Sakhaee Khashayar, Maalouf Naim M, Abrams Steven A, Pak Charles Y C
Center for Mineral Metabolism and Clinical Research, University of Texas Southwestern Medical Center, Dallas, Texas 75390-8885, USA.
J Clin Endocrinol Metab. 2005 Jun;90(6):3528-33. doi: 10.1210/jc.2004-2451. Epub 2005 Mar 8.
Potassium citrate may improve calcium balance by conferring an alkali load. Calcium supplementation slows postmenopausal bone loss by inhibiting PTH secretion. This study explores whether combined treatment with potassium citrate and calcium citrate is more effective than either agent alone in inhibiting bone loss. In a crossover study involving 18 postmenopausal women, the following treatments were compared: potassium citrate (4.3 g or 40 mmol/d), calcium citrate (800 mg or 20 mmol/d), combined treatment, and placebo. During the last 2 d of each 2-wk phase, serum and 24-h urine were collected for assessment of calcium metabolism, alkali load, and bone turnover markers. Compared with placebo, potassium citrate provided an alkali load and significantly decreased urinary calcium without changing serum PTH (sPTH) or bone turnover markers. Calcium citrate significantly increased absorbed calcium, marginally decreased sPTH, and significantly reduced bone resorption markers. Combined treatment retained key features of potassium citrate and calcium citrate. However, more alkali was delivered than with potassium citrate alone, and absorbed calcium did not differ from calcium citrate alone. Compared with placebo, combined treatment increased urinary calcium, marginally reduced sPTH, provided a clear alkali load, and reduced the bone resorption markers serum type I collagen C-telopeptide and urinary N-telopeptide by 20.4% (P < 0.0001) and 18.2% (P = 0.005), respectively. A significant trend was noted for the decrease in bone resorption markers as treatment changed from placebo to potassium citrate to calcium citrate to combined treatment. In postmenopausal women, combined treatment with potassium citrate and calcium citrate inhibits bone resorption by providing an alkali load and increasing absorbed calcium.
柠檬酸钾可通过提供碱负荷来改善钙平衡。补充钙可通过抑制甲状旁腺激素(PTH)分泌来减缓绝经后骨质流失。本研究探讨柠檬酸钾和柠檬酸钙联合治疗在抑制骨质流失方面是否比单独使用任何一种药物更有效。在一项涉及18名绝经后女性的交叉研究中,比较了以下几种治疗方法:柠檬酸钾(4.3 g或40 mmol/d)、柠檬酸钙(800 mg或20 mmol/d)、联合治疗和安慰剂。在每2周阶段的最后2天,收集血清和24小时尿液,以评估钙代谢、碱负荷和骨转换标志物。与安慰剂相比,柠檬酸钾提供了碱负荷,并显著降低了尿钙,而血清PTH(sPTH)或骨转换标志物没有变化。柠檬酸钙显著增加了钙吸收,略微降低了sPTH,并显著降低了骨吸收标志物。联合治疗保留了柠檬酸钾和柠檬酸钙的关键特性。然而,与单独使用柠檬酸钾相比,联合治疗提供了更多的碱,并且钙吸收与单独使用柠檬酸钙时没有差异。与安慰剂相比,联合治疗增加了尿钙,略微降低了sPTH,提供了明显的碱负荷,并使骨吸收标志物血清I型胶原C末端肽和尿N末端肽分别降低了20.4%(P < 0.0001)和18.2%(P = 0.005)。当治疗从安慰剂改为柠檬酸钾、柠檬酸钙再到联合治疗时,观察到骨吸收标志物有显著下降趋势。在绝经后女性中,柠檬酸钾和柠檬酸钙联合治疗通过提供碱负荷和增加钙吸收来抑制骨吸收。