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尿路上皮细胞癌的分离分析

Segregation analysis of urothelial cell carcinoma.

作者信息

Aben Katja K H, Baglietto Laura, Baffoe-Bonnie Agnes, Coebergh Jan-Willem W, Bailey-Wilson Joan E, Trink Barry, Verbeek André L M, Schoenberg Mark P, Alfred Witjes J, Kiemeney Lambertus A

机构信息

Dept. of Epidemiology & Biostatistics, Radboud University, Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

出版信息

Eur J Cancer. 2006 Jul;42(10):1428-33. doi: 10.1016/j.ejca.2005.07.039. Epub 2006 Jun 5.

Abstract

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 1 193 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.

摘要

尿路上皮细胞癌(UCC)家族史会使患UCC的风险增加近两倍。目前尚不清楚这种UCC聚集现象(部分)是否具有孟德尔遗传背景。我们对1193个家庭进行了复杂分离分析,这些家庭是通过患有膀胱、输尿管、肾盂或尿道UCC的先证者确定的,这些先证者于1995年1月1日至1997年12月31日期间新确诊,并由荷兰东南部两个基于人群的癌症登记处登记。通过邮政问卷报告了10738名一级亲属的数据;其中101名亲属患有UCC。所有报告的UCC病例均(如有可能)使用病历进行了核实。使用S.A.G.E.分离软件包进行分析。针对一般无限制模型测试了五个受限模型(孟德尔显性、孟德尔隐性、孟德尔共显性、“无主基因”模型和环境模型)。将性别和吸烟状况作为协变量纳入分析。在这1193个家庭中未发现通过单个主基因进行UCC孟德尔遗传的有力证据。然而,由于没有一个孟德尔模型可以被排除,因此不能排除UCC的遗传亚型。一个主基因可能在一些家庭中分离,但这种效应可能在高散发性发病率的背景下被掩盖了。“无主基因”(或散发性)模型似乎是描述这些家庭中UCC发生情况的最简约模型。

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