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Differences in osteogenic and apoptotic genes between osteoporotic and osteoarthritic patients

By Giner Mercè, Montoya Mª José, Vázquez Mª Angeles, Miranda Cristina and Pérez-Cano Ramón

Abstract

<p>Abstract</p> <p>Background</p> <p>Osteoporosis is a metabolic disorder characterized by a reduction in bone mass and deterioration in the microarchitectural structure of the bone, leading to a higher risk for spontaneous and fragility fractures.</p> <p>The main aim was to study the differences between human bone from osteoporotic and osteoarthritic patients about gene expression (osteogenesis and apoptosis), bone mineral density, microstructural and biomechanic parameters.</p> <p>Methods</p> <p>We analyzed data from 12 subjects: 6 with osteoporotic hip fracture (OP) and 6 with hip osteoarthritis (OA), as the control group. All subjects underwent medical history, analytical determinations, densitometry, histomorphometric and biochemical study. The expression of 86 genes of osteogenesis and 86 genes of apoptosis was studied in pool of bone samples from patients with OP and OA by PCR array.</p> <p>Results</p> <p>We observed that most of the genes of apoptosis and osteogenesis show a decrease in gene expression in the osteoporotic group in comparison with the osteoarthritic group. The histomorphometric study shows a lower bone quality in the group of patients with hip fractures compared to the osteoarthritic group.</p> <p>Conclusions</p> <p>The bone tissue of osteoporotic fracture patients is more fragile than the bone of OA patients. Our results showed an osteoporotic bone with a lower capacities for differentiation and osteoblastic activity as well as a lower rate of apoptosis than osteoarthritic bone. These results are related with structural and biochemical parameters.</p

Topics: Human bone, Osteoporosis, Osteogenesis, Apoptosis, Microstructural, Internal medicine, RC31-1245, Medicine, R, DOAJ:Internal medicine, DOAJ:Medicine (General), DOAJ:Health Sciences, Diseases of the musculoskeletal system, RC925-935
Publisher: BioMed Central
Year: 2013
DOI identifier: 10.1186/1471-2474-14-41
OAI identifier: oai:doaj.org/article:287661b0dca644be836f1a0cae3e2b65
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