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前列腺干细胞抗原基因多态性对幽门螺杆菌相关性疾病易感性的影响:一项病例对照研究。

Influence of prostate stem cell antigen gene polymorphisms on susceptibility to Helicobacter pylori-associated diseases: a case-control study.

机构信息

First Department of Medicine, Hamamatsu University School of Medicine, Hamamatsu, Japan.

出版信息

Helicobacter. 2015 Apr;20(2):106-13. doi: 10.1111/hel.12183. Epub 2015 Jan 12.

DOI:10.1111/hel.12183
PMID:25582162
Abstract

BACKGROUND

Patients with duodenal ulcer have a reduced risk of developing gastric cancer compared to those without. Recently, the prostate stem cell antigen (PSCA) rs2294008 C>T polymorphism was found to be associated with different pathogenesis of duodenal ulcer and gastric cancer developments. However, whether PSCA rs2294008 C>T polymorphism is associated with severity of gastric mucosal atrophy is unclear. We examined the influence of the PSCA rs2294008 C>T polymorphism on susceptibility to H. pylori-related diseases and the relationships between PSCA polymorphism and gastric mucosal atrophy.

METHODS

PSCA rs2294008 C>T polymorphism was assessed in H. pylori-positive Japanese patients (n = 488) with noncardia gastric cancer (n = 193), gastric ulcer (n = 84), duodenal ulcer (n = 61), and atrophic gastritis (n = 150), as well as in H. pylori-negatives (n = 266).

RESULTS

Frequency of PSCA rs2294008 C/C genotype in duodenal ulcer was 36.1%, which was significantly higher than those with gastric cancer (12.4%), gastric ulcer (19.0%), gastritis (10.7%), and H. pylori-negatives (19.5%) (p < .001). Compared with duodenal ulcer, having the T allele significantly increased the risk of gastric cancer (OR: 3.97, 95% CI: 2.02-7.80; p < .001), gastric ulcer (2.40, 1.13-5.10; p = .023), and gastritis (4.72, 2.26-9.86; p < .001). Mean pepsinogen (PG) I/PG II ratio in T allele carriers (2.17 ± 0.75) was significantly lower than that in C/C genotype (3.39 ± 1.27, p < .001).

CONCLUSIONS

The PSCA rs2294008 C>T polymorphism is associated with differing susceptibilities to H. pylori-associated diseases. The PSCA rs2294008 C>T polymorphism may be acting through induction of gastric mucosal atrophy, finally leading to development of gastric ulcer and gastric cancer in PSCA rs2294008 T allele carriers, but not duodenal ulcer.

摘要

背景

与无十二指肠溃疡患者相比,十二指肠溃疡患者发生胃癌的风险较低。最近,发现前列腺干细胞抗原(PSCA)rs2294008 C>T 多态性与十二指肠溃疡和胃癌发展的不同发病机制有关。然而,PSCA rs2294008 C>T 多态性是否与胃黏膜萎缩的严重程度有关尚不清楚。我们研究了 PSCA rs2294008 C>T 多态性对幽门螺杆菌相关疾病易感性的影响,以及 PSCA 多态性与胃黏膜萎缩之间的关系。

方法

评估了幽门螺杆菌阳性的日本患者(n = 488)中 PSCA rs2294008 C>T 多态性,这些患者患有非贲门胃癌(n = 193)、胃溃疡(n = 84)、十二指肠溃疡(n = 61)和萎缩性胃炎(n = 150),以及幽门螺杆菌阴性患者(n = 266)。

结果

十二指肠溃疡患者 PSCA rs2294008 C/C 基因型的频率为 36.1%,明显高于胃癌(12.4%)、胃溃疡(19.0%)、胃炎(10.7%)和幽门螺杆菌阴性患者(19.5%)(p<.001)。与十二指肠溃疡相比,携带 T 等位基因显著增加了胃癌(OR:3.97,95%CI:2.02-7.80;p<.001)、胃溃疡(2.40,1.13-5.10;p =.023)和胃炎(4.72,2.26-9.86;p<.001)的风险。T 等位基因携带者的胃蛋白酶原(PG)I/PG II 比值(2.17 ± 0.75)明显低于 C/C 基因型(3.39 ± 1.27,p<.001)。

结论

PSCA rs2294008 C>T 多态性与幽门螺杆菌相关疾病的易感性不同。PSCA rs2294008 C>T 多态性可能通过诱导胃黏膜萎缩,最终导致 PSCA rs2294008 T 等位基因携带者发生胃溃疡和胃癌,而不是十二指肠溃疡。

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