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Graves病患儿并存自身免疫性疾病的检出率及临床特征:一项来自中国的单中心研究

Detection rate and clinical characteristics of coexisting autoimmune diseases in children with Graves' disease: a single-center study from China.

作者信息

Li Yang, Yan Mu-Qiao, Song Yan-Ning, Zhang Qin, Gong Chun-Xiu

机构信息

Department of Endocrinology, Genetics and Metabolism, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

Department of Health Care, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, China.

出版信息

Endocrine. 2025 Apr;88(1):143-150. doi: 10.1007/s12020-024-04148-w. Epub 2025 Jan 6.

DOI:10.1007/s12020-024-04148-w
PMID:39762666
Abstract

PURPOSE

This study aimed to determine the detection rate of autoimmune polyendocrine syndrome (APS) among children with Graves' disease (GD) at a single center and to compare clinical characteristics between those with isolated GD and those GD with APS (APS-GD).

METHODS

A retrospective analysis was conducted on the clinical data of 555 patients and were categorized into isolated GD and APS-GD groups based on their progression status. The time for FT to return to normal was used as an indicator of short-term treatment effectiveness.

RESULTS

In all, 63 (11.4%) had coexisting APS; 52 (82.5%) were female. The most common component of APS was type 1 diabetes mellitus (T1DM) [24 (4.3%)]. Among APS-GD patients, after the diagnosis of the first component, the cumulative incidences of a second disease within the first, second, and third years were 63.4%, 74.6%, and 82.0%, respectively and till the end of the first decade reached 95.0%. The isolated GD group had higher levels of FT, TT, and TRAb. Under the same initial dosage, the median time for FT to normalize was 22.0 (14.0, 30.0) d for the isolated GD group and 25.0 (13.5, 31.0) d for the APS group (P = 0.936).

CONCLUSION

The study uncovered a high comorbidity rate of APS in children with GD, suggesting that patients with APS-GD have a higher risk of progression to additional endocrine gland disorders. Yet, both groups showed no significant difference in their short-term therapeutic response. These findings are crucial for guiding the clinical management and follow-up of pediatric GD patients.

摘要

目的

本研究旨在确定单中心格雷夫斯病(GD)患儿自身免疫性多内分泌腺综合征(APS)的检出率,并比较单纯GD患儿与合并APS的GD患儿(APS-GD)的临床特征。

方法

对555例患者的临床资料进行回顾性分析,根据病情进展情况分为单纯GD组和APS-GD组。以游离甲状腺素(FT)恢复正常的时间作为短期治疗效果的指标。

结果

共有63例(11.4%)合并APS;其中52例(82.5%)为女性。APS最常见的组成部分是1型糖尿病(T1DM)[24例(4.3%)]。在APS-GD患者中,在诊断出首个组成部分后,在第一、第二和第三年内第二种疾病的累积发病率分别为63.4%、74.6%和82.0%,到第一个十年末达到95.0%。单纯GD组的FT、总甲状腺素(TT)和促甲状腺素受体抗体(TRAb)水平较高。在相同初始剂量下,单纯GD组FT恢复正常的中位时间为22.0(14.0,30.0)天,APS组为25.0(13.5,31.0)天(P = 0.936)。

结论

本研究发现GD患儿中APS的合并率较高,提示APS-GD患者进展为其他内分泌腺疾病的风险更高。然而,两组在短期治疗反应上无显著差异。这些发现对于指导儿科GD患者的临床管理和随访至关重要。

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本文引用的文献

1
Autoimmune diseases and adverse pregnancy outcomes: an umbrella review.自身免疫性疾病与不良妊娠结局:伞式综述。
BMC Med. 2024 Mar 5;22(1):94. doi: 10.1186/s12916-024-03309-y.
2
Risk of recurrence at the time of withdrawal of short- or long-term methimazole therapy in patients with Graves' hyperthyroidism: a randomized trial and a risk-scoring model.Graves 甲亢患者短期或长期甲巯咪唑治疗停药时的复发风险:一项随机试验和风险评分模型。
Endocrine. 2024 May;84(2):577-588. doi: 10.1007/s12020-023-03656-5. Epub 2024 Jan 2.
3
A 20-year study of autoimmune polyendocrine syndrome type II and III in Taiwan.
台湾自身免疫性多内分泌腺综合征 II 型和 III 型的 20 年研究。
Eur Thyroid J. 2023 Nov 23;12(6). doi: 10.1530/ETJ-23-0162. Print 2023 Dec 1.
4
Graves disease is more prevalent than Hashimoto disease in children and adolescents with type 1 diabetes.Graves 病在儿童和青少年 1 型糖尿病患者中的患病率高于桥本甲状腺炎。
Front Endocrinol (Lausanne). 2023 Jan 10;13:1083690. doi: 10.3389/fendo.2022.1083690. eCollection 2022.
5
Long-term outcomes of anti-thyroid drug treatment in childhood-onset Graves' disease.儿童期发病 Graves 病抗甲状腺药物治疗的长期结局。
Clin Endocrinol (Oxf). 2023 Jun;98(6):823-831. doi: 10.1111/cen.14869. Epub 2023 Jan 31.
6
2022 European Thyroid Association Guideline for the management of pediatric Graves' disease.2022年欧洲甲状腺协会儿童格雷夫斯病管理指南
Eur Thyroid J. 2022 Jan 1;11(1):e210073. doi: 10.1530/ETJ-21-0073.
7
Biomarkers of idiosyncratic drug-induced liver injury (DILI) - a systematic review.药物性肝损伤(DILI)的个体化生物标志物:系统评价。
Expert Opin Drug Metab Toxicol. 2021 Nov;17(11):1327-1343. doi: 10.1080/17425255.2021.1999410. Epub 2021 Nov 15.
8
The clinical phenotype of Graves' disease occurring as an isolated condition or in association with other autoimmune diseases.Graves 病的临床表型,可表现为孤立性疾病,也可与其他自身免疫性疾病相关。
J Endocrinol Invest. 2020 Feb;43(2):157-162. doi: 10.1007/s40618-019-01094-7. Epub 2019 Aug 12.
9
Thyroid Dysfunction and Diabetes Mellitus: Two Closely Associated Disorders.甲状腺功能紊乱与糖尿病:两种密切相关的疾病。
Endocr Rev. 2019 Jun 1;40(3):789-824. doi: 10.1210/er.2018-00163.
10
The association of other autoimmune diseases in patients with Graves' disease (with or without ophthalmopathy): Review of the literature and report of a large series.伴有(或不伴有眼病)Graves 病患者的其他自身免疫性疾病的关联:文献复习及大型系列报告。
Autoimmun Rev. 2019 Mar;18(3):287-292. doi: 10.1016/j.autrev.2018.10.001. Epub 2019 Jan 11.