PPARGC1A rs8192678 and NRF1 rs6949152 Polymorphisms Are Associated with Muscle Fiber Composition in Women

dc.contributor.authorYvert, Thomas Paul
dc.contributor.authorMiyamoto-Mikami, Eri
dc.contributor.authorTobina, Takuro
dc.contributor.authorShiose, Keisuke
dc.contributor.authorKakigi, Ryo
dc.contributor.authorTsuzuki, Takamasa
dc.contributor.authorTakaragawa, Mizuki
dc.contributor.authorIchinoseki-Sekine, Noriko
dc.contributor.authorPérez Ruiz, Margarita
dc.contributor.authorFuku, Noriyuki
dc.contributor.authorEt al.
dc.date.accessioned2020-10-31T18:41:29Z
dc.date.available2020-10-31T18:41:29Z
dc.date.issued2020
dc.description.abstractPPARGC1A rs8192678 G/A (Gly482Ser) and NRF1 rs6949152 A/G polymorphisms have been associated with endurance athlete status, endurance performance phenotypes, and certain health-related markers of different pathologies such as metabolic syndrome, diabetes, and dyslipidemia. We hypothesized that they could be considered interesting candidates for explaining inter-individual variations in muscle fiber composition in humans. We aimed to examine possible associations of these polymorphisms with myosin heavy-chain (MHC) isoforms as markers of muscle fiber compositions in vastus lateralis muscle in a population of 214 healthy Japanese subjects, aged between 19 and 79 years. No significant associations were found in men for any measured variables. In contrast, in women, the PPARGC1A rs8192678 A/A genotype was significantly associated with a higher proportion of MHC-I (p = 0.042) and with a lower proportion of MHC-IIx (p = 0.033), and the NRF1 rs6949152 AA genotype was significantly associated with a higher proportion of MHC-I (p = 0.008) and with a lower proportion of MHC IIx (p = 0.035). In women, the genotype scores of the modes presenting the most significant results for PPARGC1A rs8192678 G/A (Gly482Ser) and NRF1 rs6949152 A/G polymorphisms were significantly associated with MHC-I (p = 0.0007) and MHC IIx (p = 0.0016). That is, women with combined PPARGC1A A/A and NRF1 A/A genotypes presented the highest proportion of MHC-I and the lowest proportion of MHC-IIx, in contrast to women with combined PPARGC1A GG+GA and NRF1 AG+GG genotypes, who presented the lowest proportion of MHC-I and the highest proportion of MHC-IIx. Our results suggest possible associations between these polymorphisms (both individually and in combination) and the inter-individual variability observed in muscle fiber composition in women, but not in men.spa
dc.description.filiationUEMspa
dc.description.impact4.096 JCR (2020) Q2, 65/175 Genetics & Heredityspa
dc.description.impact1.337 SJR (2020) Q2, 99/340 Geneticsspa
dc.description.impactNo data IDR 2019spa
dc.description.sponsorshipJSPS KAKENHI (16KK0188 to N.F)spa
dc.description.sponsorshipMEXT-Supported Program for the Strategic Research Foundation at Private Universities (to Juntendo University and Fukuoka University)spa
dc.identifier.citationYvert, T., Miyamoto-Mikami, E., Tobina, T., Shiose, K., Kakigi, R., Tsuzuki, T., Takaragawa, M., Ichinoseki-Sekine, N., Pérez Ruiz, M., Kobayashi, H., Tanaka, H., Naito, H., & Fuku, N. (2020). PPARGC1A rs8192678 and NRF1 rs6949152 Polymorphisms Are Associated with Muscle Fiber Composition in Women. Genes, 11(9), 1012. https://doi.org/10.3390/genes11091012spa
dc.identifier.doi10.3390/genes11091012
dc.identifier.issn2073-4425
dc.identifier.urihttp://hdl.handle.net/11268/9264
dc.language.isoengspa
dc.peerreviewedSispa
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internacional
dc.rights.accessRightsopen accessspa
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subject.uemGenética humanaspa
dc.subject.uemMujeresspa
dc.subject.uemFisiología humanaspa
dc.subject.unescoGenética humanaspa
dc.subject.unescoMujerspa
dc.subject.unescoFisiología humanaspa
dc.titlePPARGC1A rs8192678 and NRF1 rs6949152 Polymorphisms Are Associated with Muscle Fiber Composition in Womenspa
dc.typejournal articlespa
dspace.entity.typePublication
relation.isAuthorOfPublicationf246e4d3-82d3-4e05-bacd-ae0c4874324d
relation.isAuthorOfPublicationa5c08444-aa82-4924-a71e-de56086bcd7c
relation.isAuthorOfPublication.latestForDiscoveryf246e4d3-82d3-4e05-bacd-ae0c4874324d

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