Suppr超能文献

重度小儿桥本氏甲状腺功能减退症追赶生长情况的评估

Evaluation of catch-up growth in severe pediatric Hashimoto's hypothyroidism.

作者信息

Vincent A, Bouvattier C, Teinturier C, Rodrigue D, Busiah K, Olivier-Petit I, Bony H, Barat P, Cammas B, Coutant R, Lienhardt A, Linglart A, Lambert A-S

机构信息

Department of Pediatric Endocrinology and diabetology, Bicêtre Hospital and Paris Sud University, Le Kremlin-Bicêtre, France.

Department of Pediatric Endocrinology and diabetology, Bicêtre Hospital and Paris Sud University, Le Kremlin-Bicêtre, France.

出版信息

Arch Pediatr. 2023 Apr;30(3):142-148. doi: 10.1016/j.arcped.2023.01.001. Epub 2023 Mar 10.

Abstract

BACKGROUND

We aimed to evaluate catch-up growth in children with severe Hashimoto's hypothyroidism (HH) after thyroid hormone replacement therapy (HRT).

METHODS

A multicenter retrospective study was conducted including children referred for growth slowdown that led to the diagnosis of HH between 1998 and 2017.

RESULTS

A total of 29 patients were included, with a median age of 9.7 years (13-172 months). Median height at diagnosis was -2.7 [-4.6; -0.1] standard deviation score (SDS), with a height loss of 2.5 [0.7; 5.4] SDS compared to height before growth deflection (p<0.0001). At diagnosis, the median TSH level was 819.5 mIU/L [100; 1844], the median FT4 level was 0 pmol/L [undetectable; 5.4], and the median anti-thyroperoxidase antibody level was 1601 UI/L [47; 25,500]. In the 20 patients treated only with HRT, there were significant differences between height at diagnosis and height at 1 year (n = 19, p<0.0001), 2 years (n = 13, p = 0.0005), 3 years (n = 9, p = 0.0039), 4 years (n = 10, p = 0.0078), and 5 years (n = 10, p = 0.0018) of treatment but not in the case of final height (n = 6, p = 0.0625). Median final height was -1.4 [-2.7; 1,5] SDS (n = 6), with a significant difference between height loss at diagnosis and total catch-up growth (p = 0.003). The other nine patients were also given growth hormone (GH). They were smaller at diagnosis (p = 0.01); however, there was no difference in final height between those two groups (p = 0.68).

CONCLUSION

Severe HH can lead to a major height deficit, and catch-up growth seems to be insufficient after treatment with HRT alone. In the most severe cases, administration of GH may enhance this catch-up.

摘要

背景

我们旨在评估重度桥本甲状腺功能减退症(HH)患儿在接受甲状腺激素替代疗法(HRT)后的追赶生长情况。

方法

进行了一项多中心回顾性研究,纳入了1998年至2017年间因生长发育迟缓而被诊断为HH的患儿。

结果

共纳入29例患者,中位年龄为9.7岁(13 - 172个月)。诊断时的中位身高标准差分数(SDS)为 -2.7 [-4.6; -0.1],与生长偏离前的身高相比,身高损失了2.5 [0.7; 5.4] SDS(p<0.0001)。诊断时,中位促甲状腺激素(TSH)水平为819.5 mIU/L [100; 1844],中位游离甲状腺素(FT4)水平为0 pmol/L [不可检测; 5.4],中位抗甲状腺过氧化物酶抗体水平为1601 UI/L [47; 25,500]。在仅接受HRT治疗的20例患者中,诊断时的身高与治疗1年(n = 19,p<0.0001)、2年(n = 13,p = 0.0005)、3年(n = 9,p = 0.0039)、4年(n = 10,p = 0.0078)和5年(n = 10,p = 0.0018)时的身高存在显著差异,但最终身高(n = 6,p = 0.0625)情况无差异。中位最终身高为 -1.4 [-2.7; 1.5] SDS(n = 6),诊断时的身高损失与总追赶生长之间存在显著差异(p = 0.003)。其他9例患者还接受了生长激素(GH)治疗。他们在诊断时身材更小(p = 0.01);然而,两组之间的最终身高无差异(p = 0.68)。

结论

重度HH可导致严重的身高缺陷,仅用HRT治疗后追赶生长似乎不足。在最严重的病例中,给予GH可能会增强这种追赶生长。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验