BJSM

HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
[Advanced]

Published Online First: 21 September 2006. doi:10.1136/bjsm.2006.030866
British Journal of Sports Medicine 2006;40:998-1002
Copyright © 2006 BMJ Publishing Group Ltd & British Association of Sport and Exercise Medicine

This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
bjsm.2006.030866v1
40/12/998    most recent
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this link to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Add article to my folders
Right arrow Download to citation manager
Right arrowRequest Permissions
Citing Articles
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by He, Z
Right arrow Articles by Lucia, A
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by He, Z
Right arrow Articles by Lucia, A

ORIGINAL ARTICLE

Polymorphisms in the HBB gene relate to individual cardiorespiratory adaptation in response to endurance training

Z He1, Y Hu2, L Feng1, Y Lu1, G Liu2, Y Xi3, L Wen3, X Xu2, K Xu2

1 Biology Center, China Institute of Sport Science, Beijing, China
2 Department of Sport and Human Sciences, Beijing Sport University, Beijing, China
3 Department of Sport and Human Sciences, Tianjin Institute of Physical Education, Tianjin, China

Correspondence to:
Correspondence to:
Yang Hu
Section of Exercise Biochemistry, Department of Sport and Human Sciences, Beijing Sport University, Beijing 100084, China; bsugene{at}yahoo.com

Objective: The crucial role of haemoglobin in endurance performance has been well documented. We examined whether polymorphisms in the HBB gene modified aerobic capacity.

Methods: 102 recruits were trained by running 5000 m three times per week for 18 weeks. Exercise intensity progressively increased from an initial heart rate corresponding to 95% of the individual baseline ventilatory threshold during the first 10 weeks to 105% during the last 8 weeks. The phenotypes measured were running economy and VO2max. Running economy was determined by measuring submaximal VO2 for 5 min at a constant running speed of 12 km·h–1 and VO2max was obtained during an incremental test to exhaustion. Genomic DNA was extracted from white cells of peripheral blood and the –551C/T, intron2,+16C/G and +340 A/T genotypes were examined relative to the TAA site variants by PCR-RFLP.

Results: Genotype distributions were in Hardy-Weinberg equilibrium at three loci. None of the running economy and VO2max-related traits were associated with the three polymorphisms or haplotypes at baseline, while the training response of running economy was associated with –551C/T and intron2,+16C/G polymorphisms. Subjects homozygous for intron2,+16C/C or –551C/C had decreased oxygen cost of running compared to the other individuals.

Discussion: It was concluded that the –551C/C or intron2,+16C/C genotype might explain part of the individual variation in the cardiorespiratory adaptation to endurance training.


Abbreviations: ATP, adenosine 5'-triphosphate; LBM, lean body mass; RER, respiratory exchange ratio; TBM, total body mass; UTR, untranslated region

Keywords: haplotype; polymorphism; running economy; training; VO2max


 

Commentary

A Lucia

Universidad Europea de Madrid, Spain; alejandro.lucia{at}uem.es







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS REGISTER
Terms and conditions relating to subscriptions purchased online  ¦  Website terms and conditions  ¦  Privacy policy
Copyright © 2006 BMJ Publishing Group Ltd & British Association of Sport and Exercise Medicine