Osteoporosis: the role of genetics and the environment.

Boonsong Ongphiphadhanakul
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引用次数: 24

Abstract

Osteoporosis is partly genetically determined. The genetics of osteoporosis is polygenic in nature with multiple common polymorphic alleles interacting with each other and environmental factors to determine bone mass. A number of studies have attempted to dissect the genetic factors responsible for the pathogenesis of osteoporosis using genome-wide scanning and the candidate gene approach. However, the results of such studies among different populations have been mostly inconsistent, suggesting genetic heterogeneity of osteoporosis. It is likely that the cohort of genes indicating predisposition to the risk of osteoporosis may be different among populations with different ethnic backgrounds. The successful identification of susceptibility genes for osteoporosis should prove to be helpful in targeting preventive and therapeutic measures to individuals at higher risk and to render the effort more cost-effective. Information with regard to genetic variations is also likely to be useful in targeting preventive or therapeutic measures to subjects genetically determined to have better responsiveness. Intestinal calcium absorption is dependent on vitamin D receptor gene polymorphisms. Skeletal responsiveness to estrogen, particularly at lower doses, is related to polymorphisms in the estrogen receptor-alpha gene. Recently, circulating homocysteine levels have been shown to be associated with fracture risk. Folate and vitamin B supplements for reducing serum homocysteine and fractures in postmenopausal women have not been fully investigated. However, there is an interaction between folate status and methylenetetrahydrofolate reductase gene polymorphism on bone phenotypes. Due to recent technological advances, whole-genome association study is becoming more feasible. Genomic information with regard to the susceptibility to osteoporosis and the responsiveness to preventive or therapeutic modalities should supplement rather than replace conventional clinical information. Clinical decision should also take into account the social, health and economic perspectives in order to balance the benefit of novel clinical strategies against the associated risks and available resources.

骨质疏松症:基因和环境的作用。
骨质疏松症部分是由基因决定的。骨质疏松症的遗传本质上是多基因的,多个共同的多态等位基因相互作用并与环境因素共同决定骨量。许多研究试图利用全基因组扫描和候选基因方法来剖析骨质疏松症发病机制的遗传因素。然而,这类研究在不同人群中的结果大多不一致,提示骨质疏松症存在遗传异质性。在不同种族背景的人群中,表明易患骨质疏松症风险的基因队列可能是不同的。骨质疏松易感基因的成功鉴定将有助于针对高危人群采取针对性的预防和治疗措施,并使治疗工作更具成本效益。关于遗传变异的信息也可能有助于将预防或治疗措施的目标定位于遗传上确定具有更好反应性的受试者。肠道钙吸收依赖于维生素D受体基因多态性。骨骼对雌激素的反应性,特别是在低剂量下,与雌激素受体α基因的多态性有关。最近,循环同型半胱氨酸水平已被证明与骨折风险有关。叶酸和维生素B补充剂对降低绝经后妇女血清同型半胱氨酸和骨折的作用尚未得到充分研究。然而,叶酸状态与亚甲基四氢叶酸还原酶基因多态性对骨表型的影响存在相互作用。由于近年来的技术进步,全基因组关联研究变得更加可行。关于骨质疏松易感性和对预防或治疗方式的反应的基因组信息应该补充而不是取代传统的临床信息。临床决策还应考虑到社会、健康和经济方面的因素,以便在新的临床战略的益处与相关风险和现有资源之间取得平衡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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