Serum FGF-21 levels and stature in children and adolescents with celiac disease on a gluten-free diet.

IF 1
Fırat Kaya, Nafiye Urgancı, Ahmet Uçar, Özge Pelin Akbay, Ayşe Merve Usta, Sedanur Celik, Mustafa Safa Kasım
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Abstract

Objectives: To evaluate stature in patients with celiac disease (CD) adherent to a gluten-free diet (GFD), determine the prevalence of growth hormone deficiency (GHD), and assess the associations between stature and serum insulin-like growth factor-1 (IGF-1), insulin-like growth factor-binding protein 3 (IGFBP-3), and FGF 21 levels.

Methods: In this prospective cross-sectional study, 141 pediatric patients with CD (79 females) who had adhered to a GFD for at least 2 years were included. Anthropometric and clinical data were obtained from medical records. Serum IGF-1, IGFBP-3, and FGF21 levels were measured in fasting samples. Growth hormone stimulation tests (L-dopa and clonidine) were performed in patients with a height >1.5 SDS below target height (TH).

Results: Twelve patients (8.5 %) had persistent short stature despite long-term adherence to a GFD. Growth hormone deficiency was diagnosed in three patients (2.1 % of the entire cohort; 25 % of patients with persistent short stature). Patients with persistent short stature without GHD had significantly lower serum IGF-1 and IGFBP-3 standard deviation scores than those with normal stature, whereas serum FGF21 concentrations did not differ significantly between the groups. Serum FGF21 concentrations were not significantly correlated with height SDS, IGF-1, IGFBP-3, or other anthropometric variables.

Conclusions: Persistent short stature may occur despite long-term adherence to a GFD in a small proportion of children and adolescents with CD. GHD was identified in 2.1 % of patients, emphasizing the importance of growth monitoring. Lower IGF-1 and IGFBP-3 SDS in patients with persistent short stature without GHD suggest alterations within the GH-IGF axis. Serum FGF21 concentrations were not associated with stature, suggesting that persistent growth impairment in treated CD is likely multifactorial and is not explained by circulating FGF21 alone.

无麸质饮食中患有乳糜泻的儿童和青少年血清FGF-21水平和身材
目的:评估坚持无谷蛋白饮食(GFD)的乳糜泻(CD)患者的身高,确定生长激素缺乏症(GHD)的患病率,并评估身高与血清胰岛素样生长因子-1 (IGF-1)、胰岛素样生长因子结合蛋白3 (IGFBP-3)和FGF 21水平之间的关系。方法:在这项前瞻性横断面研究中,141名儿童CD患者(79名女性)接受了GFD治疗至少2年。人体测量和临床数据来自医疗记录。测定空腹样品血清IGF-1、IGFBP-3和FGF21水平。身高低于目标身高(TH) 1.5 SDS的患者行生长激素刺激试验(左旋多巴和可乐定)。结果:12例患者(8.5 %)尽管长期坚持GFD,但仍持续身材矮小。三名患者被诊断为生长激素缺乏症(占整个队列的2.1% %;占持续身材矮小患者的25% %)。持续身材矮小且无GHD的患者血清IGF-1和IGFBP-3标准差评分明显低于身材正常的患者,而血清FGF21浓度在组间无显著差异。血清FGF21浓度与身高SDS、IGF-1、IGFBP-3或其他人体测量变量无显著相关。结论:在一小部分患有CD的儿童和青少年中,尽管长期坚持GFD,但仍可能出现持续的身材矮小。在2.1 %的患者中发现了GHD,强调了生长监测的重要性。无GHD的持续性身材矮小患者IGF-1和IGFBP-3 SDS较低,提示GH-IGF轴发生改变。血清FGF21浓度与身高无关,这表明治疗后的CD患者持续生长障碍可能是多因素的,不能仅用循环FGF21来解释。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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