Thakkar Amruta, Huang Xiaofan, Wang Johnny, Hwu Kathy, Chinn Ivan K, Minard Charles, Hajjar Joud, Redondo Maria J
Division of Diabetes and Endocrinology, Department of Pediatrics, Texas Children's Hospital, Baylor College of Medicine, Houston, TX, USA.
Baylor College of Medicine, Houston, TX, USA.
Pediatr Diabetes. 2024 Mar 19;2024:7284088. doi: 10.1155/2024/7284088. eCollection 2024.
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.
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.
Elevated serum IgA was present in 20.3% (128/631) of the children with newly diagnosed T1D. After adjusting for other variables, A1c level (=0.029), positive insulin autoantibodies (IAA) (=0.041), negative glutamic acid decarboxylase autoantibodies (GADA) (=0.005) and Hispanic ethnicity ( < 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).
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.
在包括1型糖尿病(T1D)在内的多种自身免疫性疾病中均观察到血清IgA水平升高。然而,T1D患儿且血清IgA升高是否具有独特特征尚未得到研究。我们旨在评估儿童T1D发病时血清IgA升高的患病率及相关特征。
我们回顾性分析了631名不同种族(6个月至18岁)T1D患儿的人口统计学、临床和实验室数据,这些患儿在T1D诊断后90天内检测了血清IgA水平。采用单变量和多变量逻辑回归模型来确定与IgA升高和正常相关的显著特征。
新诊断的T1D患儿中20.3%(128/631)存在血清IgA升高。在调整其他变量后,糖化血红蛋白(A1c)水平(=0.029)、胰岛素自身抗体(IAA)阳性(=0.041)、谷氨酸脱羧酶自身抗体(GADA)阴性(=0.005)和西班牙裔种族(<0.001)与血清IgA升高显著相关。在调整混杂因素后,IAA阳性(比值比[OR]1.653,95%置信区间[CI]1.019 - 2.679)、较高的糖化血红蛋白(HbA1c)(OR 1.132,95% CI 1.014 - 1.268)和西班牙裔种族(OR 3.279,95% CI 2.003 - 5.359)使血清IgA升高的几率显著增加,而GADA阳性则使其降低(OR 0.474,95% CI 0.281 - 0.805)。
20.3%的T1D患儿在发病时血清IgA升高,且与特定的人口统计学和临床特征相关,提示一部分个体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随时间持续存在。