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Published on: August 11, 2021
Targeting MTHFR for the treatment of migraines
Innocenzo Rainero1, Alessandro Vacca1, Fausto Roveta1
1a Headache Center, Department of Neuroscience "Rita Levi Montalcini" , University of Torino , Torino , Italy.
Introduction:
Migraine is a common neurovascular disorder classified by the World Health Organization as one of the most debilitating diseases. Migraine is a complex disease and is a consequence of an interaction between genetic, epigenetic and environmental factors. The MTHFR gene is one of the few replicated genetic risk factors for migraine and encodes an enzyme that is crucial for the folate and the methionine cycles. Individuals carrying the T allele of the MTHFR C677T polymorphism have increased plasma concentrations of homocysteine which leads to endothelial cell injury and alterations in coagulant properties of blood. Areas covered: This review focuses on the recent advances in genetics and the role of the MTHFR gene and homocysteine metabolism in migraine etiopathogenesis. The article summarizes the potential of targeting MTHFR and homocysteine for disease prevention. Expert opinion: Determination of MTHFR C677T polymorphisms as well as measurement of homocysteine concentrations may be useful to migraine patients, particularly those suffering from migraine with aura. Preliminary studies support the use of folate, vitamin B6 and vitamin B12 for the prevention of migraine. However, the results of these studies await replication in larger randomized controlled clinical trials.
Insights
Migraine is linked to the MTHFR gene and elevated homocysteine levels. Targeting these factors, along with B vitamins, may help prevent debilitating migraine attacks.
Area of Science:
- Neuroscience
- Genetics
- Metabolic Disorders
Background:
- Migraine is a debilitating neurovascular disorder influenced by genetic, epigenetic, and environmental factors.
- The Methylenetetrahydrofolate reductase (MTHFR) gene plays a crucial role in folate and methionine metabolism.
- The MTHFR C677T polymorphism is a replicated genetic risk factor for migraine, associated with increased homocysteine.
Purpose of the Study:
- To review recent advances in the genetics of migraine.
- To elucidate the role of the MTHFR gene and homocysteine metabolism in migraine.
- To summarize the potential of targeting MTHFR and homocysteine for migraine prevention.
Main Methods:
- Literature review focusing on genetic and metabolic aspects of migraine.
- Analysis of the MTHFR gene's role in homocysteine metabolism.
- Synthesis of current research on MTHFR and homocysteine in migraine etiopathogenesis.
Main Results:
- Individuals with the MTHFR C677T T allele exhibit higher homocysteine, potentially causing endothelial damage.
- Elevated homocysteine levels are implicated in the altered coagulant properties of blood in migraine patients.
- Genetic variations in MTHFR and homocysteine metabolism are significant contributors to migraine.
Conclusions:
- MTHFR C677T genotyping and homocysteine measurement may benefit migraine patients, especially those with aura.
- Folate, vitamin B6, and vitamin B12 show preliminary promise for migraine prevention.
- Larger randomized controlled trials are needed to confirm the efficacy of MTHFR and homocysteine-targeted interventions.
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