Harinck H I, Bijvoet O L, Blanksma H J, Dahlinghaus-Nienhuys P J
Clin Orthop Relat Res. 1987 Apr(217):79-98.
The effects of treatment with aminobisphosphonate (APD) have been studied in a large and well-defined group of patients with Paget's disease over a period of seven years. Particular attention is given to the pharmacology of the drug, to methods of assessment of efficacy, and to the quality and the long-term persistence of the treatment results. These studies are compared to previously reported studies on bisphosphonates (P-C-Ps). The data suggest that the efficacy of P-C-Ps in Paget's disease results from a physiologic adaptation of all cellular processes involved in bone metabolism to a primary inhibition of bone resorption. The prolonged persistence of remissions may indicate that this is associated with disappearance rather than suppression of pathogenic material. If the low specific toxicity of the new generations of P-C-Ps is confirmed, it will be possible to induce complete and prolonged remissions through short oral or parenteral treatment courses that are associated with minimal side effects. Early institution of treatment in selected patients may prevent the development of deformity, fracture, and pain.
在一组大规模且明确界定的患有佩吉特病的患者中,对氨基双膦酸盐(APD)治疗的效果进行了为期七年的研究。特别关注了该药物的药理学、疗效评估方法以及治疗结果的质量和长期持续性。将这些研究与先前报道的关于双膦酸盐(P-C-Ps)的研究进行了比较。数据表明,P-C-Ps在佩吉特病中的疗效源于参与骨代谢的所有细胞过程对骨吸收的原发性抑制的生理适应。缓解期的长期持续可能表明这与致病物质的消失而非抑制有关。如果新一代P-C-Ps的低特异性毒性得到证实,那么通过与最小副作用相关的短期口服或肠胃外治疗疗程诱导完全且持久的缓解将成为可能。在选定患者中早期开始治疗可能会预防畸形、骨折和疼痛的发生。