Seno Takahiro, Yamamoto Aihiro, Kukida Yuji, Hirano Aiko, Kida Takashi, Nakabayashi Amane, Fujioka Kazuki, Nagahara Hidetake, Fujii Wataru, Murakami Ken, Oda Ryo, Fujiwara Hiroyoshi, Kohno Masataka, Kawahito Yutaka
Inflammation and Immunology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566 Japan.
Department of Orthopaedics, Graduate School of Medical Science, Kyoto Prefectural University of Medicine, Kajii-cho, Kawaramachi-Hirokoji, Kamigyo-ku, Kyoto, 602-8566 Japan.
Springerplus. 2016 Jul 11;5(1):1056. doi: 10.1186/s40064-016-2704-5. eCollection 2016.
Patients with glucocorticoid-induced osteoporosis (GIOP) are at very high risk of fracture, and patients with severe GIOP often experience fractures during treatment with bisphosphonates. Teriparatide (TPTD) is the only currently available anabolic agent expected to be effective for GIOP. Once-weekly TPTD decreased bone resorption marker with primary osteoporosis different from daily TPTD, but it has not yet been tested with GIOP.
To evaluate the efficacy of once-weekly TPTD for patients with GIOP and inadequate response to bisphosphonates.
Patients with GIOP and collagen diseases treated with prednisolone for at least 6 months with inadequate responses to bisphosphonates were administered once-weekly TPTD. Bone density of the lumbar spine and femoral neck, measured as percent young adult mean (YAM); serum concentrations of cross-linked N-terminal telopeptides of type I collagen (NTx), bone alkaline phosphatase (BAP), and calcium; and FRAX were measured at baseline and 6, 12 and 18 months after starting TPTD.
Of the 12 GIOP patients with collagen diseases enrolled, nine (seven females, two males; mean age 57.4 ± 11.1 years) completed treatment, including six with systemic lupus erythematosus, two with rheumatoid arthritis, and one with adult onset still disease. Only one new fracture event, a lumbar compression fracture, occurred during the study period, although seven patients experienced eight fracture events within 18 months before starting TPTD (p = 0.04). Lumbar spine YAM significantly improved at 18 months (p = 0.04), whereas femoral neck YAM did not (p = 0.477). Serum NTx, BAP, Ca, and FRAX were not significantly affected by TPTD treatment.
Once-weekly TPTD reduces fracture events and increases bone density of the lumbar spine of GIOP patients with inadequate response to bisphosphonates.
糖皮质激素性骨质疏松症(GIOP)患者骨折风险极高,重度GIOP患者在双膦酸盐治疗期间常发生骨折。特立帕肽(TPTD)是目前唯一有望对GIOP有效的促合成代谢药物。与每日使用的TPTD不同,每周一次的TPTD可降低原发性骨质疏松症患者的骨吸收标志物,但尚未在GIOP患者中进行测试。
评估每周一次的TPTD对GIOP且对双膦酸盐反应不足患者的疗效。
对患有GIOP且因胶原病接受泼尼松龙治疗至少6个月、对双膦酸盐反应不足的患者,给予每周一次的TPTD。在基线以及开始TPTD治疗后的6、12和18个月,测量腰椎和股骨颈的骨密度,以年轻成人平均值百分比(YAM)表示;测量血清I型胶原交联N端肽(NTx)、骨碱性磷酸酶(BAP)、钙的浓度;并计算FRAX。
纳入的12例患有胶原病的GIOP患者中,9例(7例女性,2例男性;平均年龄57.4±11.1岁)完成治疗,其中6例患有系统性红斑狼疮,2例患有类风湿关节炎,1例患有成人斯蒂尔病。研究期间仅发生1例新的骨折事件,即腰椎压缩性骨折,尽管7例患者在开始TPTD治疗前18个月内发生了8次骨折事件(p=0.04)。腰椎YAM在18个月时显著改善(p=0.04),而股骨颈YAM未改善(p=0.477)。TPTD治疗对血清NTx、BAP、钙和FRAX无显著影响。
每周一次的TPTD可减少对双膦酸盐反应不足的GIOP患者的骨折事件,并增加其腰椎骨密度。