Rheumatic Diseases Unit, Institute of Genetics and Molecular Medicine, Western General Hospital, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Calcif Tissue Int. 2014 Feb;94(2):176-82. doi: 10.1007/s00223-013-9788-5. Epub 2013 Sep 13.
Teriparatide (TPTD) is often used for the treatment of patients with severe osteoporosis, but its effectiveness in this patient group has not been specifically studied. Here, we report upon the results of an observational study involving 323 patients with severe osteoporosis (bone density T-score of -4 or less) who were treated at a specialist osteoporosis clinic with TPTD (n = 217) or standard care (n = 106) over a 5.5-year period. The standard care group did not receive TPTD because they declined to self-inject (59.4%), had a contraindication (7.5%), or were already stabilized on oral bisphosphonates (33%). The two groups were matched for the severity of osteoporosis, fracture risk, and most other clinical variables. The annual percentage change in lumbar spine bone mineral density (BMD) was greater in the TPTD group (8.2 ± 6.0 vs. 5.0 ± 8.4, p = 0.002), but there was no difference in response of hip BMD. During follow-up, 3/217 (1.38%) TPTD-treated patients had new vertebral fractures compared with 7/106 (6.6%) receiving standard care (p = 0.011), but there was no difference between the groups in the rate of nonvertebral fractures (11.1 vs. 8.5%, p = 0.47). Logistic regression analysis adjusting for baseline characteristics showed that the risk of vertebral fractures in TPTD-treated patients was significantly reduced compared with standard care (odds ratio = 0.12, 95% confidence interval 0.03-0.55, p = 0.007). Treatment of severe spinal osteoporosis with TPTD substantially reduces the risk of vertebral fractures compared with standard care and may be the preferred treatment in this patient group.
特立帕肽(TPTD)常用于治疗严重骨质疏松症患者,但尚未专门研究其在该患者群体中的疗效。在这里,我们报告了一项涉及 323 名严重骨质疏松症患者(骨密度 T 评分-4 或更低)的观察性研究结果,这些患者在一家骨质疏松症专科诊所接受了特立帕肽(n = 217)或标准护理(n = 106)治疗,为期 5.5 年。标准护理组未接受特立帕肽治疗,因为他们拒绝自行注射(59.4%)、存在禁忌症(7.5%)或已稳定接受口服双膦酸盐(33%)。两组在骨质疏松症严重程度、骨折风险和大多数其他临床变量方面相匹配。TPTD 组腰椎骨密度(BMD)的年变化率较大(8.2 ± 6.0 比 5.0 ± 8.4,p = 0.002),但髋部 BMD 反应无差异。随访期间,3/217(1.38%)接受特立帕肽治疗的患者发生新的椎体骨折,而接受标准护理的 7/106(6.6%)患者(p = 0.011),但两组非椎体骨折发生率无差异(11.1%比 8.5%,p = 0.47)。调整基线特征的逻辑回归分析显示,与标准护理相比,特立帕肽治疗患者椎体骨折的风险显著降低(比值比 = 0.12,95%置信区间 0.03-0.55,p = 0.007)。与标准护理相比,特立帕肽治疗严重脊柱骨质疏松症可显著降低椎体骨折风险,可能是该患者群体的首选治疗方法。