Paschalis Eleftherios P, Glass Emmett V, Donley David W, Eriksen Erik F
Mineralized Tissue Section, Research Division, The Hospital for Special Surgery, New York, New York 10021, USA.
J Clin Endocrinol Metab. 2005 Aug;90(8):4644-9. doi: 10.1210/jc.2004-2489. Epub 2005 May 24.
Evidence suggests that both bone mineral density and bone quality should be taken into account when assessing bone strength and fracture risk. Bone quality is a multifactor entity, of which bone architecture and material properties are two important components. Matrix mineralization, hydroxyapatite characteristics, and collagen cross-link ratio are key determinants of material properties. Fourier transform infrared imaging (FTIRI) yields data on these characteristics from bone sections.
We sought to determine collagen cross-link ratios and matrix mineralization of bone from patients randomized to teriparatide [recombinant human PTH (1-34)] treatment using FTIRI.
The Fracture Prevention Trial was randomized, double blind, and placebo-controlled.
The trial was conducted at global clinical research centers.
Patients consisted of postmenopausal women with osteoporosis.
Patients were randomized to receive daily sc injections of placebo (n = 12) or 20 microg (n = 13) or 40 microg (n = 13) teriparatide. Biopsies were obtained after 12 months of treatment or at the end of treatment (range, 19-24 months for end of treatment paired biopsies).
Biopsies were analyzed by FTIRI to determine the matrix mineralization (mineral to matrix), mineral crystallinity, and collagen cross-link ratio (pyridinoline/dehydrodihydroxylysinonorleucine) with a spatial resolution of approximately 6.3 microm.
Patients administered teriparatide 20 and 40 microg/d exhibited significantly lower matrix mineralization, mineral crystallinity, and collagen cross-link ratio when compared with placebo.
These findings indicate that the bone-forming effect of teriparatide results in bone with a molecular profile reminiscent of younger bone.
有证据表明,在评估骨强度和骨折风险时,应同时考虑骨矿物质密度和骨质量。骨质量是一个多因素的实体,其中骨结构和材料特性是两个重要组成部分。基质矿化、羟基磷灰石特性和胶原交联率是材料特性的关键决定因素。傅里叶变换红外成像(FTIRI)可从骨切片中获取这些特性的数据。
我们试图使用FTIRI确定随机接受特立帕肽[重组人甲状旁腺激素(1-34)]治疗的患者的骨胶原交联率和基质矿化情况。
骨折预防试验是随机、双盲且安慰剂对照的。
该试验在全球临床研究中心进行。
患者为患有骨质疏松症的绝经后女性。
患者被随机分配,每天皮下注射安慰剂(n = 12)或20微克(n = 13)或40微克(n = 13)特立帕肽。在治疗12个月后或治疗结束时(治疗结束时配对活检的时间范围为19 - 24个月)获取活检样本。
通过FTIRI对活检样本进行分析,以确定基质矿化(矿物质与基质的比例)、矿物结晶度和胶原交联率(吡啶啉/脱氢二羟基赖氨酰正亮氨酸),空间分辨率约为6.3微米。
与安慰剂相比,每日给予20微克和40微克特立帕肽的患者表现出显著更低的基质矿化、矿物结晶度和胶原交联率。
这些发现表明,特立帕肽的成骨作用导致骨的分子特征让人联想到年轻的骨。