The continuing overall objective of this application is to improve the understanding of early events leading to Barrett's esophagus (a risk factor for esophageal adenocarcinoma), and to identify potential targets for early intervention. Barrett's esophagus is a metaplastic change in the lining of the esophagus that is commonly considered to be a strong risk factor for and precursor to esophageal adenocarcinoma. The incidence of esophageal adenocarcinoma has been rising more rapidly than that of any malignancy in the United States for the last three decades;however, explanations for the marked incidence increase, and its marked incidence variation by ethnicity and gender (three times more common among Caucasian men than among women or African Americans) remain elusive. Obesity is a major risk factor for many cancers (including esophageal adenocarcinoma), although the mechanisms are unknown. The pathway between obesity and cancer may be through intermediary, adipose-associated hormones, such as leptin, adiponectin, ghrelin and insulin-like growth factors. These hormone systems have demonstrated experimental effects on inflammation, healing, and the risk of neoplasia and they may differ by gender and ethnicity. They therefore represent a potential mechanistic link in the individual pathway to Barrett's esophagus and may help explain why among many persons with reflux disease, only some develop Barrett's esophagus and esophageal adenocarcinoma. Thus, we propose to evaluate the associations between adipose-associated hormones, obesity, body fat distribution, and Barrett's esophagus.
The specific aims of this study will be to evaluate the associations between leptin, adiponectin, and ghrelin and the risk of Barrett's esophagus, compared with GERD controls and population controls. The project will be a continuation of a recently established, high-quality, community-based case- control study of patients with a new Barrett's esophagus diagnosis, patients with gastroesophageal reflux disease, and population controls. Subjects completed detailed interviews, physical/anthropometric examinations, food frequency questionnaires, and serum samples. Serum samples are available for 99% of subjects. The proposed research will extend a highly novel translational research effort, is supported by a substantial body of literature for similar disorders, will leverage resources from an existing productive multidisciplinary research team, and may permit elucidation of an entirely new direction in determining why patients get Barrett's esophagus and esophageal adenocarcinoma.

Public Health Relevance

Barrett's esophagus (BE) is a precancerous condition of the esophagus that is very common;it is a strong risk factor for a kind of esophageal cancer that has become much more frequent seen in recent years. The objective of this application is to improve the understanding of what causes Barrett's esophagus and identify potential targets for intervention. The proposed study explores how hormones associated with body fat may change the way the body heals after an injury, and increase the risk of cells developing precancerous changes.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
5R01DK063616-08
Application #
7869425
Study Section
Kidney, Nutrition, Obesity and Diabetes (KNOD)
Program Officer
Everhart, James
Project Start
2002-09-30
Project End
2012-06-30
Budget Start
2010-07-01
Budget End
2012-06-30
Support Year
8
Fiscal Year
2010
Total Cost
$240,395
Indirect Cost
Name
Kaiser Foundation Research Institute
Department
Type
DUNS #
150829349
City
Oakland
State
CA
Country
United States
Zip Code
94612
Corley, Douglas A; Peek Jr, Richard M (2018) When Should Guidelines Change? A Clarion Call for Evidence Regarding the Benefits and Risks of Screening for Colorectal Cancer at Earlier Ages. Gastroenterology 155:947-949
Dong, Jing; Levine, David M; Buas, Matthew F et al. (2018) Interactions Between Genetic Variants and Environmental Factors Affect Risk of Esophageal Adenocarcinoma and Barrett's Esophagus. Clin Gastroenterol Hepatol 16:1598-1606.e4
Bakr, Omar; Zhao, Wei; Corley, Douglas (2018) Gastroesophageal Reflux Frequency, Severity, Age of Onset, Family History and Acid Suppressive Therapy Predict Barrett Esophagus in a Large Population. J Clin Gastroenterol 52:873-879
Li, Nan; Petrick, Jessica Leigh; Steck, Susan Elizabeth et al. (2017) Dietary sugar/starches intake and Barrett's esophagus: a pooled analysis. Eur J Epidemiol 32:1007-1017
Gharahkhani, Puya; Tung, Joyce; Hinds, David et al. (2016) Chronic gastroesophageal reflux disease shares genetic background with esophageal adenocarcinoma and Barrett's esophagus. Hum Mol Genet 25:828-35
Ek, Weronica E; Lagergren, Katarina; Cook, Michael et al. (2016) Polymorphisms in genes in the androgen pathway and risk of Barrett's esophagus and esophageal adenocarcinoma. Int J Cancer 138:1146-52
Thrift, Aaron P; Anderson, Lesley A; Murray, Liam J et al. (2016) Nonsteroidal Anti-Inflammatory Drug Use is Not Associated With Reduced Risk of Barrett's Esophagus. Am J Gastroenterol 111:1528-1535
Kendall, Bradley J; Rubenstein, Joel H; Cook, Michael B et al. (2016) Inverse Association Between Gluteofemoral Obesity and Risk of Barrett's Esophagus in a Pooled Analysis. Clin Gastroenterol Hepatol 14:1412-1419.e3
Thomas, Stuart J; Almers, Lucy; Schneider, Jennifer et al. (2016) Ghrelin and Leptin Have a Complex Relationship with Risk of Barrett's Esophagus. Dig Dis Sci 61:70-9
Schneider, Jennifer L; Corley, Douglas A (2015) A review of the epidemiology of Barrett's oesophagus and oesophageal adenocarcinoma. Best Pract Res Clin Gastroenterol 29:29-39

Showing the most recent 10 out of 44 publications