Takagi Yasuhiko, Masamune Atsushi, Kume Kiyoshi, Satoh Akihiko, Kikuta Kazuhiro, Watanabe Takashi, Satoh Kennichi, Hirota Morihisa, Shimosegawa Tooru
Division of Gastroenterology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Hum Immunol. 2009 Mar;70(3):200-4. doi: 10.1016/j.humimm.2009.01.006.
This study evaluated the association of the polymorphisms in the Toll-like receptor (TLR)2 and TLR4 genes with acute pancreatitis (AP) in Japan. The numbers of guanine-thymine [(GT)n] repeats in intron 2 of the TLR2 gene were counted in 202 unrelated patients with AP (80 with severe and 122 with mild disease) and in 286 healthy controls, using polymerase chain reaction and Genescan analysis. The alleles were divided into three subclasses: (GT)16 or less as the S allele; between (GT)17 and (GT)22 as the M allele; and (GT)23 or more as the L allele. Asp299Gly and Thr399Ile polymorphisms in the TLR4 gene were examined by polymerase chain reaction-restriction fragment length polymorphism analysis. Patients with AP had more S alleles (p < 0.001; odds ratio = 2.37; 95% confidence interval = 1.78-3.17) and fewer M alleles (p < 0.001; odds ratio = 0.40; 95% confidence interval 0.31-0.52) than did healthy controls. Genotypes SS and SL were more common, whereas MM and ML were less common in patients with AP. In subgroup analyses, the genotypes including S alleles were more common in patients with severe AP than in controls. No Asp299Gly and Thr399Ile polymorphisms were detected. In conclusion, microsatellite polymorphism in intron 2 of the TLR2 gene was associated with susceptibility to AP and its severity in Japan.
本研究评估了日本人群中Toll样受体(TLR)2和TLR4基因多态性与急性胰腺炎(AP)的相关性。采用聚合酶链反应和基因扫描分析,对202例无亲缘关系的AP患者(80例重症患者和122例轻症患者)及286例健康对照者进行TLR2基因内含子2中鸟嘌呤 - 胸腺嘧啶[(GT)n]重复序列计数。等位基因分为三个亚类:(GT)16及以下为S等位基因;(GT)17至(GT)22为M等位基因;(GT)23及以上为L等位基因。通过聚合酶链反应 - 限制性片段长度多态性分析检测TLR4基因中的Asp299Gly和Thr399Ile多态性。与健康对照者相比,AP患者具有更多的S等位基因(p < 0.001;优势比 = 2.37;95%置信区间 = 1.78 - 3.17)和更少的M等位基因(p < 0.001;优势比 = 0.40;95%置信区间0.31 - 0.52)。在AP患者中,SS和SL基因型更为常见,而MM和ML基因型则较少见。在亚组分析中,包含S等位基因的基因型在重症AP患者中比对照者更常见。未检测到Asp299Gly和Thr399Ile多态性。总之,在日本人群中,TLR2基因内含子2中的微卫星多态性与AP易感性及其严重程度相关。