Cumulative association of five genetic variants with prostate cancer

被引：480

作者：

Zheng, S. Lilly ^{[1
]}

Sun, Jielin ^{[1
]}

Wiklund, Fredrik ^{[4
]}

Smith, Shelly ^{[1
]}

Stattin, Par ^{[5
]}

Li, Ge ^{[1
]}

Adami, Hans-Olov ^{[4
,6
]}

Hsu, Fang-Chi ^{[1
,2
]}

Zhu, Yi ^{[1
]}

Balter, Katarina ^{[4
]}

Kader, A. Karim ^{[3
]}

Turner, Aubrey R. ^{[1
]}

Liu, Wennuan ^{[1
]}

Bleecker, Eugene R. ^{[1
]}

Meyers, Deborah A. ^{[1
]}

Duggan, David ^{[7
]}

Carpten, John D. ^{[7
]}

Chang, Bao-Li ^{[1
]}

Isaacs, William B. ^{[8
]}

Xu, Jianfeng ^{[1
]}

Gronberg, Henrik ^{[4
]}

机构：

[1] Wake Forest Univ, Bowman Gray Sch Med, Ctr Human Genome, Winston Salem, NC 27157 USA

[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Biostat Sci, Winston Salem, NC 27157 USA

[3] Wake Forest Univ, Bowman Gray Sch Med, Dept Urol, Winston Salem, NC 27157 USA

[4] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden

[5] Univ Umea Hosp, Dept Urol, S-90185 Umea, Sweden

[6] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA

[7] Translat Genom Res Inst, Phoenix, AZ USA

[8] Johns Hopkins Med Inst, Baltimore, MD 21205 USA

来源：

NEW ENGLAND JOURNAL OF MEDICINE | 2008年 / 358卷 / 09期

关键词：

D O I：

10.1056/NEJMoa075819

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

Background Single-nucleotide polymorphisms (SNPs) in five chromosomal regions -- three at 8q24 and one each at 17q12 and 17q24.3 -- have been associated with prostate cancer. Each SNP has only a moderate association, but when SNPs are combined, the association may be stronger. Methods We evaluated 16 SNPs from five chromosomal regions in a Swedish population (2893 subjects with prostate cancer and 1781 control subjects) and assessed the individual and combined association of the SNPs with prostate cancer. Results Multiple SNPs in each of the five regions were associated with prostate cancer in single SNP analysis. When the most significant SNP from each of the five regions was selected and included in a multivariate analysis, each SNP remained significant after adjustment for other SNPs and family history. Together, the five SNPs and family history were estimated to account for 46% of the cases of prostate cancer in the Swedish men we studied. The five SNPs plus family history had a cumulative association with prostate cancer (P for trend, 3.93x10(-28)). In men who had any five or more of these factors associated with prostate cancer, the odds ratio for prostate cancer was 9.46 (P=1.29x10(-8)), as compared with men without any of the factors. The cumulative effect of these variants and family history was independent of serum levels of prostate-specific antigen at diagnosis. Conclusions SNPs in five chromosomal regions plus a family history of prostate cancer have a cumulative and significant association with prostate cancer.

引用

页码：910 / 919

页数：10

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