Li Zhong-wu, Tian Meng-meng, Wu Ying, Sun Yu, Feng Guo-shuang, You Wei-cheng, Li Ji-you, Zhao Ai-lian
Department of Pathology, Peking University School of Oncology, Beijing Cancer Hospital & Institute, Beijing 100142, China.
Zhonghua Zhong Liu Za Zhi. 2012 Mar;34(3):192-5. doi: 10.3760/cma.j.issn.0253-3766.2012.03.007.
To investigate the influence of ICAM-1 469K/E gene polymorphisms on the risk of atrophic gastritis and dysplasia.
The ICAM-1 469K/E gene polymorphisms in a total of 372 subjects were detected by polymerase chain reaction-direct sequencing. All of the subjects were from Linqu County, a high risk area of gastric cancer in Shandong Province of northern China. All cases were initially diagnosed as normal or superficial gastritis at the beginning of this study. After a 5-year follow-up, the cases were subdivided into no progression group (no histological progression, n=137), progression group I (progressed to severe chronic atrophic gastritis, n=194) and progression group II (progressed to low-grade dysplasia, n=41).
In all 372 subjects, the frequencies of KK, KE or EE genotype of ICAM-1 K469E were 50.5%, 39.2% and 10.2%, respectively. No significant differences were observed in the ICAM-1 469K/E genotype frequencies between the progression group I and no progression group (P>0.05). The frequencies of KK genotype (68.3%) were significantly higher in the progression group II than in the no progression group (49.6%, P=0.035), and also than in the progression group I (47.4%, P=0.015). An increased risk of the progressing to dysplasia from normal or superficial gastritis was found in the individuals with ICAM-1 469KK genotype [odds ratio (OR)=2.21, 95%CI, 1.10-4.42].
ICAM-1 469K/E gene polymorphisms are significantly associated with the risk of gastric low-grade dysplasia, but not related with severe chronic atrophic gastritis in a population with high risk of gastric cancer in Linqu County, Shandong Province, China.
探讨细胞间黏附分子-1(ICAM-1)469K/E基因多态性对萎缩性胃炎及发育异常风险的影响。
采用聚合酶链反应-直接测序法检测372例受试者的ICAM-1 469K/E基因多态性。所有受试者均来自中国北方山东省胃癌高发区临朐县。本研究开始时,所有病例最初诊断为正常或浅表性胃炎。经过5年随访,病例被分为无进展组(无组织学进展,n = 137)、进展I组(进展为重度慢性萎缩性胃炎,n = 194)和进展II组(进展为低度发育异常,n = 41)。
在372例受试者中,ICAM-1 K469E的KK、KE或EE基因型频率分别为50.5%、39.2%和10.2%。进展I组与无进展组之间的ICAM-1 469K/E基因型频率无显著差异(P>0.05)。进展II组的KK基因型频率(68.3%)显著高于无进展组(49.6%,P = 0.035),也高于进展I组(47.4%,P = 0.015)。ICAM-1 469KK基因型个体从正常或浅表性胃炎进展为发育异常的风险增加[比值比(OR)= 2.21,95%可信区间(CI),1.10 - 4.42]。
在中国山东省临朐县胃癌高危人群中,ICAM-1 469K/E基因多态性与胃低度发育异常风险显著相关,但与重度慢性萎缩性胃炎无关。