Successful treatment of a patient with mitochondrial myopathy with alirocumab

J Clin Lipidol. 2020 Sep-Oct;14(5):646-648. doi: 10.1016/j.jacl.2020.07.007. Epub 2020 Jul 24.

Abstract

A 48-year-old man presented to our lipid clinic with statin intolerance and elevated serum creatine kinase levels, being affected by mitochondrial myopathy because of heteroplasmic mitochondrial DNA missense mutation in MTCO1 gene (m.7671T>A). He had just been treated with a coronary artery bypass 4 years before because of acute coronary syndrome, and he had consistently high levels of both low-density lipoprotein cholesterol and triglycerides. Dyslipidemia was successfully treated using 75 mg of alirocumab subcutaneously every 2 weeks, 10 mg of ezetimibe daily, 2 g of marine omega-3 fatty acids daily, and 145 mg of micronized fenofibrate every 2 days. Although muscle weakness persisted, myalgia did not reoccur and serum creatine kinase levels remained almost stable over the time.

Keywords: Alirocumab; Hypercholesterolemia; Mitochondrial myopathy; PCSK9 inhibitor.

Publication types

  • Case Reports

MeSH terms

  • Antibodies, Monoclonal, Humanized / therapeutic use*
  • Electron Transport Complex IV / genetics
  • Electron Transport Complex IV / metabolism
  • Humans
  • Hyperlipidemias / drug therapy*
  • Hyperlipidemias / metabolism
  • Hyperlipidemias / pathology
  • Male
  • Middle Aged
  • Mitochondrial Myopathies / drug therapy*
  • Mitochondrial Myopathies / metabolism
  • Mitochondrial Myopathies / pathology
  • Mutation, Missense
  • Prognosis

Substances

  • Antibodies, Monoclonal, Humanized
  • Electron Transport Complex IV
  • cytochrome c oxidase subunit I, human
  • alirocumab