Risk factors for dysplasia in patients with Barrett's esophagus (BE) - Results from a multicenter consortium

被引:86
|
作者
Gopal, DV
Lieberman, DA
Magaret, N
Fennerty, MB
Sampliner, RE
Garewal, HS
Falk, GW
Faigel, DO
机构
[1] Oregon Hlth & Sci Univ, Div Gastroenterol, Portland, OR 97201 USA
[2] Portland VA Med Ctr, Portland, OR USA
[3] So Arizona VA Healthcare Syst, Tucson, AZ USA
[4] Univ Arizona, Tucson, AZ USA
[5] Cleveland Clin Fdn, Cleveland, OH 44195 USA
关键词
Barrett's esophagus; COBE; cooperative study of Barrett's esophagus; age; length; prevalence; dysplasia;
D O I
10.1023/A:1024715824149
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Studies show Barrett's esophagus prevalence increases with age, while mean length of Barrett's esophagus is unchanged. Few data are available about the relationship between age and length on the development of dysplasia. Our aim was to assess age and length as risk factors for dysplasia. Consecutive patients with Barrett's esophagus were enrolled in a multicenter study establishing a tissue bank of Barrett's esophagus patients 1994 and 1998. Demographics, length of Barrett's esophagus (centimeters), and histology were recorded. Risk factors for dysplasia were assessed, including patient age, gender, and length of Barrett's esophagus. Statistical analysis was performed comparing prevalence of dysplasia ( which included the presence of any carcinoma and high- or low-grade dysplasia) to age and length. In all, 309 patients were studied [ 278 (90%) male and 31 (10%) female]: 5 had adenocarcinoma of the esophagus, 11 had high- grade dysplasia, and 29 had low-grade dysplasia. Patients with Barrett's esophagus without dysplasia were younger than those with dysplasia [62 +/- 0.8 years vs 67 +/- 1.7 years (mean +/- SEM, P = 0.02)]. The risk of dysplasia increased by 3.3%/yr of age. Mean length of Barrett's esophagus in patients with Barrett's alone vs dysplasia was 4.0 +/- 0.2 cm vs 5.4 +/- 0.4 cm (P = 0.003). Patients with Barrett's esophagus length, 3 cm had a significantly greater prevalence of dysplasia compared to length < 3 cm ( 23% vs 9%, P = 0.0001). The risk of dysplasia increased by 14%/ cm of increased length. Multivariate analysis showed age and length to be independent risk factors. In conclusions; prevalence of dysplasia is strongly associated with age and length of Barrett's esophagus. These preliminary results can be used to develop a strategy for screening/surveillance based on age and length of Barrett's epithelium.
引用
收藏
页码:1537 / 1541
页数:5
相关论文
共 50 条
  • [21] Risk Stratification of Patients With Barrett's Esophagus and Low-grade Dysplasia or Indefinite for Dysplasia
    Thota, Prashanthi N.
    Lee, Hyun-Ju
    Goldblum, John R.
    Liu, Xiuli
    Sanaka, Madhusudhan R.
    Gohel, Tushar
    Kanadiya, Mehulkumar
    Lopez, Rocio
    CLINICAL GASTROENTEROLOGY AND HEPATOLOGY, 2015, 13 (03) : 459 - 465
  • [22] Dysplasia in Barrett’s esophagus
    Marcos Pedrosa
    Current Treatment Options in Gastroenterology, 2001, 4 (1) : 67 - 71
  • [23] ARE THERE RISK FACTORS FOR DEVELOPING BARRETT'S ESOPHAGUS IN PATIENTS WITH GASTROPARESIS?
    Panchal, Dayna
    Choi, Catherine
    Nasir, Umair M.
    Khawaja, Umar Sharif
    Feurdean, Mirela
    GASTROENTEROLOGY, 2020, 158 (06) : S319 - S319
  • [24] A survey of symptoms and risk factors in patients with Barrett's esophagus
    Desilets, D
    Nathanson, B
    Navab, F
    AMERICAN JOURNAL OF GASTROENTEROLOGY, 2005, 100 (09): : S46 - S46
  • [25] Risk Factors for Barrett's Esophagus Among Men Without GERD Symptoms: Results From the Newly Diagnosed Barrett's Esophagus Study
    Rubenstein, Joel H.
    Morgenstern, Hal
    Appelman, Henry D.
    Scheiman, James M.
    Schoenfeld, Philip S.
    McMahon, Laurence F.
    Metko, Val
    Near, Ellen
    Kellenberg, Joan E.
    Kalish, Tal
    Inadomi, John M.
    GASTROENTEROLOGY, 2012, 142 (05) : S72 - S72
  • [26] Risk Factors for Progression of Barrett's Esophagus to High Grade Dysplasia and Esophageal Adenocarcinoma
    Kambhampati, Swetha
    Tieu, Alan H.
    Luber, Brandon
    Wang, Hao
    Meltzer, Stephen J.
    SCIENTIFIC REPORTS, 2020, 10 (01)
  • [27] The Extent of Barrett's Esophagus Predicts Resistance to Successful Endoscopic Eradication Therapy for Barrett's Esophagus (BE) With Dysplasia or Early Cancer (EAC): Results From an International, Multi-Center Consortium
    Vennelaganti, Sreekar
    Seewald, Stefan
    Vennalaganti, Prashanth
    Jhun, Hye Yeon
    Brown, Jesica
    Alsop, Benjamin
    Bansal, Ajay
    Repici, Alessandro
    Gupta, Neil
    Falk, Gary W.
    Waxman, Irving
    Konda, Vani J.
    Haidry, Rehan
    Ross, Andrew S.
    Buckles, Daniel
    Mathur, Sharad
    Olyaee, Mojtaba S.
    Sharma, Prateek
    GASTROENTEROLOGY, 2016, 150 (04) : S258 - S258
  • [28] Photodynamic therapy of high grade dysplasia in Barrett's esophagus: Results from treatment of 17 patients
    Weiss, A
    Wiesinger, H
    Owen, D
    GASTROINTESTINAL ENDOSCOPY, 2005, 61 (05) : AB145 - AB145
  • [29] Clinical outcomes in patients with a diagnosis of "indefinite for dysplasia" in Barrett's esophagus: a multicenter cohort study
    Sinh, Preetika
    Anaparthy, Rajeswari
    Young, Patrick E.
    Gaddam, Srinivas
    Thota, Prashanthi
    Balasubramanian, Gokulakrishnan
    Singh, Mandeep
    Higbee, April D.
    Wani, Sachin
    Gupta, Neil
    Rastogi, Amit
    Mathur, Sharad C.
    Bansal, Ajay
    Horwhat, John D.
    Cash, Brooks D.
    Falk, Garyw.
    Lieberman, David A.
    Vargo, John J.
    Sampliner, Richard E.
    Sharma, Prateek
    ENDOSCOPY, 2015, 47 (08) : 669 - 674
  • [30] Are Clinical Outcomes in Indefinite for Dysplasia (IND) Any Different From Low Grade Dysplasia (LGD) in Patients With Barrett's Esophagus (BE)? Results From a Large Multicenter Cohort Study
    Anaparthy, Rajeswari
    Gaddam, Srinivas
    Balasubramanian, Gokulakrishnan
    Singh, Mandeep
    Higbee, April D.
    Wani, Sachin
    Gupta, Neil
    Rastogi, Amit
    Mathur, Sharad C.
    Bansal, Ajay
    Horwhat, John D.
    Young, Patrick E.
    Cash, Brooks D.
    Falk, Gary W.
    Lieberman, David A.
    Vargo, John J.
    Sampliner, Richard E.
    Sharma, Prateek
    GASTROENTEROLOGY, 2012, 142 (05) : S746 - S746