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Abstract Details

Exploring Natural Cohorts of Chronic Migraine Phenotype
Headache
P4 - Poster Session 4 (5:30 PM-6:30 PM)
13-012

To identify naturally occurring clusters of chronic migraine patients, and to examine relationships among several chronic migraine clinical features.

 

 

Chronic migraine is a complex and heterogenous disorder involving varying degrees of clinical features. Unsupervised modeling methods may be useful to help obtain impressions in phenotypic subclassification of chronic migraine. 

Agglomerative hierarchical clustering analysis wasconducted to identify natural cohorts in 87 chronic migraine patients using 13 migraine related clinical variables. Principle component analysis was used to condense the 13 clinical variables to those explaining the largest variation. Association analysis between these clinical features was conducted; Benjamini-Hochberg procedure was used to correct for multiple testing at false discovery rate of 5%.  

 

Two major clusters were identified. Higher levels of self-efficacy and exercise were found in Cluster 1, while higher levels of depression, somatic symptoms, anxiety, pain catastrophizing, poor sleep quality, post-traumatic stress disorder, and migraine-related disability were found in Cluster 2. Similarly, principle component analysis revealed one major pattern of clinical features (eigenvalue 3.8) characterized by depression, somatic symptoms, anxiety, pain catastrophizing, poor sleep quality, migraine-related disability, and negatively loaded by self-efficacy and exercise levels. Exercise levels were significantly associated with pain self-efficacy (Benjamini-Hochberg p= 0.002), while negatively correlated with depression (p= 0.001), somatic symptoms (p= 0.014), migraine-related disability (p= 0.017), poor sleep quality (p= 0.019), and anxiety (p= 0.032).     

 

Chronic migraine patients can be classified into two major groups using clustering analysis. Chronic migraine patients with higher self-efficacy and exercise levels had lower depression, somatic symptoms, disability, sleep quality, and anxiety.
Authors/Disclosures
Yohannes W. Woldeamanuel, MD (Mayo Clinic Arizona)
PRESENTER
Dr. Woldeamanuel has received personal compensation in the range of $0-$499 for serving as a Consultant for Atheneum. Dr. Woldeamanuel has received personal compensation in the range of $0-$499 for serving as a Consultant for Research Square. The institution of Dr. Woldeamanuel has received research support from NINDS.
No disclosure on file
Addie Peretz, MD (Stanford University) Dr. Peretz has nothing to disclose.
Robert Cowan, MD, FAAN (Stanford Neurosciences Health Center) Dr. Cowan has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Lundbeck. Dr. Cowan has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Teva. Dr. Cowan has received personal compensation in the range of $5,000-$9,999 for serving as a Consultant for Abbvie. Dr. Cowan has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Lilly. Dr. Cowan has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Biohaven. Dr. Cowan has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for lundbeck. Dr. Cowan has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for biohavenn. Dr. Cowan has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Abbviie. Dr. Cowan has stock in Percept. Dr. Cowan has received intellectual property interests from a discovery or technology relating to health care. Dr. Cowan has received intellectual property interests from a discovery or technology relating to health care. Dr. Cowan has received publishing royalties from a publication relating to health care.