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Is Osteoporosis Curable? Insights of the Utah Paradigm of Skeletal Physiology In 1999

机译:骨质疏松症可固化吗? 1999年骨骼生理学犹他州范例的见解

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This text summarizes things that would concern most absorptiometrists, clinicians, basic scientists and pharmaceutical companies involved in soem way with "osteoporosis". Currently available agents do not completely prevent or cure them, so a need persists for agents that do. The multidisciplinary Utah paradigm of skeletal physiology begins to change earlier ideas about the nature, causes and pathogenesis of "osteoporosis", and how to diagnose and manage them. Salient facts in that paradigm include: A) Muscle strength dominates the control of bone strength and "mass". B) It does so by causing the bone strains that directly or indirectly control the modeling and remodeling mechanisms that establish bone strength and "mass". C) Special strain thresholds, a posited mediator mechanism in marrow, and a posited mechanostat, all help to control how, where and when those things affect bone strength and "mass". D) Most nonmechanical agents (hormones, vitamin D, calcium, etc) can modulate but not duplicate those effects. E) At present indices of whole-bone strength obtained by peripheral quantitative computed tomography provide better noninvasive estimates than other methods.
机译:本文总结的东西,就最关心的absorptiometrists,临床医生,基础科学家,并参与了与“骨质疏松症” SOEM方式制药公司。目前可用的代理商并不完全防止或治愈它们,因此需要持续存在的代理人。骨骼生理学的多学科犹他州范例开始改变关于“骨质疏松症”的性质,原因和发病机制的早期思想,以及如何诊断和管理它们。范例的突出事实包括:a)肌肉力量占据骨强度和“质量”的控制。 b)通过导致直接或间接控制建立骨强度和“质量”的建模和改造机制的骨菌株来这样做。 c)特殊的应变阈值,骨髓中的一个定位的介质机制,以及一个受到的机械仓,一切都有助于控制这些东西影响骨骼强度和“质量”的方式。 d)大多数非机械剂(激素,维生素D,钙等)可以调节但不复制这些效果。 e)目前通过外围定量计算断层扫描获得的全骨强度指数提供比其他方法更好的非侵入性估计。

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