选择性免疫球蛋白A缺乏症的阿曼患者筛选乳糜泻:横断面研究。

Q2 Medicine
Oman Medical Journal Pub Date : 2025-03-31 eCollection Date: 2025-03-01 DOI:10.5001/omj.2025.60
Iman Nasr, Manal Al Kindi, Salma Al Abri, Mahmood Al Kindi, Zainab Ansari, Bushra Al Hinai, Ozay Mohamed, Salah Al Awaidy
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引用次数: 0

摘要

目的:选择性免疫球蛋白A缺乏症(SIgAD)的特点是血清IgA缺乏,而免疫球蛋白G (IgG)和免疫球蛋白M (IgM)水平保持正常。症状从无症状到复发性感染不等。我们的目的是确定在阿曼接受乳糜泻筛查的患者中IgAD和SIgAD的患病率。方法:本横断面研究纳入2005年1月至2023年12月在马斯喀特皇家医院接受抗组织转谷氨酰胺酶(anti-tTG) IgA乳糜泻筛查的1岁以上阿曼国民。IgAD定义为血清总IgA水平低于年龄相关参考范围。IgG和IgM值均在各自参考值范围内时诊断SIgAD。对IgAD和SIgAD的流行情况进行统计分析。结果:在9615名接受乳糜泻筛查的个体中,114名IgA水平较低。IgAD患病率为1.2%,其中0.4%确诊为SIgAD。其中大多数人的年龄在10到14岁之间。与1-2岁的患者相比,6-14岁和10 -14岁的患者更容易患IgAD。只有39例(34.2%)患者接受了进一步的检测以确认SIgAD,而其余75例(65.8%)未接受IgG和IgM的随访检测。在确诊为SIgAD的患者中,11例(28.2%)接受了进一步的抗ttg IgG抗体检测,只有1例(9.1%)经食管胃十二指肠镜检查(EGD)和组织病理学证实为乳糜泻阳性。抗ttg IgG和EGD患者出现低IgA水平的风险显著增加。其余28例(71.8%)患者未接受进一步的乳糜泻检查(抗ttg IgG抗体、EGD或基因检测)。结论:在阿曼诊断为乳糜泻的患者中,有1.2%存在IgAD, 0.4%确诊为SIgAD。当IgG/IgM水平较低或感染复发时,建议转诊到免疫学家。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Selective Immunoglobulin A Deficiency Among Omani Patients Screened for Celiac Disease: A Cross-sectional Study.

Objectives: Selective immunoglobulin A deficiency (SIgAD) is characterized by an isolated deficiency of serum IgA while immunoglobulin G (IgG) and immunoglobulin M (IgM) levels remain normal. Symptoms range from asymptomatic to recurrent infections. We aimed to determine the prevalence of IgAD and SIgAD among Omani patients undergoing screening for celiac disease.

Methods: This cross-sectional study included Omani nationals aged above one year, who were screened for celiac disease with anti-tissue transglutaminase (anti-tTG) IgA at Royal Hospital, Muscat, from January 2005 to December 2023. IgAD was defined as a total serum IgA level below the age-dependent reference range. SIgAD was diagnosed when both IgG and IgM values were within their respective reference limits. The prevalence of IgAD and SIgAD was statistically reviewed.

Results: Of the 9615 individuals who underwent screening for celiac disease, 114 had low IgA levels. The prevalence of IgAD was 1.2%, and among these, 0.4% were confirmed to have SIgAD. The majority were > 14 years. Patients aged 6-14 years and > 14 years were more likely to have IgAD compared to 1-2 years old. Only 39 (34.2%) patients underwent further testing to confirm SIgAD, while the remaining 75 (65.8%) did not undergo follow-up IgG and IgM testing. Among the patients with confirmed SIgAD, 11 (28.2%) underwent further testing with anti-tTG IgG antibody, with only one (9.1%) testing positive for celiac disease as confirmed by esophagogastroduodenoscopy (EGD) and histopathology. Patients with anti-tTG IgG and EGD exhibited a significantly increased risk of low IgA levels. The remaining 28 (71.8%) patients did not undergo further celiac disease workup (anti-tTG IgG antibody, EGD, or genetic testing).

Conclusions: IgAD was present in 1.2% of Omani patients evaluated for celiac disease, and 0.4% had confirmed SIgAD. Referral to an immunologist is recommended when IgG/IgM levels are low or infections are recurrent.

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来源期刊
Oman Medical Journal
Oman Medical Journal Medicine-Medicine (all)
CiteScore
3.10
自引率
0.00%
发文量
119
审稿时长
12 weeks
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