Mitochondrial dysfunction and migraine: evidence and hypotheses

Cephalalgia. 2006 Apr;26(4):361-72. doi: 10.1111/j.1468-2982.2005.01059.x.


The molecular basis of migraine is still not completely understood. An impairment of mitochondrial oxidative metabolism might play a role in the pathophysiology of this disease, by influencing neuronal information processing. Biochemical assays of platelets and muscle biopsies performed in migraine sufferers have shown a decreased activity of the respiratory chain enzymes. Studies with phosphorus magnetic resonance spectroscopy ((31)P-MRS) have demonstrated an impairment of the brain oxidative energy metabolism both during and between migraine attacks. However, molecular genetic studies have not detected specific mitochondrial DNA (mtDNA) mutations in patients with migraine, although other studies suggest that particular genetic markers (i.e. neutral polymorphisms or secondary mtDNA mutations) might be present in some migraine sufferers. Further studies are still needed to clarify if migraine is associated with unidentified mutations on the mtDNA or on nuclear genes that code mitochondrial proteins. In this paper, we review morphological, biochemical, imaging and genetic studies which bear on the hypothesis that migraine may be related to mitochondrial dysfunction at least in some individuals.

Publication types

  • Review

MeSH terms

  • Animals
  • Comorbidity
  • DNA, Mitochondrial / genetics*
  • Genetic Predisposition to Disease / epidemiology
  • Genetic Predisposition to Disease / genetics
  • Humans
  • Migraine Disorders / epidemiology*
  • Migraine Disorders / genetics*
  • Mitochondrial Diseases / epidemiology*
  • Mitochondrial Diseases / genetics*


  • DNA, Mitochondrial