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Endosc Int Open. 2021 Sep 16;9(10):E1524-E1529. doi: 10.1055/a-1526-0507. eCollection 2021 Oct.
2
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J Clin Med. 2024 Aug 14;13(16):4783. doi: 10.3390/jcm13164783.

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Microbiota Detection Patterns Correlate With Presence and Severity of Barrett's Esophagus.微生物组检测模式与巴雷特食管的存在和严重程度相关。
Front Cell Infect Microbiol. 2021 Feb 23;11:555072. doi: 10.3389/fcimb.2021.555072. eCollection 2021.
2
Meta-Analysis Reveals the Prognostic Relevance of Nuclear and Membrane-Associated Bile Acid Receptors in Gastric Cancer.Meta 分析揭示核和膜相关胆汁酸受体在胃癌中的预后相关性。
Clin Transl Gastroenterol. 2021 Jan 12;12(1):e00295. doi: 10.14309/ctg.0000000000000295.
3
Crohn's disease of esophagus, stomach and duodenum.食管、胃和十二指肠克罗恩病
World J Gastrointest Pharmacol Ther. 2019 Mar 7;10(2):35-49. doi: 10.4292/wjgpt.v10.i2.35.
4
Barrett's esophagus is associated with a distinct oral microbiome.巴雷特食管与独特的口腔微生物群有关。
Clin Transl Gastroenterol. 2018 Feb 20;9(3):135. doi: 10.1038/s41424-018-0005-8.
5
Epidemiology of Barrett's Esophagus and Esophageal Adenocarcinoma.巴雷特食管与食管腺癌的流行病学
Gastroenterol Clin North Am. 2015 Jun;44(2):203-31. doi: 10.1016/j.gtc.2015.02.001. Epub 2015 Apr 9.
6
Bile acids but not acidic acids induce Barrett's esophagus.胆汁酸而非酸性酸会诱发巴雷特食管。
Int J Clin Exp Pathol. 2015 Feb 1;8(2):1384-92. eCollection 2015.
7
Risk of neoplastic progression in Barrett's esophagus diagnosed as indefinite for dysplasia: a nationwide cohort study.诊断为不典型增生的巴雷特食管的肿瘤进展风险:一项全国性队列研究。
Endoscopy. 2015 May;47(5):409-14. doi: 10.1055/s-0034-1391091. Epub 2014 Dec 18.
8
Barrett esophagus and risk of esophageal cancer: a clinical review.巴雷特食管与食管癌风险:临床综述。
JAMA. 2013 Aug 14;310(6):627-36. doi: 10.1001/jama.2013.226450.
9
Germline mutations in MSR1, ASCC1, and CTHRC1 in patients with Barrett esophagus and esophageal adenocarcinoma.MSR1、ASCC1 和 CTHRC1 种系突变与 Barrett 食管和食管腺癌患者相关。
JAMA. 2011 Jul 27;306(4):410-9. doi: 10.1001/jama.2011.1029.
10
Barrett's esophagus.巴雷特食管。
J Gastroenterol Hepatol. 2011 Apr;26(4):639-48. doi: 10.1111/j.1440-1746.2010.06602.x.

炎症性肠病与巴雷特食管共存与食管发育异常相关:一项倾向评分匹配队列研究

Co-existing inflammatory bowel disease and Barrett's esophagus is associated with esophageal dysplasia: a propensity score-matched cohort.

作者信息

Fasullo Matthew, Sreenivasen Aditya, Holzwanger Erik, Lavender Charles, Patel Milan, Shah Tilak, Mutha Pritesh, Yacavone Robert F, Sultan Keith, Trindade Arvind J, Smallfield George

机构信息

Division of Gastroenterology, Hepatology, and Nutrition, Virginia Commonwealth University Medical Center, Richmond, Virginia, United States.

Division of Gastroenterology, Zucker School of Medicine at Hofstra/Northwell, Long Island Jewish Medical Center, New Hyde Park, New York, United States.

出版信息

Endosc Int Open. 2021 Sep 16;9(10):E1524-E1529. doi: 10.1055/a-1526-0507. eCollection 2021 Oct.

DOI:10.1055/a-1526-0507
PMID:34540545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8445678/
Abstract

Barrett's esophagus (BE) and inflammatory bowel disease (IBD) predispose to the development of dysplasia and cancer. It is unclear if the inflammatory cascade seen in IBD affects disease progression in BE. We aimed to determine if patients with BE who have co-existing IBD had a higher risk of dysplasia, nodular disease, or longer segments than BE patients without IBD.  This was a multicenter, retrospective propensity score-matched cohort study. We compared rates of dysplasia, nodular disease, and segment length in patients with BE and IBD (cases) to patients with BE who did not have IBD (controls). Controls were 1:1 propensity score matched with controls for age, sex, body mass index (BMI), smoking, and hiatal hernia.  A total of 132 patients were included in the IBD + BE group and 132 patients in the BE group. Patients with IBD + BE had higher rates of esophageal dysplasia compared to controls (15.9 % vs. 6.1 % [adjusted odds ratio [OR]: 2.9, 95 % CI: 1.2-6.9]) and more nodules (9.8 % vs. 3.0 % [adjusted OR: 3.5, 95 % CI: 1.1-11.0]). IBD + BE group was also associated with longer BE segments (43.9 % vs. 12.1 % [OR: 5.7, 95 % CI: 3.0-10.6]).  Co-existing IBD may increase the risk of dysplasia and esophageal nodules in patients with BE. Our findings may have implications for BE surveillance intervals in IBD patients. Prospective studies are needed to confirm our findings.

摘要

巴雷特食管(BE)和炎症性肠病(IBD)易发生发育异常和癌症。目前尚不清楚IBD中所见的炎症级联反应是否会影响BE的疾病进展。我们旨在确定合并IBD的BE患者发生发育异常、结节性病变的风险是否更高,或其BE段长度是否比无IBD的BE患者更长。

这是一项多中心、回顾性倾向评分匹配队列研究。我们比较了BE合并IBD患者(病例组)与无IBD的BE患者(对照组)的发育异常率、结节性病变率和段长度。对照组与病例组按年龄、性别、体重指数(BMI)、吸烟情况和食管裂孔疝进行1:1倾向评分匹配。

IBD+BE组共纳入132例患者,BE组纳入132例患者。与对照组相比,IBD+BE患者的食管发育异常率更高(15.9%对6.1%[调整优势比(OR):2.9,95%CI:1.2 - 6.9]),且结节更多(9.8%对3.0%[调整OR:3.5,95%CI:1.1 - 11.0])。IBD+BE组的BE段长度也更长(43.9%对12.1%[OR:5.7,95%CI:3.0 - 10.6])。

合并IBD可能会增加BE患者发生发育异常和食管结节的风险。我们的研究结果可能对IBD患者的BE监测间隔有影响。需要进行前瞻性研究来证实我们的发现。