Savage M O, Cohen L, Cohen A J, Cohen P, Saenger P H
Department of Endocrinology, William Harvey Research Institute, Barts and Royal London School of Medicine & Dentistry, London, UK.
Pediatr Endocrinol Rev. 2010 Jun;7(4):347-56.
Defects in the growth hormone (GH)-insulin-like growth factor (IGF)I axis may cause GH resistance characterized by IGFI deficiency and growth failure. The range of defects causing GH resistance is broad as are their biochemical and phenotypical characteristics. We propose that GH-IGFI axis defects form a continuum of clinical and biochemical effects ranging from GH deficiency to GH resistance. The pathophysiology of GH resistance is described followed by a scheme for investigation of the child with severe short stature and normal GH secretion. We critically discuss GH therapy for such patients and define acceptable growth responsiveness. Finally we discuss therapy with IGF-I within the limits of the USA Food and Drug Administration and European Medicines Agency labels for GH resistance.
生长激素(GH)-胰岛素样生长因子(IGF)-I轴的缺陷可能导致以IGF-I缺乏和生长障碍为特征的GH抵抗。导致GH抵抗的缺陷范围很广,其生化和表型特征也是如此。我们提出,GH-IGF-I轴缺陷形成了一个从GH缺乏到GH抵抗的临床和生化效应连续体。本文描述了GH抵抗的病理生理学,接着是针对严重身材矮小且GH分泌正常儿童的调查方案。我们批判性地讨论了此类患者的GH治疗,并确定了可接受的生长反应性。最后,我们在美国食品药品监督管理局和欧洲药品管理局关于GH抵抗的标签范围内讨论了IGF-I治疗。