Corder E H, Friedman G D, Vogelman J H, Orentreich N
Center for Demographic Studies, Duke University, Durham, North Carolina 27708, USA.
Cancer Epidemiol Biomarkers Prev. 1995 Sep;4(6):655-9.
Our previous study provided evidence that higher serum levels of the active form of vitamin D, 1,25-dihydroxyvitamin D (1, 25-D), might possibly slow the progression of subclinical to clinically significant prostate cancer in both black and white men, especially after age 57. This paper extends the prior study by contrasting seasonal variation in 1,25-D and its precursor, 25-hydroxyvitamin D (25-D), in case and control subjects. In addition, the risk of prostate cancer is related to serum levels of vitamin D-binding protein (VDBP) and total dehydroepiandrosterone and to polymorphic variation in VDBP. The expected elevated summer levels of 25-D were seen in case and control subjects and, as expected, 1,25-D did not vary throughout the year in the control subjects. Unexpectedly, lower case levels of 1,25-D were limited largely to the summer months (P = 0.01) in both black and white cases and to cases greater than or equal to the median age of 57 years. Levels of VDBP and dehydroepiandrosterone and the frequencies of VDBP polymorphisms were similar in case and control subjects, although striking differences were seen in allelic frequencies in black and white men. These observations provide additional evidence that vitamin D metabolism may impact the risk of prostate cancer.
我们之前的研究表明,较高的血清活性维生素D形式,即1,25-二羟基维生素D(1,25-D),可能会减缓黑人和白人男性亚临床前列腺癌发展为具有临床意义的前列腺癌的进程,尤其是在57岁之后。本文通过对比病例组和对照组中1,25-D及其前体25-羟基维生素D(25-D)的季节性变化,扩展了之前的研究。此外,前列腺癌风险与维生素D结合蛋白(VDBP)和总脱氢表雄酮的血清水平以及VDBP的多态性变异有关。病例组和对照组均出现了预期中的25-D夏季水平升高的情况,并且正如预期的那样,对照组中1,25-D全年无变化。出乎意料的是,在黑人和白人病例中,较低的1,25-D水平主要局限于夏季月份(P = 0.01),且在年龄大于或等于57岁中位数的病例中也是如此。病例组和对照组中VDBP和脱氢表雄酮的水平以及VDBP多态性的频率相似,尽管在黑人和白人男性的等位基因频率上存在显著差异。这些观察结果提供了额外的证据,表明维生素D代谢可能会影响前列腺癌风险。