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骨密度群体方差中的遗传和环境因素。

Genetic and environmental components of the population variance in bone density.

作者信息

Seeman E, Hopper J L

机构信息

Austin and Repatriation Medical Centre, University of Melbourne, Australia.

出版信息

Osteoporos Int. 1997;7 Suppl 3:S10-6. doi: 10.1007/BF03194336.

Abstract

Understanding of the genetic and environmental factors contributing to the differences in fracture rates between young and old, between women and men, and between races is limited. The reasons for this may partly relate to the lack of a detailed understanding of the structural basis of bone fragility. This information, although difficult to obtain because of the invasiveness of bone biopsy, will be required if advances are to occur. aBMD cannot be relied upon as an endpoint in the study of the pathophysiology of osteoporosis. Advances will require the description of the age-, gender and race-specific means and variances in trabecular number, thickness, spacing and orientation, cortical thickness, and bone size and shape in women and men of different racial groups. Subsequent comparison of the structures in young versus old, female versus male, and in racial groups may reveal the structural differences from which inferences may be made concerning the differences in fracture rates between these groups. By defining the structural basis for bone fragility, the genetic and modifiable environmental determinants of these structures may then be identified, providing hypotheses to be tested in randomized trials aimed at reducing the incidence of fractures in these groups.

摘要

目前对于导致年轻人与老年人、女性与男性以及不同种族之间骨折率差异的遗传和环境因素的了解有限。造成这种情况的原因可能部分与对骨脆性结构基础缺乏详细了解有关。尽管由于骨活检的侵入性而难以获取,但如果要取得进展,就需要这些信息。在骨质疏松症病理生理学研究中,骨密度(aBMD)不能作为一个终点指标。要取得进展,需要描述不同种族的女性和男性在小梁数量、厚度、间距和方向、皮质厚度以及骨骼大小和形状方面的年龄、性别和种族特异性均值及方差。随后比较年轻人与老年人、女性与男性以及不同种族群体之间的结构,可能会揭示出结构差异,从而据此推断这些群体之间骨折率的差异。通过确定骨脆性的结构基础,进而可以识别这些结构的遗传和可改变的环境决定因素,为旨在降低这些群体骨折发生率的随机试验提供有待检验的假设。

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