Very high incidence of familial colorectal cancer in Newfoundland: a comparison with Ontario and 13 other population-based studies

被引:60
作者
Green, R. C. [1 ]
Green, J. S.
Buehler, S. K.
Robb, J. D.
Daftary, D.
Gallinger, S.
McLaughlin, J. R.
Parfrey, P. S.
Younghusband, H. B.
机构
[1] Mem Univ Newfoundland, Fac Med, St John, NF A1B 3V6, Canada
[2] Canc Care Ontario, Toronto, ON, Canada
[3] Univ Toronto, Samuel Lunenfeld Res Inst, Toronto, ON, Canada
关键词
colorectal cancer; family history; founder effect; HNPCC; incidence; Lynch syndrome; meta-analysis; MYH; Newfoundland; Ontario;
D O I
10.1007/s10689-006-9104-x
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Newfoundland has the highest rate of colorectal cancer (CRC) of any Canadian province. In order to investigate the factors, especially genetic components, responsible for CRC we established the Newfoundland Colorectal Cancer Registry. In a 5-year period we examined every case of CRC diagnosed under the age of 75 years and obtained consent from 730 cases. Careful analysis of family history was used to assign a familial cancer risk, based on established criteria. We observed that 3.7% of CRC cases came from families meeting the Amsterdam II criteria and a further 0.9% of cases involved familial adenomatous polyposis (FAP). An additional 43% of cases met one or more of the revised Bethesda criteria and 31% of all cases had a first-degree relative affected with CRC. We compared the Newfoundland data with data from the province of Ontario, where the same recruitment and risk-assessment criteria were used. In all categories, the indicators of familial risk were significantly higher in Newfoundland. These data were also compared to results published from 13 other population-based studies worldwide. In every category the proportion of Newfoundland cases meeting the criteria was higher than in any other population. The mean differences were: 3.5-fold greater for FAP, 2.8-fold higher for Amsterdam criteria, 2.0-fold higher for Bethesda criteria and 1.9-fold higher for the number of affected first-degree relatives. We conclude that the high incidence of CRC in Newfoundland may be attributable to genetic, or at least familial, factors. In the high-risk families we provide evidence for the involvement of founder mutations in the APC and MSH2 genes.
引用
收藏
页码:53 / 62
页数:10
相关论文
共 49 条
[1]  
AALTONEN LA, 1994, CANCER RES, V54, P1645
[2]   Family cancer histories predictive of a high risk of hereditary non-polyposis colorectal cancer associate significantly with a genomic rearrangement in hMSH2 or hMLH1 [J].
Ainsworth, PJ ;
Koscinski, D ;
Fraser, BP ;
Stuart, JA .
CLINICAL GENETICS, 2004, 66 (03) :183-188
[3]   Evolution of the nomenclature for the hereditary colorectal cancer syndromes [J].
Boland, CR .
FAMILIAL CANCER, 2005, 4 (03) :211-218
[4]   Colorectal screening is associated with reduced colorectal cancer risk: a case-control study within the population-based Ontario Familial Colorectal Cancer Registry [J].
Cotterchio, M ;
Manno, M ;
Klar, N ;
McLaughlin, J ;
Gallinger, S .
CANCER CAUSES & CONTROL, 2005, 16 (07) :865-875
[5]  
Cotterchio M, 2000, Chronic Dis Can, V21, P81
[6]  
Cravo ML, 1999, CANCER, V85, P779, DOI 10.1002/(SICI)1097-0142(19990215)85:4<779::AID-CNCR4>3.3.CO
[7]  
2-3
[8]   Association between biallelic and monoallelic germline MYH gene mutations and colorectal cancer risk [J].
Croitoru, ME ;
Cleary, SP ;
Di Nicola, N ;
Manno, M ;
Selander, T ;
Aronson, M ;
Redston, M ;
Cotterchio, M ;
Knight, J ;
Gryfe, R ;
Gallinger, S .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 2004, 96 (21) :1631-1634
[9]   The frequency of hereditary defective mismatch repair in a prospective series of unselected colorectal carcinomas [J].
Cunningham, JM ;
Kim, CY ;
Christensen, ER ;
Tester, DJ ;
Parc, Y ;
Burgart, LJ ;
Halling, KC ;
McDonnell, SK ;
Schaid, DJ ;
Vockley, CW ;
Kubly, V ;
Nelson, H ;
Michels, VV ;
Thibodeau, SN .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (04) :780-790
[10]   Hereditary colorectal cancer in the general population: from cancer registration to molecular diagnosis [J].
de Leon, MP ;
Pedroni, M ;
Benatti, P ;
Percesepe, A ;
Di Gregorio, C ;
Foroni, M ;
Rossi, G ;
Genuardi, M ;
Neri, G ;
Leonardi, F ;
Viel, A ;
Capozzi, E ;
Boiocchi, M ;
Roncucci, L .
GUT, 1999, 45 (01) :32-38