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Longitudinal effects of FTO gene polymorphism on body composition, cardiorespiratory fitness, physical activity, inflammatory markers, and cardiovascular risk in children and adolescents. “The UP & DOWN study”

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URI: http://hdl.handle.net/10498/31225

DOI: 10.1111/sms.14469

ISSN: 0905-7188

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Scandinavian Med Sci Sports - Mier‐Mota.pdf (1.712Mb)
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Author/s
Mier Mota, Julián; Ponce González, Jesús GustavoAuthority UCA; Perez Bey, Alejandro; Cabanas Sánchez, Verónica; Veiga Núñez, Oscar; Santiago Dorrego, Catalina; Gómez Gallego, Félix; Castro Piñero, JoséAuthority UCA
Date
2023-08-30
Department
Didáctica de la Educación Física, Plástica y Musical
Source
Scandinavian Journal of Medicine and Science in Sports. Vol. 33, nº 11, November 2023, pp. 2261 - 2272
Abstract
The role of polymorphism rs9939609 of the FTO gene has been related with fat mass and cardiovascular risk in adults, but it remains unclear in children and adolescents. Hence, the main aim of this study was to determine the FTO polymorphism effects on body composition, cardiorespiratory fitness (CRF), physical activity (PA), inflammatory markers, and cardiovascular risk both in cross-sectional analysis and after two-years of follow-up in children and adolescents. A total of 2129 participants were included in this study. The rs9939609 polymorphism was genotyped. Body composition measurements, CRF, and moderate-to-vigorous PA (MVPA) were determined at baseline and after two-year of follow-up. Moreover, plasma leptin and adiponectin were also determined as inflammatory markers. Furthermore, an index of cardiovascular disease risk factors (CVDRF-I) was calculated. Codominant (TT vs. TA vs. AA) and dominant (AA+AT vs. TT) models were applied for statistical analysis. The results showed a main effect of the FTO genotype on body composition measures in both first and third year (p < 0.05), with lower adiposity in TT compared with AA or AA+AT group. These differences were maintained after accounting for pubertal maturity, sex, age, VO2max, and MVPA. Moreover, lower leptin level was observed in TT compared to AA+AT group in the third year. An interaction in Gene*Time*Sex was found in height and neck circumference in dominant model (p = 0.047; p = 0.020, respectively). No differences were found in CRF, MVPA nor CVDRF-I between groups. Hence, homozygous TT allele could be a protective factor against weight gain from early childhood.
Subjects
cardiovascular disease; childhood obesity; FTO; genotype
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