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EPIDEMIOLOGY OF BARRETTS ESOPHAGUS

EPIDEMIOLOGY OF BARRETTS ESOPHAGUS
Barrett 食管的流行病学
批准号:
6172847
负责人:
THOMAS L VAUGHAN
金额:
$54.27万
依托单位国家:
美国
项目类别:
财政年份:
1997
资助国家:
美国
项目状态:
已结题
起止时间:
1997-09-05 至 2003-06-30

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中文摘要
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英文摘要
DESCRIPTION: Barrett's esophagus is a metaplastic condition that develops in an estimated 10-20% of persons with long-standing gastroesophageal reflux disease (GERD). Patients with this condition are at high risk, estimated at 1-2% per year, of developing esophageal adenocarcinoma, a rapidly fatal cancer that, for unknown reasons, has risen sharply in incidence since the mid-1970s. Although much research has been directed toward identifying predictors of progression i patients with Barrett's esophagus, there is little information about the causes of the conditions itself. The first Specific Aim of this case-control study is to compare cases with newly diagnosed Barrett's esophagus (N=335) to controls from the general population (N=335) to test the hypothesis that specific environmental exposures and host factors increase risk of Barrett's metaplasia, and to estimate the fraction of cases attributable to them. Also to be examined will be the role of obesity, diet high in fat and low in fruits and vegetables, low serum vitamin C, vitamin E, carotenoids and selenium, tobacco use, alcohol consumption, use of medications that promote reflux and family history. The second Specific Aim is to identify determinant of Barrett's esophagus among individuals with severe and persistent GERD, by comparing cases to patients undergoing upper endoscopy for reflux symptoms, but who are biopsy-proven negative for Barrett's esophagus (N=335). Specifically, the hypothesis to be tested is that among patients with GERD: 1) cigarette smoking, alcohol consumption and dietary intake of nitrosamines are associated with increased risk of Barrett's esophagus, and that higher dietary intake and serum levels of antioxidants are associated with decreased risk; and 2) duodenogastric reflux (measured as the concentration of bile in fasting gastric juice) is associated with an increased risk of metaplasia. The prevalence of short-segment Barrett's will be estimated among patients undergoing endoscopy for GERD, using the largest sample of endoscoped patients, to date, all biopsied according to a standard protocol. Given that 95% of persons with Barrett's esophagus remain undiagnosed and that esophageal adenocarcinoma survival rates are dismal, the most direct means of reducing esophageal adenocarcinoma incidence amy be by preventing metaplasia, rather than by the surveillance and treatment of patients already diagnosed with the condition.
期刊论文(16)
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会议论文
Alcohol and the risk of Barrett's esophagus: a pooled analysis from the International BEACON Consortium.
酒精和巴雷特食管的风险:来自国际标准联盟的合并分析。
DOI: 10.1038/ajg.2014.206
发表时间: 2014-10
期刊: AMERICAN JOURNAL OF GASTROENTEROLOGY
影响因子: 9.8
作者: [Thrift, Aaron P., Cook, Michael B., Vaughan, Thomas L., Anderson, Lesley A., Murray, Liam J., Whiteman, David C., Shaheen, Nicholas J., Corley, Douglas A.]
通讯作者: Corley, Douglas A.
DOI: 10.1016/s1470-2045(16)30240-6
发表时间: 2016-10
期刊: LANCET ONCOLOGY
影响因子: 51.1
作者: [Gharahkhani, Puya, Fitzgerald, Rebecca C., Vaughan, Thomas L., Palles, Claire, Gockel, Ines, Tomlinson, Ian, Buas, Matthew F., May, Andrea, Gerges, Christian, Anders, Mario, Becker, Jessica, Kreuser, Nicole, Noder, Tania, Venerito, Marino, Veits, Lothar, Schmidt, Thomas, Manner, Hendrik, Schmidt, Claudia, Hess, Timo, Boehmer, Anne C., Izbicki, Jakob R., Hoelscher, Arnulf H., Lang, Hauke, Lorenz, Dietmar, Schumacher, Brigitte, Hackelsberger, Andreas, Mayershofer, Rupert, Pech, Oliver, Vashist, Yogesh, Ott, Katja, Vieth, Michael, Weismueller, Josef, Noethen, Markus M., Attwood, Stephen, Barr, Hugh, Chegwidden, Laura, de Caestecker, John, Harrison, Rebecca, Love, Sharon B., MacDonald, David, Moayyedi, Paul, Prenen, Hans, Watson, R. G. Peter, Iyer, Prasad G., Anderson, Lesley A., Bernstein, Leslie, Chow, Wong-Ho, Hardie, Laura J., Lagergren, Jesper, Liu, Geoffrey, Risch, Harvey A., Wu, Anna H., Ye, Weimin, Bird, Nigel C., Shaheen, Nicholas J., Gammon, Marilie D., Corley, Douglas A., Caldas, Carlos, Moebus, Susanne, Knapp, Michael, Peters, Wilbert H. M., Neuhaus, Horst, Roesch, Thomas, Ell, Christian, MacGregor, Stuart, Pharoah, Paul, Whiteman, David C., Jankowski, Janusz, Schumacher, Johannes]
通讯作者: Schumacher, Johannes
DOI: 10.1136/gutjnl-2016-311622
发表时间: 2017-10
期刊: Gut
影响因子: 24.5
作者: [Buas MF, He Q, Johnson LG, Onstad L, Levine DM, Thrift AP, Gharahkhani P, Palles C, Lagergren J, Fitzgerald RC, Ye W, Caldas C, Bird NC, Shaheen NJ, Bernstein L, Gammon MD, Wu AH, Hardie LJ, Pharoah PD, Liu G, Iyer P, Corley DA, Risch HA, Chow WH, Prenen H, Chegwidden L, Love S, Attwood S, Moayyedi P, MacDonald D, Harrison R, Watson P, Barr H, deCaestecker J, Tomlinson I, Jankowski J, Whiteman DC, MacGregor S, Vaughan TL, Madeleine MM]
通讯作者: Madeleine MM
DOI: 10.1038/ng.2408
发表时间: 2012-10
期刊: Nature genetics
影响因子: 30.8
作者: [Su Z, Gay LJ, Strange A, Palles C, Band G, Whiteman DC, Lescai F, Langford C, Nanji M, Edkins S, van der Winkel A, Levine D, Sasieni P, Bellenguez C, Howarth K, Freeman C, Trudgill N, Tucker AT, Pirinen M, Peppelenbosch MP, van der Laan LJ, Kuipers EJ, Drenth JP, Peters WH, Reynolds JV, Kelleher DP, McManus R, Grabsch H, Prenen H, Bisschops R, Krishnadath K, Siersema PD, van Baal JW, Middleton M, Petty R, Gillies R, Burch N, Bhandari P, Paterson S, Edwards C, Penman I, Vaidya K, Ang Y, Murray I, Patel P, Ye W, Mullins P, Wu AH, Bird NC, Dallal H, Shaheen NJ, Murray LJ, Koss K, Bernstein L, Romero Y, Hardie LJ, Zhang R, Winter H, Corley DA, Panter S, Risch HA, Reid BJ, Sargeant I, Gammon MD, Smart H, Dhar A, McMurtry H, Ali H, Liu G, Casson AG, Chow WH, Rutter M, Tawil A, Morris D, Nwokolo C, Isaacs P, Rodgers C, Ragunath K, MacDonald C, Haigh C, Monk D, Davies G, Wajed S, Johnston D, Gibbons M, Cullen S, Church N, Langley R, Griffin M, Alderson D, Deloukas P, Hunt SE, Gray E, Dronov S, Potter SC, Tashakkori-Ghanbaria A, Anderson M, Brooks C, Blackwell JM, Bramon E, Brown MA, Casas JP, Corvin A, Duncanson A, Markus HS, Mathew CG, Palmer CN, Plomin R, Rautanen A, Sawcer SJ, Trembath RC, Viswanathan AC, Wood N, Trynka G, Wijmenga C, Cazier JB, Atherfold P, Nicholson AM, Gellatly NL, Glancy D, Cooper SC, Cunningham D, Lind T, Hapeshi J, Ferry D, Rathbone B, Brown J, Love S, Attwood S, MacGregor S, Watson P, Sanders S, Ek W, Harrison RF, Moayyedi P, de Caestecker J, Barr H, Stupka E, Vaughan TL, Peltonen L, Spencer CC, Tomlinson I, Donnelly P, Jankowski JA, Esophageal Adenocarcinoma Genetics Consortium, Wellcome Trust Case Control Consortium 2]
通讯作者: Wellcome Trust Case Control Consortium 2
10
    METABOLITE BIOIMARKERS IN THE DEVELOPMENT OF ESOPHAGEAL ADENOCARCINOMA
    METABOLITE BIOIMARKERS IN THE DEVELOPMENT OF ESOPHAGEAL ADENOCARCINOMA
    Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
    Barrett's and Esophageal Adenocarcinoma Genetic Susceptibility Study (BEAGESS)
    海外基金