Ohtaka Y, Azuma T, Konishi J, Ito S, Kuriyama M
Second Department of Internal Medicine, Fukui Medical School, Japan.
Gut. 1997 Oct;41(4):469-74. doi: 10.1136/gut.41.4.469.
The genetic trait plays a part in the pathogenesis of peptic ulcer disease. To identify a DNA marker for peptic ulcer disease, the association between the restriction fragment length polymorphism (RFLP) of the pepsinogen C (PGC) gene and peptic ulcer disease was investigated.
One hundred and seventy seven unrelated controls, 75 patients with gastric ulcer, and 70 with duodenal ulcer were studied. PGC-RFLP was analysed by polymerase chain reaction (PCR), and the association between PGC-RFLP and peptic ulcer disease was examined. The relation between the genetic association of PGC polymorphism with peptic ulcer and Helicobacter pylori infection was also examined.
Four alleles, 480 (allele 1), 450 (allele 2), 400 (allele 3), and 310 bp (allele 4), were detected by PCR. The frequency of allele 4 was significantly higher in patients with gastric body ulcer than in controls (chi (2) = 9.92, p < 0.005). Genotypes containing allele 4 were significantly more frequent in patients with gastric body ulcer than in controls and patients with gastric angular or antral ulcer. The relative risk of gastric body ulcer associated with the presence of allele 4, compared with its absence, was 4.63 and was statistically significant (chi (2) = 14.84, p < 0.005). There were no significant differences in the allelic frequencies between H pylori positive and H pylori negative groups in controls, patients with gastric body ulcer, or patients with gastric angular or antral ulcer. Both in H pylori negative and H pylori positive cases, there was an increased frequency of allele 4 in patients with gastric body ulcer compared with controls.
These results suggest that there is a significant association between this genetic polymorphism at the PGC gene locus and gastric body ulcer. There are differences in the genetic aetiology between gastric body ulcer and gastric angular or antral ulcer. PGC-RFLP may be used as a genetic marker for a genetic predisposition to gastric body ulcer; this genetic predisposition is not associated with H pylori infection.
遗传特性在消化性溃疡病的发病机制中起作用。为了确定消化性溃疡病的DNA标记物,研究了胃蛋白酶原C(PGC)基因的限制性片段长度多态性(RFLP)与消化性溃疡病之间的关联。
研究了177名无关对照、75名胃溃疡患者和70名十二指肠溃疡患者。通过聚合酶链反应(PCR)分析PGC-RFLP,并检测PGC-RFLP与消化性溃疡病之间的关联。还检测了PGC多态性与消化性溃疡的遗传关联和幽门螺杆菌感染之间的关系。
通过PCR检测到4个等位基因,480(等位基因1)、450(等位基因2)、400(等位基因3)和310bp(等位基因4)。胃体溃疡患者中,等位基因4的频率显著高于对照组(χ² = 9.92,p < 0.005)。含有等位基因4的基因型在胃体溃疡患者中比在对照组以及胃角或胃窦溃疡患者中更为常见。与不存在等位基因4相比,胃体溃疡与等位基因4存在相关的相对风险为4.63,具有统计学意义(χ² = 14.84,p < 0.005)。在对照组、胃体溃疡患者或胃角或胃窦溃疡患者中,幽门螺杆菌阳性组和幽门螺杆菌阴性组之间的等位基因频率没有显著差异。在幽门螺杆菌阴性和阳性病例中,胃体溃疡患者的等位基因4频率均高于对照组。
这些结果表明,PGC基因位点的这种遗传多态性与胃体溃疡之间存在显著关联。胃体溃疡与胃角或胃窦溃疡的遗传病因存在差异。PGC-RFLP可作为胃体溃疡遗传易感性的遗传标记物;这种遗传易感性与幽门螺杆菌感染无关。