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Tytuł pozycji:

Systematic review with meta-analysis: the effects of family history on the risk of Barrett's oesophagus and oesophageal adenocarcinoma.

Tytuł:
Systematic review with meta-analysis: the effects of family history on the risk of Barrett's oesophagus and oesophageal adenocarcinoma.
Autorzy:
Peters Y; Department of Gastroenterology and Hepatology, Radboud Institute for Health Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
van Grinsven E; Department of Gastroenterology and Hepatology, Radboud Institute for Health Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
Siersema PD; Department of Gastroenterology and Hepatology, Radboud Institute for Health Sciences, Radboud University Medical Centre, Nijmegen, The Netherlands.
Źródło:
Alimentary pharmacology & therapeutics [Aliment Pharmacol Ther] 2021 Oct; Vol. 54 (7), pp. 868-879. Date of Electronic Publication: 2021 Aug 12.
Typ publikacji:
Journal Article; Meta-Analysis; Systematic Review
Język:
English
Imprint Name(s):
Publication: Oxford : Wiley-Blackwell
Original Publication: [Oxford, OX] : Blackwell Scientific Publications, [c1987-
MeSH Terms:
Adenocarcinoma*/diagnosis
Adenocarcinoma*/epidemiology
Adenocarcinoma*/genetics
Barrett Esophagus*/diagnosis
Barrett Esophagus*/epidemiology
Barrett Esophagus*/genetics
Esophageal Neoplasms*/diagnosis
Esophageal Neoplasms*/epidemiology
Esophageal Neoplasms*/genetics
Early Diagnosis ; Humans ; Risk Factors
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Entry Date(s):
Date Created: 20210812 Date Completed: 20210916 Latest Revision: 20220731
Update Code:
20240105
PubMed Central ID:
PMC9292032
DOI:
10.1111/apt.16558
PMID:
34383966
Czasopismo naukowe
Background: Current guidelines recommend different screening approaches for individuals with a family history of Barrett's oesophagus (BO) or oesophageal adenocarcinoma (OAC), varying from no screening to screening all individuals with a positive family history.
Aims: To determine evidence-based risk estimates for individuals with a family history of BO or OAC METHODS: We systematically searched Pubmed, Embase and Cochrane Library until October 2020 to identify all studies that reported on the association between family history and the risk of BO and OAC. Pooled summary estimates of adjusted relative risks and prevalence of familial BO/OAC with 95% confidence intervals (CIs) were calculated using a random effects model.
Results: Fourteen studies comprising 16 189 BO/OAC patients were analysed. Familial clustering was seen in 8.84% (95% CI: 5.54-13.82) and 4.37% (95% CI: 2.15-8.69) of patients with BO and OAC, respectively (nine studies). Screening first-degree relatives of BO patients had a diagnostic yield between 12% and 44% for BO (four studies). However, the yield for high-grade dysplasia and OAC was low (<2%). Individuals with a positive family history had a higher risk of having BO (aRR 3.26; 95% CI 1.43-7.40; I 2  = 46%; three studies) and OAC (aRR 2.19; 95% CI 1.14-4.21; I 2  = 48%; five studies) compared to individuals without a family history.
Conclusions: A verified family history of BO or OAC is a strong risk factor for both BO and OAC. A positive family history could be a clinically meaningful way to identify high-risk individuals who may benefit from early detection strategies.
(© 2021 The Authors. Alimentary Pharmacology & Therapeutics published by John Wiley & Sons Ltd.)
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