Aimaretti Gianluca, Baldelli Roberto, Corneli Ginevra, Bellone Simonetta, Rovere Silvia, Croce Chiara, Ragazzoni Federico, Giordano Roberta, Arvat Emanuela, Bona Gianni, Ghigo Ezio
Division of Endocrinology and Metabolic Diseases, Department of Internal Medicine, University of Turin, Italy.
Pediatr Endocrinol Rev. 2004 Nov;2 Suppl 1:86-92.
The diagnosis and treatment of growth hormone deficiency (GHD), as well as the possibility of counteracting somatopause and age-related changes in body composition, structural functions, and metabolism, prompted interest in potential clinical uses of GH-releasing hormone (GHRH) and GH secretagogues (GHS). GHD often reflects hypothalamic GHRH deficiency and it has been clearly demonstrated that the age-related decline in the function of the GH/IGF-I axis reflects a reduction in hypothalamic function as evidenced by the preservation of the releasable pool of pituitary GH in aged subjects. The effectiveness of recombinant human GH (rhGH) is well established, but it is also recognized that GH replacement does not mimic physiological GH secretion which theoretically would be restored by GHRH and/or GHS. At present, it has been clearly demonstrated that GHRH and/or GHS represent reliable tools for the diagnosis of GHD. On the other hand, neither GHRH nor GHS has been shown to provide effective alternatives to rhGH for the treatment of GHD. Although GHRH and/or GHS represent the most logical approaches for the restoration of the GH/IGF-I axis to a youthful level of activity and for counteracting the somatopause, this hypothesis has never been proven definitively. Conceptually, GHRH replacement would be the most physiological approach and its safety is guaranteed, provided an appropriate dose is used, in order to avoid hyperactivity of the GH/IGF-I axis. However, a long-acting preparation is needed. On the other hand, GHS, e.g., ghrelin analogues, could be considered as a function of their selectivity of action. However, ghrelin has a wide spectrum of endocrine and non-endocrine actions at both central and peripheral levels. Thus, non-selective GHS, although available in orally active forms, could elicit unforeseen side effects. Previous studies with GHRH and/or GHS in aging patients provided encouraging results. However, it still remains to be definitively demonstrated that aged subjects would benefit from chronic treatment with these molecules.
生长激素缺乏症(GHD)的诊断与治疗,以及对抗生长停滞和身体成分、结构功能及新陈代谢方面与年龄相关变化的可能性,引发了人们对生长激素释放激素(GHRH)和生长激素促分泌素(GHS)潜在临床用途的兴趣。GHD通常反映下丘脑GHRH缺乏,并且已经明确表明,生长激素/胰岛素样生长因子-Ⅰ(GH/IGF-I)轴功能的年龄相关性下降反映了下丘脑功能的减退,这一点在老年受试者中垂体GH可释放池得以保留的情况中得到了证明。重组人生长激素(rhGH)的有效性已得到充分证实,但人们也认识到,生长激素替代并不能模拟生理性生长激素分泌,理论上这种分泌可通过GHRH和/或GHS得以恢复。目前,已经明确表明GHRH和/或GHS是诊断GHD的可靠工具。另一方面,对于GHD的治疗,GHRH和GHS均未被证明是rhGH的有效替代物。尽管GHRH和/或GHS是将GH/IGF-I轴恢复到年轻活性水平以及对抗生长停滞的最合理方法,但这一假设从未得到确凿证实。从概念上讲,GHRH替代将是最符合生理的方法,并且只要使用适当剂量以避免GH/IGF-I轴过度活跃,其安全性是有保障的。然而,需要一种长效制剂。另一方面,GHS,例如胃饥饿素类似物,可根据其作用的选择性来考虑。然而,胃饥饿素在中枢和外周水平均具有广泛的内分泌和非内分泌作用。因此,非选择性GHS尽管有口服活性形式,但可能会引发不可预见的副作用。先前对老年患者使用GHRH和/或GHS的研究取得了令人鼓舞的结果。然而,仍有待确凿证明老年受试者会从这些分子的长期治疗中获益。