共 50 条
Low Risk of Progression of Barrett's Esophagus to Neoplasia in Women
被引:11
|作者:
Allen, James E.
[1
]
Desai, Madhav
[2
]
Roumans, Carlijn A. M.
[3
]
Vennalaganti, Sreekar
[2
]
Vennalaganti, Prashanth
[2
]
Bansal, Ajay
[1
]
Falk, Gary
[4
]
Lieberman, David
[5
]
Sampliner, Richard
[6
]
Thota, Prashanthi
[7
]
Vargo, John
[7
]
Gupta, Neil
[8
]
Moawad, Fouad
[9
]
Bruno, Marco
[3
]
Kennedy, Kevin F.
[2
]
Gaddam, Srinivas
[10
]
Young, Patrick
[9
]
Mathur, Sharad
[2
]
Cash, Brooks
[11
]
Spaander, Manon
[3
]
Sharma, Prateek
[1
,2
]
机构:
[1] Univ Kansas, Med Ctr, Dept Gastroenterol & Hepatol, Kansas City, KS 66103 USA
[2] Vet Affairs Med Ctr, Dept Gastroenterol & Hepatol, Kansas City, MO USA
[3] Erasmus MC, Dept Gastroenterol, Rotterdam, Netherlands
[4] Univ Penn, Perelman Sch Med, Div Gastroenterol, Philadelphia, PA 19104 USA
[5] Oregon Hlth & Sci Univ, Div Gastroenterol & Hepatol, Portland, OR 97201 USA
[6] Univ Arizona, Dept Gastroenterol & Hepatol, Tucson, AZ USA
[7] Cleveland Clin, Dept Gastroenterol & Hepatol, Cleveland, OH 44106 USA
[8] Loyola Univ Med Ctr, Div Gastroenterol, Maywood, IL 60153 USA
[9] Walter Reed Natl Mil Med Ctr, Dept Gastroenterol, Bethesda, MD USA
[10] Cedars Sinai Med Ctr, Div Gastroenterol, Los Angeles, CA 90048 USA
[11] Univ Texas Hlth Sci Ctr Houston, Div Gastroenterol Hepatol & Nutr, Houston, TX 77030 USA
关键词:
Barrett’
s esophagus;
gender disparity;
adenocarcinoma;
INCREASING INCIDENCE;
ADENOCARCINOMA;
DIAGNOSIS;
DYSPLASIA;
STATIN;
REPRODUCIBILITY;
EPIDEMIOLOGY;
SURVEILLANCE;
CARCINOMA;
ESTROGEN;
D O I:
10.1097/MCG.0000000000001362
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
Background and Aims: Men are at a higher risk for Barrett's esophagus (BE) and esophageal adenocarcinoma (EAC), but little is known about BE progression to dysplasia and EAC in women. We performed a retrospective, multicenter cohort study to assess risk of BE progression to dysplasia and EAC in women compared with men. We also investigated comorbidities, medication use, and endoscopic features that contribute to sex differences in risk of BE progression. Methods: We collected data from large cohort of patients with BE seen at 6 centers in the United States and Europe, followed for a median 5.7 years. We obtained demographic information (age, sex, ethnicity), clinical history (tobacco use, body mass index, comorbidities), endoscopy results (procedure date, BE segment length), and histopathology findings. Neoplasia was graded as low-grade dysplasia, high-grade dysplasia (HGD), or EAC. Rates of disease progression between women and men were compared using chi(2) analysis and the Student t test. Multivariable logistic regression was used to assess the association between sex and disease progression after adjusting for possible confounding variables. Results: Of the total 4263 patients in the cohort, 2145 met the inclusion criteria, including 324 (15%) women. There was a total of 34 (1.6%) incident EACs, with an overall annual incidence of 0.3% (95% confidence interval: 0.2%-0.4%). We found significant differences between women and men in annual incidence rates of EAC (0.05% for women vs. 0.3% in men; P=0.04) and in the combined endpoint of HGD or EAC (0.1% for women vs. 1.1% for men; P<0.001). Female gender was an independent predictor for reduced progression to HGD or EAC when rates of progression were adjusted for body mass index, smoking history, race, use of aspirin, nonsteroidal anti-inflammatory drugs, proton-pump inhibitors, or statins, hypertriglyceridemia, BE length, and histology findings at baseline (hazard ratio: 0.11; 95% confidence interval: 0.03-0.45; P=0.002). Conclusions: In a multicenter study of men versus women with BE, we found a significantly lower risk of disease progression to cancer and HGD in women. The extremely low risk of EAC in women with BE (0.05%/y) indicates that surveillance endoscopy may not be necessary for this subgroup of patients with BE.
引用
收藏
页码:321 / 326
页数:6
相关论文