Prostate cancer risk and prediagnostic serum 25-hydroxyvitamin D levels (Finland)

Citation
Mh. Ahonen et al., Prostate cancer risk and prediagnostic serum 25-hydroxyvitamin D levels (Finland), CANC CAUSE, 11(9), 2000, pp. 847-852
Citations number
24
Categorie Soggetti
Envirnomentale Medicine & Public Health
Journal title
CANCER CAUSES & CONTROL
ISSN journal
09575243 → ACNP
Volume
11
Issue
9
Year of publication
2000
Pages
847 - 852
Database
ISI
SICI code
0957-5243(200011)11:9<847:PCRAPS>2.0.ZU;2-3
Abstract
Objectives: The aim was to evaluate the association between serum vitamin D (25-hydroxyvitamin D) level and risk of prostate cancer. Methods: The nested case-control study was based on a 13-year follow-up of about 19,000 middle-aged men who attended the first screening visit within the Helsinki Heart Study and were free of clinically verified prostate canc er at baseline. Through record linkage with the files of the Finnish Cancer Registry, 149 prostate cancer cases were identified in the cohort. They we re matched (1:4) to probability density sampled controls for age, time of s ample retrieval, and residence. Serum levels of 25-hydroxyvitamin D (25-VD) at entry were measured for cases and controls. The relative risks of prost ate cancer were derived using conditional logistic regression analysis. Results: Prostate cancer risk, analyzed by quartiles of the 25-VD levels, w as inversely related to 25-VD. Men with 25-VD concentration below the media n had an adjusted relative risk (OR) of 1.7 compared to men with 25-VD leve l above the median. The prostate cancer risk was highest among younger men (< 52 years) at entry and low serum 25-VD (OR 3.1 nonadjusted and 3.5 adjus ted). Among those younger men (< 52 years), low 25-VD entailed a higher ris k of non-localized cancers (OR 6.3). The mean age at diagnosis of the patie nts with 25-VD concentration above the median was 1.8 years higher than tha t of patients with vitamin D below the median (63.1 vs 61.3 years). Conclusions: We conclude that low levels of 25-VD associated with an increa sed risk for subsequent earlier exposure and more aggressive development of prostate cancer, especially before the andropause.