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地夫可特治疗青少年慢性关节炎。

Deflazacort in juvenile chronic arthritis.

作者信息

Loftus J K, Reeve J, Hesp R, David J, Ansell B M, Woo P M

机构信息

MRC Clinical Research Centre, Harrow, UK.

出版信息

J Rheumatol Suppl. 1993 Apr;37:40-2.

PMID:8501751
Abstract

Vertebral crush fracture associated with glucocorticoid therapy causes major morbidity in juvenile chronic arthritis (JCA). Deflazacort (DFZ) may have an advantage over prednisone (PRED) because of its alleged bone sparing properties. Of 34 children with JCA receiving more than 5 mg PRED/day, 31 completed a 1-year, double blind, randomized, comparative trial of DFZ and PRED. Patient characteristics at trial entry were well matched. DFZ and PRED were prescribed in equivalent amounts. DFZ achieved similar disease control to PRED, and was not associated with untoward effects. Joint counts, hematological indices and biochemical values did not differ between treatment groups initially or during the trial. Bone density trends (velocities) in the lumbar spine were measured using dual photon absorptiometry at 3-monthly intervals and trends in bone and soft tissue growth calculated. Lumbar spine bone growth correlated with indices of somatic growth, with wide ranges in each group. Co-variance analysis showed a significant advantage (p < 0.007) of DFZ over PRED when spinal bone density was compared to body surface area and weight. Children taking DFZ showed less weight gain but similar height gain to children taking PRED. Children with poor or no somatic growth showed significant lumbar bone loss only in the PRED group. Of the children originally treated with PRED; 11 were switched to DFZ after completing the double blind study. Data for 26 children treated with DFZ for 1 year were thus available and confirmed a significantly greater rate of spinal bone growth relative to somatic growth, p < 0.002.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

与糖皮质激素治疗相关的椎体压缩性骨折在青少年慢性关节炎(JCA)中会导致严重的发病情况。由于据称地夫可特(DFZ)具有保护骨骼的特性,它可能比泼尼松(PRED)更具优势。在34名每日接受超过5毫克PRED治疗的JCA患儿中,31名完成了一项为期1年的DFZ与PRED双盲、随机、对照试验。试验开始时患者的特征匹配良好。DFZ和PRED的给药剂量相当。DFZ实现了与PRED相似的疾病控制,且未出现不良反应。治疗组之间的关节计数、血液学指标和生化值在初始阶段及试验期间均无差异。每隔3个月使用双能光子吸收法测量腰椎的骨密度趋势(速度),并计算骨骼和软组织生长趋势。腰椎骨生长与身体生长指标相关,每组范围较广。当将脊柱骨密度与体表面积和体重进行比较时,协方差分析显示DFZ比PRED具有显著优势(p < 0.007)。服用DFZ的儿童体重增加较少,但身高增长与服用PRED的儿童相似。身体生长不良或无生长的儿童仅在PRED组出现明显的腰椎骨丢失。在最初接受PRED治疗的儿童中,11名在完成双盲研究后改用DFZ。因此,有26名接受DFZ治疗1年的儿童的数据,这些数据证实相对于身体生长,脊柱骨生长速率显著更高,p < 0.002。(摘要截短于250字)

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