Elevated Serum IgA at Onset of Type 1 Diabetes in Children.

IF 3.9 3区 医学 Q2 ENDOCRINOLOGY & METABOLISM
Pediatric Diabetes Pub Date : 2024-03-19 eCollection Date: 2024-01-01 DOI:10.1155/2024/7284088
Amruta Thakkar, Xiaofan Huang, Johnny Wang, Kathy Hwu, Ivan K Chinn, Charles Minard, Joud Hajjar, Maria J Redondo
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引用次数: 0

Abstract

Background: Elevated serum IgA levels have been observed in various autoimmune conditions, including type 1 diabetes (T1D). However, whether children with T1D and elevated serum IgA have unique features has not been studied. We aimed to evaluate the prevalence and characteristics associated with elevated serum IgA at the onset of pediatric T1D.

Materials and methods: We analyzed demographic, clinical, and laboratory data retrospectively collected from 631 racially diverse children (6 months-18 years of age) with T1D who had serum IgA levels measured within 90 days of T1D diagnosis. Univariable and multivariable logistic regression models were used to identify characteristics that were significantly associated with elevated versus normal IgA.

Results: Elevated serum IgA was present in 20.3% (128/631) of the children with newly diagnosed T1D. After adjusting for other variables, A1c level (p=0.029), positive insulin autoantibodies (IAA) (p=0.041), negative glutamic acid decarboxylase autoantibodies (GADA) (p=0.005) and Hispanic ethnicity (p  < 0.001) were significantly associated with elevated serum IgA. After adjustment for confounders, the odds of elevated serum IgA were significantly increased with positive IAA (OR 1.653, 95% CI 1.019-2.679), higher HbA1c (OR 1.132, 95% CI 1.014-1.268) and Hispanic ethnicity (OR 3.279, 95% CI 2.003-5.359) but decreased with GADA positivity (OR 0.474, 95% CI 0.281-0.805).

Conclusions: Elevated serum IgA is present in 20.3% of the children at T1D onset and is associated with specific demographic and clinical characteristics, suggesting a unique pathogenesis in a subset of individuals. Further studies are warranted to investigate the IgA response, its role in T1D pathogenesis, and whether these associations persist over time.

儿童1型糖尿病发病时血清IgA升高
背景:血清IgA水平升高已在多种自身免疫性疾病中观察到,包括1型糖尿病(T1D)。然而,T1D和血清IgA升高的儿童是否有其独特的特征尚未研究。我们的目的是评估儿童T1D发病时血清IgA升高的患病率和相关特征。材料和方法:我们回顾性分析了631名不同种族的T1D儿童(6个月-18岁)的人口统计学、临床和实验室数据,这些儿童在T1D诊断后90天内测量了血清IgA水平。使用单变量和多变量逻辑回归模型来确定与IgA升高和正常显著相关的特征。结果:20.3%(128/631)的新诊断T1D患儿血清IgA升高。在校正其他变量后,A1c水平(p=0.029)、胰岛素自身抗体(IAA)阳性(p=0.041)、谷氨酸脱羧酶自身抗体(GADA)阴性(p=0.005)和西班牙裔(p < 0.001)与血清IgA升高显著相关。校正混杂因素后,IAA阳性(OR 1.653, 95% CI 1.019-2.679)、HbA1c升高(OR 1.132, 95% CI 1.014-1.268)和西班牙裔(OR 3.279, 95% CI 2.003-5.359)患者血清IgA升高的几率显著增加,但GADA阳性患者血清IgA升高的几率降低(OR 0.474, 95% CI 0.281-0.805)。结论:20.3%的T1D发病患儿血清IgA升高,与特定的人口学和临床特征相关,提示在一部分个体中存在独特的发病机制。有必要进一步研究IgA反应,其在T1D发病机制中的作用,以及这些关联是否持续存在。
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来源期刊
Pediatric Diabetes
Pediatric Diabetes 医学-内分泌学与代谢
CiteScore
6.60
自引率
14.70%
发文量
141
审稿时长
4-8 weeks
期刊介绍: Pediatric Diabetes is a bi-monthly journal devoted to disseminating new knowledge relating to the epidemiology, etiology, pathogenesis, management, complications and prevention of diabetes in childhood and adolescence. The aim of the journal is to become the leading vehicle for international dissemination of research and practice relating to diabetes in youth. Papers are considered for publication based on the rigor of scientific approach, novelty, and importance for understanding mechanisms involved in the epidemiology and etiology of this disease, especially its molecular, biochemical and physiological aspects. Work relating to the clinical presentation, course, management and outcome of diabetes, including its physical and emotional sequelae, is considered. In vitro studies using animal or human tissues, whole animal and clinical studies in humans are also considered. The journal reviews full-length papers, preliminary communications with important new information, clinical reports, and reviews of major topics. Invited editorials, commentaries, and perspectives are a regular feature. The editors, based in the USA, Europe, and Australasia, maintain regular communications to assure rapid turnaround time of submitted manuscripts.
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