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本文引用的文献

1
Hereditary and familial colon cancer.遗传性和家族性结直肠癌。
Gastroenterology. 2010 Jun;138(6):2044-58. doi: 10.1053/j.gastro.2010.01.054.
2
A segregation analysis of Barrett's esophagus and associated adenocarcinomas.巴雷特食管及其相关腺癌的分离分析。
Cancer Epidemiol Biomarkers Prev. 2010 Mar;19(3):666-74. doi: 10.1158/1055-9965.EPI-09-1136. Epub 2010 Mar 3.
3
Predictors of progression in Barrett's esophagus: current knowledge and future directions.巴雷特食管进展的预测因素:现有知识和未来方向。
Am J Gastroenterol. 2010 Jul;105(7):1490-1502. doi: 10.1038/ajg.2010.2. Epub 2010 Jan 26.
4
Assessment of familiality, obesity, and other risk factors for early age of cancer diagnosis in adenocarcinomas of the esophagus and gastroesophageal junction.评估食管癌和胃食管交界腺癌中家族性、肥胖及其他癌症早期诊断风险因素。
Am J Gastroenterol. 2009 Aug;104(8):1913-21. doi: 10.1038/ajg.2009.241. Epub 2009 Jun 2.
5
Lifestyle factors and risk for symptomatic gastroesophageal reflux in monozygotic twins.单卵双胞胎的生活方式因素与症状性胃食管反流风险
Gastroenterology. 2007 Jan;132(1):87-95. doi: 10.1053/j.gastro.2006.11.019. Epub 2006 Nov 17.
6
Familiality in Barrett's esophagus, adenocarcinoma of the esophagus, and adenocarcinoma of the gastroesophageal junction.巴雷特食管、食管腺癌和胃食管交界腺癌的家族聚集性。
Cancer Epidemiol Biomarkers Prev. 2006 Sep;15(9):1668-73. doi: 10.1158/1055-9965.EPI-06-0293.
7
Hereditary breast and ovarian cancer: review and future perspectives.遗传性乳腺癌和卵巢癌:综述与未来展望
J Mol Med (Berl). 2006 Jan;84(1):16-28. doi: 10.1007/s00109-005-0696-7. Epub 2005 Nov 11.
8
Epidemiologic risk factors for Barrett's esophagus and associated adenocarcinoma.巴雷特食管及其相关腺癌的流行病学危险因素。
Clin Gastroenterol Hepatol. 2005 Jan;3(1):1-10. doi: 10.1016/s1542-3565(04)00602-0.
9
Accuracy of reporting of family history of colorectal cancer.结直肠癌家族史报告的准确性。
Gut. 2004 Feb;53(2):291-5. doi: 10.1136/gut.2003.027896.
10
Demographic and phenotypic features of 70 families segregating Barrett's oesophagus and oesophageal adenocarcinoma.70个存在巴雷特食管和食管腺癌分离现象的家族的人口统计学和表型特征。
J Med Genet. 2003 Sep;40(9):651-6. doi: 10.1136/jmg.40.9.651.

家族性和散发性 Barrett 食管患者的内镜和临床特征比较。

Comparison of endoscopic and clinical characteristics of patients with familial and sporadic Barrett's esophagus.

机构信息

Department of Medicine, University of Washington School of Medicine, Seattle, WA, USA.

出版信息

Dig Dis Sci. 2011 Jun;56(6):1702-6. doi: 10.1007/s10620-011-1620-3. Epub 2011 Feb 24.

DOI:10.1007/s10620-011-1620-3
PMID:21347561
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3144147/
Abstract

BACKGROUND

A proportion of Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC) displays familial aggregation, known as familial Barrett's esophagus (FBE). Pedigrees and characteristics of EAC in these families have been previously described.

AIMS

We aimed to evaluate endoscopic and clinical characteristics of Barrett's esophagus in FBE.

METHODS

A cohort of 979 BE patients were retrospectively evaluated for FBE, defined as having a first-degree relative with BE or esophageal cancer, confirmed when possible by interview. FBE and sporadic BE were compared regarding demographic, clinical, and endoscopic characteristics. Potential FBE probands were contacted and interviewed to obtain full family pedigrees.

RESULTS

Of 603 BE probands (61.6% of total cohort) with a documented family history, 35 (5.8%) had FBE. There was no difference between FBE and non-FBE probands with regard to BE length (median: 3 cm, IQR 2-5 vs. 3 cm, IQR 1-6 cm, respectively; p = 0.78) or hiatal hernia size (p = 0.90). FBE probands were younger (mean, 58.4 vs. 63.8; p = 0.02) and had a significant association with less-advanced neoplasia (adjusted OR 0.41, 95% CI 0.19-0.90). There was no obvious association between FBE and other malignancies.

CONCLUSIONS

There were no differences in endoscopic characteristics between FBE and non-FBE probands. While FBE patients were younger and had less-advanced neoplasia, we speculate that these findings may have been the result of more aggressive screening due to the family history. Further studies are warranted to determine whether familial clustering is due to genetic predisposition to development of BE or to risk of neoplastic progression.

摘要

背景

一部分 Barrett 食管(BE)和食管腺癌(EAC)表现出家族聚集性,称为家族性 Barrett 食管(FBE)。这些家族中 EAC 的家系和特征之前已经有描述。

目的

我们旨在评估 FBE 中 Barrett 食管的内镜和临床特征。

方法

回顾性评估了 979 例 BE 患者的 FBE,定义为一级亲属患有 BE 或食管癌,如有可能通过访谈进行确认。比较了 FBE 和散发性 BE 在人口统计学、临床和内镜特征方面的差异。联系并访谈了潜在的 FBE 先证者,以获得完整的家族系谱。

结果

在有明确家族史的 603 例 BE 先证者(总队列的 61.6%)中,有 35 例(5.8%)患有 FBE。FBE 和非 FBE 先证者的 BE 长度(中位数:3cm,IQR 2-5 与 3cm,IQR 1-6cm,分别;p=0.78)或食管裂孔疝大小(p=0.90)没有差异。FBE 先证者更年轻(平均年龄 58.4 岁与 63.8 岁;p=0.02),且与进展期较低的肿瘤有显著关联(调整后的 OR 0.41,95%CI 0.19-0.90)。FBE 与其他恶性肿瘤之间没有明显的关联。

结论

FBE 和非 FBE 先证者的内镜特征没有差异。尽管 FBE 患者更年轻,且肿瘤进展程度较低,但我们推测这些发现可能是由于家族史而进行了更积极的筛查。需要进一步的研究来确定家族聚集是否是由于发生 BE 的遗传易感性,还是由于肿瘤进展的风险增加所致。