Rituximab in the treatment of anti-HMGCR immune-mediated necrotizing myopathy: Two cases successfully treated

Abstract

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A](#j_rir-2025-0014_fig_001)). Anti-HMGCR antibodies were strongly positive on an enzyme-linked immunosorbent assay (ELISA) in both cases (315 and 402 U, respectively; reference range < 20 U). Initial treatment included high-dose intravenous steroids and IVIG followed by oral high-dose corticosteroids and MTX, with a rapid CK reduction and progressive improvement of muscle strength. However, CK and anti-HMGCR antibody levels remained elevated, and symptoms persisted, especially in case 1. In this patient a muscle biopsy was performed and discrete inhomogeneity in fibres calibre, nuclear intern

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Dear Editor,

Anti-HMGCR-positive myositis is an immune-mediated necrotizing myopathy (IMNM) characterized by the presence of antibodies directed against hydroxymethylglutaryl-CoA reductase (HMGCR), a key enzyme involved in cholesterol metabolism. Clinically, it presents with symmetric proximal muscle weakness, markedly elevated serum creatine kinase (CK) levels, abnormal findings on electromyography (EMG) and histopathological evidence of muscle fibre necrosis with macrophage infiltrate. A history of statins exposure is often reported, although the disease can also develop in statin-naïve individuals.^[1,2]^ Myositis persists even after drug discontinuation and requires immunosuppressive/immunomodulatory therapies, mainly represented by glucocorticoids, methotrexate (MTX) and high-dose intravenous immunoglobulins (IVIG).^[3]^ Although the response to treatment is generally good, some patients do not respond to initial therapy or relapse after steroid discontinuation. Rituximab (RTX) has been successfully used as second-line therapy, due to the putative pathogenic role of anti-HMGCR antibodies.^[4,5]^ Herein, we report two patients with anti-HMGCR-positive IMNM successfully treated with rituximab, in addition to standard therapy.

A 57-year-old man (case 1) and a 70-year-old woman (case 2) presented with progressive asthenia and limb muscle weakness. Both showed significantly elevated serum CK levels (12,946 and 11,344 U/L, respectively; reference range 39–308 U/L). Only case 2 had a history of statin use, but both had taken red yeast rice supplements prior to symptom onset. EMG revealed myositic and myopathic changes in both patients. In case 1, magnetic resonance image (MRI) was showed hyperintensities on FAT-suppressed images (Figure 1A). Anti-HMGCR antibodies were strongly positive on an enzyme-linked immunosorbent assay (ELISA) in both cases (315 and 402 U, respectively; reference range < 20 U). Initial treatment included high-dose intravenous steroids and IVIG followed by oral high-dose corticosteroids and MTX, with a rapid CK reduction and progressive improvement of muscle strength. However, CK and anti-HMGCR antibody levels remained elevated, and symptoms persisted, especially in case 1. In this patient a muscle biopsy was performed and discrete inhomogeneity in fibres calibre, nuclear internalizations, isolated nicotinamide adenine dinucleotide (NADH)-positive hypotrophic and diverse regenerating fibres, diffuse modest CD68 expression and increased expression of membrane attack complex (MAC) and major histocompatibility complex (MHC) class I on cellular surfaces in a picture of myopathic damage were found. For this reason, RTX therapy was proposed (1000 mg two weeks apart and then every 6 months for 3 times). Following RTX therapy, case 1 achieved full recovery, with normalization of CK, complete negativization of anti-HMGCR antibodies, resolution of MRI findings, and discontinuation of IVIG (Figure 1B, 2A-B). No adverse events occurred during and after treatment. Case 2 improved clinically, discontinued MTX and IVIG, and achieved reduction of anti-HMGCR antibody levels (Figure 2C-D). In this patient, a mild IgG1 deficiency occurred after RTX, without increased infections.

Anti-HMGCR myopathy is a rare subtype of IMNM.^[6,7]^ To date, prospective studies and randomized clinical trials specifically addressing the optimal therapeutic approach for this entity are limited. Anti-HMGCR antibody titres have been reported to correlate with disease severity, supporting a potential pathogenic role.^[8,9]^ Accordingly, B-cell depletion with RTX has emerged as a promising effective therapeutic strategy. However, published data on RTX efficacy in this subset of myopathies remain limited with currently no consensus regarding the optimal RTX protocol.^[10,11]^ In conclusion, the few retrospective studies published to date show substantial heterogeneity in the patient characteristics, treatment regimens, timing of RTX initiation, and biomarkers used to monitor response. Our findings contribute to the growing evidence supporting the use of RTX in anti-HMGCR-positive IMNM and emphasize the urgent need for prospective randomized clinical trials to evaluate its efficacy and safety in this context.