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生长激素治疗:生长激素缺乏症儿童与小于胎龄儿短期和长期结局的比较

Growth Hormone Therapy: Comparison of Short- and Long-Term Outcomes between Children with Growth Hormone Deficiency and Small for Gestational Age.

作者信息

Gleiss Andreas, Raimann Adalbert, Haufler Florentina, Ertl Diana-Alexandra, Sagmeister Susanne, Hartmann Gabriele

机构信息

Institute of Clinical Biometrics, Center for Medical Data Science, Medical University of Vienna, Vienna, Austria.

Department of Pediatrics and Adolescent Medicine, Medical University of Vienna, Vienna, Austria.

出版信息

Horm Res Paediatr. 2025;98(3):344-356. doi: 10.1159/000538798. Epub 2024 Apr 18.

Abstract

INTRODUCTION

Direct comparisons of both short-term and long-term auxological outcomes of growth hormone therapy (GHT) between growth hormone deficiency (GHD) and small for gestational age (SGA) are scarce.

METHODS

One hundred three patients with GHD and 53 patients with SGA treated at our tertiary center were investigated. Short-term and long-term outcomes were compared between these groups using multivariable linear regression models with adjustment for age, sex, and height at therapy start, also allowing for sex-specific group comparisons.

RESULTS

Mean delta height standard deviation scores (SDS) after 1 year of treatment were significantly higher in GHD (0.90, CI: 0.82-0.99) compared to SGA (0.67, CI: 0.54-0.79) (p = 0.003) with no sex difference. As expected, the mean increase in height SDS at final height (FH) was significantly higher in GHD (2.21, CI: 2.00-2.42) compared to SGA (1.05, CI: 0.75-1.35) (p < 0.001), leading to a target height corrected FH of -0.39 SDS (CI: -0.62 to -0.15) in GHD and -1.22 SDS (CI: -1.57 to -0.87) in SGA (p < 0.001). Girls with GHD had a better long-term outcome, as did boys with SGA when compared to the respective opposite sex. The cut-off of delta height of 0.5 SDS during the first year had a low sensitivity to detect long-term non-responders. We found a relation between short-term and long-term outcomes in GHD but not in SGA (adjusted R2 = 0.66 vs. 0.01).

CONCLUSION

In contrast to GHD, we observed practically no relationship between 1st-year and long-term outcomes in SGA patients treated with GH.

摘要

引言

生长激素缺乏症(GHD)和小于胎龄儿(SGA)之间生长激素治疗(GHT)的短期和长期生长学结果的直接比较很少见。

方法

对在我们三级中心接受治疗的103例GHD患者和53例SGA患者进行了调查。使用多变量线性回归模型对这些组之间的短期和长期结果进行比较,该模型对治疗开始时的年龄、性别和身高进行了调整,还进行了性别特异性组比较。

结果

治疗1年后,GHD组的平均身高标准差评分(SDS)(0.90,CI:0.82 - 0.99)显著高于SGA组(0.67,CI:0.54 - 0.79)(p = 0.003),且无性别差异。正如预期的那样,GHD组最终身高(FH)时身高SDS的平均增加(2.21,CI:2.00 - 2.42)显著高于SGA组(1.05,CI:0.75 - 1.35)(p < 0.001),导致GHD组目标身高校正后的FH为 - 0.39 SDS(CI: - 0.62至 - 0.15),SGA组为 - 1.22 SDS(CI: - 1.57至 - 0.87)(p < 0.001)。与各自相反性别的患者相比,GHD女孩的长期结果更好,SGA男孩也是如此。第一年身高变化0.5 SDS的临界值对检测长期无反应者的敏感性较低。我们发现GHD组的短期和长期结果之间存在关联,而SGA组则没有(调整后的R2 = 0.66对0.01)。

结论

与GHD相反,我们观察到接受GH治疗的SGA患者的第一年和长期结果之间几乎没有关系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c06b/12133120/1bf93c64554c/hrp-2025-0098-0003-538798_F01.jpg

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