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[血清成纤维细胞生长因子23在儿童低磷性佝偻病诊断中的价值]

[Value of serum fibroblast growth factor 23 in diagnosis of hypophosphatemic rickets in children].

作者信息

Dong Sha-Sha, Che Ruo-Chen, Zheng Bi-Xia, Zhang Ai-Hua, Wang Chun-Li, Bai Mi, Chen Ying

机构信息

Department of Nephrology, Children's Hospital of Nanjing Medical University, Nanjing 210000, China.

出版信息

Zhongguo Dang Dai Er Ke Za Zhi. 2023 Jul 15;25(7):705-710. doi: 10.7499/j.issn.1008-8830.2303016.

DOI:10.7499/j.issn.1008-8830.2303016
PMID:37529952
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10414175/
Abstract

OBJECTIVES

To study the value of serum fibroblast growth factor 23 (FGF23) in the diagnosis of hypophosphatemic rickets in children.

METHODS

A total of 28 children who were diagnosed with hypophosphatemic rickets in Children's Hospital of Nanjing Medical University from January 2016 to June 2021 were included as the rickets group. Forty healthy children, matched for sex and age, who attended the Department of Child Healthcare of the hospital were included as the healthy control group. The serum level of FGF23 was compared between the two groups, and the correlations of the serum FGF23 level with clinical characteristics and laboratory test results were analyzed. The value of serum FGF23 in the diagnosis of hypophosphatemic rickets was assessed.

RESULTS

The rickets group had a significantly higher serum level of FGF23 than the healthy control group (<0.05). In the rickets group, the serum FGF23 level was positively correlated with the serum alkaline phosphatase level (=0.38, <0.05) and was negatively correlated with maximum renal tubular phosphorus uptake/glomerular filtration rate (=-0.64, <0.05), while it was not correlated with age, height Z-score, sex, and parathyroid hormone (>0.05). Serum FGF23 had a sensitivity of 0.821, a specificity of 0.925, an optimal cut-off value of 55.77 pg/mL, and an area under the curve of 0.874 in the diagnosis of hypophosphatemic rickets (<0.05).

CONCLUSIONS

Serum FGF23 is of valuable in the diagnosis of hypophosphatemic rickets in children, which providing a theoretical basis for early diagnosis of this disease in clinical practice.

摘要

目的

探讨血清成纤维细胞生长因子23(FGF23)在儿童低磷性佝偻病诊断中的价值。

方法

选取2016年1月至2021年6月在南京医科大学附属儿童医院确诊为低磷性佝偻病的28例患儿作为佝偻病组。选取同期在该院儿童保健科就诊的40例性别、年龄相匹配的健康儿童作为健康对照组。比较两组血清FGF23水平,并分析血清FGF23水平与临床特征及实验室检查结果的相关性。评估血清FGF23在低磷性佝偻病诊断中的价值。

结果

佝偻病组血清FGF23水平显著高于健康对照组(<0.05)。在佝偻病组中,血清FGF23水平与血清碱性磷酸酶水平呈正相关(=0.38,<0.05),与最大肾小管磷重吸收/肾小球滤过率呈负相关(=-0.64,<0.05),而与年龄、身高Z评分、性别及甲状旁腺激素无相关性(>0.05)。血清FGF23诊断低磷性佝偻病的敏感度为0.821,特异度为0.925,最佳截断值为55.77 pg/mL,曲线下面积为0.874(<0.05)。

结论

血清FGF23对儿童低磷性佝偻病的诊断具有重要价值,为临床早期诊断该病提供了理论依据。

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本文引用的文献

1
Clinical and genetic characteristics of 29 Chinese patients with X-linked hypophosphatemia.29 例 X 连锁低磷血症患者的临床和遗传学特征。
Front Endocrinol (Lausanne). 2022 Aug 19;13:956646. doi: 10.3389/fendo.2022.956646. eCollection 2022.
2
Efficacy of Burosumab in Adults with X-linked Hypophosphatemia (XLH): A Post Hoc Subgroup Analysis of a Randomized Double-Blind Placebo-Controlled Phase 3 Study.布罗索尤单抗治疗 X 连锁低磷血症(XLH)成人患者的疗效:一项随机双盲安慰剂对照 3 期研究的事后亚组分析。
Calcif Tissue Int. 2022 Oct;111(4):409-418. doi: 10.1007/s00223-022-01006-7. Epub 2022 Aug 4.
3
Interdisciplinary management of FGF23-related phosphate wasting syndromes: a Consensus Statement on the evaluation, diagnosis and care of patients with X-linked hypophosphataemia.成纤维细胞生长因子 23(FGF23)相关磷代谢紊乱的综合管理:X 连锁低磷血症患者评估、诊断和治疗的专家共识声明。
Nat Rev Endocrinol. 2022 Jun;18(6):366-384. doi: 10.1038/s41574-022-00662-x. Epub 2022 Apr 28.
4
Clinical performance of a novel chemiluminescent enzyme immunoassay for FGF23.新型化学发光酶免疫分析法检测 FGF23 的临床性能。
J Bone Miner Metab. 2021 Nov;39(6):1066-1075. doi: 10.1007/s00774-021-01250-1. Epub 2021 Jul 13.
5
Intact and C-Terminal FGF23 Assays-Do Kidney Function, Inflammation, and Low Iron Influence Relationships With Outcomes?完整和 C 端 FGF23 检测——肾功能、炎症和低铁如何影响与结果的关系?
J Clin Endocrinol Metab. 2020 Dec 1;105(12):e4875-85. doi: 10.1210/clinem/dgaa665.
6
Efficacy and safety of burosumab in children aged 1-4 years with X-linked hypophosphataemia: a multicentre, open-label, phase 2 trial.布罗索尤单抗治疗 1-4 岁 X 连锁低磷血症儿童的疗效和安全性:一项多中心、开放标签、2 期临床试验。
Lancet Diabetes Endocrinol. 2019 Mar;7(3):189-199. doi: 10.1016/S2213-8587(18)30338-3. Epub 2019 Jan 9.
7
Mineral and bone disorders in conventional hemodialysis: Challenges and solutions.常规血液透析中的矿物质与骨代谢紊乱:挑战与解决方案
Semin Dial. 2018 Nov;31(6):592-598. doi: 10.1111/sdi.12729. Epub 2018 Jun 13.
8
X-Linked Hypophosphatemia and FGF23-Related Hypophosphatemic Diseases: Prospect for New Treatment.X 连锁低磷血症和 FGF23 相关低磷血症疾病:新治疗方法的前景。
Endocr Rev. 2018 Jun 1;39(3):274-291. doi: 10.1210/er.2017-00220.
9
Method-specific differences in plasma fibroblast growth factor 23 measurement using four commercial ELISAs.四种商业 ELISA 检测血浆成纤维细胞生长因子 23 的方法特异性差异。
Clin Chem Lab Med. 2013 Oct;51(10):1971-81. doi: 10.1515/cclm-2013-0208.
10
Dosage effect of a Phex mutation in a murine model of X-linked hypophosphatemia.X 连锁低磷血症小鼠模型中 Phex 突变的剂量效应。
Calcif Tissue Int. 2013 Aug;93(2):155-62. doi: 10.1007/s00223-013-9736-4. Epub 2013 May 23.