Division of Epidemiology and Prevention, Aichi Cancer Center Research Institute, Nagoya, Japan.
Cancer Sci. 2011 May;102(5):1076-80. doi: 10.1111/j.1349-7006.2011.01907.x. Epub 2011 Mar 14.
Several studies have investigated a possible association between the ABO blood group and the risk of pancreatic cancer (PC), but this association has not been fully evaluated in Asian populations. The present study aimed to assess the impact of genotype-derived ABO blood types, particularly ABO alleles, on the risk of PC in a Japanese population. We conducted a case-control study using 185 PC and 1465 control patients who visited Aichi Cancer Center in Nagoya, Japan. Using rs8176719 as a marker for the O allele, and rs8176746 and rs8176747 for the B allele, all participants' two ABO alleles were inferred. The impact of ABO blood type on PC risk was examined by multivariate analysis, with adjustment for potential confounders to estimate odds ratios (OR) and 95% confidence intervals (CI). An increased risk of PC was observed with the addition of any non-O allele (trend P = 0.012). Compared with subjects with the OO genotype, those with AO and BB genotypes had significantly increased OR of 1.67 (CI, 1.08-2.57) and 3.28 (CI, 1.38-7.80), respectively. Consistent with earlier reports showing a higher risk of PC for individuals with the non-O blood type, the previously reported protective allele (T) for rs505922 was found to be strongly correlated (r(2) = 0.96) with the O allele. In conclusion, this case-control study showed a statistically significant association between ABO blood group and PC risk in a Japanese population. Further studies are necessary to define the mechanisms by which the ABO gene or closely linked genetic variants influence PC risk.
几项研究调查了 ABO 血型与胰腺癌(PC)风险之间的可能关联,但这种关联在亚洲人群中尚未得到充分评估。本研究旨在评估基因型衍生的 ABO 血型,特别是 ABO 等位基因,对日本人群中 PC 风险的影响。我们使用来自日本名古屋市爱知癌症中心的 185 名 PC 患者和 1465 名对照患者进行了病例对照研究。使用 rs8176719 作为 O 等位基因的标记,使用 rs8176746 和 rs8176747 作为 B 等位基因的标记,推断所有参与者的两个 ABO 等位基因。通过多元分析检查 ABO 血型对 PC 风险的影响,调整潜在混杂因素以估计比值比(OR)和 95%置信区间(CI)。观察到添加任何非 O 等位基因会增加 PC 的风险(趋势 P = 0.012)。与 OO 基因型的受试者相比,AO 和 BB 基因型的受试者的 OR 分别显著增加了 1.67(CI,1.08-2.57)和 3.28(CI,1.38-7.80)。与先前报告的非 O 血型个体患 PC 的风险较高一致,先前报道的 rs505922 的保护性等位基因(T)与 O 等位基因强烈相关(r(2) = 0.96)。综上所述,这项病例对照研究表明在日本人群中 ABO 血型与 PC 风险之间存在统计学显著关联。需要进一步的研究来确定 ABO 基因或紧密连锁的遗传变异如何影响 PC 风险的机制。