3 Growth hormone therapy and fracture risk in the growth hormone-deficient adult

Gudmundur Johannsson MD, PhD (Researcher), Claes Ohlsson MD, PhD (Researcher)
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引用次数: 16

Abstract

Adults with childhood-onset growth hormone deficiency (GHD) and younger adults with adult-onset GHD have a reduced bone mineral content (BMC). Recent trials with prolonged GH replacement therapy have demonstrated increased BMC in such patients.

GH treatment in animals increases the amount of bone and the total strength while the density (BMC per unit volume) and the quality of the bone is not increased. A sensitive non-invasive parameter for the detection of effects of GH on bone in clinical studies is therefore to use the BMC from dual-energy X-ray absorption (DEXA) analysis.

Bone density is strongly related to fracture risk in women. A number of other risk factors for fractures can be identified in adult GHD patients which, collectively, might explain the increased fracture frequency observed in these patients.

The increase in BMC in response to long-term GH replacement therapy is promising. Whether more prolonged treatment will result in a normalization of the bone mass and reduced fracture frequency remains to be established.

生长激素缺乏成人的生长激素治疗与骨折风险
患有儿童期生长激素缺乏症(GHD)的成年人和患有成年期生长激素缺乏症(GHD)的年轻人的骨矿物质含量(BMC)降低。最近延长生长激素替代治疗的试验表明,这些患者的BMC增加。动物生长激素处理增加了骨量和总强度,而骨密度(单位体积BMC)和骨质量没有增加。因此,在临床研究中,使用双能x射线吸收(DEXA)分析的BMC是检测生长激素对骨骼影响的一种敏感的非侵入性参数。骨密度与女性骨折风险密切相关。在成人GHD患者中可以发现许多其他骨折危险因素,这些因素可能解释了这些患者中观察到的骨折频率增加。长期生长激素替代治疗的BMC增加是有希望的。更长时间的治疗是否会导致骨量的正常化和骨折频率的降低仍有待确定。
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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