OsteoRheuma Bern, Bahnhofplatz 1, Bern, Switzerland; Department of Rheumatology and Immunology, University Hospital, Bern, Switzerland.
OsteoRheuma Bern, Bahnhofplatz 1, Bern, Switzerland.
J Clin Densitom. 2022 Jul-Sep;25(3):293-298. doi: 10.1016/j.jocd.2022.03.001. Epub 2022 Mar 24.
Denosumab discontinuation can lead to bone loss despite subsequent bisphosphonate therapy. This bone loss is more severe in patients treated with denosumab for longer than 3 years. We aimed to evaluate the bone mass changes after only a single denosumab injection followed by zoledronate administration. We screened all of our patients who received a single denosumab injection and who were included in the osteoporosis register from the Swiss Society of Rheumatology between August 1, 2010, and January 31, 2022. This case series assessed the outcome of patients who were consecutively treated with one denosumab injection followed by a single infusion of zoledronate 6 months later. Bone mineral density (BMD) and bone turnover markers (BTM) changes were analysed before therapy and 18 months later. Percentage BMD changes and T-scores were compared with those of registered patients who received 2.5 years of denosumab treatment and one subsequent infusion of zoledronate. Thirty-two patients (31 female, 1 male) received a single denosumab injection and one zoledronate infusion 6 months later. BTM decreased significantly in this period (p = 0.035). Percentage BMD changes from baseline to 1 year after zoledronate treatment were 7.6% [IQR 3.2, 9.4] at the lumbar spine, 3.5% [1.8, 5.9] at the total hip and 4.6% [1.3, 6.0] at the femoral neck. In contrast, percentage changes from baseline in 110 patients with 2.5 years of denosumab treatment and one zoledronate infusion were 5.6% [3.0, 9.1], 2.3% [0.2, 4.9] and 2.3% [-0.9, 4.7], respectively. Differences between the 2 groups were significant at the lumbar spine (p = 0.014), total hip (p = 0.010) and femoral neck (p = 0.010). A single denosumab injection followed by zoledronate led to a remarkable gain of BMD at the lumbar spine and hip within a short time. This observation could help to identify a new short treatment sequence for patients with osteoporosis.
地舒单抗停药后,尽管随后使用双膦酸盐治疗,仍会导致骨质流失。对于接受地舒单抗治疗超过 3 年的患者,骨质流失更为严重。我们旨在评估单次地舒单抗注射后仅接受唑来膦酸治疗的患者的骨量变化。我们筛选了 2010 年 8 月 1 日至 2022 年 1 月 31 日期间在瑞士风湿病学会骨质疏松登记处接受单次地舒单抗注射且纳入的所有患者。该病例系列评估了连续接受单次地舒单抗注射后 6 个月再单次输注唑来膦酸治疗的患者的结局。在治疗前和 18 个月后分析了骨矿物质密度(BMD)和骨转换标志物(BTM)的变化。将百分比 BMD 变化和 T 评分与接受 2.5 年地舒单抗治疗和随后单次输注唑来膦酸的登记患者进行比较。32 名患者(31 名女性,1 名男性)接受了单次地舒单抗注射和 6 个月后的单次唑来膦酸输注。在此期间,BTM 显著下降(p=0.035)。唑来膦酸治疗 1 年后与基线相比的 BMD 百分比变化在腰椎为 7.6%[IQR 3.2,9.4],在全髋为 3.5%[1.8,5.9],在股骨颈为 4.6%[1.3,6.0]。相比之下,在接受 2.5 年地舒单抗治疗和单次唑来膦酸输注的 110 名患者中,与基线相比的百分比变化分别为 5.6%[3.0,9.1]、2.3%[0.2,4.9]和 2.3%[-0.9,4.7]。两组在腰椎(p=0.014)、全髋(p=0.010)和股骨颈(p=0.010)的差异均有统计学意义。单次地舒单抗注射后紧接着唑来膦酸治疗在短时间内显著增加了腰椎和髋部的 BMD。这一观察结果有助于为骨质疏松症患者确定新的短期治疗方案。