Journal
PROSTATE
Volume 56, Issue 1, Pages 30-36Publisher
WILEY-LISS
DOI: 10.1002/pros.10220
Keywords
luteinizing hormone; polymorphism; prostate cancer
Categories
Funding
- NCI NIH HHS [CA92818, CA64220] Funding Source: Medline
- NIAMS NIH HHS [AR30582] Funding Source: Medline
- NIDDK NIH HHS [DK58859] Funding Source: Medline
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BACKGROUND. Circulating testosterone plays an important role in maintenance and growth of prostate cells. Luteinizing hormone (LH), secreted from the anterior pituitary, signals testicular Leydig cells to secrete testosterone. A genetic variant of the LH-beta protein, LH-betaV, exists in up to 40% of Caucasians and is more bioactive than the wild-type protein. We hypothesized that genetically determined variation in LH function might affect susceptibility to prostate cancer via altered testosterone secretion. METHODS. We determined the frequency of the LH-betaV polymorphism (two linked polymorphisms: Trp(8) Arg and Ile 15 --> Thr) in familial prostate cancer patients (n = 446), in sporadic prostate cancer patients (n = 388), and in population-based controls without prostate cancer (n = 510) to assess the role of this polymorphism in susceptibility to prostate cancer. RESULTS. A higher frequency of this variant genotype (LH-betaV: Arg(8)/Thr(15)) was observed in familial prostate cancer patients (18.6%) than in controls (13.7%), and after taking into account the correlation of the familial cases and adjusting for age and body mass index (BMI), there was a weak positive association between the variant LH-beta genotype, and risk of familial prostate cancer (OR = 1.29; 95% CI 0.96-1.75). The sporadic case group was also slightly more likely to have a variant genotype (15.2%) compared to the controls (13.7%), and after adjustment for age and BMI, a similar association with this variant was found (OR= 1.33; 95% CI 0.86-02.07). Surgical cases showed a slightly stronger association for the variant LH-beta genotype compared to non-surgical cases, but among the surgical cases there was little variability in risk across nodal status, stage, and tumor grade. CONCLUSIONS. These data are consistent with the hypothesis that the LH-beta variant is a weak risk factor for prostate cancer. Prostate 56: 30-36, 2003. (C) 2003Wiley-Liss, Inc.
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