The genetics and chronobiology of cluster headache

Author:

Belin Andrea Carmine1ORCID,Barloese Mads Christian23

Affiliation:

1. Centre for Cluster Headache, Department of Neuroscience, Karolinska Institutet, Stockholm, Sweden

2. Department of Functional and Diagnostic Imaging, Hvidovre Hospital, Hvidovre, Denmark

3. Danish Headache Center, Department of Neurology, Rigshospitalet-Glostrup, University of Copenhagen, Glostrup, Denmark

Abstract

Background/Hypothesis Cluster headache displays uniquely rhythmic patterns in its attack manifestation. This strong chronobiological influence suggests that part of the pathophysiology of cluster headache is distinctly different from migraine and has prompted genetic investigations probing these systems. Methods This is a narrative overview of the cluster headache chronobiological phenotype from the point of view of genetics covering existing knowledge, highlighting the specific challenges in cluster headache and suggesting novel research approaches to overcome these. Results The chronobiological features of cluster headache are a hallmark of the disorder and while discrepancies between study results do exist, the main findings are highly reproducible across populations and time. Particular findings in subgroups indicate that the heritability of the disorder is linked to chronobiological systems. Meanwhile, genetic markers of circadian rhythm genes have been implicated in cluster headache, but with conflicting results. However, in two recently published genome wide association studies two of the identified four loci include genes with an involvement in circadian rhythm, MER proto-oncogene, tyrosine kinase and four and a half LIM domains 5. These findings strengthen the involvement of circadian rhythm in cluster headache pathophysiology. Conclusion/Interpretation Studying chronobiology and genetics in cluster headache presents challenges unique to the disorder. Researchers are overcoming these challenges by pooling various data from different cohorts and performing meta-analyses providing novel insights into a classically enigmatic disorder. Further progress can likely be made by combining deep pheno- and genotyping.

Funder

Swedish Brain Foundation

The Mellby Gård Foundation

Publisher

SAGE Publications

Subject

Neurology (clinical),General Medicine

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