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1000 Titel
  • Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology
1000 Autor/in
  1. Siegert, Elise |
  2. Uruha, Akinori |
  3. Goebel, Hans-Hilmar |
  4. Preuße, Corinna |
  5. Casteleyn, Vincent |
  6. Kleefeld, Felix |
  7. Alten, Rieke |
  8. Burmester, Gerd R. |
  9. Schneider, Udo |
  10. Höppner, Jakob |
  11. Hahn, Kathrin |
  12. Dittmayer, Carsten |
  13. Stenzel, Werner |
1000 Erscheinungsjahr 2021
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2021-04-17
1000 Erschienen in
1000 Quellenangabe
  • 141(6):917-927
1000 Copyrightjahr
  • 2021
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-021-02305-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8113184/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • 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.
1000 Sacherschließung
lokal Systemic sclerosis
lokal Original Paper
lokal Myositis
lokal Large-scale electron microscopy
lokal Capillary pathology
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U2llZ2VydCwgRWxpc2U=|https://frl.publisso.de/adhoc/uri/VXJ1aGEsIEFraW5vcmk=|https://frl.publisso.de/adhoc/uri/R29lYmVsLCBIYW5zLUhpbG1hcg==|https://frl.publisso.de/adhoc/uri/UHJldcOfZSwgQ29yaW5uYQ==|https://frl.publisso.de/adhoc/uri/Q2FzdGVsZXluLCBWaW5jZW50|https://frl.publisso.de/adhoc/uri/S2xlZWZlbGQsIEZlbGl4|https://frl.publisso.de/adhoc/uri/QWx0ZW4sIFJpZWtl|https://frl.publisso.de/adhoc/uri/QnVybWVzdGVyLCBHZXJkIFIu|https://frl.publisso.de/adhoc/uri/U2NobmVpZGVyLCBVZG8=|https://frl.publisso.de/adhoc/uri/SMO2cHBuZXIsIEpha29i|https://frl.publisso.de/adhoc/uri/SGFobiwgS2F0aHJpbg==|https://frl.publisso.de/adhoc/uri/RGl0dG1heWVyLCBDYXJzdGVu|https://orcid.org/0000-0002-1143-2103
1000 Hinweis
  • DeepGreen-ID: 0bb33203ff6847f1b30408b809d64334 ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 @id frl:6450716.rdf
1000 Erstellt am 2023-05-11T10:44:23.273+0200
1000 Erstellt von 322
1000 beschreibt frl:6450716
1000 Zuletzt bearbeitet 2023-10-21T03:56:03.101+0200
1000 Objekt bearb. Sat Oct 21 03:56:03 CEST 2023
1000 Vgl. frl:6450716
1000 Oai Id
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