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遗传学、钙摄入与骨质疏松症

Genetics, calcium intake and osteoporosis.

作者信息

Eisman J A

机构信息

Bone and Mineral Research Program, Garvan Institute of Medical Research, St Vincent's Hospital, Sydney, NSW, Australia.

出版信息

Proc Nutr Soc. 1998 May;57(2):187-93. doi: 10.1079/pns19980031.

Abstract

Genetic factors explain a high proportion of the age-specific differences in bone density, size and turnover. The potential for interaction between hormonal, diet and lifestyle factors is likely to be important. Common allelic variation in the VDR is an example of normal gene variants altering Ca homoeostasis, with effects on body and bone size as well as bone density. The VDR findings suggesting interactions between genetic and nutritional factors are an important target for future research. These studies are complicated by the potential for effects of gene-gene interactions and of undefined environmental factors. These problems notwithstanding, considerations of environmental and nutritional contributions, such as Ca intake and vitamin D status, will be critical in interpreting these genetic pathways and in 'personalizing' nutritional recommendations.

摘要

遗传因素在很大程度上解释了骨密度、骨骼大小和骨转换在不同年龄阶段的差异。激素、饮食和生活方式因素之间相互作用的可能性可能很重要。维生素D受体(VDR)的常见等位基因变异是正常基因变体改变钙稳态的一个例子,对身体和骨骼大小以及骨密度都有影响。VDR的研究结果表明遗传因素与营养因素之间存在相互作用,这是未来研究的一个重要目标。基因与基因之间的相互作用以及不明环境因素的潜在影响使这些研究变得复杂。尽管存在这些问题,但考虑环境和营养因素的作用,如钙摄入量和维生素D状况,对于解释这些遗传途径以及“个性化”营养建议至关重要。

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