Final height of adults with childhood-onset steroid-responsive idiopathic nephrotic syndrome

被引:27
作者
Donatti, Teresinha Lermen [1 ]
Koch, Vera Hermina [1 ]
机构
[1] Univ Sao Paulo, Sch Med, Inst Crianca, Pediat Nephrol Unit,Hosp Clin, Sao Paulo, Brazil
关键词
Nephrotic syndrome; Growth; Final height; Glucocorticoid; Children; Adolescent; CATCH-UP GROWTH; HORMONE-RELEASING-HORMONE; CHILDREN;
D O I
10.1007/s00467-009-1301-z
中图分类号
R72 [儿科学];
学科分类号
100202 [儿科学];
摘要
The aim of this study was to evaluate the final stature of adults with childhood-onset steroid-responsive idiopathic nephrotic syndrome (INS) and the influence of disease-related issues on the achievement of their target heights. We analyzed 60 (41 male) patients and/or their records, with a minimum age of 19 years or at a Tanner's pubertal stage 4 for boys or status postmenarche for girls, and normal glomerular filtration rate. Mean age at first and last consultation was 5.3 +/- 2.4 years and 20.5 +/- 3.1 years, respectively. Mean follow-up period was 15.10 years. Mean cumulative dose of prednisone was 1254 +/- 831.40 mg/kg. Mean initial and final height Z scores (HtZ) were, respectively, -0.60 +/- 1.0 and -0.64 +/- 0.92 (p = 0.72). The final HtZ showed a significant correlation only with the initial HtZ and the target HtZ (THZ). Six patients achieved a final HtZ below -2, which in male patients correlated strongly to the initial HtZ and THZ. A strong correlation was demonstrated between final HtZ, initial HtZ, and THZ. INS-related issues did not prevent the final stature to reach the predicted target height.
引用
收藏
页码:2401 / 2408
页数:8
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