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PPARGC1A gene polymorphism is associated with exercise-induced fat loss

Mazur, II, Drozdovska, S, Andrieieva, O, Vinnichuk, Y, Polishchuk, A, Dosenko, V, Andreev, I, Pickering, C and Ahmetov, II (2020) PPARGC1A gene polymorphism is associated with exercise-induced fat loss. Molecular Biology Reports, 47 (10). pp. 7451-7457. ISSN 0301-4851

PPARGC1A gene polymorphism is associated with exercise-induced fat loss.pdf - Accepted Version

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Obesity is a widespread problem within modern society, serving to increase the risk of cardiovascular, metabolic, and neurodegenerative disorders. Peroxisome proliferator-activated receptor gamma (PPARγ) and PPARγ coactivator 1 α (PGC1α) play a key role in the regulation of cellular energy metabolism and is implicated in the pathology of these diseases. This study examined the association between polymorphisms of the PPARG and PPARGC1A genes and individual variability in weight loss in response to physical activity intervention. 39 obese Ukrainian women (44.4 ± 7.5 years, BMI > 30.0 kg/m2) undertook a 3-month fitness program whilst following a hypocaloric diet (~ 1500 cal). Anthropometric and biochemical measurements took place before and after the program. Single nucleotide polymorphisms within or near PPARG (n = 94) and PPARGC1A (n = 138) were identified and expression of PPARG mRNA was measured via reverse transcription and amplification. The association between DNA polymorphisms and exercise-induced weight loss, initial body mass, biochemistry and PPARG expression was determined using one-way analysis of variance (ANOVA). The present intervention induced significant fat loss in all participants (total fat: 40.3 ± 5.3 vs 36.4 ± 5.7%; P < 0.00001). Only one polymorphism (rs17650401 C/T) within the PPARGC1A gene was found to be associated with fat loss efficiency after correction for multiple testing, with T allele carriers showing the greatest reduction in body fat percentage (2.5-fold; P = 0.00013) compared to non-carriers. PPARGC1A (rs17650401) is associated with fat loss efficiency of the fitness program in obese women. Further studies are warranted to test whether this variation is associated with fat oxidation.

Item Type: Article
Additional Information: This is a post-peer-review, pre-copyedit version of an article published in Molecular Biology Reports. The final authenticated version is available online at: http://dx.doi.org/10.1007/s11033-020-05801-z
Uncontrolled Keywords: 0601 Biochemistry and Cell Biology
Subjects: R Medicine > RC Internal medicine > RC1200 Sports Medicine
Divisions: Sport & Exercise Sciences
Publisher: Springer
Related URLs:
Date Deposited: 26 Nov 2020 12:24
Last Modified: 10 Sep 2021 00:50
DOI or ID number: 10.1007/s11033-020-05801-z
URI: https://researchonline.ljmu.ac.uk/id/eprint/14087
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