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一项关于胃化生亚型与肿瘤发生风险的荟萃分析及系统评价。

A meta-analysis and systematic review on subtypes of gastric intestinal metaplasia and neoplasia risk.

作者信息

Wei Ning, Zhou Mengyue, Lei Siyu, Zhong Zhiheng, Shi Ruihua

机构信息

Medical School of Southeast University, Nanjing, 210009, China.

Department of Gastroenterology, Southeast University Affiliated Zhongda Hospital, No. 87 Dingjiaqiao, Nanjing, 210009, China.

出版信息

Cancer Cell Int. 2021 Mar 17;21(1):173. doi: 10.1186/s12935-021-01869-0.

Abstract

BACKGROUND

Gastric intestinal metaplasia (GIM) is a significant risk factor for gastric cancer. Risk of gastric cancer/dysplasia between complete intestinal metaplasia (CIM) and incomplete intestinal metaplasia (IIM) was controversial. Our study aimed to pool relative risk (RR) of cancer/dysplasia of IIM compared with CIM in GIM patients.

METHODS

PubMed, EMBASE, Cochrane Library and Web of Science were searched for studies concerning cancer/dysplasia in GIM patients. Random-effects or fixed-effects model was utilized for pooling RR. Sensitivity and publication bias analyses were conducted. Stability of results would be evaluated in case of publication bias.

RESULTS

12 studies were included. Compared with CIM, pooled RR of cancer/dysplasia in IIM patients was 4.48 (95% CI 2.50-8.03), and the RR was 4.96 (95% CI 2.72-9.04) for cancer, and 4.82 (95% CI 1.45-16.0) for dysplasia. The pooled RR for cancer/dysplasia in type III IM was 6.27 (95% CI 1.89-20.77) compared with type II + I IM, while it was 5.55 (95% CI 2.07-14.92) compared with type II IM. Pooled RR between type II IM and type I IM was 1.62 (95% CI 1.16-2.27). Subgroup analyses showed that IIM was associated with a higher risk of gastric cancer/dysplasia in Western population (pooled RR = 4.65 95% CI 2.30-9.42), but not in East Asian population (pooled RR = 4.01 95% CI 0.82-19.61).

CONCLUSIONS

IIM was related to a higher risk of cancer/dysplasia compared with CIM. Risk of developing cancer/dysplasia from type I, II, and III intestinal metaplasia increased gradually.

摘要

背景

胃黏膜肠化生(GIM)是胃癌的一个重要危险因素。完全性肠化生(CIM)和不完全性肠化生(IIM)之间的胃癌/发育异常风险存在争议。我们的研究旨在汇总GIM患者中IIM与CIM相比的癌症/发育异常相对风险(RR)。

方法

检索PubMed、EMBASE、Cochrane图书馆和Web of Science,查找有关GIM患者癌症/发育异常的研究。采用随机效应或固定效应模型汇总RR。进行敏感性和发表偏倚分析。若存在发表偏倚,将评估结果的稳定性。

结果

纳入12项研究。与CIM相比,IIM患者癌症/发育异常的汇总RR为4.48(95%CI 2.50 - 8.03),癌症的RR为4.96(95%CI 2.72 - 9.04),发育异常的RR为4.82(95%CI 1.45 - 16.0)。与II + I型IM相比,III型IM中癌症/发育异常的汇总RR为6.27(95%CI 1.89 - 它与II型IM相比,汇总RR为5.(95%CI 2.07 - 14.92)。II型IM和I型IM之间的汇总RR为1.62(95%CI 1.16 - 2.27)。亚组分析显示,IIM在西方人群中与较高的胃癌/发育异常风险相关(汇总RR = 4.65,95%CI 2.30 - 9.42),但在东亚人群中并非如此(汇总RR = 4.01,95%CI 0.82 - 19.61)。

结论

与CIM相比,IIM与较高的癌症/发育异常风险相关。从I型、II型和III型肠化生发展为癌症/发育异常的风险逐渐增加。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff41/7968216/74a40818ce05/12935_2021_1869_Fig1_HTML.jpg

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