Burke Eoghan, Harkins Patricia, Arumugasamy Mayilone
The Royal College of Surgeons in Ireland, Dublin, Ireland.
Mater Misericordiae University Hospital, Dublin, Ireland.
J Gastrointest Cancer. 2025 Aug 19;56(1):174. doi: 10.1007/s12029-025-01291-z.
Gastric atrophy (GA) is a pre-neoplastic condition leading to gastric cancer (GC). Early GA detection is critical for guiding surveillance and preventing advanced GC. Histology is the current gold standard for GA diagnosis, but is considered not cost-effective for routine screening in Western populations. Serological methods offer a potentially affordable alternative. Understanding GA prevalence, symptom impact, and optimal detection strategies in low-risk Western populations is essential before integrating GA screening into GC prevention programs.
This systematic review and meta-analysis assessed GA prevalence in Northern and Western European populations. Key outcomes included GA prevalence (any topographical distribution in the stomach and corpus-specific), effects of symptomatology on prevalence, and differences between serological and histological prevalence.
Twenty-two cross-sectional studies (n = 62,520) were included; 13 used histology and 9 used serology. Overall GA prevalence of any topographical distribution was 13% (95% confidence interval (CI) 7-18%). Histology-based studies reported 21% (95% CI 11-30%) versus 5% (95% CI 3-7%) by serology. Corpus-involving GA had a pooled prevalence of 6% (95% CI 4-9%), with histology detecting higher rates (10-15%) than serology (4-5%). In symptomatic populations, GA prevalence rose to 47%, compared to 6-10% in asymptomatic groups. Corpus GA reached 20% in symptomatic patients versus 6-8% in asymptomatic ones.
GA, especially corpus-involving GA, is more prevalent in Western and Northern European populations than previously thought. These findings suggest that screening for GA in these populations may be a viable route to increasing early GC detection rates and improving outcomes.
胃萎缩(GA)是一种癌前病变,可导致胃癌(GC)。早期检测GA对于指导监测和预防晚期GC至关重要。组织学是目前GA诊断的金标准,但在西方人群中进行常规筛查时,其成本效益不高。血清学方法提供了一种潜在的经济实惠的替代方案。在将GA筛查纳入GC预防计划之前,了解低风险西方人群中GA的患病率、症状影响和最佳检测策略至关重要。
本系统评价和荟萃分析评估了北欧和西欧人群中GA的患病率。主要结果包括GA患病率(胃内任何部位分布及胃体特定部位分布)、症状对患病率的影响以及血清学和组织学患病率之间的差异。
纳入了22项横断面研究(n = 62,520);13项使用组织学方法,9项使用血清学方法。胃内任何部位分布的总体GA患病率为13%(95%置信区间(CI)7 - 18%)。基于组织学的研究报告患病率为21%(95% CI 11 - 30%),而血清学研究报告的患病率为5%(95% CI 3 - 7%)。累及胃体的GA合并患病率为6%(95% CI 4 - 9%),组织学检测率(10 - 15%)高于血清学检测率(4 - 5%)。有症状人群中,GA患病率升至47%,无症状组为6 - 10%。有症状患者胃体GA患病率达20%,无症状患者为6 - 8%。
GA(尤其是累及胃体的GA)在北欧和西欧人群中的患病率比之前认为的更高。这些发现表明,在这些人群中筛查GA可能是提高早期GC检测率和改善预后的可行途径。