Saha Marja-Terttu, Haapasaari Jarkko, Hannula Sirpa, Sarna Seppo, Lenko Hanna Liisa
Tampere University Hospital, Department of Paediatrics, PO Box 2000, FIN 33521 Tampere, Finland.
J Rheumatol. 2004 Jul;31(7):1413-7.
To assess the efficacy of growth hormone (GH) treatment in severe growth retardation in prepubertal children with juvenile chronic arthritis (JCA).
In a randomized, double-blind placebo-controlled study, we treated 25 prepubertal children (7 boys, 18 girls, mean age 9.0 yrs) with severe growth retardation due to JCA with human recombinant GH (6 months) and placebo (6 months).
A significant response to GH treatment, compared with placebo, was seen in most children. The median height velocity standard deviation score was +2.09 (range -7.18 to +9.49) during the 6 month period of GH therapy and -1.11 (range -10.00 to +1.11) during placebo treatment (p = 0.0002). The median height standard deviation score increased from -2.08 to -1.79 during GH treatment and from -2.18 to -2.02 during placebo (p = 0.0268). All children except one completed the study, showing high compliance. The treatment was well tolerated, and no significant alterations in the disease activity were recorded during the study.
We conclude that human recombinant GH may be of benefit in the treatment of severe growth retardation in children with JCA. The response was seen after only 6 months and was independent of initial growth hormone status of the child.
评估生长激素(GH)治疗幼年慢性关节炎(JCA)青春期前儿童严重生长迟缓的疗效。
在一项随机、双盲、安慰剂对照研究中,我们用重组人生长激素(6个月)和安慰剂(6个月)治疗了25名因JCA导致严重生长迟缓的青春期前儿童(7名男孩,18名女孩,平均年龄9.0岁)。
与安慰剂相比,大多数儿童对GH治疗有显著反应。在GH治疗的6个月期间,身高速度标准差评分中位数为+2.09(范围-7.18至+9.49),而在安慰剂治疗期间为-1.11(范围-10.00至+1.11)(p = 0.0002)。在GH治疗期间,身高标准差评分中位数从-2.08增加到-1.79,而在安慰剂治疗期间从-2.18增加到-2.02(p = 0.0268)。除一名儿童外,所有儿童均完成了研究,显示出高依从性。治疗耐受性良好,研究期间未记录到疾病活动的显著变化。
我们得出结论,重组人生长激素可能对治疗JCA儿童的严重生长迟缓有益。仅6个月后就观察到了反应,且与儿童的初始生长激素状态无关。