乳糜泻患儿兄弟姐妹中HLA-DQ2/DQ8单倍型的分布及乳糜泻发病率

Yasin Sahin, Serdar Mermer
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引用次数: 3

摘要

背景:乳糜泻是一种多因素疾病,遗传因素在其发病中起主要作用。已知人类白细胞抗原(HLA)-DQ2/DQ8单倍型是最重要的易感遗传因素之一。乳糜泻患者的一级亲属特别是兄弟姐妹罹患乳糜泻的风险很高,因为他们具有相同的HLA单倍型。目的:评价乳糜泻患者兄弟姐妹中乳糜泻的发病频率及HLA-DQ2/DQ8单倍型的分布。方法:将活检证实的乳糜泻患者及其兄弟姐妹纳入研究;那些没有HLA基因分型的人被排除在研究之外。所有的兄弟姐妹都吃含谷蛋白的食物。所有受试者均进行HLA基因分型、组织转谷氨酰胺酶抗体IgA抗体检测和总IgA检测。结果:共有57名乳糜泻患者及其112名兄弟姐妹被纳入研究。乳糜泻患者及其兄弟姐妹的平均年龄分别为10.30±3.87岁和9.90±6.11岁。在98.2%的乳糜泻患者和90.2%的乳糜泻患者的兄弟姐妹中检测到HLA-DQ2/DQ8等位基因。所有诊断为乳糜泻的兄弟姐妹中均存在HLA-DQ基因型。16名兄弟姐妹中发现组织转谷氨酰胺酶抗体IgA测试呈阳性。12名兄弟姐妹(10.7%)通过肠道活检确诊为乳糜泻。结论:本研究发现乳糜泻患者的兄弟姐妹乳糜泻患病率为10.7%。三分之一被诊断为乳糜泻的兄弟姐妹无症状。我们在98.2%的乳糜泻患者和100%诊断为乳糜泻的兄弟姐妹中检测到HLA-DQ等位基因。此外,2个兄弟姐妹中有1个在1年后诊断为乳糜泻,另一个在4年后诊断为乳糜泻。因此,我们建议对乳糜泻患者的兄弟姐妹进行临床随访,并进行HLA分析和血清学检查。由于无症状的兄弟姐妹患乳糜泻的风险要高得多,我们建议即使兄弟姐妹没有症状,也应该进行乳糜泻筛查。
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Frequency of celiac disease and distribution of HLA-DQ2/DQ8 haplotypes among siblings of children with celiac disease.

Background: Celiac disease (CD) is a multifactorial disease, but genetic factors play a major role in its etiology. It has been known that human leucocyte antigen (HLA)-DQ2/DQ8 haplotypes are one of the most important predisposing genetic factors. The risk of developing CD in first-degree relatives and especially siblings of celiac patients is quite high because of having the same HLA haplotypes.

Aim: To evaluate the frequency of CD and the distribution of the HLA-DQ2/DQ8 haplotypes in siblings of celiac patients.

Methods: Patients with biopsy-proven CD and their siblings were included in the study; those who did not have HLA genotyping were excluded from the study. All siblings were on a gluten-containing diet. The HLA genotyping, tissue transglutaminase antibody IgA antibody test, and total IgA test were performed in all participants.

Results: A total of 57 celiac patients and their 112 siblings were included in the study. The mean age of celiac patients and siblings were 10.30 ± 3.87 years and 9.90 ± 6.11 years, respectively. HLA-DQ2/DQ8 alleles were detected in 98.2% of patients with CD and 90.2% of siblings of celiac patients. HLA-DQ genotypes were present in all siblings diagnosed with CD. Tissue transglutaminase antibody IgA test was found to be positive in 16 siblings. CD was diagnosed in 12 siblings (10.7%) by intestinal biopsy.

Conclusion: The prevalence of CD was found to be 10.7% in siblings of celiac patients in our study. One-third of the siblings diagnosed with CD were asymptomatic. We detected HLA-DQ alleles in 98.2% of celiac patients and 100% in siblings diagnosed with CD. In addition, 1 of the 2 siblings was diagnosed with CD 1 year later and the other 4 years later. Therefore, we suggest that siblings of celiac patients should be followed up with clinical findings as well as HLA analysis and serological examination. Since the risk of developing CD is much higher in asymptomatic siblings, we recommend that siblings should be screened for CD even if they are asymptomatic.

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