Baron John A, Beach Michael, Wallace Kristin, Grau Maria V, Sandler Robert S, Mandel Jack S, Heber David, Greenberg E Robert
Department of Medicine, Dartmouth Medical School, Hanover, New Hampshire, USA.
Cancer Epidemiol Biomarkers Prev. 2005 Mar;14(3):586-9. doi: 10.1158/1055-9965.EPI-04-0319.
In some studies, high calcium intake has been associated with an increased risk of prostate cancer, but no randomized studies have investigated this issue.
We randomly assigned 672 men to receive either 3 g of calcium carbonate (1,200 mg of calcium), or placebo, daily for 4 years in a colorectal adenoma chemoprevention trial. Participants were followed for up to 12 years and asked periodically to report new cancer diagnoses. Subject reports were verified by medical record review. Serum samples, collected at randomization and after 4 years, were analyzed for 1,25-(OH)2 vitamin D, 25-(OH) vitamin D, and prostate-specific antigen (PSA). We used life table and Cox proportional hazard models to compute rate ratios for prostate cancer incidence and generalized linear models to assess the relative risk of increases in PSA levels.
After a mean follow-up of 10.3 years, there were 33 prostate cancer cases in the calcium-treated group and 37 in the placebo-treated group [unadjusted rate ratio, 0.83; 95% confidence interval (95% CI), 0.52-1.32]. Most cases were not advanced; the mean Gleason's score was 6.2. During the first 6 years (until 2 years post-treatment), there were significantly fewer cases in the calcium group (unadjusted rate ratio, 0.52; 95% CI, 0.28-0.98). The calcium risk ratio for conversion to PSA >4.0 ng/mL was 0.63 (95% CI, 0.33-1.21). Baseline dietary calcium intake, plasma 1,25-(OH)2 vitamin D and 25-(OH) vitamin D levels were not materially associated with risk.
In this randomized controlled clinical trial, there was no increase in prostate cancer risk associated with calcium supplementation and some suggestion of a protective effect.
在一些研究中,高钙摄入量与前列腺癌风险增加有关,但尚无随机研究对此问题进行调查。
在一项结直肠腺瘤化学预防试验中,我们将672名男性随机分为两组,一组每天服用3克碳酸钙(含钙1200毫克),另一组服用安慰剂,为期4年。对参与者进行长达12年的随访,并定期要求他们报告新的癌症诊断情况。通过查阅医疗记录核实受试者的报告。在随机分组时和4年后采集血清样本,分析其中1,25 - (OH)2维生素D、25 - (OH)维生素D和前列腺特异性抗原(PSA)的含量。我们使用生命表和Cox比例风险模型计算前列腺癌发病率的比率,并使用广义线性模型评估PSA水平升高的相对风险。
平均随访10.3年后,钙治疗组有33例前列腺癌病例,安慰剂治疗组有37例[未调整的比率,0.83;95%置信区间(95%CI),0.52 - 1.32]。大多数病例并非晚期;平均Gleason评分为6.2。在前6年(直到治疗后2年),钙组的病例明显较少(未调整的比率,0.52;95%CI,0.28 - 0.98)。钙组转换为PSA>4.0 ng/mL的风险比率为0.63(95%CI,0.33 - 1.21)。基线饮食钙摄入量、血浆1,25 - (OH)2维生素D和25 - (OH)维生素D水平与风险无实质性关联。
在这项随机对照临床试验中,补钙与前列腺癌风险增加无关,且有一定的保护作用迹象。