| Literature DB >> 35391603 |
Manuela Stella1,2, Erica Biassoni3,4,5, Chiara Fiorillo4,6, Marina Grandis4,5, Francesca Mattioli7,8, Massimo Del Sette5.
Abstract
Inflammatory myopathies, including immune-mediated necrotizing myopathy (IMNM), are a rare and heterogeneous group of autoimmune diseases which can even involve extramuscular districts and seriously impact patients' quality of life. We report the case of a 76-year-old woman who developed muscle weakness, fatigue, and increased CK, following treatment with dapagliflozin, a sodium/glucose co-transporter 2 (SGLT2) inhibitor, and metformin. Neurophysiology, muscle biopsy, and antibody dosage confirmed the diagnosis of IMNM. The temporal correlation between the onset of clinical manifestations and the increase in the dosage of antidiabetic drugs, the improvement of symptoms with the dechallenge of dapagliflozin, and the exclusion of other possible causes triggering myopathy suggests that this may be the first case of dapagliflozin-induced myopathy, different from the former one associated with the use of SGLT2 inhibitors.Entities:
Keywords: Anti-HMGCR antibodies; Dapagliflozin; Drug-induced myopathy; IMNM
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Year: 2022 PMID: 35391603 DOI: 10.1007/s10072-022-06046-3
Source DB: PubMed Journal: Neurol Sci ISSN: 1590-1874 Impact factor: 3.307