Correspondence: "Effect of early treatment with zoledronic acid on prevention of bone loss in patients with acute spinal cord injury: a randomized controlled trial".
Correspondence: "Effect of early treatment with zoledronic acid on prevention of bone loss in patients with acute spinal cord injury: a randomized controlled trial".
复制标题
通讯:“唑来膦酸早期治疗对预防急性脊髓损伤患者骨质流失的效果:一项随机对照试验”。
DOI:
10.1038/s41393-018-0221-9
复制
发表时间:
2018
期刊:
影响因子:
2.2
通讯作者:
Beaupre,GaryS
中科院分区:
文献类型:
--
作者:
Beaupre,GaryS
It was with great interest that I read the recent article by Goenka et al.[1] on the use of zoledronic acid (ZA) to treat acute bone loss in patients with spinal cord injury (SCI). The authors are to be congratulated for their important contribution to the literature. Their randomized controlled trial (RCT), which included 60 subjects divided into two groups, is three to four times larger than previous studies on the same topic [2–4]. The associated improvement in statistical power with such a large RCT represents a substantial benefit to the research field.One aspect of the authors' study that deserves comment is their choice of skeletal sites for bone density measurements. In their Introduction, the authors correctly note that fragility fractures post SCI most commonly occur in the distal femur and proximal tibia. Given that recognition, it is unfortunate that the authors chose to limit their bone density measurements to the hip. Bauman et al.[3] and Schnitzer et al.[4] have previously examined bone changes in the distal femur and proximal tibia in studies of ZA treatment in patients with SCI. Those two studies of ZA treatment post SCI are the only ones to date that have reported bone density near the knee. What is perplexing about those two studies is they show contradictory trends. The results of Schnitzer et al. suggest a benefit of ZA treatment in the distal femur, although the effect was not statistically significant. The results of Bauman et al. suggest a negative effect of ZA on knee BMD. If the counterintuitive results of Bauman et al. are replicated, it would raise a serious question about the use of ZA tor treating post-SCI bone loss. It