Alkaddour Ahmad, Palacio Carlos, Vega Kenneth J
Department of Medicine, University of Florida/Jacksonville, Jacksonville, FL, USA.
Division of Gastroenterology, National Jewish Health, Denver, CO, USA.
United European Gastroenterol J. 2018 Feb;6(1):22-28. doi: 10.1177/2050640617707862. Epub 2017 May 7.
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.
The objective of this article is to determine the degree of histologic BE risk difference between AA and nHw.
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.
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.
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.
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。
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。
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。
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。
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。