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Abstract
Context: Polymorphisms in the ESR1 gene encoding estrogen receptor (ER)-{alpha} may be associated with fat mass in adults.
Objectives: The objective of the study was to establish whether ESR1 polymorphisms influence fat mass in childhood.
Design: This was a cross-sectional analysis after genotyping of rs9340799, rs2234693, and rs7757956 ESR1 polymorphisms.
Setting: The Avon Longitudinal Study of Parents and Children (ALSPAC) was a population-based prospective study.
Participants: Participants included 3097 11-yr-old children with results for ESR1 genotyping, puberty measures, and dual-energy x-ray absorptiometry results.
Outcomes: Relationships between ESR1 polymorphisms and indices of body composition were measured.
Results: The rs7757956 polymorphism was associated with fat mass (P = 0.002). Total body fat mass (adjusted for height) was reduced by 6% in children with TA/AA genotypes, and risk of being overweight (≥85th centile of fat mass) was decreased by 20%. This genetic effect appeared to interact with puberty in girls (P = 0.05 for interaction): in those with the TT genotype, total body fat mass (adjusted for height) was 18% higher in Tanner stages 3–5 vs. stages 1–2; the equivalent difference was 7% in those with TA/AA genotypes. Furthermore, the risk of being overweight was 36% lower in girls with TA/AA genotypes in Tanner stages 3–5, but no reduction was seen in those in stages 1–2. Neither rs9340799 nor rs2234693 polymorphisms were associated with body composition measures.
Conclusions: Fat mass in 11-yr-old children was related to the rs7757956 ESR1 polymorphism. This association was strongest in girls in more advanced puberty, in whom the risk of being overweight was reduced by 36% in those with the TA/AA genotype.
Translated title of the contribution | Effect of an Estrogen Receptor-α Intron 4 Polymorphism on Fat Mass in 11-Year-Old Children |
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Original language | English |
Pages (from-to) | 2286 - 2291 |
Number of pages | 6 |
Journal | Journal of Clinical Endocrinology and Metabolism |
Volume | 92 (6) |
DOIs | |
Publication status | Published - Jun 2007 |
Bibliographical note
Publisher: Endocrine SocietyFingerprint
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