Miller Paul D, Delmas Pierre D, Lindsay Robert, Watts Nelson B, Luckey Marjorie, Adachi Jonathan, Saag Kenneth, Greenspan Susan L, Seeman Ego, Boonen Steven, Meeves Suzanne, Lang Thomas F, Bilezikian John P
Colorado Center for Bone Research, Lakewood, Colorado 80227, USA.
J Clin Endocrinol Metab. 2008 Oct;93(10):3785-93. doi: 10.1210/jc.2008-0353. Epub 2008 Aug 5.
Anabolic responsiveness to teriparatide can be blunted or delayed in patients previously treated with alendronate. The extent of this effect is different for other antiresorptives. This study evaluated the early anabolic effects of teriparatide in postmenopausal women with osteoporosis previously treated with alendronate or risedronate.
Patients treated for at least 24 months with alendronate or risedronate discontinued their bisphosphonate and received teriparatide for 12 months. The primary endpoint was a comparison of changes from baseline in N-terminal propeptide of type 1 collagen after 3 months between prior bisphosphonate groups. We also examined changes in other bone turnover markers, bone mineral density (BMD), and relationships between early changes in bone turnover markers and 12-month areal and volumetric BMD.
In the prior risedronate group, the N-terminal propeptide of type 1 collagen increase was significantly greater after 3 months of teriparatide than in the prior alendronate group (mean +/- se, 86.0 +/- 5.6 vs. 61.2 +/- 5.3 ng/ml, respectively; P < 0.001). Findings were similar for the other bone turnover markers. The changes in areal BMD and trabecular spine volumetric BMD were also greater in the prior risedronate group (P < 0.05). Early changes in bone turnover markers correlated with changes in trabecular spine volumetric BMD at 12 months (Spearman r = 0.45). Teriparatide was well tolerated.
This nonrandomized but prospective study suggests that there may be differences in anabolic responsiveness to teriparatide as a function of the type of prior bisphosphonate exposure.
曾接受阿仑膦酸钠治疗的患者对特立帕肽的合成代谢反应可能会减弱或延迟。其他抗吸收药物的这种作用程度有所不同。本研究评估了特立帕肽对曾接受阿仑膦酸钠或利塞膦酸钠治疗的绝经后骨质疏松症女性的早期合成代谢作用。
接受阿仑膦酸钠或利塞膦酸钠治疗至少24个月的患者停用双膦酸盐,并接受特立帕肽治疗12个月。主要终点是比较3个月后先前双膦酸盐治疗组之间1型胶原N端前肽相对于基线的变化。我们还检查了其他骨转换标志物、骨密度(BMD)的变化,以及骨转换标志物早期变化与12个月时面积骨密度和体积骨密度之间的关系。
在先前使用利塞膦酸钠的组中,特立帕肽治疗3个月后1型胶原N端前肽的增加显著大于先前使用阿仑膦酸钠的组(分别为平均±标准误,86.0±5.6与61.2±5.3 ng/ml;P<0.001)。其他骨转换标志物的结果相似。先前使用利塞膦酸钠的组中面积骨密度和小梁骨体积骨密度的变化也更大(P<0.05)。骨转换标志物的早期变化与12个月时小梁骨体积骨密度的变化相关(Spearman相关系数r=0.45)。特立帕肽耐受性良好。
这项非随机但前瞻性的研究表明,根据先前双膦酸盐暴露类型的不同,对特立帕肽的合成代谢反应可能存在差异。