首页> 外文期刊>Journal of Pharmaceutical and Biomedical Analysis: An International Journal on All Drug-Related Topics in Pharmaceutical, Biomedical and Clinical Analysis >Evaluation of modal damping factor as a diagnostic tool for osteoporosis and its relation with serum osteocalcin and collagen I N-telopeptide for monitoring the efficacy of alendronate in ovariectomized rats.
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Evaluation of modal damping factor as a diagnostic tool for osteoporosis and its relation with serum osteocalcin and collagen I N-telopeptide for monitoring the efficacy of alendronate in ovariectomized rats.

机译:模态阻尼因子作为骨质疏松症诊断工具的评估及其与血清骨钙蛋白和胶原I N-端肽的关系,以监测去卵巢大鼠中阿仑膦酸盐的疗效。

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摘要

Osteoporosis is a metabolic bone disease characterized by reduced bone mass and deterioration of bone microarchitecture. It results from the shift of the osteoblast-osteoclast activity equilibrium in favor of the later. Although, a number of biochemical markers, such as collagen I N-telopeptide (NTx) and osteocalcin (OC), have been used for monitoring bone remodeling, a new, monitoring, non-invasive method, which is based on the measurement of the dynamic characteristic of bone and is known as modal damping factor (MDF), has not been evaluated as a diagnostic tool for osteoporosis. Bisphosphonates, such as alendronate, have an established role in the treatment of osteoporosis. The aim of the present study was, therefore, to evaluate the effects of alendronate on the levels of MDF, serum NTx and OC on osteoporosis induced by ovariectomy in rats. Furthermore, the effects of alendronate on osteoporosis have been histologically evaluated. Fifteen adult female Wistar rats were bilaterally ovariectomized andosteoporosis was histologically confirmed and by the use of peripheral quantitative computerized tomography (pQCT). MDF was applied to assess the bone structural integrity. The serum levels of NTx (37.4+/-0.5 nM bone collagen equivalents, BCE) and OC (111.0+/-8.2 ng/mL) were found to significantly increase following ovariectomy (72.0+/-2.9 nM BCE and 213.5+/-12.1 ng/mL, respectively, p<0.001). As assessed by histology and the levels of NTx and OC in sera, animals treated with alendronate presented a statistically significant deceleration in the progression of the disease in comparison to the no-therapy control group (alendronate group NTx levels: 146.3+/-8.9 nM BCE versus no-therapy control group NTx levels: 265.3+/-14.0 nM BCE, p<0.001, alendronate group OC levels: 205.6+/-18.2 ng/mL versus no-therapy group OC levels: 353.9+/-26.1 ng/mL, p<0.001). Data obtained from the vibration analysis performed illustrated that the change in damping was equal or greater to the change in total and trabecular density, respectively. Damping increased with decreasing bone density, as expected, given that damping accounts for the structural integrity of bone (MDF value before ovariectomy: 0.058+/-0.003 versus MDF value after ovariectomy: 0.098+/-0.003, p<0.001). The higher damping values correspond to more deteriorated structures. In particular, both total and trabecular density were significantly decreased following ovariectomy (total density before ovariectomy: 702.4+/-19.0 versus total density after ovariectomy: 542.2+/-12.8, p<0.001, trabecular density before ovariectomy: 445.3+/-13.0 versus trabecular density after ovariectomy: 396.7+/-8.4, p<0.05). MDF value of the alendronate group (0.07+/-0.002) was significantly lower (p<0.001) as compared to MDF value after ovariectomy (0.098+/-0.003) and that of the no-therapy group (0.1+/-0.004, p<0.001). The administration of alendronate seemed to have no effect on either total or trabecular density, since both parameters continued to decrease (alendronate group total density: 549.4+/-12.3, alendronate group trabecular density: 368.4+/-14.7). However, when this was compared to the no-therapy group, a statistically significant difference of total density at the 0.05 level was observed (no-therapy total density: 464.8+/-9.1). The results of this study suggest that combined measurements of MDF, NTx and OC may be a potential diagnostic tool for osteoporosis and monitoring bone integrity during treatment with bisphosphonates. Furthermore, administration of alendronate showed to offer a critical deceleration in the progression of osteoporosis.
机译:骨质疏松症是一种代谢性骨疾病,其特征是骨量减少和骨微结构恶化。这是由于成骨细胞-破骨细胞活性平衡的改变而导致的。尽管许多生化标记物(例如胶原蛋白I N-端肽(NTx)和骨钙蛋白(OC))已被用于监测骨重塑,但它是一种新的,监测性的,非侵入性的方法,该方法基于骨的动态特性,被称为模态阻尼因子(MDF),尚未被评估为骨质疏松症的诊断工具。双膦酸盐(例如阿仑膦酸盐)在骨质疏松症的治疗中具有确定的作用。因此,本研究的目的是评估阿仑膦酸盐对大鼠卵巢切除术引起的骨质疏松症中MDF,血清NTx和OC水平的影响。此外,已经从组织学上评价了阿仑膦酸盐对骨质疏松的作用。十五只成年雌性Wistar大鼠经双侧卵巢切除术,并通过外围定量计算机断层扫描(pQCT)进行组织学证实为骨质疏松。使用MDF评估骨结构完整性。发现卵巢切除术后血清NTx(37.4 +/- 0.5 nM骨胶原当量,BCE)和OC(111.0 +/- 8.2 ng / mL)显着增加(72.0 +/- 2.9 nM BCE和213.5 +/-)分别为12.1 ng / mL,p <0.001)。根据组织学和血清中NTx和OC的水平评估,与非治疗对照组相比,用阿仑膦酸盐治疗的动物在疾病进展方面具有统计学上显着的减速作用(阿仑膦酸盐组NTx水平:146.3 +/- 8.9 nM BCE与未治疗对照组的NTx水平:265.3 +/- 14.0 nM BCE,p <0.001,阿仑膦酸盐组OC水平:205.6 +/- 18.2 ng / mL与未治疗组OC水平:353.9 +/- 26.1 ng / mL ,p <0.001)。从振动分析获得的数据表明,阻尼的变化分别等于或大于总密度和小梁密度的变化。如预期的那样,阻尼随着骨密度的降低而增加,这是由于阻尼说明了骨骼的结构完整性(卵巢切除术前的MDF值:0.058 +/- 0.003,而卵巢切除术后的MDF值:0.098 +/- 0.003,p <0.001)。较高的阻尼值对应于更恶化的结构。特别是,卵巢切除后总密度和小梁密度均显着降低(卵巢切除前的总密度:702.4 +/- 19.0,而卵巢切除后的总密度:542.2 +/- 12.8,p <0.001,卵巢切除前的小梁密度:445.3 +/- 13.0与卵巢切除后的小梁密度比较:396.7 +/- 8.4,p <0.05)。阿仑膦酸盐组的MDF值(0.07 +/- 0.002)与卵巢切除术后的MDF值(0.098 +/- 0.003)和非治疗组的MDF值(0.1 +/- 0.004)相比均显着降低(p <0.001), p <0.001)。阿仑膦酸盐的施用似乎对总密度或小梁密度没有影响,因为两个参数都持续降低(阿仑膦酸盐组总密度:549.4 +/- 12.3,阿仑膦酸盐组小梁密度:368.4 +/- 14.7)。然而,当将其与非治疗组进行比较时,观察到总密度在0.05水平上具有统计学上的显着差异(非治疗总密度:464.8 +/- 9.1)。这项研究的结果表明,MDF,NTx和OC的组合测量可能是骨质疏松和监测双膦酸盐治疗期间骨完整性的潜在诊断工具。此外,阿仑膦酸盐的施用显示出在骨质疏松症进展中提供关键的减速。

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