Ahonen M H, Tenkanen L, Teppo L, Hakama M, Tuohimaa P
University of Tampere, Medical School, Finland.
Cancer Causes Control. 2000 Oct;11(9):847-52. doi: 10.1023/a:1008923802001.
The aim was to evaluate the association between serum vitamin D (25-hydroxyvitamin D) level and risk of prostate cancer.
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 cancer at baseline. Through record linkage with the files of the Finnish Cancer Registry, 149 prostate cancer cases were identified in the cohort. They were matched (1:4) to probability density sampled controls for age, time of sample retrieval, and residence. Serum levels of 25-hydroxyvitamin D (25-VD) at entry were measured for cases and controls. The relative risks of prostate cancer were derived using conditional logistic regression analysis.
Prostate cancer risk, analyzed by quartiles of the 25-VD levels, was inversely related to 25-VD. Men with 25-VD concentration below the median had an adjusted relative risk (OR) of 1.7 compared to men with 25-VD level 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 adjusted). Among those younger men (< 52 years), low 25-VD entailed a higher risk of non-localized cancers (OR 6.3). The mean age at diagnosis of the patients with 25-VD concentration above the median was 1.8 years higher than that of patients with vitamin D below the median (63.1 vs 61.3 years).
We conclude that low levels of 25-VD associated with an increased risk for subsequent earlier exposure and more aggressive development of prostate cancer, especially before the andropause.
旨在评估血清维生素D(25-羟基维生素D)水平与前列腺癌风险之间的关联。
这项巢式病例对照研究基于对约19000名中年男性进行的13年随访,这些男性参加了赫尔辛基心脏研究的首次筛查,且基线时无经临床证实的前列腺癌。通过与芬兰癌症登记处的档案进行记录链接,在该队列中确定了149例前列腺癌病例。按照年龄、样本采集时间和居住地,将病例与概率密度抽样的对照进行匹配(1:4)。测量病例组和对照组入组时的血清25-羟基维生素D(25-VD)水平。使用条件逻辑回归分析得出前列腺癌的相对风险。
按25-VD水平四分位数分析,前列腺癌风险与25-VD呈负相关。25-VD浓度低于中位数的男性与25-VD水平高于中位数的男性相比,调整后的相对风险(OR)为1.7。入组时年龄较轻(<52岁)且血清25-VD水平较低的男性前列腺癌风险最高(未调整的OR为3.1,调整后的OR为3.5)。在那些年龄较轻(<52岁)的男性中,低25-VD导致非局限性癌症的风险更高(OR为6.3)。25-VD浓度高于中位数的患者诊断时的平均年龄比维生素D低于中位数的患者高1.8岁(63.1岁对61.3岁)。
我们得出结论,低水平的25-VD与随后前列腺癌更早暴露和更具侵袭性发展的风险增加相关,尤其是在男性更年期之前。