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生长激素缺乏症患者接受生长激素治疗后的生长模式与骨骼成熟:影响治疗结果的因素

Growth pattern and skeletal maturation following growth hormone therapy in growth hormone deficiency: factors influencing outcome.

作者信息

Bajpai Anurag, Kabra Madhulika, Gupta Arun Kumar, Menon P S N

机构信息

Division of Pediatric Endocrinology, Department of Pediatrics, All India Institute of Medical Sciences, New Delhi 110 029, India.

出版信息

Indian Pediatr. 2006 Jul;43(7):593-9.

Abstract

OBJECTIVE

To evaluate pattern of growth and skeletal maturation following growth hormone (GH) therapy in children with GH deficiency (GHD) with special emphasis on factors influencing outcome.

METHODS

Records of ninety-six children (67 boys, 29 girls) with GHD treated with GH for 2.3 +/-2.1 years were reviewed.

RESULTS

Height SDS at the end of treatment was significantly higher than that at initiation (-3.4 +/- 1.7 versus -4.8 +/-1.6, P < 0.001); it was however lower than target height SDS (corrected height SDS (1.8 +/- 1.6, P < 0.001). The greatest increase in height SDS was observed during the first two years of treatment. Kaplan Meier survival analysis showed that 92%; of all subjects achieving end height SDS in the target height range did so within the first two years of treatment. Height SDS for bone age increased by 0.7 +/-0.9 during treatment (from -2.5 +/- 1.0 to -1.8 +/- 1.5, P < 0.001); the increase was however lower compared to that for height SDS for chronological age (P < 0.01) suggesting inadvertent skeletal maturation. End height SDS was influenced by duration of treatment and corrected height SDS on multivariate analysis.

CONCLUSION

GH treatment improves growth parameters in GHD; height however still remains compromised. Most of the catch-up growth occurs within two years of treatment emphasizing the need of optimal treatment during this period. Inadvertent skeletal maturation during treatment indicates a need for evaluating the role of agents effective in retarding skeletal maturation.

摘要

目的

评估生长激素(GH)缺乏症(GHD)患儿接受GH治疗后的生长模式和骨骼成熟情况,特别强调影响治疗效果的因素。

方法

回顾了96例接受GH治疗2.3±2.1年的GHD患儿(67例男孩,29例女孩)的记录。

结果

治疗结束时的身高标准差得分(SDS)显著高于治疗开始时(-3.4±1.7对-4.8±1.6,P<0.001);然而,仍低于目标身高SDS(矫正身高SDS为1.8±1.6,P<0.001)。治疗的前两年身高SDS增加最为显著。Kaplan-Meier生存分析显示,所有达到目标身高范围内最终身高SDS的受试者中,92%是在治疗的前两年内实现的。治疗期间骨龄的身高SDS增加了0.7±0.9(从-2.5±1.0增至-1.8±1.5,P<0.001);然而,与按实际年龄计算的身高SDS增加相比,该增加幅度较低(P<0.01),提示存在意外的骨骼成熟。多因素分析显示,最终身高SDS受治疗持续时间和矫正身高SDS的影响。

结论

GH治疗可改善GHD患儿的生长参数;然而身高仍受影响。大多数追赶性生长发生在治疗的两年内,这强调了在此期间进行最佳治疗的必要性。治疗期间意外的骨骼成熟表明需要评估有效延缓骨骼成熟的药物的作用。

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