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本文引用的文献

1
Common Variants Confer Susceptibility to Barrett's Esophagus: Insights from the First Genome-Wide Association Studies.常见变异增加巴雷特食管易感性:来自首批全基因组关联研究的见解
Adv Exp Med Biol. 2016;908:265-90. doi: 10.1007/978-3-319-41388-4_13.
2
Reduced Risk of Barrett's Esophagus in Statin Users: Case-Control Study and Meta-Analysis.他汀类药物使用者患巴雷特食管的风险降低:病例对照研究与荟萃分析。
Dig Dis Sci. 2016 Jan;61(1):238-46. doi: 10.1007/s10620-015-3869-4. Epub 2015 Sep 19.
3
Risk factors for Barrett's esophagus compared between African Americans and non-Hispanic Whites.非裔美国人和非西班牙裔白人之间 Barrett 食管的风险因素比较。
Am J Gastroenterol. 2014 Dec;109(12):1870-80. doi: 10.1038/ajg.2014.351. Epub 2014 Nov 25.
4
Central adiposity is associated with increased risk of esophageal inflammation, metaplasia, and adenocarcinoma: a systematic review and meta-analysis.中心性肥胖与食管炎症、化生和腺癌风险增加相关:系统评价和荟萃分析。
Clin Gastroenterol Hepatol. 2013 Nov;11(11):1399-1412.e7. doi: 10.1016/j.cgh.2013.05.009. Epub 2013 May 22.
5
Sex-specific associations between body mass index, waist circumference and the risk of Barrett's oesophagus: a pooled analysis from the international BEACON consortium.性别特异性体重指数、腰围与巴雷特食管风险的关系:国际 BEACON 联盟的荟萃分析。
Gut. 2013 Dec;62(12):1684-91. doi: 10.1136/gutjnl-2012-303753. Epub 2013 Jan 26.
6
Body mass index in relation to oesophageal and oesophagogastric junction adenocarcinomas: a pooled analysis from the International BEACON Consortium.体质量指数与食管和食管胃交界腺癌的关系:来自国际 BEACON 联盟的合并分析。
Int J Epidemiol. 2012 Dec;41(6):1706-18. doi: 10.1093/ije/dys176. Epub 2012 Nov 12.
7
The incidence of esophageal adenocarcinoma continues to rise: analysis of period and birth cohort effects on recent trends.食管腺癌的发病率持续上升:对近期趋势的时期和出生队列效应分析。
Ann Oncol. 2012 Dec;23(12):3155-3162. doi: 10.1093/annonc/mds181. Epub 2012 Jul 30.
8
Hiatal hernia and the risk of Barrett's esophagus.食管裂孔疝与巴雷特食管的风险。
J Gastroenterol Hepatol. 2013 Mar;28(3):415-31. doi: 10.1111/j.1440-1746.2012.07199.x.
9
The association between Barrett's esophagus and Helicobacter pylori infection: a meta-analysis.巴雷特食管与幽门螺杆菌感染的相关性:荟萃分析。
Helicobacter. 2012 Jun;17(3):163-75. doi: 10.1111/j.1523-5378.2011.00931.x. Epub 2012 Mar 20.
10
Risk factors and chemoprevention in Barrett's esophagus--an update.巴雷特食管的危险因素与化学预防——最新进展
Scand J Gastroenterol. 2012 Apr;47(4):397-406. doi: 10.3109/00365521.2012.667145.

非裔美国人和非西班牙裔白人之间组织学巴雷特食管的风险:一项荟萃分析。

Risk of histologic Barrett's esophagus between African Americans and non-Hispanic whites: A meta-analysis.

作者信息

Alkaddour Ahmad, Palacio Carlos, Vega Kenneth J

机构信息

Department of Medicine, University of Florida/Jacksonville, Jacksonville, FL, USA.

Division of Gastroenterology, National Jewish Health, Denver, CO, USA.

出版信息

United European Gastroenterol J. 2018 Feb;6(1):22-28. doi: 10.1177/2050640617707862. Epub 2017 May 7.

DOI:10.1177/2050640617707862
PMID:29435310
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5802672/
Abstract

BACKGROUND

Barrett's esophagus (BE) is rare in African Americans (AA). However, the risk difference magnitude in histologic BE prevalence between AA and non-Hispanic whites (nHw) has not been quantified to date.

OBJECTIVE

The objective of this article is to determine the degree of histologic BE risk difference between AA and nHw.

METHODS

PubMed, Web of Science and EMBASE were searched for studies reporting histologic BE in AA/nHw for inclusion. Pooled odds ratios (ORs) with risk estimates of histologic BE occurrence between AA/nHw were calculated along with 95% confidence intervals (CIs). Forest plots were used to quantify heterogeneity. Funnel plots and the Cochrane Collaboration Risk of Bias tool were used to assess bias risk.

RESULTS

Eight studies reported BE histologic confirmation in AA/nHw. Analysis demonstrated a nearly 400% increased histologic BE risk in nHw patients compared to AA (OR 3.949, 95% CI 3.069-5.082). In the model without the case-control study, histologic BE risk remained elevated at approximately 360% in nHw compared to AA (OR 3.618, 95% CI 2.769-4.726). Heterogeneity was not present in either model. Risk of bias was significant.

CONCLUSIONS

Histologic BE risk is elevated in nHw by 3.6-4 times compared to AA. Investigation into understanding any clinical, molecular or genetic mechanisms underlying this risk disparity is warranted.

摘要

背景

巴雷特食管(BE)在非裔美国人(AA)中较为罕见。然而,迄今为止,非裔美国人和非西班牙裔白人(nHw)之间组织学确诊的BE患病率的风险差异幅度尚未得到量化。

目的

本文的目的是确定非裔美国人和非西班牙裔白人之间组织学确诊的BE风险差异程度。

方法

检索PubMed、科学网和EMBASE,查找报告非裔美国人/非西班牙裔白人中组织学确诊的BE的研究以纳入分析。计算非裔美国人/非西班牙裔白人之间组织学确诊的BE发生风险估计值的合并比值比(OR)以及95%置信区间(CI)。采用森林图量化异质性。采用漏斗图和Cochrane协作偏倚风险工具评估偏倚风险。

结果

八项研究报告了非裔美国人/非西班牙裔白人中BE的组织学确诊情况。分析表明,与非裔美国人相比,非西班牙裔白人患者组织学确诊的BE风险增加了近400%(OR 3.949,95%CI 3.069 - 5.082)。在不包括病例对照研究的模型中,与非裔美国人相比,非西班牙裔白人组织学确诊的BE风险仍升高约360%(OR 3.618,95%CI 2.769 - 4.726)。两个模型均不存在异质性。偏倚风险显著。

结论

与非裔美国人相比,非西班牙裔白人组织学确诊的BE风险升高了3.6至4倍。有必要对这种风险差异背后的任何临床、分子或遗传机制进行研究。