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Low Risk of Progression of Barrett's Esophagus to Neoplasia in Women.
Allen, James E; Desai, Madhav; Roumans, Carlijn A M; Vennalaganti, Sreekar; Vennalaganti, Prashanth; Bansal, Ajay; Falk, Gary; Lieberman, David; Sampliner, Richard; Thota, Prashanthi; Vargo, John; Gupta, Neil; Moawad, Fouad; Bruno, Marco; Kennedy, Kevin F; Gaddam, Srinivas; Young, Patrick; Mathur, Sharad; Cash, Brooks; Spaander, Manon; Sharma, Prateek.
Afiliação
  • Allen JE; Department of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, KS.
  • Desai M; Department of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO.
  • Roumans CAM; Department of Gastroenterology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Vennalaganti S; Department of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO.
  • Vennalaganti P; Department of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO.
  • Bansal A; Department of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, KS.
  • Falk G; Division of Gastroenterology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA.
  • Lieberman D; Division of Gastroenterology and Hepatology, Oregon Health and Science University, Portland, OR.
  • Sampliner R; Department of Gastroenterology and Hepatology, University of Arizona, Tucson, AZ.
  • Thota P; Department of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH.
  • Vargo J; Department of Gastroenterology and Hepatology, Cleveland Clinic, Cleveland, OH.
  • Gupta N; Division of Gastroenterology, Loyola University Medical Center, Maywood, IL.
  • Moawad F; Department of Gastroenterology, Walter Reed National Military Medical Center, Bethesda, MD.
  • Bruno M; Department of Gastroenterology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Kennedy KF; Department of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO.
  • Gaddam S; Division of Gastroenterology, Cedars-Sinai Medical Center, Los Angeles, CA.
  • Young P; Department of Gastroenterology, Walter Reed National Military Medical Center, Bethesda, MD.
  • Mathur S; Department of Gastroenterology and Hepatology, Veterans Affairs Medical Center, Kansas City, MO.
  • Cash B; Division of Gastroenterology, Hepatology and Nutrition, University of Texas Health Science Center, Houston, TX.
  • Spaander M; Department of Gastroenterology, Erasmus Medical Centre, Rotterdam, The Netherlands.
  • Sharma P; Department of Gastroenterology and Hepatology, University of Kansas Medical Center, Kansas City, KS.
J Clin Gastroenterol ; 55(4): 321-326, 2021 04 01.
Article em En | MEDLINE | ID: mdl-32379085
ABSTRACT
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 χ2 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.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Esôfago de Barrett / Neoplasias Esofágicas Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: America do norte / Europa Idioma: En Revista: J Clin Gastroenterol Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Lesões Pré-Cancerosas / Esôfago de Barrett / Neoplasias Esofágicas Tipo de estudo: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Female / Humans / Male País/Região como assunto: America do norte / Europa Idioma: En Revista: J Clin Gastroenterol Ano de publicação: 2021 Tipo de documento: Article