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Vitamin D and prostate cancer prognosis: a Mendelian randomization study
Authors:Olivia Trummer  Uwe Langsenlehner  Sabine Krenn-Pilko  Thomas R Pieber  Barbara Obermayer-Pietsch  Armin Gerger  Wilfried Renner  Tanja Langsenlehner
Institution:1.Division of Endocrinology and Metabolism, Department of Internal Medicine,Medical University of Graz,Graz,Austria;2.Division of Internal Medicine,GKK Outpatient Department,Graz,Austria;3.Department of Therapeutic Radiology and Oncology,Medical University of Graz,Graz,Austria;4.Division of Oncology, Department of Internal Medicine,Medical University of Graz,Graz,Austria;5.Clinical Institute of Medical and Chemical Laboratory Diagnostics,Medical University of Graz,Graz,Austria
Abstract:

Purpose

Decreased vitamin D levels have been associated with prostate cancer, but it is unclear whether this association is causal. A functional single-nucleotide polymorphism (SNP) in the group-specific component (GC) gene (T > G, rs2282679) has been associated with 25-hydroxy (25-OH) vitamin D and 1.25 dihydroxy (1.25-OH2) vitamin D levels.

Methods

To examine the hypothesized inverse relationship between vitamin D status and prostate cancer, we studied the association between this SNP and prostate cancer outcome in the prospective PROCAGENE study comprising 702 prostate cancer patients with a median follow-up of 82 months.

Results

GC rs2282679 genotypes were not associated with biochemical recurrence hazard ratios (HR) 0.91, 95 % confidence interval (CI) 0.73–1.12; p = 0.36], development of metastases (HR 1.20, 95 % CI 0.88–1.63; p = 0.25) or overall survival (HR 1.10; 95 % CI 0.84–1.43; p = 0.50).

Conclusions

A causal role of vitamin D status, as reflected by GC rs2282679 genotype, in disease progression and mortality in prostate cancer patients is unlikely.
Keywords:
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