Objective: Calcitonin-gene-related-peptide monoclonal antibodies (CGRP-MABs) are newly-introduced but widelyused treatments for migraine. We aimed to characterize some predictors of clinical response to CGRP-MABs.
Methods:This was a retrospective chart review of patients started on CGRP-MABs at our academic headache practice in a 3 year-period. All patients met the criteria for migraine with or without aura, and/or chronic migraine as per the international headache classification ICHD-III.We collected demographics, migraine characteristics, phenotypical features of the headache, and response to CGRP-MABs. Responders had a 50% or more reduction in headache days. We performed multi-variate analyses and a logistic regression model to determine if any baseline characteristics or phenotypical features aided in predicting CGRP-MAB response.Results: 76 subjects were enrolled, 82% female (63/76), with a mean age of 40.2 ± 13.1. We had 64% (49/76) of the patients experience a response. Having autonomic symptoms (such as lacrimation, rhinorrhea, congestion) was associated with lower likelihood of response to CGRP MABs (OR 0.12, 95% CI [0.02 to 0.60, p = 0.015]), as was increased age with a lower effect size (OR 0.94 95% CI [0.88-0.99], p = 0.020). Increased BMI was not statistically significant as a predictor although there may have been a trend towards and effect (OR 0.40 95% CI [0.11-1.33], p = 0.142).
Conclusions:The presence of autonomic symptoms in migraine headaches may predict lack of response to CGRP-MABs. This study is limited by the small sample size. However, it is biologically plausible that presence of autonomic features is predictive of a decreased response to CGRP MABs as migraine patients with autonomic symptoms have higher levels of VIP correlated to this, and not CGRP(3). Our study raises the possibility that migraines with autonomic features may be at least in part VIP driven. Larger prospective studies are needed to confirm these findings.