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• W3199040141 abstract "Abstract Hirschsprung disease (HSCR) is an infrequent congenital intestinal dysplasia. The known genetic variations are unable to fully explain the pathogenesis of HSCR. The α/β‐hydratase domain 1 (ABHD1) interferes with the proliferation and migration of intestinal stem cells. Docking protein 6 ( DOK6 ) is involved in neurodevelopment through RET signalling pathway. We examined the association of ABHD1 and DOK6 genetic variants with HSCR using 1470 controls and 1473 HSCR patients from Southern Chinese children. The results clarified that DOK6 rs12968648 G allele significantly increased HSCR susceptibility, in the allelic model ( p = 0.034; OR = 1.12, 95%CI = 1.01~1.24) and the dominant model ( p = 0.038; OR = 1.12, 95%CI = 1.01~1.25). Clinical stratification analysis showed that rs12968648 G allele was associated with increased risk of short‐segment HSCR (S‐HSCR), in the allelic model ( p = 0.028; OR = 1.14, 95%CI = 1.01~1.28) and the additive model ( p = 0.030; OR = 1.14, 95%CI = 1.01~1.28). ABHD1 rs2304678 C allele had higher risk to develop total colonic aganglionosis (TCA) in the allelic model ( p = 7.04E‐03; OR = 1.67, 95%CI = 1.15~2.43) and the dominant model ( p = 4.12E‐03; OR = 1.93, 95%CI = 1.23~3.04). DOK6 rs12968648 and ABHD1 rs2304678 had significant intergenic synergistic effect according to logical regression ( p = 0.0081; OR = 0.76, 95%CI = 0.63~0.93) and multifactor dimensionality reduction (MDR, p = 0.0045; OR = 1.25, 95%CI = 1.07~1.46). This study verified two susceptible variations of HSCR on ABHD1 and DOK6 . Their roles in HSCR should be conducted in further studies." @default.
• W3199040141 created "2021-09-27" @default.
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• W3199040141 date "2021-09-20" @default.
• W3199040141 modified "2023-10-12" @default.
• W3199040141 title "Association between <i>ABHD1</i> and <i>DOK6</i> polymorphisms and susceptibility to Hirschsprung disease in Southern Chinese children" @default.
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• W3199040141 doi "https://doi.org/10.1111/jcmm.16905" @default.
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