Department of Epidemiology, University of Iowa College of Public Health, Iowa City, IA 52242, USA.
Am J Clin Nutr. 2011 Jul;94(1):270-7. doi: 10.3945/ajcn.110.003350. Epub 2011 Apr 27.
The Women's Health Initiative (WHI) randomized clinical trial (RCT) of calcium plus vitamin D (CaD) supplements found a 17% excess in urinary tract stone incidence in the supplemented group. This study evaluated whether this risk is modified by participant characteristics.
We examined the correlates of urinary tract stone occurrence in the CaD arm of the WHI trial.
We analyzed an RCT involving 36,282 postmenopausal women aged 50-79 y from 40 WHI centers: 18,176 women received 500 mg calcium carbonate plus 200 IU vitamin D(3) twice daily (1000 mg and 400 IU daily, respectively), and 18,106 women received a matching placebo for an average of 7.0 y. The incidence of urinary tract stones was determined.
The incidence of self-reported clinically diagnosed urinary tract stones was more common in the active CaD medication group than in the placebo group (hazard ratio: 1.17; 95% CI: 1.02, 1.34): 449 women in the CaD group and 381 women in the placebo group reported a stone during the trial. The rates of self-reported stones did not differ between various demographic, anthropomorphic, dietary, and other hypothesized risk factors according to randomization assignment. Neither the total calcium intake nor the use of calcium supplements at baseline was associated with the risk of stones. In sensitivity analyses that censored participants who were below 80% adherence, the findings were similar.
Daily supplementation with CaD for 7 y was associated with an increase in the number of self-reported urinary tract stones. These findings have implications for CaD supplement use. This trial was registered with the WHI at clinicaltrials.gov as NCT00000611.
妇女健康倡议(WHI)的钙加维生素 D(CaD)补充剂随机临床试验(RCT)发现补充组中尿路结石发病率增加 17%。本研究评估了该风险是否受参与者特征的影响。
我们检查了 WHI 试验 CaD 臂中尿路结石发生的相关因素。
我们分析了一项涉及 40 个 WHI 中心的 36282 名绝经后 50-79 岁女性的 RCT:18176 名女性每天接受 500mg 碳酸钙加 200IU 维生素 D3(分别为 1000mg 和 400IU),18106 名女性接受匹配的安慰剂,平均随访 7.0 年。确定尿路结石的发生率。
与安慰剂组相比,活性 CaD 药物组中自我报告的临床诊断尿路结石的发生率更高(风险比:1.17;95%CI:1.02,1.34):CaD 组中有 449 名女性和安慰剂组中有 381 名女性报告在试验期间有结石。根据随机分组,各种人口统计学、人体测量学、饮食和其他假设的危险因素之间的自我报告结石率没有差异。总钙摄入量或基线时钙补充剂的使用与结石风险无关。在对低于 80%依从性的参与者进行 censored 的敏感性分析中,结果相似。
7 年每日补充 CaD 与自我报告尿路结石数量的增加有关。这些发现对 CaD 补充剂的使用有影响。该试验在 clinicaltrials.gov 上作为 NCT00000611 注册于 WHI。