Segregation analysis of urothelial cell carcinoma

被引:28
作者
Aben, Katja K. H.
Baglietto, Laura
Baffoe-Bonnie, Agnes
Coebergh, Jan-Willem W.
Bailey-Wilson, Joan E.
Trink, Barry
Verbeek, Andre L. M.
Schoenberg, Mark P.
Witjes, J. Alfred
Kiemeney, Lambertus A.
机构
[1] Radboud Univ Nijmegen, Nijmegen Med Ctr, Dept Epidemiol & Biostat, NL-6500 HB Nijmegen, Netherlands
[2] Ctr Comprehens Canc, IKO, Nijmegen, Netherlands
[3] Canc Council Victoria, Canc Epidemiol Ctr, Melbourne, Vic, Australia
[4] Fox Chase Canc Ctr, Div Populat Sci, Philadelphia, PA 19111 USA
[5] NHGRI, State Genet Sect, NIH, Baltimore, MD USA
[6] IKZ, Comprehens Canc Ctr, Eindhoven, Netherlands
[7] Johns Hopkins Univ, Sch Med, Dept Otolaryngol Head & Neck Surg, Div Head & Neck Canc Res, Baltimore, MD USA
[8] Johns Hopkins Univ Hosp, James Buchanan Brady Urol Inst, Baltimore, MD 21287 USA
[9] Radboud Univ Nijmegen Med Ctr, Dept Urol, Nijmegen, Netherlands
关键词
urothelial cell carcinoma; segregation analysis; familial aggregation;
D O I
10.1016/j.ejca.2005.07.039
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
A family history of urothelial cell carcinoma (UCC) confers an almost two-fold increased risk of developing UCC. It is unknown whether (part of) this aggregation of UCC has a Mendelian background. We performed complex segregation analyses on 1193 families ascertained through a proband with UCC of the bladder, ureter, renal pelvis or urethra, who were newly diagnosed between January 1, 1995 and December 31, 1997 and registered by two population-based cancer registries in the southeastern part of the Netherlands. Data were reported on 10 738 first-degree relatives by postal questionnaire; 101 of these relatives had UCC. All reported occurrences of UCC were verified (if possible) using medical records. Analyses were performed with the S.A.G.E. segregation package. Five restricted models (Mendelian dominant, Mendelian recessive, Mendelian co-dominant, 'no major gene' model and environmental model) were tested against the general unrestricted model. Sex and smoking status were incorporated as covariates. Strong evidence of Mendelian inheritance of UCC through a single major gene was not found in these 1193 families. However, since none of the Mendelian models could be rejected, an inherited subtype of UCC cannot be excluded. A major gene may segregate in some families but this effect may have been masked in a background of high sporadic incidence. The 'no major gene' (or sporadic) model appeared to be the most parsimonious one to describe the occurrence of UCC in these families. (c) 2006 Elsevier Ltd. All rights reserved.
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页码:1428 / 1433
页数:6
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