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Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations

Although an inverse relationship between osteoarthritis (OA) and osteoporosis (OP) has been shown by some studies, other reports supported their coexistence. To clarify this relationship, we analyzed the interplay between clinical and histomorphometric features. Bone mineral density (BMD) and histom...

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Autores principales: Tarantino, Umberto, Celi, Monica, Rao, Cecilia, Feola, Maurizio, Cerocchi, Irene, Gasbarra, Elena, Ferlosio, Amedeo, Orlandi, Augusto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009293/
https://www.ncbi.nlm.nih.gov/pubmed/24829574
http://dx.doi.org/10.1155/2014/372021
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author Tarantino, Umberto
Celi, Monica
Rao, Cecilia
Feola, Maurizio
Cerocchi, Irene
Gasbarra, Elena
Ferlosio, Amedeo
Orlandi, Augusto
author_facet Tarantino, Umberto
Celi, Monica
Rao, Cecilia
Feola, Maurizio
Cerocchi, Irene
Gasbarra, Elena
Ferlosio, Amedeo
Orlandi, Augusto
author_sort Tarantino, Umberto
collection PubMed
description Although an inverse relationship between osteoarthritis (OA) and osteoporosis (OP) has been shown by some studies, other reports supported their coexistence. To clarify this relationship, we analyzed the interplay between clinical and histomorphometric features. Bone mineral density (BMD) and histomorphometric structure were assessed in 80 patients of four different age-matched groups undergoing hip arthroplasty for severe OA or OP-related femoral fracture. Harris Hip Score was also performed. Surgical double osteotomy of the femoral head was performed and microscopic bone slice samples analysis was performed by using a BioQuant Osteo software. Bone volume fraction (BV/TV) was lower (P < 0.01) in subjects with femoral neck fracture (20.77 ± 4.34%) than in subjects with nonosteopenic OA (36.49 ± 7.73%) or osteopenic OA (32.93 ± 6.83%), whereas no difference was detected between subjects with femoral neck fractures and those with combined OA and OP (20.71 ± 5.23%). Worse Harris Hip Score was found in those patients with the lowest BMD and BV/TV values. Our data support recent evidences indicating the possibility of impaired bone volume fraction in OA patients, with a high risk of developing OP, likely for their decreased mobility. Further studies are needed in order to investigate biomolecular pathway and/or growth factors involved in bone volume impairment in OA patients.
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spelling pubmed-40092932014-05-14 Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations Tarantino, Umberto Celi, Monica Rao, Cecilia Feola, Maurizio Cerocchi, Irene Gasbarra, Elena Ferlosio, Amedeo Orlandi, Augusto Int J Endocrinol Clinical Study Although an inverse relationship between osteoarthritis (OA) and osteoporosis (OP) has been shown by some studies, other reports supported their coexistence. To clarify this relationship, we analyzed the interplay between clinical and histomorphometric features. Bone mineral density (BMD) and histomorphometric structure were assessed in 80 patients of four different age-matched groups undergoing hip arthroplasty for severe OA or OP-related femoral fracture. Harris Hip Score was also performed. Surgical double osteotomy of the femoral head was performed and microscopic bone slice samples analysis was performed by using a BioQuant Osteo software. Bone volume fraction (BV/TV) was lower (P < 0.01) in subjects with femoral neck fracture (20.77 ± 4.34%) than in subjects with nonosteopenic OA (36.49 ± 7.73%) or osteopenic OA (32.93 ± 6.83%), whereas no difference was detected between subjects with femoral neck fractures and those with combined OA and OP (20.71 ± 5.23%). Worse Harris Hip Score was found in those patients with the lowest BMD and BV/TV values. Our data support recent evidences indicating the possibility of impaired bone volume fraction in OA patients, with a high risk of developing OP, likely for their decreased mobility. Further studies are needed in order to investigate biomolecular pathway and/or growth factors involved in bone volume impairment in OA patients. Hindawi Publishing Corporation 2014 2014-04-14 /pmc/articles/PMC4009293/ /pubmed/24829574 http://dx.doi.org/10.1155/2014/372021 Text en Copyright © 2014 Umberto Tarantino et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Tarantino, Umberto
Celi, Monica
Rao, Cecilia
Feola, Maurizio
Cerocchi, Irene
Gasbarra, Elena
Ferlosio, Amedeo
Orlandi, Augusto
Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title_full Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title_fullStr Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title_full_unstemmed Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title_short Hip Osteoarthritis and Osteoporosis: Clinical and Histomorphometric Considerations
title_sort hip osteoarthritis and osteoporosis: clinical and histomorphometric considerations
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009293/
https://www.ncbi.nlm.nih.gov/pubmed/24829574
http://dx.doi.org/10.1155/2014/372021
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