Peacock Munro, Bilezikian John P, Klassen Preston S, Guo Matthew D, Turner Stewart A, Shoback Dolores
Department of Medicine, Indiana University School of Medicine, Indianapolis, Indiana 46202, USA.
J Clin Endocrinol Metab. 2005 Jan;90(1):135-41. doi: 10.1210/jc.2004-0842. Epub 2004 Nov 2.
Calcimimetics increase the sensitivity of parathyroid calcium-sensing receptors to extracellular calcium, thereby reducing PTH secretion. This multicenter, randomized, double-blind, placebo-controlled study assessed the ability of the oral calcimimetic cinacalcet HCl to achieve long-term reductions in serum calcium and PTH concentrations in patients with primary hyperparathyroidism (HPT). Patients (n = 78) were randomized to cinacalcet or placebo. Cinacalcet was titrated from 30-50 mg twice daily during a 12-wk dose-titration phase. Efficacy was assessed during 12-wk maintenance and 28-wk follow-up phases. The primary endpoint was the achievement of normocalcemia [serum calcium </= 10.3 mg/dl (2.57 mmol/liter)] with at least 0.5 mg/dl (0.12-mmol/liter) reduction from baseline. Plasma PTH, serum and urine biochemistry, biochemical measures of bone turnover, bone mineral density, and safety were also assessed. Seventy-three percent of cinacalcet-treated patients vs. only 5% of placebo-treated patients achieved the primary endpoint (P < 0.001). Fasting predose plasma PTH decreased 7.6% in cinacalcet patients but increased 7.7% in placebo patients (P < 0.01). Bone mineral density was unchanged by cinacalcet, but bone resorption and formation markers increased (P < 0.05). Adverse events were mild and similar between treatment groups. Cinacalcet rapidly normalizes serum calcium and reduces PTH in patients with primary HPT, and these effects are maintained with long-term treatment. Cinacalcet may be an effective, nonsurgical approach for management of primary HPT.
拟钙剂可提高甲状旁腺钙敏感受体对细胞外钙的敏感性,从而减少甲状旁腺激素(PTH)的分泌。这项多中心、随机、双盲、安慰剂对照研究评估了口服拟钙剂盐酸西那卡塞使原发性甲状旁腺功能亢进症(HPT)患者的血清钙和PTH浓度长期降低的能力。患者(n = 78)被随机分为西那卡塞组或安慰剂组。在为期12周的剂量滴定阶段,西那卡塞从每日两次、每次30 - 50毫克开始滴定。在12周的维持期和28周的随访期评估疗效。主要终点是实现血钙正常[血清钙≤10.3毫克/分升(2.57毫摩尔/升)],且较基线至少降低0.5毫克/分升(0.12毫摩尔/升)。还评估了血浆PTH、血清和尿液生化指标、骨转换的生化指标、骨矿物质密度及安全性。接受西那卡塞治疗的患者中有73%达到主要终点,而接受安慰剂治疗的患者中只有5%达到主要终点(P < 0.001)。西那卡塞组患者空腹给药前血浆PTH下降了7.6%,而安慰剂组患者则升高了7.7%(P < 0.01)。西那卡塞对骨矿物质密度无影响,但骨吸收和形成标志物增加(P < 0.05)。不良事件轻微,且治疗组之间相似。西那卡塞可使原发性HPT患者的血清钙迅速恢复正常并降低PTH,且这些作用在长期治疗中得以维持。西那卡塞可能是一种治疗原发性HPT的有效非手术方法。