A review of myositis in the NEJM, authored by two French experts

In line with their research over several decades and the advances they have already spearheaded, Professors Olivier Benveniste and Yves Allenbach (the Inflammatory Myopathies & Innovative Targeted Therapies team at the Center for Research in Myology of the Institute of Myology) have published a review on inflammatory myopathies in the New England Journal of Medicine, in which they advocate:

  • the adoption of a clinical-serological classification of myositis, in which autoantibodies (present in around 70 per cent of patients) are no longer a secondary parameter but a key element in establishing the diagnosis of myositis, identifying its type and assessing the prognosis;
  • the existence of five main types of myositis: immune-mediated necrotising myopathy, inclusion body myositis, dermatomyositis, antisynthetase syndrome and myositis overlapping with other autoimmune diseases, the latter three being systemic;
  • the virtual disappearance of polymyositis, with the majority of cases actually being inclusion body myositis, immune-mediated necrotising myopathy, antisynthetase syndrome or myositis overlapping with other autoimmune diseases;
  • the implementation of increasingly personalised treatments, made possible by improved understanding of the mechanisms underlying the various forms of myositis.

 

Inflammatory Myopathies. Allenbach Y, Benveniste O. N Engl J Med. 2026 May 14;394(19):1925-1938.