Zhang Li, Li Delin, Zhang Yongsheng, Hu Wenqi, Lv Haoyue, Zhang Xiaodong, Zhang Hongyu
Department of Pharmacology, Jinan Central Hospital Affiliated to Shandong First Medical University, Jinan, China.
Department of Medical Equipment, Jinan Mental Health Center, Jinan, China.
Front Oncol. 2024 Aug 29;14:1366975. doi: 10.3389/fonc.2024.1366975. eCollection 2024.
This study conducts a systematic review through meta-analysis, comparing the composition and diversity of the gut microbiome in patients with esophageal cancer and healthy individuals, and explores the relationship between risk factors and related factors of esophageal cancer.
According to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA), we comprehensively searched the databases of PubMed, Web of Science, Embase, Cochrane Library. In addition, we applied the R programming language version 4.0.3 and Stata 15.1 software for data analysis. We also implemented the Newcastle-Ottawa Scale (NOS), funnel plot analysis, Egger's test, and Begg's test to assess the risk of bias.
In this study, a total of 328 studies were identified through the literature search. Among them, 117 duplicate studies were removed, and 202 studies were excluded based on inclusion and exclusion criteria. Finally, 9 studies were included in the analysis, involving a total of 216 patients with esophageal carcinoma and 352 healthy controls. Four studies provided Chao1 index for quantitative consolidation (ES = 637.41, 95% CI: 549.16 to 725.66, p = 0.000, I = 98.2%). Two studies [27, 29] reported ACE index (ES = 438.89, 95% CI: 362.42 to 515.35, p = 0.000, I = 97%). Seven studies [26,27,29,30,32] reported the Shannon index for quantitative consolidation (ES = 4.38, 95% CI: 3.95 to 4.81, p = 0.000, I = 99%). At the phylum level, the abundance of Bacteroidetes(ES = 37.8, 95% CI: 25.75 to 49.85, p = 0.000, I2 = 87.2%) and Proteobacteria(ES = 7.48, 95% CI: 5.02 to 8.85, p = 0.04, I = 2.4%) have statistical difference between ESCC and HC. There was no significant difference between ESCC and HC in the abundance of genera(p>0.05).
This observational meta-analysis revealed that changes in the GM were correlated with esophageal carcinoma, and variations in some advantageous GM might involve regional differences. Additionally, the study aims to facilitate early diagnosis of esophageal cancer and improve screening and diagnostic efficiency.
本研究通过荟萃分析进行系统评价,比较食管癌患者与健康个体肠道微生物群的组成和多样性,并探讨食管癌的危险因素及相关因素之间的关系。
根据系统评价和荟萃分析的首选报告项目(PRISMA),我们全面检索了PubMed、Web of Science、Embase、Cochrane图书馆等数据库。此外,我们应用R编程语言版本4.0.3和Stata 15.1软件进行数据分析。我们还采用纽卡斯尔-渥太华量表(NOS)、漏斗图分析、Egger检验和Begg检验来评估偏倚风险。
在本研究中,通过文献检索共识别出328项研究。其中,去除117项重复研究,并根据纳入和排除标准排除202项研究。最终,9项研究纳入分析,共涉及216例食管癌患者和352例健康对照。四项研究提供了Chao1指数用于定量合并(ES = 637.41,95%CI:549.16至725.66,p = 0.000,I² = 98.2%)。两项研究[27, 29]报告了ACE指数(ES = 438.89,95%CI:362.42至515.35,p = 0.000,I² = 97%)。七项研究[26,27,29,30,32]报告了Shannon指数用于定量合并(ES = 4.38,95%CI:3.95至4.81,p = 0.000,I² = 99%)。在门水平上,食管鳞状细胞癌(ESCC)与健康对照(HC)之间拟杆菌门(ES = 37.8,95%CI:25.75至49.85,p = 0.000,I² = 87.2%)和变形菌门(ES = 7.48,95%CI:5.02至8.85,p = 0.04,I² = 2.4%)的丰度存在统计学差异。ESCC与HC在属的丰度上无显著差异(p>0.05)。
这项观察性荟萃分析表明,肠道微生物群的变化与食管癌相关,一些有益肠道微生物群的变化可能存在地区差异。此外,该研究旨在促进食管癌的早期诊断并提高筛查和诊断效率。