dc.contributor.author
Siegert, Elise
dc.contributor.author
Uruha, Akinori
dc.contributor.author
Goebel, Hans-Hilmar
dc.contributor.author
Preuße, Corinna
dc.contributor.author
Casteleyn, Vincent
dc.contributor.author
Kleefeld, Felix
dc.contributor.author
Alten, Rieke
dc.contributor.author
Burmester, Gerd R.
dc.contributor.author
Schneider, Udo
dc.contributor.author
Höppner, Jakob
dc.contributor.author
Hahn, Kathrin
dc.contributor.author
Dittmayer, Carsten
dc.contributor.author
Stenzel, Werner
dc.date.accessioned
2023-06-08T12:33:24Z
dc.date.available
2023-06-08T12:33:24Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/39781
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-39499
dc.description.abstract
Systemic sclerosis represents a chronic connective tissue disease featuring fibrosis, vasculopathy and autoimmunity, affecting skin, multiple internal organs, and skeletal muscles. The vasculopathy is considered obliterative, but its pathogenesis is still poorly understood. This may partially be due to limitations of conventional transmission electron microscopy previously being conducted only in single patients. The aim of our study was therefore to precisely characterize immune inflammatory features and capillary morphology of systemic sclerosis patients suffering from muscle weakness. In this study, we identified 18 individuals who underwent muscle biopsy because of muscle weakness and myalgia in a cohort of 367 systemic sclerosis patients. We performed detailed conventional and immunohistochemical analysis and large-scale electron microscopy by digitizing entire sections for in-depth ultrastructural analysis. Muscle biopsies of 12 of these 18 patients (67%) presented minimal features of myositis but clear capillary alteration, which we termed minimal myositis with capillary pathology (MMCP). Our study provides novel findings in systemic sclerosis-associated myositis. First, we identified a characteristic and specific morphological pattern termed MMCP in 67% of the cases, while the other 33% feature alterations characteristic of other overlap syndromes. This is also reflected by a relatively homogeneous clinical picture among MMCP patients. They have milder disease with little muscle weakness and a low prevalence of interstitial lung disease (20%) and diffuse skin involvement (10%) and no cases of either pulmonary arterial hypertension or renal crisis. Second, large-scale electron microscopy, introducing a new level of precision in ultrastructural analysis, revealed a characteristic capillary morphology with basement membrane thickening and reduplications, endothelial activation and pericyte proliferation. We provide open-access pan-and-zoom analysis to our datasets, enabling critical discussion and data mining. We clearly highlight characteristic capillary pathology in skeletal muscles of systemic sclerosis patients.
en
dc.rights.uri
https://creativecommons.org/licenses/by/4.0/
dc.subject
Systemic sclerosis
en
dc.subject
Capillary pathology
en
dc.subject
Large-scale electron microscopy
en
dc.subject.ddc
600 Technik, Medizin, angewandte Wissenschaften::610 Medizin und Gesundheit::610 Medizin und Gesundheit
dc.title
Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.doi
10.1007/s00401-021-02305-3
dcterms.bibliographicCitation.journaltitle
Acta Neuropathologica
dcterms.bibliographicCitation.number
6
dcterms.bibliographicCitation.originalpublishername
Springer Nature
dcterms.bibliographicCitation.pagestart
917
dcterms.bibliographicCitation.pageend
927
dcterms.bibliographicCitation.volume
141
refubium.affiliation
Charité - Universitätsmedizin Berlin
refubium.funding
Springer Nature DEAL
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.bibliographicCitation.pmid
33864496
dcterms.isPartOf.issn
0001-6322
dcterms.isPartOf.eissn
1432-0533