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Associations between the Pubertal Timing-Related Variant in LIN28B and BMI Vary Across the Life Course

机译:LIN28B中与青春期相关的变体与BMI在整个生命过程中的关联

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Context: The common C allele of rs314276 in LIN28B has been robustly associated with earlier age at menarche in girls and associated with earlier timing of other pubertal traits in both sexes.Objective: Our objective was to explore the associations between rs314276, as a marker of earlier pubertal timing, and body mass index (BMI), weight, and height across the life course.Methods: The rs314276 in LIN28B was genotyped in 1242 men and 1209 women born in 1946 and participating in the Medical Research Council National Survey of Health and Development. Birth weight was recorded, and height and weight were measured or self-reported repeatedly at 11 time points between ages 2 and 53 yr. Polynomial mixed models were used to test whether additive genetic associations with sd scores (SDS) for BMI and height changed with age between 0 and 53 yr.Results: Longitudinal analyses revealed age-dependent associations between rs314276 genotype and BMI ( P < 0.001 for genotype-by-age~(2) interaction) and body weight ( P < 0.001 for genotype-by-age~(2) interaction) in women, but not in men. In women only, the C allele at rs314276 was associated with higher BMI SDS from ages 15–43 yr. In contrast, C allele associations with shorter height SDS were apparent in both men and women and did not vary with age.Conclusion: A common genetic variant in LIN28B that confers earlier puberty was associated with a prolonged increase in BMI during adolescence and early to mid-adulthood in women only. Such genetic associations may provide insights into the direct effects of pubertal timing on obesity risk.
机译:语境:LIN28B中rs314276的常见C等位基因与女孩初潮年龄早以及与其他性别的其他青春期特征的早期发生密切相关。目的:我们的目的是探索rs314276之间的关联,作为方法:在LIN28B中的rs314276在1946年出生的1242名男性和1209名女性中进行了基因分型,并参加了医学研究委员会国家健康与健康调查。发展。记录出生体重,并在2至53岁之间的11个时间点重复测量身高和体重或自我报告。多项式混合模型用于检验BMI和身高的sd评分(SDS)的加性遗传关联是否随年龄在0至53岁之间变化。结果:纵向分析显示rs314276基因型与BMI之间存在年龄相关性(基因型P <0.001) (2)相互作用)和体重(基因型(2)相互作用的P <0.001)在女性中而不是在男性中。仅在女性中,rs314276的C等位基因与15-43岁的较高BMI SDS相关。与此相反,在男性和女性中,C等位基因与高度SDS较短的关联均很明显,并且不随年龄而变化。结论:LIN28B中常见的遗传变异赋予青春期提前,与青春期和早期至中期的BMI持续升高有关-仅在女性中成年。这样的遗传关联可以提供对青春期时机对肥胖风险的直接影响的见解。

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