Abstract

IntroductionCalcified 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.MethodsSurgically-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.ResultsSome 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.ConclusionsThe 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.

Highlights

  • Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM

  • Our analyses revealed that the mineral present in the calcinosis lesions of juvenile and adult myositis patients consists of carbonate apatite and not hydroxyapatite or fluoroapatite, as it was referred to in earlier case reports of surgically removed calcinosis specimens from patients with calcinosis cutis, juvenile dermatomyositis (JDM) and DM, using X-ray diffraction (XRD) [9,10,11,12]

  • The information that was obtained from the complementary Fourier Transform Infrared microspectroscopy in reflectance mode (FTIR-RM), SEM/SDD-EDS, XRD, μCT, quantitative backscattered electron (qBSE) imaging, nanoindentation and polarized light microscopy (PLM) methods increase our understanding of the dystrophic mineralization process in DM

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Summary

Introduction

Calcified deposits (CDs) in skin and muscles are common in juvenile dermatomyositis (DM), and less frequent in adult DM. 30% of patients with juvenile dermatomyositis (JDM) develop dystrophic calcification, which is associated with increased functional disability and a chronic illness course [1,2,3]. Calcinosis has been reported, but less frequently in adult patients [4]. These calcified deposits often develop in sites of microtrauma, including the joint extensor surfaces, digits and extremities, they may occur anywhere [1]. Limited information is available about the microstructure and composition of the calcified deposits in DM specimens and most of the studies were case reports or included small number of patients [8,9,10,11,12]. There are no reports on their mineral density (MD), stiffness and elemental composition mapping

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