Reeve J, Davies U M, Hesp R, McNally E, Katz D
Department of Radiology, Northwick Park Hospital, Harrow.
BMJ. 1990 Aug 11;301(6747):314-8. doi: 10.1136/bmj.301.6747.314.
To evaluate the need for a randomised study of treatment of spinal osteoporosis with human parathyroid peptide in the secondary prevention of crush fractures; to study the effect of human parathyroid hormone peptide 1-34 plus sex hormones on vertebral body cancellous bone; and, separately, to determine the effect of relatively low doses of sodium fluoride plus calcium on spinal bone mineral density.
Open study of patients with primary or postmenopausal osteoporosis. All patients had serial bone densitometry of the spine by quantitative computed tomography and dual photon absorptiometry as well as serial densitometry of the radial midshaft (cortical) and radial distal (trabecular) bone by quantitative computed tomography. Changes in the spinal bone not forming the spongiosa of the vertebral bodies ("cortical" bone) were determined from the difference between the two axial measurements, after correction to the same units of measurement.
Northwick Park Hospital and Medical Research Council Clinical Research Centre.
24 Patients who fulfilled the conventional criteria for type 1 (vertebral) osteoporosis not secondary to recognised causes other than sex hormone deficiency and with at least one crush or wedge vertebral fracture and a spinal bone density (quantitative computed tomography) less than 80 mg/cm3 or two or more fractures. Twelve patients received human parathyroid peptide and 12 sodium fluoride; they were not randomised.
Trends in axial and peripheral bone mass values determined by linear, time dependent regression analyses.
The patients receiving the peptide showed a substantial increase in vertebral spongiosa (mean 25.6 mg/cm2 two years after the start of treatment). No significant changes were seen in spinal cortical or radial bone density. The patients receiving sodium fluoride showed roughly equal increases in cancellous and cortical bone over the same period (mean increase in vertebral spongiosa 16.1 mg/cm3). No significant changes were seen in radial bone.
Treatment of postmenopausal women with human parathyroid peptide selectively increases spinal cancellous bone density by amounts that may prove useful in secondary prevention. Peptide treatment should now be tested in a randomised study in which the important end point is prevention of fractures as the usefulness of sodium fluoride in this context is doubtful.
评估开展一项关于人甲状旁腺肽治疗脊柱骨质疏松症以预防椎体压缩性骨折的随机研究的必要性;研究人甲状旁腺激素肽1 - 34联合性激素对椎体松质骨的影响;另外,确定相对低剂量的氟化钠加钙剂对脊柱骨密度的影响。
对原发性或绝经后骨质疏松症患者进行的开放性研究。所有患者均通过定量计算机断层扫描和双能光子吸收法对脊柱进行系列骨密度测量,以及通过定量计算机断层扫描对桡骨骨干中段(皮质骨)和桡骨远端(小梁骨)进行系列骨密度测量。在将两个轴向测量值校正为相同测量单位后,通过两者差值确定未形成椎体松质骨的脊柱骨(“皮质”骨)的变化。
诺斯威克公园医院和医学研究理事会临床研究中心。
24例符合1型(椎体)骨质疏松症传统标准的患者,非因除性激素缺乏以外的其他公认原因所致,且至少有一处椎体压缩或楔形骨折,脊柱骨密度(定量计算机断层扫描)低于80mg/cm³或有两处或更多骨折。12例患者接受人甲状旁腺肽治疗,12例接受氟化钠治疗;未进行随机分组。
通过线性、时间依赖性回归分析确定轴向和外周骨量值的变化趋势。
接受肽治疗的患者椎体松质骨显著增加(治疗开始后两年平均增加25.6mg/cm²)。脊柱皮质骨或桡骨骨密度未见明显变化。接受氟化钠治疗的患者在同一时期松质骨和皮质骨的增加大致相同(椎体松质骨平均增加16.1mg/cm³)。桡骨骨密度未见明显变化。
用人甲状旁腺肽治疗绝经后女性可选择性增加脊柱松质骨密度,增加的幅度可能对二级预防有用。现在应该通过一项随机研究来测试肽治疗,其中重要的终点是预防骨折,因为在此背景下氟化钠的有效性值得怀疑。