Human Leukocyte Antigen-DQ Genotyping in Pediatric Celiac Disease.

IF 1.3 Q3 PEDIATRICS
Stuti Pareek, Raj Kumar Gupta, Abhinav Sharma, Sandhya Gulati
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Abstract

Purpose: The purpose of this study was to determine the pattern of human leukocyte antigen (HLA)-DQ genotype in children diagnosed with celiac disease (CD) (biopsy proven), and to compare this with a control group; and secondarily, to correlate HLA genotypes with clinical profiles of CD.

Methods: This cross-sectional comparative observational study included 26 controls and 52 patients diagnosed with CD who presented at Sir Padampat Mother and Child Health Institute, Jaipur, from May, 2017 to October, 2018. HLA DQ genotype was assessed for each patients and correlated with clinical profiles.

Results: HLA DQ2/DQ8 genotypes were significantly more common in CD (present in 100.0% cases) than in controls (23.1%) in Northern India (Rajasthan). When HLA DQ2.5 and DQ8 were present together, individuals had significantly more atypical presentations and severe findings on duodenal biopsy. Similarly, patients with the HLA DQ 2.5 genotype were also predisposed to more severe endoscopic findings, while HLA DQ2.2 predisposed them to less severe biopsy findings. HLA DQ8 was significantly associated with later age at diagnosis (>5 years) and shorter stature. The highest HLA DQ relative risk (RR) for CD development was associated with HLA DQ2.5 and DQ2.2 in combination, followed by HLA DQ2.5 and DQ8 in combination, while HLA DQx.5 and HLA DQ2.2 together had the lowest risk.

Conclusion: HLA DQ2/DQ8 genotypes are strongly associated with pediatric CD patients in northern India. These genotypes and their combinations may be associated with different clinical presentations of CD, and may help predict severity of CD.

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儿童乳糜泻的人白细胞抗原- dq基因分型
目的:本研究的目的是确定诊断为乳糜泻(CD)(活检证实)的儿童中人类白细胞抗原(HLA)-DQ基因型的模式,并将其与对照组进行比较;方法:本横断面比较观察研究包括2017年5月至2018年10月在斋浦尔Sir Padampat母婴健康研究所就诊的26名对照组和52名诊断为CD的患者。评估每位患者的HLA DQ基因型,并与临床资料相关联。结果:HLA DQ2/DQ8基因型在印度北部(拉贾斯坦邦)的CD患者中(100.0%)比对照组(23.1%)明显更常见。当HLA DQ2.5和DQ8同时存在时,个体在十二指肠活检中有明显更多的不典型表现和严重的结果。同样,HLA dq2.5基因型患者也易出现更严重的内窥镜检查结果,而HLA DQ2.2基因型患者易出现较轻的活检结果。HLA DQ8与诊断年龄较晚(>5岁)和身材较矮显著相关。发生CD的最高HLA DQ相对风险(RR)与HLA DQ2.5和DQ2.2联合相关,其次是HLA DQ2.5和DQ8联合,而HLA DQx。HLA 5和HLA DQ2.2的风险最低。结论:HLA DQ2/DQ8基因型与印度北部儿童CD患者密切相关。这些基因型及其组合可能与乳糜泻的不同临床表现有关,并可能有助于预测乳糜泻的严重程度。
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来源期刊
CiteScore
3.90
自引率
0.00%
发文量
43
期刊介绍: Pediatric Gastroenterology, Hepatology and Nutrition (Pediatr Gastroenterol Hepatol Nutr), an official journal of The Korean Society of Pediatric Gastroenterology, Hepatology and Nutrition, is issued bimonthly and published in English. The aim of Pediatr Gastroenterol Hepatol Nutr is to advance scientific knowledge and promote child healthcare by publishing high-quality empirical and theoretical studies and providing a recently updated knowledge to those practitioners and scholars in the field of pediatric gastroenterology, hepatology and nutrition. Pediatr Gastroenterol Hepatol Nutr publishes review articles, original articles, and case reports. All of the submitted papers are peer-reviewed. The journal covers basic and clinical researches on molecular and cellular biology, pathophysiology, epidemiology, diagnosis, and treatment of all aspects of pediatric gastrointestinal diseases and nutritional health problems.
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