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Mathematical modeling of the effects of CK2.3 on mineralization in osteoporotic bone

机译:CK2.3对骨质疏松性骨矿化影响的数学模型

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摘要

Osteoporosis is caused by decreased bone mineral density (BMD) and new treatments for this disease are desperately needed. Bone morphogenetic protein 2 (BMP2) is crucial for bone formation. The mimetic peptide CK2.3 acts downstream of BMP2 and increases BMD when injected systemically into the tail vein of mice. However, the most effective dosage needed to induce BMD in humans is unknown. We developed a mathematical model for CK2.3‐dependent bone mineralization. We used a physiologically based pharmacokinetic (PBPK) model to derive the CK2.3 concentration needed to increase BMD. Based on our results, the ideal dose of CK2.3 for a healthy individual to achieve the maximum increase of mineralization was about 409 µM injected in 500 µL volume, while dosage for osteoporosis patients was about 990 µM. This model showed that CK2.3 could increase the average area of bone mineralization in patients and in healthy adults.
机译:骨质疏松症是由骨矿物质密度(BMD)降低引起的,迫切需要针对这种疾病的新疗法。骨形态发生蛋白2(BMP2)对于骨骼形成至关重要。模拟肽CK2.3在BMP2的下游起作用,并在全身注入小鼠尾静脉时增加BMD。然而,尚不清楚在人中诱导BMD所需的最有效剂量。我们为CK2.3依赖性骨矿化开发了数学模型。我们使用基于生理学的药代动力学(PBPK)模型来得出增加BMD所需的CK2.3浓度。根据我们的结果,对于一个健康个体,实现最大程度矿化的理想CK2.3剂量约为409 µM(500 µL注射量),而骨质疏松症患者的剂量约为990 µM。该模型表明,CK2.3可以增加患者和健康成年人的平均骨矿化面积。

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