4.6 Article

Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathology

Journal

ACTA NEUROPATHOLOGICA
Volume 141, Issue 6, Pages 917-927

Publisher

SPRINGER
DOI: 10.1007/s00401-021-02305-3

Keywords

Systemic sclerosis; Myositis; Capillary pathology; Large-scale electron microscopy

Funding

  1. Projekt DEAL

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Systemic sclerosis patients with muscle weakness were found to have a characteristic capillary pathology called minimal myositis with capillary pathology (MMCP) in approximately 67% of cases. This study used large-scale electron microscopy to reveal specific capillary morphology in skeletal muscles, introducing a new level of precision in ultrastructural analysis. The findings suggest a relatively homogeneous clinical picture among MMCP patients, with milder disease and specific patterns of organ involvement.
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.

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