Clinical Trial Service Unit & Epidemiological Studies Unit (CTSU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Medical Research Council Population Health Research Unit (MRC PHRU), Nuffield Department of Population Health, University of Oxford, Oxford, UK.
Int J Epidemiol. 2023 Aug 2;52(4):1197-1208. doi: 10.1093/ije/dyad007.
Helicobacter pylori infection is a major cause of non-cardia gastric cancer (NCGC), but uncertainty remains about the associations between sero-positivity to different H. pylori antigens and risk of NCGC and cardia gastric cancer (CGC) in different populations.
A case-cohort study in China included ∼500 each of incident NCGC and CGC cases and ∼2000 subcohort participants. Sero-positivity to 12 H. pylori antigens was measured in baseline plasma samples using a multiplex assay. Hazard ratios (HRs) of NCGC and CGC for each marker were estimated using Cox regression. These were further meta-analysed with studies using same assay.
In the subcohort, sero-positivity for 12 H. pylori antigens varied from 11.4% (HpaA) to 70.8% (CagA). Overall, 10 antigens showed significant associations with risk of NCGC (adjusted HRs: 1.33 to 4.15), and four antigens with CGC (HRs: 1.50 to 2.34). After simultaneous adjustment for other antigens, positive associations remained significant for NCGC (CagA, HP1564, HP0305) and CGC (CagA, HP1564, HyuA). Compared with CagA sero-positive only individuals, those who were positive for all three antigens had an adjusted HR of 5.59 (95% CI 4.68-6.66) for NCGC and 2.17 (95% CI 1.54-3.05) for CGC. In the meta-analysis of NCGC, the pooled relative risk for CagA was 2.96 (95% CI 2.58-3.41) [Europeans: 5.32 (95% CI 4.05-6.99); Asians: 2.41 (95% CI 2.05-2.83); Pheterogeneity<0.0001]. Similar pronounced population differences were also evident for GroEL, HP1564, HcpC and HP0305. In meta-analyses of CGC, two antigens (CagA, HP1564) were significantly associated with a higher risk in Asians but not Europeans.
Sero-positivity to several H. pylori antigens was significantly associated with an increased risk of NCGC and CGC, with varying effects between Asian and European populations.
幽门螺杆菌感染是导致非贲门胃癌(NCGC)的主要原因,但不同人群中针对不同幽门螺杆菌抗原的血清阳性与 NCGC 和贲门胃癌(CGC)风险之间的关联仍存在不确定性。
在中国进行的一项病例-队列研究中,包括约 500 例新发 NCGC 和 CGC 病例和约 2000 名亚队列参与者。使用多重分析在基线血浆样本中测量 12 种幽门螺杆菌抗原的血清阳性率。使用 Cox 回归估计每个标志物的 NCGC 和 CGC 的风险比(HR)。这些结果进一步与使用相同检测方法的研究进行了荟萃分析。
在亚队列中,12 种幽门螺杆菌抗原的血清阳性率从 11.4%(HpaA)到 70.8%(CagA)不等。总体而言,有 10 种抗原与 NCGC 风险显著相关(调整后的 HR:1.33 至 4.15),4 种抗原与 CGC 相关(HR:1.50 至 2.34)。在同时调整其他抗原后,CagA、HP1564 和 HP0305 与 NCGC 之间的阳性关联仍然显著,CagA、HP1564 和 HyuA 与 CGC 之间的阳性关联仍然显著。与仅 CagA 血清阳性个体相比,同时检测到所有三种抗原的个体患 NCGC 的调整 HR 为 5.59(95%CI 4.68-6.66),患 CGC 的调整 HR 为 2.17(95%CI 1.54-3.05)。在 NCGC 的荟萃分析中,CagA 的 pooled 相对风险为 2.96(95%CI 2.58-3.41)[欧洲人:5.32(95%CI 4.05-6.99);亚洲人:2.41(95%CI 2.05-2.83);P 异质性<0.0001]。在 GroEL、HP1564、HcpC 和 HP0305 中也明显存在类似的人群差异。在 CGC 的荟萃分析中,两种抗原(CagA 和 HP1564)在亚洲人群中与更高的风险显著相关,但在欧洲人群中则不相关。
针对几种幽门螺杆菌抗原的血清阳性与 NCGC 和 CGC 的风险增加显著相关,并且在亚洲人和欧洲人之间存在不同的影响。