Suzuki Takako, Nakamura Yukio, Kato Hiroyuki
a Department of Orthopaedic Surgery , Shinshu University School of Medicine , Matsumoto , Japan.
b Department of Orthopedic Surgery , Showa-Inan General Hospital , Komagane , Japan.
Mod Rheumatol. 2019 Jul;29(4):676-681. doi: 10.1080/14397595.2018.1524997. Epub 2018 Nov 28.
This extended randomized prospective study aimed to compare the 4-year clinical outcomes of denosumab treatment alone or in combination with teriparatide in treatment-naïve postmenopausal Japanese patients with osteoporosis. Between July 2013 and December 2016, 30 eligible women from our previous study were enrolled. After newly adding 17 randomly assigned patients, 47 patients were classified into the denosumab alone group (denosumab group, = 22) or denosumab plus teriparatide group (combination group, = 25). Serum bone-specific alkaline phosphatase (BAP), serum tartrate-resistant acid phosphatase (TRACP)-5b, urinary cross-linked N-terminal telopeptide of type I collagen (NTX), and bone mineral density (BMD) of the lumbar 1-4 vertebrae (L-BMD) and bilateral total hips (H-BMD) were determined at the first visit and at regular time points up to 48 months of treatment to determine percentage changes. BAP was significantly decreased from baseline in both groups from 24 to 48 months, with significant differences at all time points between the groups. TRACP-5b and urinary NTX were comparably decreased at every time point in both groups versus pretreatment levels. L-BMD was significantly more increased by combination therapy over denosumab alone at 24 and 30 months (21.1% increase vs. 14.2% increase at 48 months). There were no significant differences in H-BMD between the groups, although levels tended to be higher in the combination group throughout the study period (9.7% increase vs. 6.8% increase at 48 months). Long-term denosumab and teriparatide combination therapy represents an effective treatment option for primary osteoporosis patients with low L-BMD.
这项扩展的随机前瞻性研究旨在比较在初治的绝经后日本骨质疏松症患者中,单独使用地诺单抗或地诺单抗联合特立帕肽治疗的4年临床结局。2013年7月至2016年12月期间,我们从之前的研究中招募了30名符合条件的女性。新加入17名随机分配的患者后,47名患者被分为单独使用地诺单抗组(地诺单抗组,n = 22)或地诺单抗加特立帕肽组(联合治疗组,n = 25)。在首次就诊时以及治疗长达48个月的定期时间点,测定血清骨特异性碱性磷酸酶(BAP)、血清抗酒石酸酸性磷酸酶(TRACP)-5b、尿I型胶原交联N末端肽(NTX)以及第1-4腰椎(L-BMD)和双侧全髋部(H-BMD)的骨密度,以确定百分比变化。两组在24至48个月时,BAP均较基线显著降低,且各时间点两组间均存在显著差异。与治疗前水平相比,两组在每个时间点TRACP-5b和尿NTX均有相当程度的降低。联合治疗组在24个月和30个月时L-BMD的增加显著高于单独使用地诺单抗组(48个月时增加21.1% vs. 14.2%)。两组间H-BMD无显著差异,尽管在整个研究期间联合治疗组的水平往往更高(48个月时增加9.7% vs. 6.8%)。长期地诺单抗和特立帕肽联合治疗是L-BMD较低的原发性骨质疏松症患者的一种有效治疗选择。