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Refractory Statin-Induced Immune-Mediated Necrotizing Myositis: Challenges and Perils in Its Management
Chong Hsien Yeo1, Aziman Yaakub1, Margaret Choon Lee Wang1
1Department of Medicine, Raja Isteri Pengiran Anak Saleha Hospital, Bandar Seri Begawan, BRN.
Insights
This case report details a refractory statin-induced immune-mediated necrotizing myositis (IMNM) successfully treated with rituximab. However, long-term steroid therapy led to severe coronary artery disease, underscoring treatment challenges.
Area of Science:
- Immunology
- Neurology
- Pharmacology
Background:
- Statins (3-hydroxy-3-methylglutaryl-coenzyme A reductase inhibitors) are crucial for managing cardiovascular and cerebrovascular diseases.
- While generally safe, statins can rarely cause immune-mediated necrotizing myositis (IMNM), an autoimmune condition targeting muscle tissue.
Observation:
- A 55-year-old female with diabetes and hyperlipidemia developed refractory IMNM associated with statin use.
- The patient exhibited resistance to multiple immunosuppressive agents including prednisolone, methotrexate, azathioprine, and immunoglobulin.
Findings:
- Introduction of rituximab led to successful tapering of steroid dosage in the refractory IMNM case.
- Despite IMNM treatment success, the patient later developed severe coronary artery disease (CAD).
Implications:
- This case highlights the complex management of statin-induced IMNM, particularly in patients with pre-existing cardiovascular risk factors.
- Long-term immunosuppressive therapy, especially corticosteroids, poses significant risks, including cardiovascular complications like CAD, necessitating careful risk-benefit assessment.
Abstract:
Statin or 3-hydroxy-3-methylglutaryl-coenzyme A reductase (HMGCR) inhibitor is widely used and plays a vital role in the management of cardiovascular and cerebrovascular diseases. Statin is generally safe and its side effects are mostly mild and self-limiting. Immune-mediated necrotizing myositis (IMNM) is a rare and serious side effect characterized by the presence of anti-HMGCR inhibitor and myositis. Long-term immunosuppressive therapy is often required to manage it, and in refractory cases, the treatment can be very challenging. We report the case of a 55-year-old female with underlying diabetes mellitus and hyperlipidemia who developed refractory statin-induced IMNM despite being administered prednisolone, methotrexate, azathioprine, and immunoglobulin. After the introduction of rituximab, steroids were able to be tapered down to the lowest maintenance dose. Unfortunately, the patient subsequently succumbed to severe coronary artery disease (CAD) likely caused by the long-term steroid therapy, highlighting the difficulty and complications associated with the treatment of IMNM, especially in patients with cardiovascular risk factors.
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