Shared genetics in epilepsy and migraine: A scoping review
Prachi Sahu1, Anjana Munshi1, Gagandeep Singh2,3
1Department of Human Genetics and Molecular Medicine, Central University of Punjab, Bathinda, India.
Epileptic Disorders : International Epilepsy Journal with Videotape
|December 17, 2025
Summary
Migraine and epilepsy share genetic links, increasing occurrence in affected individuals. Further research into shared genetic susceptibility is crucial for understanding these neurological disorders.
Area of Science:
- Neurology
- Genetics
Background:
- Migraine and epilepsy are distinct neurological disorders with overlapping prevalence.
- Clinical, mechanistic, and genetic studies suggest a convergence between migraine and epilepsy.
- Both conditions exhibit higher co-occurrence in families and individuals than expected by chance.
Purpose of the Study:
- To investigate the shared genetic susceptibility between migraine and epilepsy.
- To understand the common mechanisms underlying the co-occurrence of these neurological disorders.
- To explore the genetic basis of both conditions individually and collectively.
Main Methods:
- Review of clinical, mechanistic, and genetic studies.
- Analysis of polygenic bases for common epilepsies and migraines.
- Examination of rare monogenic disorders like familial hemiplegic migraine with seizure features.
Main Results:
- Migraine is more frequent in epilepsy patients, and vice versa.
- Common forms of both disorders have polygenic inheritance.
- Familial hemiplegic migraine can present with seizures and epilepsy, though not universally.
Conclusions:
- Shared genetic factors likely contribute to the co-occurrence of migraine and epilepsy.
- Further investigation into shared genetic bases is warranted, utilizing advanced computational and genetic approaches.
- Functional studies in monogenic familial hemiplegic migraine cases are needed to elucidate shared mechanisms.
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