Myasthenia gravis following statin therapy: evidence from target trial emulation and self-controlled case series study

Nat Commun. 2024 Nov 28;15(1):10317. doi: 10.1038/s41467-024-54097-1.

Abstract

Several international pharmacovigilance agencies have issued warnings regarding the potential risk of myasthenia gravis (MG) following statin therapy. Our study investigated this association using population-based electronic health records in Hong Kong. We conducted a sequence of target trial emulation (TTE) for interpersonal comparison and a self-controlled case series (SCCS) study for intrapersonal comparison. In the TTE for MG onset, the incidence rates (per 100,000 person-years) and adjusted HRs were 51.91(31.80, 84.74)[HR:6.11 (3.73, 10.01)] in month 1, 16.27(9.81, 26.99)[HR:1.92(1.15, 3.19) in months 2-4, and 15.27(9.05, 25.79)[HR:1.80(1.06, 3.04)] in months 5-7. For risk of exacerbation, the adjusted HRs were 10.69(5.48, 20.84) in month 1, 1.50(0.55, 4.06) in months 2-4, and 2.79(1.33, 5.84) in months 5-7. No increased risks were found during the subsequent 18 months. A similar pattern was observed in SCCS analysis. Our findings recommend a minimum monitoring period of approximately six months for MG symptoms for patients starting using statin.

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Electronic Health Records
  • Female
  • Hong Kong / epidemiology
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / adverse effects
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / therapeutic use
  • Incidence
  • Male
  • Middle Aged
  • Myasthenia Gravis* / chemically induced
  • Myasthenia Gravis* / drug therapy
  • Myasthenia Gravis* / epidemiology
  • Risk Factors

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors