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HLA-DQ 基因型与阿拉伯人乳糜泻的相对风险:一项病例对照研究。

HLA-DQ genotypes relative risks for celiac disease in Arabs: A case-control study.

机构信息

Division of Pediatric Gastroenterology, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia.

College of Medicine, Alfaisal University, Riyadh, Saudi Arabia.

出版信息

J Dig Dis. 2019 Nov;20(11):602-608. doi: 10.1111/1751-2980.12817. Epub 2019 Oct 22.

Abstract

OBJECTIVES

It remains unknown what degree of risk is conferred by celiac disease (CD)-predisposing human leukocyte antigen (HLA)-DQ genotypes in Saudi Arabia compared with in Western countries. In this study, we aimed to determine the CD risk gradient associated with the HLA-DQ genotypes and to compare HLA-DQ genotypes between symptomatic patients with CD and screening-identified asymptomatic CD patients.

METHODS

We enrolled three groups of subjects, including 46 CD children diagnosed consecutively over the past 10 years, 54 CD children diagnosed during a mass screening of schoolchildren, and 192 healthy controls. All the participants were typed for the HLA-DQA1 and HLA-DQB1 genes by polymerase chain reaction sequence-specific oligonucleotide probes.

RESULTS

Comparing the patients with CD to controls, we identified 5 groups in the CD risk gradient: (i) very high risk associated with the DQ2.5/DQ8 genotype (odds ratio [OR] 46.93); (ii) high risk (homozygous DQ2.5, DQ2.5/DQ2.2; OR 4.12-5.04); (iii) intermediate risk (heterozygous DQ2.5, DQ8/DQ2.2; OR 1.61 and 1.67); (iv) low risk (DQ8, DQ2.2); and (v) very low risk (DQ2.x, DQX.5, DQX.x). Heterozygous DQ8 was more common in screening-identified group compared to symptomatic patients (13.0% vs 2.2%); however, other genotypes were very similar between the two groups.

CONCLUSION

The highest risk of developing CD in our Saudi Arabia population is associated with the DQ2.5/DQ8 genotype.

摘要

目的

目前尚不清楚与西方国家相比,沙特阿拉伯的乳糜泻(CD)易感人类白细胞抗原(HLA)-DQ 基因型赋予了多大程度的风险。在这项研究中,我们旨在确定与 HLA-DQ 基因型相关的 CD 风险梯度,并比较有症状的 CD 患者和筛查确定的无症状 CD 患者之间的 HLA-DQ 基因型。

方法

我们招募了三组受试者,包括过去 10 年连续诊断的 46 名 CD 儿童、在学童大规模筛查中诊断的 54 名 CD 儿童和 192 名健康对照。所有参与者均通过聚合酶链反应序列特异性寡核苷酸探针进行 HLA-DQA1 和 HLA-DQB1 基因分型。

结果

将 CD 患者与对照组进行比较,我们在 CD 风险梯度中发现了 5 个组:(i)与 DQ2.5/DQ8 基因型相关的极高风险(比值比[OR]46.93);(ii)高风险(纯合 DQ2.5、DQ2.5/DQ2.2;OR 4.12-5.04);(iii)中风险(杂合 DQ2.5、DQ8/DQ2.2;OR 1.61 和 1.67);(iv)低风险(DQ8、DQ2.2);和(v)极低风险(DQ2.x、DQX.5、DQX.x)。与有症状的患者相比,筛查确定的组中杂合 DQ8 更为常见(13.0%比 2.2%);然而,两组之间的其他基因型非常相似。

结论

在我们的沙特阿拉伯人群中,CD 发病的最高风险与 DQ2.5/DQ8 基因型相关。

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