Cesareo R, Di Stasio E, Vescini F, Campagna G, Cianni R, Pasqualini V, Romitelli F, Grimaldi F, Manfrini S, Palermo A
Thyroid Diseases Center, Department of Internal Medicine, "S.M.Goretti" Hospital, Latina, Italy.
Osteoporos Int. 2015 Apr;26(4):1295-302. doi: 10.1007/s00198-014-3000-2. Epub 2014 Dec 19.
No data on the pharmacological treatment of normocalcemic hyperparathyroidism (NPHPT) are available. We treated 30 NPHPT postmenopausal women with alendronate/cholecalciferol (treated group) or vitamin D alone (control group). Over 1 year, bone mineral density (BMD) increased significantly in treated group, but not in control group. Both treatments did not affect serum or urinary calcium.
Normocalcemic primary hyperparathyroidism (NPHPT) is defined by normal serum calcium and consistently elevated PTH levels after ruling out the causes of secondary hyperparathyroidism. It is likely that subjects with NPHPT may develop kidney and bone disease. As no data on the pharmacological treatment of NPHPT are available, we aimed to investigate the effects of alendronate and cholecalciferol on both BMD and bone biochemical markers in postmenopausal women with NPHPT. Safety of vitamin D was evaluated as secondary endpoint.
The study was a prospective open label randomized trial comparing 15 postmenopausal women with NPHPT (PMW-NPHPT), treated with oral alendronate plus cholecalciferol (treated group) and 15 PMW-NPHPT treated only with cholecalciferol (control group). Blood samples were obtained at baseline and after 3, 6, and 12 months. Bone turnover markers (BTM) were measured at baseline, 3, and 6 months, respectively. BMD was assessed at baseline and after 12 months.
After 1 year of treatment, BMD increased significantly at the lumbar, femoral neck, and hip level in the treated group, but not in the control group (p = 0.001). No differences were found between or within groups in serum calcium, PTH, and urinary calcium levels. BTM significantly decreased in the treated group but not in the control group, at 3 and 6 months (p < 0.001), respectively. No cases of hypercalcemia or hypercalciuria were detected during the study.
The results of this study indicate that alendronate/cholecalciferol increases BMD in postmenopausal women with NPHPT. Alendronate/cholecalciferol or vitamin D alone does not affect serum or urinary calcium.
目前尚无关于正常血钙性原发性甲状旁腺功能亢进症(NPHPT)药物治疗的数据。我们用阿仑膦酸钠/胆钙化醇治疗了30名绝经后NPHPT女性(治疗组),或仅用维生素D治疗(对照组)。在1年多的时间里,治疗组的骨密度(BMD)显著增加,而对照组没有。两种治疗方法均未影响血清或尿钙水平。
正常血钙性原发性甲状旁腺功能亢进症(NPHPT)的定义是血清钙正常,在排除继发性甲状旁腺功能亢进的病因后,甲状旁腺激素(PTH)水平持续升高。NPHPT患者可能会发展为肾脏和骨骼疾病。由于尚无关于NPHPT药物治疗的数据,我们旨在研究阿仑膦酸钠和胆钙化醇对绝经后NPHPT女性的骨密度和骨生化标志物的影响。将维生素D的安全性作为次要终点进行评估。
该研究是一项前瞻性开放标签随机试验,比较了15名接受口服阿仑膦酸钠加胆钙化醇治疗的绝经后NPHPT女性(PMW-NPHPT)(治疗组)和15名仅接受胆钙化醇治疗的PMW-NPHPT女性(对照组)。在基线以及3、6和12个月后采集血样。分别在基线、3个月和6个月时测量骨转换标志物(BTM)。在基线和12个月后评估骨密度。
治疗1年后,治疗组的腰椎、股骨颈和髋部骨密度显著增加,而对照组没有(p = 0.001)。组间或组内的血清钙、PTH和尿钙水平没有差异。治疗组在3个月和6个月时BTM显著下降,而对照组没有(p < 0.001)。在研究期间未检测到高钙血症或高钙尿症病例。
本研究结果表明,阿仑膦酸钠/胆钙化醇可增加绝经后NPHPT女性的骨密度。阿仑膦酸钠/胆钙化醇或单独使用维生素D均不影响血清或尿钙水平。