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G protein β3 subunit, interleukin‐10, and tumor necrosis factor‐α gene polymorphisms in Koreans with irritable bowel syndrome
Author(s) -
Lee H.j.,
Lee S.y.,
Choi J. E.,
Kim J. H.,
Sung I.k.,
Park H. S.,
Jin C. J.
Publication year - 2010
Publication title -
neurogastroenterology and motility
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.489
H-Index - 105
eISSN - 1365-2982
pISSN - 1350-1925
DOI - 10.1111/j.1365-2982.2010.01496.x
Subject(s) - irritable bowel syndrome , allele , gastroenterology , genotype , medicine , multifactor dimensionality reduction , allele frequency , gene polymorphism , immunology , gene , biology , genetics , single nucleotide polymorphism
Background The association between irritable bowel syndrome (IBS) based on Rome III criteria and G protein β3 subunit (GNB3), interleukin (IL)‐10, and tumor necrosis factor (TNF)‐α gene polymorphisms is uncertain. Methods Case and control subjects were recruited from Korean visitors to the Health Promotion Center and Digestive Disease Center for gastrointestinal endoscopy. G protein β3 subunit, IL‐10, and TNF‐α gene polymorphisms were genotyped using a polymerase chain reaction‐based method. Multifactor dimensionality reduction (MDR) analysis was used to assess gene–gene interactions. Key Results Genotype and allele frequencies of GNB3 showed marginal significance between the healthy controls and IBS patients (χ 2 = 5.92, P = 0.052; χ 2 = 3.76, P = 0.053). G protein β3 subunit T allele was more strongly correlated with IBS with constipation (12 of constipation‐dominant type and 31 of mixed type) than with 51 diarrhea‐dominant type and 88 normal subjects (χ 2 = 13.91, P = 0.008). Multifactor dimensionality reduction analysis revealed that there were no significant interactions of GNB3, IL‐10, and TNF‐α gene variants with susceptibility to IBS ( P > 0.05). Conclusions & Inferences The results suggest that GNB3 825T allele might be associated with IBS with constipation in Koreans.