Calcinosis biomarkers in and Juvenile Dermatomyositis. Autoimmunity reviews Chung, M. P., Richardson, C., Kirakossian, D., Orandi, A. B., Saketkoo, L. A., Rider, L. G., Schiffenbauer, A., von Muhlen, C. A., Chung, L., International Myositis Assessment, Clinical Studies Group (IMACS) Calcinosis Scientific Interest Group 2020: 102533


Dermatomyositis (DM) is a rare idiopathic inflammatory myopathy characterized by muscle weakness and cutaneous manifestations in adults and children. Calcinosis, a complication of DM, is the abnormal deposition of insoluble calcium salts in tissues, including skin, subcutaneous tissue, tendons, fascia, and muscle. Calcinosis is more commonly seen in juvenile DM (JDM), but also develops in adult DM. Although the mechanism of calcinosis remains unclear, several pathogenic hypotheses have been proposed, including intracellular accumulation of calcium secondary to an alteration of the cellular membrane by trauma and inflammation, local vascular ischemia, dysregulation of mechanisms controlling the deposition and solubility of calcium and phosphate, and mitochondrial damage of muscle cells. Identifying calcinosis biomarkers is important for early disease detection and risk assessment, and may lead to novel therapeutic targets for the prevention and treatment of DM-associated calcinosis. In this review, we summarize myositis autoantibodies associated with calcinosis in DM, histopathology and chemical composition of calcinosis, genetic and inflammatory markers that have been studied in adult DM and JDM-associated calcinosis, as well as potential novel biomarkers.

View details for DOI 10.1016/j.autrev.2020.102533

View details for PubMedID 32234404