Cargando…

Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies

INTRODUCTION: Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM. Limited information exists about the microstructure and composition of these deposits, and no information is available on their elemental composition and contents, m...

Descripción completa

Detalles Bibliográficos
Autores principales: Eidelman, Naomi, Boyde, Alan, Bushby, Andrew J, Howell, Peter GT, Sun, Jirun, Newbury, Dale E, Miller, Frederick W, Robey, Pamela G, Rider, Lisa G
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787294/
https://www.ncbi.nlm.nih.gov/pubmed/19857267
http://dx.doi.org/10.1186/ar2841
_version_ 1782174902035415040
author Eidelman, Naomi
Boyde, Alan
Bushby, Andrew J
Howell, Peter GT
Sun, Jirun
Newbury, Dale E
Miller, Frederick W
Robey, Pamela G
Rider, Lisa G
author_facet Eidelman, Naomi
Boyde, Alan
Bushby, Andrew J
Howell, Peter GT
Sun, Jirun
Newbury, Dale E
Miller, Frederick W
Robey, Pamela G
Rider, Lisa G
author_sort Eidelman, Naomi
collection PubMed
description INTRODUCTION: Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM. Limited information exists about the microstructure and composition of these deposits, and no information is available on their elemental composition and contents, mineral density (MD) and stiffness. We determined the microstructure, chemical composition, MD and stiffness of CDs obtained from DM patients. METHODS: Surgically-removed calcinosis specimens were analyzed with fourier transform infrared microspectroscopy in reflectance mode (FTIR-RM) to map their spatial distribution and composition, and with scanning electron microscopy/silicon drift detector energy dispersive X-ray spectrometry (SEM/SDD-EDS) to obtain elemental maps. X-ray diffraction (XRD) identified their mineral structure, X-ray micro-computed tomography (μCT) mapped their internal structure and 3D distribution, quantitative backscattered electron (qBSE) imaging assessed their morphology and MD, nanoindentation measured their stiffness, and polarized light microscopy (PLM) evaluated the organic matrix composition. RESULTS: Some specimens were composed of continuous carbonate apatite containing small amounts of proteins with a mineral to protein ratio much higher than in bone, and other specimens contained scattered agglomerates of various sizes with similar composition (FTIR-RM). Continuous or fragmented mineralization was present across the entire specimens (μCT). The apatite was much more crystallized than bone and dentin, and closer to enamel (XRD) and its calcium/phophorous ratios were close to stoichiometric hydroxyapatite (SEM/SDD-EDS). The deposits also contained magnesium and sodium (SEM/SDD-EDS). The MD (qBSE) was closer to enamel than bone and dentin, as was the stiffness (nanoindentation) in the larger dense patches. Large mineralized areas were typically devoid of collagen; however, collagen was noted in some regions within the mineral or margins (PLM). qBSE, FTIR-RM and SEM/SDD-EDS maps suggest that the mineral is deposited first in a fragmented pattern followed by a wave of mineralization that incorporates these particles. Calcinosis masses with shorter duration appeared to have islands of mineralization, whereas longstanding deposits were solidly mineralized. CONCLUSIONS: The properties of the mineral present in the calcinosis masses are closest to that of enamel, while clearly differing from bone. Calcium and phosphate, normally present in affected tissues, may have precipitated as carbonate apatite due to local loss of mineralization inhibitors.
format Text
id pubmed-2787294
institution National Center for Biotechnology Information
language English
publishDate 2009
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-27872942009-12-02 Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies Eidelman, Naomi Boyde, Alan Bushby, Andrew J Howell, Peter GT Sun, Jirun Newbury, Dale E Miller, Frederick W Robey, Pamela G Rider, Lisa G Arthritis Res Ther Research article INTRODUCTION: Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM. Limited information exists about the microstructure and composition of these deposits, and no information is available on their elemental composition and contents, mineral density (MD) and stiffness. We determined the microstructure, chemical composition, MD and stiffness of CDs obtained from DM patients. METHODS: Surgically-removed calcinosis specimens were analyzed with fourier transform infrared microspectroscopy in reflectance mode (FTIR-RM) to map their spatial distribution and composition, and with scanning electron microscopy/silicon drift detector energy dispersive X-ray spectrometry (SEM/SDD-EDS) to obtain elemental maps. X-ray diffraction (XRD) identified their mineral structure, X-ray micro-computed tomography (μCT) mapped their internal structure and 3D distribution, quantitative backscattered electron (qBSE) imaging assessed their morphology and MD, nanoindentation measured their stiffness, and polarized light microscopy (PLM) evaluated the organic matrix composition. RESULTS: Some specimens were composed of continuous carbonate apatite containing small amounts of proteins with a mineral to protein ratio much higher than in bone, and other specimens contained scattered agglomerates of various sizes with similar composition (FTIR-RM). Continuous or fragmented mineralization was present across the entire specimens (μCT). The apatite was much more crystallized than bone and dentin, and closer to enamel (XRD) and its calcium/phophorous ratios were close to stoichiometric hydroxyapatite (SEM/SDD-EDS). The deposits also contained magnesium and sodium (SEM/SDD-EDS). The MD (qBSE) was closer to enamel than bone and dentin, as was the stiffness (nanoindentation) in the larger dense patches. Large mineralized areas were typically devoid of collagen; however, collagen was noted in some regions within the mineral or margins (PLM). qBSE, FTIR-RM and SEM/SDD-EDS maps suggest that the mineral is deposited first in a fragmented pattern followed by a wave of mineralization that incorporates these particles. Calcinosis masses with shorter duration appeared to have islands of mineralization, whereas longstanding deposits were solidly mineralized. CONCLUSIONS: The properties of the mineral present in the calcinosis masses are closest to that of enamel, while clearly differing from bone. Calcium and phosphate, normally present in affected tissues, may have precipitated as carbonate apatite due to local loss of mineralization inhibitors. BioMed Central 2009 2009-10-26 /pmc/articles/PMC2787294/ /pubmed/19857267 http://dx.doi.org/10.1186/ar2841 Text en Copyright ©2009 Eidelman et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research article
Eidelman, Naomi
Boyde, Alan
Bushby, Andrew J
Howell, Peter GT
Sun, Jirun
Newbury, Dale E
Miller, Frederick W
Robey, Pamela G
Rider, Lisa G
Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title_full Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title_fullStr Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title_full_unstemmed Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title_short Microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
title_sort microstructure and mineral composition of dystrophic calcification associated with the idiopathic inflammatory myopathies
topic Research article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2787294/
https://www.ncbi.nlm.nih.gov/pubmed/19857267
http://dx.doi.org/10.1186/ar2841
work_keys_str_mv AT eidelmannaomi microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT boydealan microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT bushbyandrewj microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT howellpetergt microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT sunjirun microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT newburydalee microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT millerfrederickw microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT robeypamelag microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies
AT riderlisag microstructureandmineralcompositionofdystrophiccalcificationassociatedwiththeidiopathicinflammatorymyopathies