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性别特异性遗传因素对骨质疏松症风险的影响。

Contribution of gender-specific genetic factors to osteoporosis risk.

作者信息

Karasik D, Ferrari S L

机构信息

Hebrew SeniorLife/IFAR and Harvard Medical School, Boston, MA 02131, USA.

出版信息

Ann Hum Genet. 2008 Sep;72(Pt 5):696-714. doi: 10.1111/j.1469-1809.2008.00447.x. Epub 2008 May 8.

Abstract

Common diseases result from the complex relationship between genetic and environmental factors. The aim of this review is to provide perspective for a conceptual framework aimed at studying the interplay of gender-specific genetic and environmental factors in the etiology of complex disease, using osteoporosis as an example. In recent years, gender differences in the heritability of the osteoporosis-related phenotypes have been reported and sex-specific quantitative-trait loci were discovered by linkage studies in humans and mice. Results of numerous allelic association studies also differed by gender. In most cases, it was not clear whether or not this phenomenon should be attributed to the effect of sex-chromosomes, sex hormones, or other intrinsic or extrinsic differences between the genders, such as the level of bioavailable estrogen and of physical activity. We conclude that there is need to consider gender-specific genetic and environmental factors in the planning of future association studies on the etiology of osteoporosis and other complex diseases prevalent in the general population.

摘要

常见疾病源于遗传和环境因素之间的复杂关系。本综述的目的是提供一个概念框架的视角,该框架旨在以骨质疏松症为例,研究复杂疾病病因中性别特异性遗传和环境因素的相互作用。近年来,已有关于骨质疏松症相关表型遗传力的性别差异报道,并且通过人类和小鼠的连锁研究发现了性别特异性数量性状位点。众多等位基因关联研究的结果也因性别而异。在大多数情况下,尚不清楚这种现象是否应归因于性染色体、性激素的作用,或两性之间的其他内在或外在差异,如生物可利用雌激素水平和身体活动水平。我们得出结论,在规划未来关于骨质疏松症和普通人群中其他常见复杂疾病病因的关联研究时,有必要考虑性别特异性遗传和环境因素。

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