Division of Endocrinology, Department of Medicine, Columbia University College of Physicians and Surgeons, New York, New York 10032, USA.
J Clin Endocrinol Metab. 2011 Nov;96(11):3457-65. doi: 10.1210/jc.2011-1448. Epub 2011 Aug 17.
Bone loss and fracture are serious sequelae of organ transplantation, particularly in the first posttransplant year. Most interventional studies have been inadequately powered to detect effects on fracture.
The objective of the study was to determine whether treatment with bisphosphonates (BP) or active vitamin D analogs (vitD) during the first year after transplantation reduces fracture risk and estimate the effect of these interventions on bone loss.
Sources included PUBMED, MEDLINE, Cochrane Library, and abstracts from scientific meetings (presented 2003-2010).
Randomized controlled clinical trials of BP or vitD in solid organ transplant recipients were included if treatment was initiated at the time of transplantation and fracture data were collected.
Two investigators independently extracted data and rated study quality. Fixed effect and random-effects models were used to obtain pooled estimates.
Eleven studies of 780 transplant recipients (134 fractures) were included. Treatment with BP or vitD reduced the number of subjects with fracture [odds ratio (OR) 0.50 (0.29, 0.83)] and number of vertebral fractures, [OR 0.24 (0.07, 0.78)]. An increase in bone mineral density at the lumbar spine [2.98% (1.31, 4.64)] and femoral neck [3.05% (2.16, 3.93)] was found with treatment. When BP trials (nine studies, 625 subjects) were examined separately, there was a reduction in number of subjects with fractures [OR 0.53 (0.30, 0.91)] but no significant reduction in vertebral fractures [OR 0.34 (0.09, 1.24)].
Treatment with BP or vitD during the first year after solid organ transplant was associated with a reduction in the number of subjects with fractures and fewer vertebral fractures.
骨丢失和骨折是器官移植的严重后遗症,尤其是在移植后的第一年。大多数介入研究在检测骨折方面的效果时,其效力都不足。
本研究旨在确定在移植后第一年使用双膦酸盐(BP)或活性维生素 D 类似物(vitD)治疗是否降低骨折风险,并估计这些干预措施对骨丢失的影响。
包括 PUBMED、MEDLINE、Cochrane 图书馆以及科学会议摘要(2003-2010 年发表)。
如果在移植时开始治疗且收集了骨折数据,则将使用 BP 或 vitD 治疗的实体器官移植受者的随机对照临床试验纳入研究。
两名研究者独立提取数据并对研究质量进行评分。使用固定效应和随机效应模型来获得汇总估计值。
纳入了 11 项研究共 780 名移植受者(134 例骨折)。BP 或 vitD 治疗减少了骨折患者的数量[比值比(OR)0.50(0.29,0.83)]和椎体骨折数量[OR 0.24(0.07,0.78)]。治疗后腰椎[2.98%(1.31,4.64)]和股骨颈[3.05%(2.16,3.93)]的骨密度增加。单独检查 BP 试验(9 项研究,625 名患者)时,骨折患者的数量减少[OR 0.53(0.30,0.91)],但椎体骨折无显著减少[OR 0.34(0.09,1.24)]。
在实体器官移植后第一年使用 BP 或 vitD 治疗与骨折患者数量减少和椎体骨折减少相关。