Simon D, Bechtold S
Department of Endocrinology and Diabetology, Hôpital Robert Debré, Paris FR-75019, France.
Horm Res. 2009 Nov;72 Suppl 1:55-9. doi: 10.1159/000229765. Epub 2009 Nov 27.
Several therapeutic trials have been conducted over the past decade to evaluate the role of exogenous growth hormone (GH) as a means of correcting the growth deficiency seen in children with juvenile idiopathic arthritis (JIA). Early studies showed the benefit of GH treatment with respect to final height in patients with JIA. Of 13 patients receiving GH, 84% (11 patients) achieved a final height within their target range compared with only 22% (4 of 18 patients) of untreated patients. There are, however, factors that may limit the statural gains achieved with GH therapy including severe inflammation, severe statural deficiency at GH therapy initiation, long disease duration and delayed puberty. Data on the efficacy of GH replacement therapy in children with JIA and factors that influence the statural growth response will be reviewed.
Results from therapeutic trials show that treatment with GH can decrease the statural deficit that occurs during the active phase of JIA, producing an adult height that is close to the genetically determined target height.
在过去十年中进行了多项治疗试验,以评估外源性生长激素(GH)作为纠正幼年特发性关节炎(JIA)患儿生长缺陷手段的作用。早期研究显示,GH治疗对JIA患者的最终身高有益。在接受GH治疗的13例患者中,84%(11例患者)达到了其目标范围内的最终身高,而未治疗的患者中只有22%(18例患者中的4例)达到。然而,存在一些因素可能会限制GH治疗所取得的身高增长,包括严重炎症、开始GH治疗时严重的身高不足、病程长和青春期延迟。将对JIA患儿GH替代治疗的疗效以及影响身高生长反应的因素的数据进行综述。
治疗试验结果表明,GH治疗可减少JIA活动期出现的身高不足,使成人身高接近基因决定的目标身高。