Rueda B, Pascual M, López-Nevot M A, Koeleman B P C, Ortega E, Maldonado J, López M, Martín J
Instituto de Parasitología y Biomedicina López-Neyra, CSIC, Granada, Spain.
Am J Gastroenterol. 2003 Feb;98(2):359-62. doi: 10.1111/j.1572-0241.2003.07228.x.
The aim of this study was to analyze the role of the major histocompatibility complex class I chain-related gene A (MICA) transmembrane polymorphism in celiac disease (CD) susceptibility.
Sixty-one celiac Spanish families were genotyped for MICA transmembrane polymorphism by a polymerase chain reaction method combined with fluorescent technology. A transmission disequilibrium test was performed to investigate the preferential transmission of MICA alleles to the affected offspring.
The MICA A5.1 allele was shown to be significantly transmitted to the affected siblings. This association was independent of the CD-predisposing DQ2 haplotype. Additionally, we classified our celiac families into typical and atypical groups as we found a significant association with MICA A5.1 in typical celiac families. There was also an association tendency with atypical families.
Our data suggest that the MICA A5.1 allele is associated with CD development independently of DQ2-extended haplotype and clinical forms of CD.
本研究旨在分析主要组织相容性复合体 I 类链相关基因 A(MICA)跨膜多态性在乳糜泻(CD)易感性中的作用。
采用聚合酶链反应法结合荧光技术,对61个西班牙乳糜泻家庭的MICA跨膜多态性进行基因分型。进行传递不平衡检验,以研究MICA等位基因向患病后代的优先传递情况。
MICA A5.1等位基因被证明显著传递给患病同胞。这种关联独立于CD易感的DQ2单倍型。此外,由于我们发现典型乳糜泻家庭中MICA A5.1存在显著关联,因此将我们的乳糜泻家庭分为典型和非典型组。非典型家庭也有一定的关联趋势。
我们的数据表明,MICA A5.1等位基因与CD的发生相关,独立于DQ2扩展单倍型和CD的临床形式。