Drake W M, Brown J P, Banville C, Kendler D L
Osteoporosis Research Center, University of British Columbia, Vancouver, Canada.
Osteoporos Int. 2002 Mar;13(3):249-56. doi: 10.1007/s001980200022.
In women with postmenopausal osteoporosis (PMO), response to therapy with bisphosphonates is conventionally monitored using central-site (hip and spine) bone mineral density (BMD), but more convenient alternatives are desirable. During a randomized parallel-group study of the efficacy of once-weekly (80 mg vs 160 mg) oral alendronate in the treatment of PMO, 81 women (mean age 70.2 years +/- 4.6 SD) had BMD measurements of total hip (TH) and lumbar spine (LS) (L1-L4, Hologic); and of the middle phalanx of the middle digit of the non-dominant hand (accuDXA) at baseline and after 6 and 12 months of therapy with alendronate. At the same timepoints, subjects also had measurements of speed of sound (SOS) through bone at four sites (distal 1/3 radius, proximal phalanx of the third finger, midshaft of the tibia and fifth metatarsal) using the Sunlight Omnisense Ultrasound Bone Sonometer. Data from both patient groups were pooled for this analysis. Mean TH BMD at baseline was 0.705 g/cm2 +/- 0.093 (SD) and increased by 1.7% +/- 2.3% and 2.5% +/- 2.3% at 6 and 12 months respectively (p = 0.09 and p<0.0001). Mean LS BMD at baseline was 0.718 +/- 0.076 g/cm2 and increased by 3.9% +/- 3.6% and 6.1% +/- 3.5% at 6 and 12 months respectively (both p<0.0001). There was no statistically significant change from baseline in mean BMD by accuDXA at either 6 or 12 months. The only statistically significant changes in SOS were at the radius (decrease in SOS at 12 months, p= 0.04) and tibia (increase at 6 months, p<0.01, but no change between baseline and 12 months). Baseline correlation coefficients between accuDXA and LS and TH DXA were 0.22 (p = 0.05) and 0.27 (p = 0.02) respectively. Correlation coefficients between SOS and LS DXA ranged from 0.05 to 0.22; and between SOS and TH DXA ranged from -0.08 to 0.10 (all p = NS). These data suggest that the response to alendronate therapy over this time period cannot be measured by accuDXA or Sunlight SOS at the sites studied.
在绝经后骨质疏松症(PMO)女性中,传统上使用中心部位(髋部和脊柱)骨密度(BMD)来监测双膦酸盐治疗的反应,但更便捷的替代方法是可取的。在一项关于每周一次(80毫克对160毫克)口服阿仑膦酸钠治疗PMO疗效的随机平行组研究中,81名女性(平均年龄70.2岁±4.6标准差)在基线时以及接受阿仑膦酸钠治疗6个月和12个月后,测量了全髋(TH)和腰椎(LS)(L1 - L4,Hologic)的骨密度;以及非优势手中间手指中节指骨的骨密度(accuDXA)。在相同时间点,受试者还使用Sunlight Omnisense超声骨声速仪测量了四个部位(桡骨远端1/3、第三指近节指骨、胫骨骨干中部和第五跖骨)的骨声速(SOS)。将两个患者组的数据汇总进行此分析。基线时TH的平均骨密度为0.705克/平方厘米±0.093(标准差),在6个月和12个月时分别增加了1.7%±2.3%和2.5%±2.3%(p = 0.09和p<0.0001)。基线时LS的平均骨密度为0.718±0.076克/平方厘米,在6个月和12个月时分别增加了3.9%±3.6%和6.1%±3.5%(两者p<0.0001)。在6个月或12个月时,accuDXA测量的平均骨密度与基线相比无统计学显著变化。SOS唯一的统计学显著变化发生在桡骨(12个月时SOS降低,p = 0.04)和胫骨(6个月时增加,p<0.01,但基线与12个月之间无变化)。accuDXA与LS和TH DXA之间的基线相关系数分别为0.22(p = 0.05)和0.27(p = 0.02)。SOS与LS DXA之间的相关系数范围为0.05至0.22;SOS与TH DXA之间的相关系数范围为 - 0.08至0.10(所有p =无统计学意义)。这些数据表明,在此时间段内阿仑膦酸钠治疗的反应无法通过所研究部位的accuDXA或Sunlight SOS来测量。