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Neovascularization of osteoporotic metaphyseal bone defects: A morphometric micro-CT study. | LitMetric

Neovascularization of osteoporotic metaphyseal bone defects: A morphometric micro-CT study.

Microvasc Res

Laboratory of Experimental Radiology, Justus Liebig University Giessen, Germany; Department of Diagnostic and Interventional Radiology, BG Trauma Hospital Frankfurt/Main, Germany.

Published: May 2016

AI Article Synopsis

  • - This study examines how blood vessel structure and growth affect bone healing in osteoporosis by using an animal model, specifically focusing on the microvascular features in both healthy and injured femurs.
  • - A group of female rats underwent ovariectomy and a deficient diet to simulate osteoporosis, after which a critical bone defect was created, but no healing was seen after six weeks.
  • - The research found significant changes in blood vessel volume and thickness in the damaged area compared to healthy bone, highlighting the importance of blood vessel formation for successful bone regeneration, which could guide future studies on bone repair materials.

Article Abstract

Purpose: Neovascularization is essential for bone regeneration in fractures. This study aimed to investigate the microvascular morphology and distribution in the non-injured femur and the neovascularization of the metaphyseal critical size defect in a small animal model of osteoporosis.

Materials And Methods: Female rats (n=7) were ovariectomized (OVX) and received a multideficiency diet. Three months after OVX, a 5mm wedge shaped critical size defect was cut at the distal femoral metaphysis and stabilized with a T-shaped mini-plate. After six weeks, the animals were euthanized, and femora were removed and decalcified for micro-CT measurement of fracture neovascularization.

Results: No fracture healing was observed along the critical size defects. In the non-injured bone, micro-vessel distribution showed a specific pattern, thereby enabling a differentiation between epi-, meta- and diaphysis. Micro-CT based morphometry revealed a significant reduction of the vascular volume fraction as well as the vascular thickness (p<0.001) in the critical size defect compared to the intact contralateral femur. Blood volume related vascular surface (vascular surface/volume) increased significantly (p<0.001). Connectivity density and tissue volume related vascular surface (vascular surface density) did not change significantly.

Conclusions: Micro-CT based vascular morphometry demonstrated differences between epi-, meta- and diaphysis in the non-injured bone as well as differences between the critical size defect and the non-injured metaphysis. As angiogenesis is a crucial prerequisite that precedes osteogenesis, our results may influence further evaluation of osteoconductive or osteogenic biomaterials in this small animal model of osteoporosis.

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Source
http://dx.doi.org/10.1016/j.mvr.2015.10.005DOI Listing

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