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PINP 可作为监测特立帕肽治疗患者的辅助手段。

PINP as an aid for monitoring patients treated with teriparatide.

机构信息

Lilly Research Laboratories Japan, Eli Lilly Japan K.K., Sannomiya Plaza Building, 7-1-5 Isogamidori, Kobe 651-0086, Japan.

出版信息

Bone. 2011 Apr 1;48(4):798-803. doi: 10.1016/j.bone.2010.12.006. Epub 2010 Dec 17.

Abstract

Biochemical markers of bone turnover may be useful aids for managing patients with osteoporosis. A 12-month, phase 3, multicenter trial of Japanese patients at high risk of fracture was conducted to assess the effects of teriparatide 20 μg/day on BMD, serum markers of bone turnover, and safety. Two-hundred and seven subjects (93% female; median age 70 years) were randomized in double-blind fashion 2:1 to teriparatide versus placebo. Bone turnover markers including procollagen type I N-terminal propeptide (PINP), bone-specific alkaline phosphatase (bone ALP) and type I collagen cross-linked C-telopeptide (CTX) were collected at baseline, 1, 3, 6, and 12 months. Lumbar spine, femoral neck, and total hip BMD were measured at baseline, 3, 6, and 12 months. Increases in PINP at 1 month correlated best with increases in lumbar spine BMD at 12 months (r=0.76; P<0.01). The proportions of patients with an increase from baseline in PINP >10 μg/L at 1, 3, and 6 months were 3%, 0%, and 2% in the placebo, and 93%, 87%, and 83% in the teriparatide group. The proportions of patients with an increase in PINP >10 μg/L at either 1 or 3 months were 3% in the placebo and 95% in the teriparatide group (P<0.001). The proportions of patients with a significant increase in lumbar spine BMD (increase from baseline ≥3%) at 12 months were 20% in the placebo and 94% in the teriparatide group. The proportions of patients with an increase in PINP >10 μg/L at 1 or 3 months and an increase in lumbar spine BMD ≥3% at 12 months was 0% of placebo group patients and 92% of teriparatide group patients (P<0.001). These data confirm a strong relationship between early change in PINP and later change in lumbar spine BMD during teriparatide therapy. Also, these results suggest that monitoring with PINP and lumbar spine BMD successfully identifies positive responses in most patients taking teriparatide and negative responses in most patients not taking teriparatide. PINP monitoring may be a useful aid in the management of patients with osteoporosis during teriparatide treatment.

摘要

骨转换生化标志物可能有助于骨质疏松症患者的治疗管理。我们进行了一项为期 12 个月、多中心、针对骨折高风险日本患者的 3 期临床试验,以评估每日 20μg 特立帕肽对骨密度、骨转换血清标志物和安全性的影响。207 例患者(93%为女性;中位年龄 70 岁)以 2:1 的比例随机双盲接受特立帕肽或安慰剂治疗。基线时、第 1、3、6 和 12 个月采集骨转换标志物,包括Ⅰ型前胶原 N 端前肽(PINP)、骨碱性磷酸酶(骨 ALP)和Ⅰ型胶原交联 C 端肽(CTX)。基线、第 3、6 和 12 个月测量腰椎、股骨颈和全髋骨密度。第 1 个月 PINP 的增加与第 12 个月腰椎骨密度的增加相关性最好(r=0.76;P<0.01)。第 1、3 和 6 个月时基线 PINP 增加>10μg/L 的患者比例,安慰剂组分别为 3%、0%和 2%,特立帕肽组分别为 93%、87%和 83%。第 1 个月或第 3 个月时 PINP 增加>10μg/L 的患者比例,安慰剂组为 3%,特立帕肽组为 95%(P<0.001)。第 12 个月时腰椎骨密度增加≥3%的患者比例,安慰剂组为 20%,特立帕肽组为 94%。第 1 个月或第 3 个月时 PINP 增加>10μg/L 和第 12 个月时腰椎骨密度增加≥3%的患者比例,安慰剂组为 0%,特立帕肽组为 92%(P<0.001)。这些数据证实了特立帕肽治疗期间,PINP 的早期变化与腰椎骨密度的后期变化之间存在很强的相关性。此外,这些结果表明,通过 PINP 和腰椎骨密度监测可成功识别大多数接受特立帕肽治疗的患者的阳性反应和大多数未接受特立帕肽治疗的患者的阴性反应。在特立帕肽治疗期间,PINP 监测可能有助于骨质疏松症患者的治疗管理。

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