Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, University of Melbourne, Melbourne, Victoria, Australia.
Cancer Epidemiology Division, Cancer Council Victoria, Melbourne, Victoria, Australia.
Cancer Epidemiol Biomarkers Prev. 2022 Aug 2;31(8):1630-1637. doi: 10.1158/1055-9965.EPI-22-0234.
Mechanisms for how Helicobacter pylori infection affects risk of gastroesophageal reflux disease (GERD) and Barrett's esophagus are incompletely understood and might differ by sex.
In a case-control study nested in the Melbourne Collaborative Cohort Study with 425 GERD cases and 169 Barrett's esophagus cases (identified at 2007-2010 follow-up), we estimated sex-specific odds ratios for participants who were H. pylori seronegative versus seropositive at baseline (1990-1994). To explore possible mechanisms, we (i) compared patterns of H. pylori-induced gastritis by sex using serum pepsinogen-I and gastrin-17 data and (ii) quantified the effect of H. pylori seronegativity on Barrett's esophagus mediated by GERD using causal mediation analysis.
For men, H. pylori seronegativity was associated with 1.69-fold [95% confidence interval (CI), 1.03-2.75] and 2.28-fold (95% CI, 1.27-4.12) higher odds of GERD and Barrett's esophagus, respectively. No association was observed for women. H. pylori-induced atrophic antral gastritis was more common in men (68%) than in women (56%; P = 0.015). For men, 5 of the 15 per 1,000 excess Barrett's esophagus risk from being seronegative were mediated by GERD.
Men, but not women, who were H. pylori seronegative had increased risks of GERD and Barrett's esophagus. A possible explanation might be sex differences in patterns of H. pylori-induced atrophic antral gastritis, which could lead to less erosive reflux for men. Evidence of GERD mediating the effect of H. pylori on Barrett's esophagus risk among men supports this proposed mechanism.
The findings highlight the importance of investigating sex differences in the effect of H. pylori on risk of GERD and Barrett's esophagus in future studies.
幽门螺杆菌感染如何影响胃食管反流病(GERD)和 Barrett 食管的风险机制尚不完全清楚,并且可能因性别而异。
在一项病例对照研究中,该研究嵌套在 1990 年至 1994 年基线时进行的墨尔本合作队列研究中,共有 425 例 GERD 病例和 169 例 Barrett 食管病例(在 2007 年至 2010 年的随访中发现),我们估计了基线时 H. pylori 血清阴性与阳性的参与者的性别特异性比值比(OR)。为了探讨可能的机制,我们(i)使用血清胃蛋白酶原-I 和胃泌素-17 数据比较了 H. pylori 引起的胃炎的性别模式,(ii)使用因果中介分析量化了 H. pylori 血清阴性对 GERD 介导的 Barrett 食管的影响。
对于男性,H. pylori 血清阴性与 GERD 和 Barrett 食管的 OR 分别为 1.69 倍(95%CI,1.03-2.75)和 2.28 倍(95%CI,1.27-4.12)。对于女性,没有观察到相关性。H. pylori 引起的萎缩性胃炎在男性中更为常见(68%),而在女性中则较少(56%;P = 0.015)。对于男性,H. pylori 血清阴性导致的每 1000 人中有 5 例 Barrett 食管风险的增加是由 GERD 介导的。
H. pylori 血清阴性的男性,而非女性,GERD 和 Barrett 食管的风险增加。可能的解释可能是 H. pylori 引起的萎缩性胃炎的性别差异,这可能导致男性的侵蚀性反流减少。GERD 介导 H. pylori 对男性 Barrett 食管风险的影响的证据支持这一假设机制。
这些发现强调了在未来研究中调查 H. pylori 对 GERD 和 Barrett 食管风险的影响中的性别差异的重要性。