{"title":"HLA-DQ 分型是否有助于筛查阿拉伯 1 型糖尿病患者中的乳糜泻?一项病例对照研究。","authors":"Abdulrahman Al-Hussaini, Abdulhameed Alsaheel, Mussa AlMalki, Riccardo Troncone, Hanan Alharthi, Nezar Eltayeb-Elsheikh, Ghadeer Alshammari, Shawana Zaheer Allah, Ghadeer Aldossari, Norah AlRajhi, Fatimah Abdulkareem, Ahmed Alzahrani, Ola AlNemer, Lulwa AlMazrou, Muhammed Salman Bashir","doi":"10.1002/jpn3.12385","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>The data on the usefulness of DQ-typing in screening for celiac disease (CD) among type 1 diabetic (T1D) patients came from the West. We conducted this study among T1D patients to: (1) determine the frequency of DQ-genotypes, (2) assess the risk associated with human leukocyte antigen (HLA)-DQ genotypes, and (3) identify the cost-effective screening strategy.</p><p><strong>Methods: </strong>HLA-DQ genotyping was performed on 67 T1D patients with CD (cases) (mean age 15 years) and 224 T1D patients without CD (controls) (mean age 18.29 years) (2021-2023). The entry criterion for the control group was duration of T1D ≥5 years and negative annual celiac serology assay.</p><p><strong>Results: </strong>On comparison of the cases versus controls, T1D patients carrying homozygous DQ2.5 genotype (30% vs. 13.8%) or DR3-DQ2.5 haplotype (81.3% vs. 65.7%) showed significantly \"higher risk\" (odds ratio [OR] = 2.64, p = 0.002; OR = 2.3, p = 0.008, respectively) to develop CD. Only 4% do not harbor any of the CD-at risk genotypes (DQ2.5, DQ8, or DQ2.2) and none developed CD. Heterozygous DQ8 was associated with a significantly lower risk of developing CD with OR of 0.123 (1.5% in cases vs. 10.3% in controls, p = 0.022).</p><p><strong>Conclusion: </strong>Only 4% of Saudi patients with T1D carry DQ-genotypes at no risk to develop CD, which supports the European guidelines that recommend celiac serology test as the most cost-effective screening method. We identified the risk gradient associated with DQ-genotypes to develop CD in our population which could help in counseling patients for the risk to develop CD and planning follow-up serology tests.</p>","PeriodicalId":16694,"journal":{"name":"Journal of Pediatric Gastroenterology and Nutrition","volume":" ","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Is HLA-DQ typing useful in screening for celiac disease among Arabs with type 1 diabetes? A case-control study.\",\"authors\":\"Abdulrahman Al-Hussaini, Abdulhameed Alsaheel, Mussa AlMalki, Riccardo Troncone, Hanan Alharthi, Nezar Eltayeb-Elsheikh, Ghadeer Alshammari, Shawana Zaheer Allah, Ghadeer Aldossari, Norah AlRajhi, Fatimah Abdulkareem, Ahmed Alzahrani, Ola AlNemer, Lulwa AlMazrou, Muhammed Salman Bashir\",\"doi\":\"10.1002/jpn3.12385\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>The data on the usefulness of DQ-typing in screening for celiac disease (CD) among type 1 diabetic (T1D) patients came from the West. We conducted this study among T1D patients to: (1) determine the frequency of DQ-genotypes, (2) assess the risk associated with human leukocyte antigen (HLA)-DQ genotypes, and (3) identify the cost-effective screening strategy.</p><p><strong>Methods: </strong>HLA-DQ genotyping was performed on 67 T1D patients with CD (cases) (mean age 15 years) and 224 T1D patients without CD (controls) (mean age 18.29 years) (2021-2023). The entry criterion for the control group was duration of T1D ≥5 years and negative annual celiac serology assay.</p><p><strong>Results: </strong>On comparison of the cases versus controls, T1D patients carrying homozygous DQ2.5 genotype (30% vs. 13.8%) or DR3-DQ2.5 haplotype (81.3% vs. 65.7%) showed significantly \\\"higher risk\\\" (odds ratio [OR] = 2.64, p = 0.002; OR = 2.3, p = 0.008, respectively) to develop CD. Only 4% do not harbor any of the CD-at risk genotypes (DQ2.5, DQ8, or DQ2.2) and none developed CD. Heterozygous DQ8 was associated with a significantly lower risk of developing CD with OR of 0.123 (1.5% in cases vs. 10.3% in controls, p = 0.022).</p><p><strong>Conclusion: </strong>Only 4% of Saudi patients with T1D carry DQ-genotypes at no risk to develop CD, which supports the European guidelines that recommend celiac serology test as the most cost-effective screening method. We identified the risk gradient associated with DQ-genotypes to develop CD in our population which could help in counseling patients for the risk to develop CD and planning follow-up serology tests.</p>\",\"PeriodicalId\":16694,\"journal\":{\"name\":\"Journal of Pediatric Gastroenterology and Nutrition\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2024-10-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Pediatric Gastroenterology and Nutrition\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1002/jpn3.12385\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pediatric Gastroenterology and Nutrition","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1002/jpn3.12385","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
目的:有关 DQ 型在 1 型糖尿病(T1D)患者中筛查乳糜泻(CD)的实用性的数据来自西方。方法:对 67 名患有 CD 的 T1D 患者(病例)(平均年龄 15 岁)和 224 名未患有 CD 的 T1D 患者(对照组)(平均年龄 18.29 岁)(2021-2023 年)进行 HLA-DQ 基因分型。对照组的入选标准是 T1D 病程≥5 年且每年乳糜泻血清检测结果为阴性:病例与对照组相比,携带同型DQ2.5基因型(30%对13.8%)或DR3-DQ2.5单倍型(81.3%对65.7%)的T1D患者罹患CD的风险明显更高(几率比[OR]=2.64,P=0.002;OR=2.3,P=0.008)。只有 4% 的人不携带任何一种 CD 高危基因型(DQ2.5、DQ8 或 DQ2.2),且无一人发展为 CD。杂合子 DQ8 与罹患 CD 的风险显著降低有关,OR 值为 0.123(病例为 1.5%,对照组为 10.3%,P = 0.022):结论:只有 4% 的沙特 T1D 患者携带 DQ 基因型,没有患 CD 的风险,这支持了欧洲指南的建议,即乳糜泻血清学检测是最具成本效益的筛查方法。我们发现了我国人群中与 DQ 基因型相关的 CD 发病风险梯度,这有助于为患者提供 CD 发病风险咨询并计划后续血清学检测。
Is HLA-DQ typing useful in screening for celiac disease among Arabs with type 1 diabetes? A case-control study.
Objectives: The data on the usefulness of DQ-typing in screening for celiac disease (CD) among type 1 diabetic (T1D) patients came from the West. We conducted this study among T1D patients to: (1) determine the frequency of DQ-genotypes, (2) assess the risk associated with human leukocyte antigen (HLA)-DQ genotypes, and (3) identify the cost-effective screening strategy.
Methods: HLA-DQ genotyping was performed on 67 T1D patients with CD (cases) (mean age 15 years) and 224 T1D patients without CD (controls) (mean age 18.29 years) (2021-2023). The entry criterion for the control group was duration of T1D ≥5 years and negative annual celiac serology assay.
Results: On comparison of the cases versus controls, T1D patients carrying homozygous DQ2.5 genotype (30% vs. 13.8%) or DR3-DQ2.5 haplotype (81.3% vs. 65.7%) showed significantly "higher risk" (odds ratio [OR] = 2.64, p = 0.002; OR = 2.3, p = 0.008, respectively) to develop CD. Only 4% do not harbor any of the CD-at risk genotypes (DQ2.5, DQ8, or DQ2.2) and none developed CD. Heterozygous DQ8 was associated with a significantly lower risk of developing CD with OR of 0.123 (1.5% in cases vs. 10.3% in controls, p = 0.022).
Conclusion: Only 4% of Saudi patients with T1D carry DQ-genotypes at no risk to develop CD, which supports the European guidelines that recommend celiac serology test as the most cost-effective screening method. We identified the risk gradient associated with DQ-genotypes to develop CD in our population which could help in counseling patients for the risk to develop CD and planning follow-up serology tests.
期刊介绍:
The Journal of Pediatric Gastroenterology and Nutrition (JPGN) provides a forum for original papers and reviews dealing with pediatric gastroenterology and nutrition, including normal and abnormal functions of the alimentary tract and its associated organs, including the salivary glands, pancreas, gallbladder, and liver. Particular emphasis is on development and its relation to infant and childhood nutrition.