Department of Rheumatology and Physical Therapy, Kenézy Gyula Hospital, BartókBéla u 2-26, 4043 Debrecen, Hungary.
Rheumatol Int. 2009 Nov;30(1):25-31. doi: 10.1007/s00296-009-0892-9.
This study intended to determine whether the replacement of vitamin D3 with alfacalcidol results in any bone mineral density (BMD) increase in 76 patients unresponsive to the combination of alendronate and conventional vitamin D3 treatment. In these patients the conventional vitamin D3 had been replaced with alfacalcidol (0.5 μg/day), and then the patients were followed up for a year. After treatment for 1 year, Wilcoxon test revealed a small but statistically significant (P < 0.001) increase in the BMD values of the forearm and lumbar vertebrae, in the serum calcium and urinary calcium/creatinine ratio in first-voided morning urine. However, the serum alkaline phosphatase activity, phosphorus, parathormone, osteocalcin levels and the urinary d-pyr/creatinine ratio decreased significantly (P < 0.001). As suggested by our results, combination therapy with alendronate and alfacalcidol increases bone density and improves the biochemical markers of bone turnover, without any substantial increase in the incidence of adverse effects.
本研究旨在确定在 76 例对阿仑膦酸钠和常规维生素 D3 联合治疗无反应的患者中,用阿尔法骨化醇替代维生素 D3 是否会导致骨矿物质密度(BMD)增加。这些患者的常规维生素 D3 已被阿尔法骨化醇(0.5μg/天)替代,然后对患者进行了为期一年的随访。治疗 1 年后,Wilcoxon 检验显示前臂和腰椎 BMD 值、血清钙和晨尿中钙/肌酐比值有较小但有统计学意义的(P<0.001)增加。然而,血清碱性磷酸酶活性、磷、甲状旁腺激素、骨钙素水平和尿 d-吡咯/肌酐比值显著降低(P<0.001)。根据我们的结果,阿仑膦酸钠和阿尔法骨化醇联合治疗可增加骨密度并改善骨转换的生化标志物,而不良反应发生率无明显增加。