Comparison of Endoscopic and Clinical Characteristics  of Patients with Familial and Sporadic Barrett’s Esophagus

Comparison of Endoscopic and Clinical Characteristics of Patients with Familial and Sporadic Barrett’s Esophagus

  • نوع فایل : کتاب
  • زبان : انگلیسی
  • مؤلف : Samuel Ash Benjamin J. Vaccaro Mary Kay Dabney Wendy K. Chung Charles J. Lightdale Julian A. Abrams
  • چاپ و سال / کشور: 2011

Description

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 lessadvanced 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
Dig Dis Sci (2011) 56:1702–1706 DOI 10.1007/s10620-011-1620-3 Received: 13 January 2011 / Accepted: 5 February 2011 / Published online: 24 February 2011
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