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Bone mineral density in high-level endurance runners: Part B-genotype-dependent characteristics.
Herbert, A J; Williams, A G; Lockey, S J; Erskine, R M; Sale, C; Hennis, P J; Day, S H; Stebbings, G K.
Afiliação
  • Herbert AJ; School of Health Sciences, Birmingham City University, Birmingham, UK. adam.herbert@bcu.ac.uk.
  • Williams AG; Sports Genomics Laboratory, Department of Sport and Exercise Sciences, Manchester Metropolitan University, Manchester, UK.
  • Lockey SJ; Institute of Sport, Exercise and Health, University College London, London, UK.
  • Erskine RM; Faculty of Health, Education, Medicine and Social Care, Anglia Ruskin University, Chelmsford, UK.
  • Sale C; School of Sport and Exercise Science, Liverpool John Moores University, Liverpool, UK.
  • Hennis PJ; Institute of Sport, Exercise and Health, University College London, London, UK.
  • Day SH; Musculoskeletal Physiology Research Group, Sport, Health and Performance Enhancement Research Centre, School of Science and Technology, Nottingham Trent University, Nottingham, UK.
  • Stebbings GK; Musculoskeletal Physiology Research Group, Sport, Health and Performance Enhancement Research Centre, School of Science and Technology, Nottingham Trent University, Nottingham, UK.
Eur J Appl Physiol ; 122(1): 71-80, 2022 Jan.
Article em En | MEDLINE | ID: mdl-34550467
ABSTRACT

PURPOSE:

Inter-individual variability in bone mineral density (BMD) exists within and between endurance runners and non-athletes, probably in part due to differing genetic profiles. Certainty is lacking, however, regarding which genetic variants may contribute to BMD in endurance runners and if specific genotypes are sensitive to environmental factors, such as mechanical loading via training.

METHOD:

Ten single-nucleotide polymorphisms (SNPs) were identified from previous genome-wide and/or candidate gene association studies that have a functional effect on bone physiology. The aims of this study were to investigate (1) associations between genotype at those 10 SNPs and bone phenotypes in high-level endurance runners, and (2) interactions between genotype and athlete status on bone phenotypes.

RESULTS:

Female runners with P2RX7 rs3751143 AA genotype had 4% higher total-body BMD and 5% higher leg BMD than AC + CC genotypes. Male runners with WNT16 rs3801387 AA genotype had 14% lower lumbar spine BMD than AA genotype non-athletes, whilst AG + GG genotype runners also had 5% higher leg BMD than AG + GG genotype non-athletes.

CONCLUSION:

We report novel associations between P2RX7 rs3751143 genotype and BMD in female runners, whilst differences in BMD between male runners and non-athletes with the same WNT16 rs3801387 genotype existed, highlighting a potential genetic interaction with factors common in endurance runners, such as high levels of mechanical loading. These findings contribute to our knowledge of the genetic associations with BMD and improve our understanding of why some runners have lower BMD than others.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resistência Física / Corrida / Densidade Óssea / Polimorfismo de Nucleotídeo Único / Proteínas Wnt / Receptores Purinérgicos P2X7 Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Appl Physiol Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Resistência Física / Corrida / Densidade Óssea / Polimorfismo de Nucleotídeo Único / Proteínas Wnt / Receptores Purinérgicos P2X7 Tipo de estudo: Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Revista: Eur J Appl Physiol Ano de publicação: 2022 Tipo de documento: Article