Inzucchi S E, Robbins R J
Neuroendocrinology Program, Yale University School of Medicine, New Haven, Connecticut 06520.
J Clin Endocrinol Metab. 1994 Sep;79(3):691-4. doi: 10.1210/jcem.79.3.8077348.
GH has considerable importance in the normal development and growth of bone. An additional role in the maintenance of the adult skeleton is suggested by the alterations in bone mineral density observed in states of deficient or excess GH secretion and in the bone formation response to GH replacement in GHD patients. Deficiency in the secretion of GH is also observed, with increasing and striking frequency after middle-age despite the lack of any defined pituitary disease or injury. Although a causal relationship between hyposomatotropism and osteopenia in normal elderly patients is hypothetical, intriguing therapeutic questions are raised. Preliminary trials of hGH in osteoporosis have not resulted in increases in BMD, but such studies suffer from methodological limitations, chief of which is the failure to account for the GH/IGF-I status of their subjects. Osteopenic patients with the lowest IGF-I levels may need to be assessed independently. The utility of hGH may be in preventing the senile component of osteoporosis, which appears to result mainly from defective bone formation. Such studies will require appropriate patient selection, longer treatment periods, and more sensitive measures of bone density. Combination and/or coherence therapy with other agents, particularly those that attenuate bone resorption, may also prove useful.
生长激素(GH)在骨骼的正常发育和生长中具有相当重要的作用。生长激素分泌不足或过多状态下观察到的骨矿物质密度变化以及生长激素缺乏症(GHD)患者对生长激素替代治疗的骨形成反应表明,生长激素在维持成人骨骼方面还具有额外作用。尽管没有任何明确的垂体疾病或损伤,但中年后生长激素分泌不足的情况也日益常见且愈发明显。虽然正常老年患者中生长激素分泌不足与骨质减少之间的因果关系只是一种假设,但这引发了一些有趣的治疗问题。骨质疏松症患者使用重组人生长激素(hGH)的初步试验并未导致骨密度(BMD)增加,但此类研究存在方法学上的局限性,其中主要问题是未能考虑研究对象的生长激素/胰岛素样生长因子-I(IGF-I)状态。可能需要对胰岛素样生长因子-I水平最低的骨质减少患者进行单独评估。重组人生长激素的作用可能在于预防骨质疏松症的衰老成分,这似乎主要是由骨形成缺陷导致的。此类研究将需要进行适当的患者选择、更长的治疗周期以及更敏感的骨密度测量方法。与其他药物联合和/或协同治疗,特别是那些能减少骨吸收的药物,可能也会被证明是有用的。