Watts Nelson B, Aggers Deborah, McCarthy Edward F, Savage Tina, Martinez Stephanie, Patterson Rachel, Carrithers Erin, Miller Paul D
Mercy Health Osteoporosis and Bone Health Services, Cincinnati, OH, USA.
Colorado Center for Bone Research at Centura Health, Lakewood, CO, USA.
J Bone Miner Res. 2017 May;32(5):1027-1033. doi: 10.1002/jbmr.3081. Epub 2017 Feb 7.
If oversuppression of bone turnover explained the association between bisphosphonate use and atypical subtrochanteric femur fractures (AFF), this could be reversed with anabolic treatment such as teriparatide. We conducted a prospective, open-label study in patients previously treated with bisphosphonates who sustained AFF, examining the response to 24-month treatment with teriparatide on bone mineral density (BMD), trabecular bone score (TBS), bone turnover markers (BTM), and fracture healing as well as quantitative histomorphometry. We studied 14 patients. Baseline BMD, BTM, and TBS varied widely. On initial bone biopsies, 12 of 14 patients showed tetracycline labels, but mineralizing surface/bone surface was below published normal values in all but 2. Lumbar spine BMD increased significantly at month 24 (6.1% ± 4.3%, p < 0.05 versus baseline), whereas total hip BMD and TBS did not change significantly. Changes in BTM occurred as reported previously for patients without AFF treated with teriparatide after prior bisphosphonate treatment. At month 24, fractures were healed in 6 patients, showed partial healing in 3, were unchanged in 2, and showed nonunion in 1. In a patient with two fractures, the fracture that occurred before teriparatide treatment was reported as healed, but the fracture that occurred while on treatment showed only partial healing. Bisphosphonate-treated patients who sustain AFF show heterogeneity of bone turnover. Treatment with teriparatide resulted in increases in BTM and lumbar spine BMD, as has been reported for patients without AFF. There was no significant effect of teriparatide on hip BMD, mineralizing surface to bone surface (MS/BS), or TBS and no consistent effect on fracture healing. In the context of a patient who has experienced an AFF after receiving bisphosphonate treatment, therapy with teriparatide for 24 months would be expected to increase BMD and BTM (and probably reduce the risk of fractures resulting from osteoporosis) but should not be relied on to aid in healing of the AFF. © 2017 American Society for Bone and Mineral Research.
如果骨转换过度抑制解释了双膦酸盐使用与非典型股骨转子下骨折(AFF)之间的关联,那么这种情况可以通过诸如特立帕肽等促合成治疗来逆转。我们对既往接受双膦酸盐治疗后发生AFF的患者进行了一项前瞻性、开放标签研究,观察24个月特立帕肽治疗对骨密度(BMD)、骨小梁骨评分(TBS)、骨转换标志物(BTM)、骨折愈合以及定量组织形态计量学的影响。我们研究了14例患者。基线时BMD、BTM和TBS差异很大。在最初的骨活检中,14例患者中有12例显示四环素标记,但除2例之外,所有患者的矿化表面/骨表面均低于已发表的正常值。腰椎BMD在第24个月时显著增加(6.1%±4.3%,与基线相比p<0.05),而全髋BMD和TBS无显著变化。BTM的变化与先前报道的既往接受双膦酸盐治疗后接受特立帕肽治疗的非AFF患者的情况一致。在第24个月时,6例患者骨折愈合,3例部分愈合,2例无变化,1例不愈合。在一名有两处骨折的患者中,特立帕肽治疗前发生的骨折报告已愈合,但治疗期间发生的骨折仅部分愈合。发生AFF的双膦酸盐治疗患者显示骨转换存在异质性。与非AFF患者的报道一样,特立帕肽治疗导致BTM和腰椎BMD增加。特立帕肽对髋部BMD、矿化表面与骨表面(MS/BS)或TBS无显著影响,对骨折愈合也无一致影响。在接受双膦酸盐治疗后发生AFF的患者中,预计24个月的特立帕肽治疗会增加BMD和BTM(并可能降低骨质疏松性骨折的风险),但不应依赖其促进AFF的愈合。©2017美国骨与矿物质研究学会。