# Statin-Induced Necrotizing Autoimmune Myositis Presenting With Progressive Limb-Girdle Weakness Following Low-Dose Atorvastatin Use

**Authors:** Layla Annous, Osama Mahmoud

PMC · DOI: 10.7759/cureus.102783 · Cureus · 2026-02-01

## TL;DR

A 72-year-old man developed a rare muscle disease after low-dose statin use, requiring aggressive treatment for recovery.

## Contribution

First documented case of SINAM associated with low-dose atorvastatin.

## Key findings

- SINAM can occur with low-dose atorvastatin, not just high doses.
- Anti-HMGCR antibodies confirmed the diagnosis in this patient.
- IVIG was effective in improving function after initial treatments failed.

## Abstract

Statins are a mainstay in the prevention of cardiovascular disease and are associated with rare adverse effects, including statin-induced necrotizing autoimmune myositis (SINAM). This condition is characterized by progressive, symmetric, proximal muscle weakness and elevated creatine kinase (CK), persisting despite discontinuation of the statin, and is confirmed by the presence of anti-HMG-CoA reductase (HMGCR) antibodies. We present a case of a 72-year-old male who presented with three months of progressive limb-girdle weakness with chronic use of low-dose atorvastatin (10 mg). Our review of the literature suggests that this is the first documented case of SINAM in the setting of low-dose atorvastatin usage. Diagnosis was confirmed by anti-HMGCR antibodies. The patient was initially managed with corticosteroids and methotrexate but required escalation to intravenous immunoglobulin (IVIG), which led to functional improvement. This case underscores the need for high clinical suspicion for SINAM and highlights the importance of consideration for early aggressive immunosuppression.

## Linked entities

- **Proteins:** HMG1 (hydroxy methylglutaryl CoA reductase 1), HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase)
- **Chemicals:** atorvastatin (PubChem CID 60823), methotrexate (PubChem CID 4112)
- **Diseases:** cardiovascular disease (MONDO:0004995)

## Full-text entities

- **Genes:** PCAT2 (prostate cancer associated transcript 2) [NCBI Gene 103164619] {aka CARLO4, CARLo-4, PCA2, TCONS_00015167}, RNPC3 (RNA binding region (RNP1, RRM) containing 3) [NCBI Gene 55599] {aka CPHD7, IGHD5, RBM40, RNP, SNRNP65}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, AMPH (amphiphysin) [NCBI Gene 273] {aka AMPH1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, HMGCR (3-hydroxy-3-methylglutaryl-CoA reductase) [NCBI Gene 3156] {aka LDLCQ3, LGMDR28, MYPLG}, TRIM21 (tripartite motif containing 21) [NCBI Gene 6737] {aka RNF81, RO52, Ro/SSA, SSA, SSA1, TRIM21/Ro52}, PCAT1 (prostate cancer associated transcript 1) [NCBI Gene 100750225] {aka PCA1, PCAT-1, PiHL}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, SSB (small RNA binding exonuclease protection factor La) [NCBI Gene 6741] {aka LARP3, La, La/SSB, SSB/La}, DPYSL5 (dihydropyrimidinase like 5) [NCBI Gene 56896] {aka CRAM, CRMP-5, CRMP5, CV2, RTSC4, Ulip6}, KLK3 (kallikrein related peptidase 3) [NCBI Gene 354] {aka APS, KLK2A1, PSA, hK3}, CMPK1 (cytidine/uridine monophosphate kinase 1) [NCBI Gene 51727] {aka CK, CMK, CMPK, UMK, UMP-CMPK, UMPK}
- **Diseases:** atrophy (MESH:D001284), edema (MESH:D004487), Sjogren's syndrome (MESH:D012859), Cancer (MESH:D009369), sensory deficits (MESH:D012678), -Girdle Weakness (MESH:D018908), muscle (MESH:D019042), inflammation (MESH:D007249), trauma (MESH:D014947), SLE (MESH:D008180), Paraneoplastic (MESH:D010257), dermatomyositis (MESH:D003882), systemic sclerosis (MESH:D012595), PE (MESH:D011655), respiratory distress (MESH:D012128), fatiguability (MESH:D005221), Myositis (MESH:D009220), IMNM (MESH:C567355), Limb-Girdle Weakness (MESH:D049288), autoimmune antibody (MESH:D001327), toxicity (MESH:D064420), polymyositis (MESH:D017285), DVT (MESH:D020246), cardiovascular disease (MESH:D002318), connective tissue disease (MESH:D003240), Hypothyroid myopathy (MESH:D007037), hypertension (MESH:D006973), atrial flutter (MESH:D001282), Dysphagia (MESH:D003680), rhabdomyolysis (MESH:D012206), thrombotic (MESH:D013927), functional impairment (MESH:D003072), Autoimmune Myositis (MESH:D020721), lower extremity weakness (MESH:D020335), muscular necrosis (MESH:D009336), muscle fiber necrosis (MESH:D009135), thromboembolic (MESH:D013923), sensory loss (MESH:C580162), coronary artery disease (MESH:D003324), myalgia (MESH:D063806)
- **Chemicals:** azathioprine (MESH:D001379), mycophenolate mofetil (MESH:D009173), apixaban (MESH:C522181), metformin (MESH:D008687), methotrexate (MESH:D008727), hydrochlorothiazide (MESH:D006852), rituximab (MESH:D000069283), Atorvastatin (MESH:D000069059), T4 (MESH:D013974), alcohol (MESH:D000438), lipid (MESH:D008055), prednisone (MESH:D011241), steroid (MESH:D013256)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

19 references — full list in the complete paper: https://tomesphere.com/paper/PMC12955321/full.md

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Source: https://tomesphere.com/paper/PMC12955321