Kato Ikuko, Canzian Federico, Franceschi Silvia, Plummer Martyn, van Doorn Leen-Jan, Lu Yanhui, Gioia-Patricola Lydie, Vivas Jorge, Lopez Gladys, Severson Richard K, Schwartz Ann G, Muñoz Nubia
Karmanos Cancer Institute, 110 East Warren Avenue, Detroit, MI, 48201, USA.
Cancer Causes Control. 2006 Nov;17(9):1183-91. doi: 10.1007/s10552-006-0060-4.
The aim of the study was to assess the effects of genetic polymorphisms in anti-inflammatory mediators, i.e., IL10, IL4 and IL4R on the prevalence of gastric precancerous lesions and their interactions with other environmental factors.
The study population consisted of 2,033 Venezuelan subjects known to have extremely high Helicobacter Pylori (HP) infection rates. The odds ratios (OR) and 95% confidence intervals (CI) associated with these polymorphisms were estimated by multinominal logistic regression models for gastric precursor lesions.
We found a 60% increase in risk of intestinal metaplasia (IM) and dysplasia combined (OR 1.62, 95% CI: 1.10-2.38) among the carriers of the IL10-1082 low activity allele. This increased risk was more pronounced for dysplasia than for IM. On the other hand, homozygotes with the low activity allele of the A398G polymorphism in the IL4R gene had a modest increase in risk of atrophic gastritis (OR = 1.52, 95% CI: 1.05-2.21), compared with homozygotes of the high activity allele. There were no statistically significant synergetic interactions between these polymorphisms and environmental risk factors (low fruit intake, high starchy vegetable intake and cigarette smoking) for these lesions.
While the results of the present study suggest roles of genetic variability in these anti-inflammatory mediators in different stages of gastric carcinogenesis, there is high likelihood that they were chance findings due to multiple comparisons.
本研究旨在评估抗炎介质(即白细胞介素10、白细胞介素4和白细胞介素4受体)基因多态性对胃癌前病变患病率的影响,及其与其他环境因素的相互作用。
研究人群包括2033名已知幽门螺杆菌(HP)感染率极高的委内瑞拉受试者。通过多分类逻辑回归模型估计这些多态性与胃前驱病变相关的比值比(OR)和95%置信区间(CI)。
我们发现白细胞介素10 - 1082低活性等位基因携带者发生肠化生(IM)和发育异常合并症的风险增加60%(OR 1.62,95% CI:1.10 - 2.38)。这种风险增加在发育异常中比在肠化生中更为明显。另一方面,白细胞介素4受体基因A398G多态性低活性等位基因的纯合子与高活性等位基因纯合子相比,萎缩性胃炎风险有适度增加(OR = 1.52,95% CI:1.05 - 2.21)。这些多态性与这些病变的环境风险因素(低水果摄入量、高淀粉类蔬菜摄入量和吸烟)之间没有统计学上显著的协同相互作用。
虽然本研究结果表明这些抗炎介质的基因变异性在胃癌发生的不同阶段发挥作用,但由于进行了多次比较,很有可能这些结果是偶然发现。