Anti-MDA5 Amyopathic Dermatomyositis-A Diagnostic and Therapeutic Challenge.
Anca BobircăCristina AlexandruAnca Emanuela MusetescuFlorin BobircaAnca Teodora FlorescuMaria-Magdalena ConstantinTiberiu TebeicaAlesandra FlorescuSebastian IsacMihai BojincaIoan AncutaPublished in: Life (Basel, Switzerland) (2022)
Clinically amyopathic Dermatomyositis (CADM) is a rare subtype of idiopathic inflammatory myositis, associated with no muscular manifestations, which is more frequent in Asian women. Anti-melanoma differentiation-associated gene 5 (MDA5) antibodies are a recently discovered type of specific autoantibodies associated with myositis. The anti-MDA5 DM was initially described in Japan and later it was discovered that the target antigen was a protein implicated in the innate immune response against viruses, that is encoded by the melanoma differentiation-associated gene 5. Anti-MDA5 DM is characteristically associated with distinguished mucocutaneus and systemic manifestations, including skin ulcerations, palmar papules, arthritis, and interstitial-lung disease. Patients with anti-MDA5 positivity have a high risk of developing rapid progressive interstitial-lung disease (RP-ILD), with a poor outcome. As a result, despite high mortality, diagnosis is often delayed, necessitating increased awareness of this possible condition. Despite a severe course of lung disease and an increased mortality rate, there is currently no standard treatment. Recent insights based on observational studies and case reports support combined therapy with immunosuppressive drugs and corticotherapy, as soon as the symptoms appear. The aim of this paper is to describe anti-MDA5 DM, focusing on the recent literature about the unique clinical manifestations and therapeutic options, starting from a severe clinical case diagnosed in our Rheumatology Department.
Keyphrases
- interstitial lung disease
- systemic sclerosis
- rheumatoid arthritis
- idiopathic pulmonary fibrosis
- breast cancer cells
- immune response
- cell cycle arrest
- stem cells
- multiple sclerosis
- copy number
- systematic review
- disease activity
- drug induced
- systemic lupus erythematosus
- dna methylation
- cell death
- pregnant women
- glycemic control
- type diabetes
- polycystic ovary syndrome
- soft tissue
- bone marrow
- cell proliferation
- transcription factor
- adipose tissue
- weight loss
- coronary artery disease
- quantum dots
- pregnancy outcomes