with muscular fitness, and skeletal muscle TL was associated with higher fat-free mass and greater thigh muscle area (Lee et al., 2013; Loprinzi and Loenneke, 2016; Sillanpaä et al., 2017). On the other hand, in a cross-sectional study with powerlifters, TL remained within the range of values found in subjects with no history of regular strength training (Kadi et al., 2008), suggesting that muscular fitness was not associated with TL. The cross-sectional and prospective observational study showed that grip strength was not significantly associated with TL in the prospective analysis (Soares-Miranda et al., 2015).
Nine studies examining the association between muscular fitness and TL were identified. Overall, five studies reported that TL was positively associated with muscular fitness, including gait speed, grip strength, lower extremity muscular strength, fat-free mass, and thigh muscle area. On the other hand, the other four studies described inconclusive results.
TL shortening is associated with increased all-cause mortality risk (Wang et al., 2018) and limitations in physical function (Montiel Rojas et al., 2018). In turn, muscular fitness is positively associated with physical function and is negatively associated with all-cause mortality (Liu et al., 2014; Garcia-Hermoso et al., 2018). Accordingly, slightly more than half of the studies included in this review presented a positive association between TL and muscular fitness measures (Lee et al., 2013; Baylis et al., 2014; Loprinzi and Loenneke, 2016; Sillanpaä et al., 2017; Chang et al., 2020). These studies were mainly focused on middle-aged and older adults, strengthening evidence that points to TL being a biological marker of cellular senescence and physical aging (von Zglinicki and Martin-Ruiz, 2005). Especially among middle-aged and older adults, physical function is an important determinant of disease (O'Neill and Forman, 2020). Reinforcing this idea, in three of those studies, grip strength or gait speed were shown to be associated with TL (Lee et al., 2013; Baylis et al., 2014; Chang et al., 2020). On the other hand, two of the studies included in the review also focused on older adults, presented dissimilar findings, not sustaining the hypothesis of a direct association between TL and muscular fitness (Woo et al., 2014; Soares-Miranda et al., 2015).
It was observed that the association between TL and sarcopenia among Chinese older adults was not strong (Woo et al., 2014). Nevertheless, longer TL was still associated with a slower decline in grip strength. Also, among older adults from the USA, it was identified that grip strength was not directly associated with TL (Soares-Miranda et al., 2015). In summary, results from most studies performed in middle-aged and older adults seem to indicate a positive association between TL and muscular fitness, suggesting a possible connection between TL and healthy aging. Notwithstanding, more studies are warranted to better understand this association and the role of muscular fitness in the interaction with TL.
The shortening of TL is associated with cellular aging and can represent biological age (Arsenis et al., 2017). Thus, as people age, telomeres naturally shorten. However, their attrition is relatively stable from childhood to adulthood (Oeseburg et al., 2010). Two of the studies included in this review were conducted among younger adults (~30 years old), having presented non-significant or inconsistent findings (Kadi et al., 2008; Williams et al., 2017). In one study conducted in Sweden, it was found that the TL values of powerlifters (individuals regularly performing strength training) were similar to those with no history of regular strength training (Kadi et al., 2008). The second study, conducted in Finland, showed that longer TL was associated with higher aerobic fitness and trunk muscle endurance, but not grip strength (Williams et al., 2017). The interaction between TL and aging may explain these results among younger adults, as telomeres in younger ages are less likely to have experienced attrition. Therefore, behavioral factors such as physical inactivity and sedentariness (Arsenis et al., 2017).
Changing TL has been proposed to be one of the mechanisms through which muscular fitness is related to all-cause mortality and disease (Loprinzi and Loenneke, 2016). Mitochondrial dysfunction with age can in part explain the association between muscular fitness and TL, which is further supported by the relationship between sarcopenia, oxidative stress, and chronic inflammation (Marzetti et al., 2013). Notwithstanding, even when adjusting for inflammation (C-reactive protein) and antioxidant status (uric acid), the relationship between strength and TL remained significant (Loprinzi and Loenneke, 2016), suggesting that strength may influence TL through other mechanisms, which are still open to interpretation.
This review has some limitations that must be acknowledged and taken into account when interpreting the findings. Differences across the included studies (sample size, tissue sources, methods of evaluation of telomeres, and methods of muscular fitness evaluation) can influence the association between TL and muscular fitness and, therefore, may contribute to the variety of observed results. Also, some of the studies included in the review had small sample sizes. Nonetheless, the small number of empirical studies on the topic existing so far does not allow establishing a stratification of evidence by those additional factors. Additionally, the variety of study methodologies and outcome measures makes it impossible to adequately perform a meta-analysis.
The existing empirical evidence on the relationship between TL and muscular fitness is mixed and may be influenced by additional factors, such as individuals' age. In this regard, it seems that there is a positive association between TL and muscular fitness in middle-aged and older adults. However, among younger adults, such a relationship may not be evident.
Data Availability Statement
The original contributions presented in the study are included in the article/supplementary material, further inquiries can be directed to the corresponding author.
AM, MP, DH-N, and AI: conceptualization. AM, MP, and DH-N: methodology development. MP and PM: formal analysis. MP and DH-N: investigation. AM, MP, and PM: writing original draft. EG, GF, JM, HS, and AI: writing review and editing. EG, GF, HS, and AI: visualization. HS and AI: supervision. All authors contributed to the article and approved the submitted version.
This work was supported by the Swiss National Centre of Competence in Research LIVES—Overcoming vulnerability: life course perspectives, granted by the Swiss National Science Foundation (grant number: 51NF40-185901). AI acknowledges support from the Swiss National Science Foundation (grant number: 10001C_189407).
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Arsenis, N. C., You, T., Ogawa, E. F., Tinsley, G. M., and Zuo, L. (2017). Physical activity and telomere length: impact of aging and potential mechanisms of action. Oncotarget 8, 45008–45019. doi: 10.18632/oncotarget.16726
Baylis, D., Ntani, G., Edwards, M. H., Syddall, H. E., Bartlett, D. B., Dennison, E. M., et al. (2014). Inflammation, telomere length, and grip strength: a 10-year longitudinal study. Calcif. Tissue Int. 95, 54–63. doi: 10.1007/s00223-014-9862-7
Chang, X., Chua, K. Y., Wang, L., Liu, J., Yuan, J. M., Khor, C. C., et al. (2020). Mid-life leukocyte telomere length as an indicator for handgrip strength in late-life. J. Gerontol. A. Biol. Sci. Med. Sci. 76, 172–175. doi: 10.1093/gerona/glaa260
Codd, V., Nelson, C. P., Albrecht, E., Mangino, M., Deelen, J., Buxton, J. L., et al. (2013). Identification of seven loci affecting mean telomere length and their association with disease. Nature Genet. 45, 422–427. doi: 10.1038/ng.2528
Garcia-Hermoso, A., Cavero-Redondo, I., Ramirez-Velez, R., Ruiz, J. R., Ortega, F. B., Lee, D. C., et al. (2018). Muscular strength as a predictor of all-cause mortality in an apparently healthy population: a systematic review and meta-analysis of data from ~2 million men and women. Arch. Phys. Med. Rehabil. 99, 2100–2113. doi: 10.1016/j.apmr.2018.01.008
Kadi, F., and Ponsot, E. (2010). The biology of satellite cells and telomeres in human skeletal muscle: effects of aging and physical activity. Scand. J. Med. Sci. Sports 20, 39–48. doi: 10.1111/j.1600-0838.2009.00966.x
Kadi, F., Ponsot, E., Piehl-Aulin, K., Mackey, A., Kjaer, M., Oskarsson, E., et al. (2008). The effects of regular strength training on telomere length in human skeletal muscle. Med. Sci. Sports Exerc. 40, 82–87. doi: 10.1249/mss.0b013e3181596695
Lee, J. Y., Bang, H. W., Ko, J. H., Kim, J. H., and Lee, D. C. (2013). Leukocyte telomere length is independently associated with gait speed in elderly women. Maturitas 75, 165–169. doi: 10.1016/j.maturitas.2013.03.008
Lin, X., Zhou, J., and Dong, B. (2019). Effect of different levels of exercise on telomere length: a systematic review and meta-analysis. J. Rehabil. Med. 51, 473–478. doi: 10.2340/16501977-2560
Liu, C. J., Shiroy, D. M., Jones, L. Y., and Clark, D. O. (2014). Systematic review of functional training on muscle strength, physical functioning, and activities of daily living in older adults. Eur. Rev. Aging Phys. Act. 11, 95–106. doi: 10.1007/s11556-014-0144-1
Liu, Y., Bloom, S. I., and Donato, A. J. (2019). The role of senescence, telomere dysfunction and shelterin in vascular aging. Microcirculation 26, e12487. doi: 10.1111/micc.12487
Loprinzi, P. D., and Loenneke, J. P. (2016). Lower extremity muscular strength and leukocyte telomere length: implications of muscular strength in attenuating age-related chronic disease. J. Phys. Act. Health 13, 454–457. doi: 10.1123/jpah.2015-0120
Lu, W., Zhang, Y., Liu, D., Songyang, Z., and Wan, M. (2013). Telomeres-structure, function, and regulation. Exp. Cell Res. 319, 133–141. doi: 10.1016/j.yexcr.2012.09.005
Marques, A., Gouveira, É., R., Peralta, M., Martins, J., Venturini, J., et al. (2020). Cardiorespiratory fitness and telomere length: a systematic review. J. Sports Sci. 38, 1690–1697. doi: 10.1080/02640414.2020.1754739
Marzetti, E., Calvani, R., Cesari, M., Buford, T. W., Lorenzi, M., Behnke, B. J., et al. (2013). Mitochondrial dysfunction and sarcopenia of aging: from signaling pathways to clinical trials. Int. J. Biochem. Cell Biol. 45, 2288–2301. doi: 10.1016/j.biocel.2013.06.024
Mather, K. A., Jorm, A. F., Parslow, R. A., and Christensen, H. (2010). Is telomere length a biomarker of aging? a review. J. Gerontol. Ser. A 66A, 202–213. doi: 10.1093/gerona/glq180
Moher, D., Liberati, A., Tetzlaff, J., Altman, D. G., and Group, P. (2009). Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Ann. Intern. Med. 151, 264–269. doi: 10.7326/0003-4819-151-4-200908180-00135
Montiel Rojas, D., Nilsson, A., Ponsot, E., Brummer, R. J., Fairweather-Tait, S., Jennings, A., et al. (2018). Short telomere length is related to limitations in physical function in elderly European adults. Front. Physiol. 9:1110. doi: 10.3389/fphys.2018.01110
Mundstock, E., Sarria, E. E., Zatti, H., Mattos Louzada, F., Kich Grun, L., Herbert Jones, M., et al. (2015a). Effect of obesity on telomere length: systematic review and meta-analysis. Obesity 23, 2165–2174. doi: 10.1002/oby.21183
Mundstock, E., Zatti, H., Louzada, F. M., Oliveira, S. G., Guma, F. T. C. R., Paris, M. M., et al. (2015b). Effects of physical activity in telomere length: systematic review and meta-analysis. Ageing Res. Rev. 22, 72–80. doi: 10.1016/j.arr.2015.02.004
Oeseburg, H., de Boer, R. A., van Gilst, W. H., and van der Harst, P. (2010). Telomere biology in healthy aging and disease. Pflugers Arch. 459, 259–268. doi: 10.1007/s00424-009-0728-1
O'Neill, D., and Forman, D. E. (2020). The importance of physical function as a clinical outcome: assessment and enhancement. Clin. Cardiol. 43, 108–117. doi: 10.1002/clc.23311
Polidori, M. C., Mecocci, P., Cherubini, A., and Senin, U. (2000). Physical activity and oxidative stress during aging. Int. J. Sports Med. 21, 154–157. doi: 10.1055/s-2000-8881
Sillanpaä, E., Niskala, P., Laakkonen, E. K., Ponsot, E., Alén, M., Kaprio, J., et al. (2017). Leukocyte and skeletal muscle telomere length and body composition in monozygotic twin pairs discordant for long-term hormone replacement therapy. Twin Res. Hum. Genet. 20, 119–131. doi: 10.1017/thg.2017.1
Simioni, C., Zauli, G., Martelli, A. M., Vitale, M., Sacchetti, G., Gonelli, A., et al. (2018). Oxidative stress: role of physical exercise and antioxidant nutraceuticals in adulthood and aging. Oncotarget 9, 17181–17198. doi: 10.18632/oncotarget.24729
Soares-Miranda, L., Imamura, F., Siscovick, D., Jenny, N. S., Fitzpatrick, A. L., and Mozaffarian, D. (2015). Physical activity, physical fitness, and leukocyte telomere length: the cardiovascular health study. Med. Sci. Sports Exerc. 47, 2525–2534. doi: 10.1249/MSS.0000000000000720
Tucker, L. A. (2017). Physical activity and telomere length in U.S. men and women: an NHANES investigation. Prev. Med. 100, 145–151. doi: 10.1016/j.ypmed.2017.04.027
von Zglinicki, T., and Martin-Ruiz, C. M. (2005). Telomeres as biomarkers for ageing and age-related diseases. Curr. Mol. Med. 5, 197–203. doi: 10.2174/1566524053586545
Wang, Q., Zhan, Y., Pedersen, N. L., Fang, F., and Hägg, S. (2018). Telomere length and all-cause mortality: a meta-analysis. Ageing Res. Rev. 48, 11–20. doi: 10.1016/j.arr.2018.09.002
Williams, D. M., Buxton, J. L., Kantomaa, M. T., Tammelin, T. H., Blakemore, A. I. F., and Järvelin, M. R. (2017). Associations of leukocyte telomere length with aerobic and muscular fitness in young adults. Am. J. Epidemiol. 185, 529–537. doi: 10.1093/aje/kww123
Woo, J., Yu, R., Tang, N., and Leung, J. (2014). Telomere length is associated with decline in grip strength in older persons aged 65 years and over. Age 36:9711. doi: 10.1007/s11357-014-9711-7
Zhang, L., Hu, X. Z., Li, X., Li, H., Smerin, S., Russell, D., et al. (2014). Telomere length - a cellular aging marker for depression and post-traumatic stress disorder. Med. Hypotheses 83, 182–185. doi: 10.1016/j.mehy.2014.04.033
Keywords: handgrip, physical fitness, leukocyte, genetics, muscle
Citation: Marques A, Peralta M, Marconcin P, Henriques-Neto D, Gouveia ÉR, Ferrari G, Martins J, Sarmento H and Ihle A (2021) A Systematic Review of the Association Between Muscular Fitness and Telomere Length Across the Adult Lifespan. Front. Physiol. 12:706189. doi: 10.3389/fphys.2021.706189
Received: 07 May 2021; Accepted: 25 June 2021;
Published: 15 July 2021.
Edited by:Hamdi Chtourou, University of Sfax, Tunisia
Reviewed by:Raouf Hammami, University of Manouba, Tunisia
Morteza Taheri, Imam Khomeini International University, Iran
Copyright © 2021 Marques, Peralta, Marconcin, Henriques-Neto, Gouveia, Ferrari, Martins, Sarmento and Ihle. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Adilson Marques, firstname.lastname@example.org