PPARα gene variation and physical performance in Russian athletes

Peroxisome proliferator-activated receptor a (PPAR alpha ) regulates genes responsible for skeletal and heart muscle fatty acid oxidation. Previous studies have shown that the PPARa intron 7 G/C polymorphism was associated with left ventricular growth in response to exercise. We speculated that GG h...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:European journal of applied physiology 2006-05, Vol.97 (1), p.103-108
Hauptverfasser: Ahmetov, Ildus I, Mozhayskaya, Irina A, Flavell, David M, Astratenkova, Irina V, Komkova, Antonina I, Lyubaeva, Ekaterina V, Tarakin, Pavel P, Shenkman, Boris S, Vdovina, Anastasia B, Netreba, Aleksei I, Popov, Daniil V, Vinogradova, Olga L, Montgomery, Hugh E, Rogozkin, Viktor A
Format: Artikel
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
Zusammenfassung:Peroxisome proliferator-activated receptor a (PPAR alpha ) regulates genes responsible for skeletal and heart muscle fatty acid oxidation. Previous studies have shown that the PPARa intron 7 G/C polymorphism was associated with left ventricular growth in response to exercise. We speculated that GG homozygotes should be more prevalent within a group of endurance-oriented athletes, have normal fatty acid metabolism, and increased percentages of slow-twitch fibers. We have tested this hypothesis in the study of a mixed cohort of 786 Russian athletes in 13 different sporting disciplines prospectively stratified by performance (endurance-oriented athletes, power-oriented athletes and athletes with mixed endurance/power activity). PPARa intron 7 genotype and allele frequencies were compared to 1,242 controls. We found an increasing linear trend of C allele with increasing anaerobic component of physical performance (P=0.029). GG genotype frequencies in endurance-oriented and power-oriehted athletes were 80.3 and 50.6%, respectively, and were significantly (P
ISSN:1439-6319
1439-6327
DOI:10.1007/s00421-006-0154-4