Levels of Beta-Microseminoprotein in Blood and Risk of Prostate Cancer in Multiple Populations.

Christopher A Haiman, Daniel O Stram, Andrew J Vickers, Lynne R Wilkens, Katharina Braun, Camilla Valtonen-André, Mari Peltola, Kim Pettersson, Kevin M Waters, Loic Le Marchand, Laurence N Kolonel, Brian E Henderson, Hans Lilja

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Abstract

BackgroundA common genetic variant (rs10993994) in the 5' region of the gene encoding β-microseminoprotein (MSP) is associated with circulating levels of MSP and prostate cancer risk. Whether MSP levels are predictive of prostate cancer risk has not been evaluated.MethodsWe investigated the prospective relationship between circulating plasma levels of MSP and prostate cancer risk in a nested case-control study of 1503 case subjects and 1503 control subjects among black, Latino, Japanese, Native Hawaiian, and white men from the Multiethnic Cohort study. We also examined the ability of MSP to serve as a biomarker for discriminating prostate cancer case subjects from control subjects. All statistical tests are two-sided.ResultsIn all racial and ethnic groups, men with lower MSP levels were at greater risk of developing prostate cancer (odds ratio = 1.02 per one unit decrease in MSP, P < .001 in the prostate-specific antigen [PSA]-adjusted analysis). Compared with men in the highest decile of MSP, the multivariable PSA-adjusted odds ratio was 3.64 (95% confidence interval = 2.41 to 5.49) for men in the lowest decile. The positive association with lower MSP levels was observed consistently across racial and ethnic populations, by disease stage and Gleason score, for men with both high and low levels of PSA and across all genotype classes of rs10993994. However, we did not detect strong evidence of MSP levels in improving prostate cancer prediction beyond that of PSA.ConclusionsRegardless of race and ethnicity or rs10993994 genotype, men with low blood levels of MSP have increased risk of prostate cancer.
Original languageEnglish
JournalJournal of the National Cancer Institute
Early online date2012 Dec 3
DOIs
Publication statusPublished - 2012

Subject classification (UKÄ)

  • Cancer and Oncology

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