Osteoporosis Research Center, Creighton University, Omaha, NE, USA.
Am J Clin Nutr. 2010 Jul;92(1):101-5. doi: 10.3945/ajcn.2009.29085. Epub 2010 May 19.
Calcium is an essential cotherapy in osteoporosis treatment. The relative effectiveness of various calcium salts for this purpose is uncertain. Many older women with osteoporosis have phosphorus intakes of <70% of the Recommended Dietary Allowance.
Our objective was to test the hypothesis that calcium phosphate would better support anabolic bone building than would calcium carbonate.
This study was a 12-mo, randomized, positive-comparator, 2-arm, single-blind clinical trial in 211 patients treated with teriparatide who consumed <1000 mg phosphorus/d. Participants were randomly assigned to receive, in addition to teriparatide and 1000 IU cholecalciferol, 1800 mg calcium/d as either tricalcium phosphate or calcium carbonate. The primary endpoints were changes in lumbar spine and total hip bone mineral densities (BMDs); secondary endpoints were changes in bone resorption biomarkers and serum and urine calcium and phosphorus concentrations.
In the combined group, the lumbar spine BMD increased by 7.2%, and total hip BMD increased by 2.1% (P < 0.01 for both). However, there was no significant difference between calcium-treatment groups, and there were no significant between-group differences in serum calcium and phosphorus concentrations or in urine calcium concentrations. Bone resorption biomarkers increased in both groups, as expected with teriparatide, but the increases in the 2 calcium groups did not differ significantly.
Tricalcium phosphate and calcium carbonate appear to be approximately equally effective in supporting bone building with a potent anabolic agent; phosphate salt may be preferable in patients with restricted phosphorus intakes. This trial was registered at clinicaltrials.gov as NCT00074711.
钙是骨质疏松治疗的基本辅助治疗药物。各种钙盐在这方面的相对有效性尚不确定。许多患有骨质疏松症的老年女性的磷摄入量<推荐膳食允许量的 70%。
我们的目的是检验这样一个假设,即磷酸钙在促进合成代谢性骨形成方面优于碳酸钙。
这是一项为期 12 个月的、随机的、阳性对照、双盲临床试验,共纳入 211 名接受特立帕肽治疗且磷摄入量<1000mg/d 的患者。参与者被随机分为两组,除了接受特立帕肽和 1000IU 胆钙化醇治疗外,分别每天额外补充 1800mg 钙,补充形式为磷酸三钙或碳酸钙。主要终点为腰椎和全髋骨矿物质密度(BMD)的变化;次要终点为骨吸收生物标志物以及血清和尿钙、磷浓度的变化。
在联合组中,腰椎 BMD 增加了 7.2%,全髋 BMD 增加了 2.1%(均<0.01)。然而,两组间无显著差异,且两组间血清钙、磷浓度或尿钙浓度无显著差异。与特立帕肽治疗预期的情况一样,两组的骨吸收生物标志物均增加,但两组间的增加幅度无显著差异。
磷酸钙和碳酸钙在与一种有效的合成代谢药物一起使用时似乎具有相似的促进骨形成的效果;在磷摄入量受限的患者中,使用磷酸盐盐可能更为理想。本试验在 clinicaltrials.gov 注册,编号为 NCT00074711。