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父母调整后的身高不足作为生长激素(GH)缺乏症儿童GH治疗效果的预后因素。

Parentally-adjusted deficit of height as a prognostic factor of the effectiveness of growth hormone (GH) therapy in children with GH deficiency.

作者信息

Hilczer Maciej, Smyczyńska Joanna, Lewiński Andrzej

机构信息

Department of Endocrinology and Metabolic Diseases, Medical University of Lodz, Polish Mother's Memorial Hospital--Research Institute, Lodz, Poland.

出版信息

Neuro Endocrinol Lett. 2006 Feb-Apr;27(1-2):149-52.

PMID:16648787
Abstract

INTRODUCTION

Parental height is the most important identifiable factor influencing final height (FH) of children with growth hormone (GH) deficiency (GHD), treated with GH.

AIM

Assessment of FH of patients with GHD--classified into familial short stature (FSS) and non-familial short stature (non-FSS) according to parentally adjusted deficit of height.

PATIENTS AND METHODS

The analysis comprised 101 patients (76 boys) with childhood-onset GHD. Final height was compared with patients' height before GH therapy, predicted adult height (PAH) and target height (TH).

RESULTS

Both GH peak in stimulating tests and height standard deviation score (SDS) before the therapy were significantly lower in non-FSS than in FSS. Target height was significantly lower in FSS than in non-FSS. Parentally-adjusted deficit of height was significantly more profound in non-FSS than in FSS. The prognosis of adult height was very similar in both groups of patients, being significantly worse in non-FSS than in FSS while corrected by TH. The absolute FH was similar in FSS and non-FSS, being, however, significantly lower in non-FSS than in FSS while corrected by TH. Improvement of height was significantly better in non-FSS than in FSS. In both groups, FH SDS was significantly better than height SDS before the therapy (H0SDS). In FSS group, PAH was similar to TH, moreover, FH corresponded to both PAH and TH. In non-FSS group FH was significantly higher than PAH, but both FH and PAH were significantly lower than TH.

CONCLUSIONS

  1. Growth hormone therapy was more effective in the patients with non-FSS than in those with FSS. 2) Parentally-adjusted deficit of height is an important prognostic factor of GH therapy effectiveness.
摘要

引言

父母身高是影响接受生长激素(GH)治疗的生长激素缺乏症(GHD)患儿最终身高(FH)的最重要可识别因素。

目的

评估GHD患者的最终身高——根据父母调整后的身高不足分为家族性矮小(FSS)和非家族性矮小(非FSS)。

患者和方法

分析包括101例儿童期起病的GHD患者(76例男孩)。将最终身高与GH治疗前患者的身高、预测成人身高(PAH)和靶身高(TH)进行比较。

结果

非FSS组刺激试验中的GH峰值和治疗前的身高标准差评分(SDS)均显著低于FSS组。FSS组的靶身高显著低于非FSS组。非FSS组父母调整后的身高不足比FSS组明显更严重。两组患者成人身高的预后非常相似,经TH校正后,非FSS组明显比FSS组差。FSS组和非FSS组的绝对FH相似,但经TH校正后,非FSS组明显低于FSS组。非FSS组的身高改善明显优于FSS组。两组中,FH SDS均显著优于治疗前的身高SDS(H0SDS)。在FSS组中,PAH与TH相似,此外,FH与PAH和TH均相符。在非FSS组中,FH显著高于PAH,但FH和PAH均显著低于TH。

结论

1)生长激素治疗对非FSS患者比对FSS患者更有效。2)父母调整后的身高不足是生长激素治疗效果的重要预后因素。

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