Department of Orthopaedic Surgery, Graduate School of Medicine, Osaka University, 2-2 Yamadaoka, Suita, Osaka, 565-0871, Japan.
Department of Rheumatology, National Hospital Organization, Osaka Minami Medical Center, 2-1 Kidohigashi, Kawachinagano, Osaka, 586-8521, Japan.
J Bone Miner Metab. 2018 Jul;36(4):478-487. doi: 10.1007/s00774-017-0861-4. Epub 2017 Aug 1.
The aim of this observational, non-randomized study was to clarify the unknown effects of switching oral bisphosphonates (BPs) to denosumab (DMAb) or daily teriparatide (TPTD) in patients with rheumatoid arthritis (RA). The characteristics of the 194 female patients included in the study were 183 postmenopausal, age 65.9 years, lumbar spine (LS) T score -1.8, femoral neck (FN) T score -2.3, dose and rate of taking oral prednisolone (3.6 mg/day) 75.8%, and prior BP treatment duration 40.0 months. The patients were allocated to (1) the BP-continue group (n = 80), (2) the switch-to-DMAb group (n = 74), or (3) the switch-to-TPTD group (n = 40). After 18 months, the increase in bone mineral density (BMD) was significantly greater in the switch-to-DMAb group than in the BP-continue group (LS 5.2 vs 2.3%, P < 0.01; FN 3.8 vs 0.0%, P < 0.01) and in the switch-to-TPTD group than in the BP-continue group (LS 9.0 vs 2.3%, P < 0.001; FN 4.9 vs 0.0%, P < 0.01). Moreover, the switch-to-TPTD group showed a higher LS BMD (P < 0.05) and trabecular bone score (TBS) (2.1 vs -0.7%; P < 0.05) increase than the switch-to-DMAb group. Clinical fracture incidence during this period was 8.8% in the BP-continue group, 4.1% in the switch-to-DMAb group, and 2.5% in the switch-to-TPTD group. Both the switch-to-DMAb group and the switch-to-TPTD group showed significant increases in LS and FN BMD, and the switch-to-TPTD group showed a higher increase in TBS compared to the BP-continue group at 18 months. Switching BPs to DMAb or TPTD in female RA may provide some useful osteoporosis treatment options.
这项观察性、非随机研究的目的是阐明在类风湿关节炎(RA)患者中将口服双膦酸盐(BPs)转换为地舒单抗(DMAb)或每日特立帕肽(TPTD)的未知影响。纳入研究的 194 名女性患者的特征为:183 名绝经后,年龄 65.9 岁,腰椎(LS)T 评分-1.8,股骨颈(FN)T 评分-2.3,口服泼尼松龙剂量和频率 75.8%(3.6mg/天),以及之前的 BP 治疗持续时间 40.0 个月。患者被分配至(1)BP 继续组(n=80)、(2)转换至 DMAb 组(n=74)或(3)转换至 TPTD 组(n=40)。18 个月后,与 BP 继续组相比,转换至 DMAb 组的骨密度(BMD)增加更显著(LS 5.2%对 2.3%,P<0.01;FN 3.8%对 0.0%,P<0.01),与 BP 继续组相比,转换至 TPTD 组的 BMD 增加也更显著(LS 9.0%对 2.3%,P<0.001;FN 4.9%对 0.0%,P<0.01)。此外,与转换至 DMAb 组相比,转换至 TPTD 组的 LS BMD(P<0.05)和骨小梁评分(TBS)(2.1%对-0.7%;P<0.05)升高更显著。在此期间,BP 继续组的临床骨折发生率为 8.8%,转换至 DMAb 组为 4.1%,转换至 TPTD 组为 2.5%。转换至 DMAb 组和转换至 TPTD 组的 LS 和 FN BMD 均显著增加,与 BP 继续组相比,转换至 TPTD 组的 TBS 增加更高,在 18 个月时。在女性 RA 患者中,将 BPs 转换为 DMAb 或 TPTD 可能提供一些有用的骨质疏松症治疗选择。