Key result
Chronic αCGRP antagonism may blunt exercise-induced cardioprotection, preclinical evidence suggests.
Why the study?
The cardiovascular protective effects of exercise are mediated by αCGRP, but the cardiovascular safety of long-term αCGRP antagonism in patients with cardiovascular diseases remains unestablished.
αCGRP appears to mediate the cardiovascular benefits of exercise, raising theoretical safety concerns regarding the long-term use of CGRP antagonists for migraine in patients with cardiovascular disease.
Raises theoretical safety concerns for chronic CGRP antagonism in cardiovascular patients; leaves open clinical translation of preclinical exercise benefits.
Regular physical activity exerts cardiovascular protective effects in healthy individuals and those with chronic cardiovascular diseases. Exercise is accompanied by an increased plasma concentration of α-calcitonin gene-related peptide (αCGRP), a 37-amino acid peptide with vasodilatory effects and causative roles in migraine. Moreover, mouse models revealed that loss of αCGRP disrupts physiological adaptation of the cardiovascular system to exercise in normotension and aggravates cardiovascular impairment in primary chronic hypertension, both can be reversed by αCGRP administration. This suggests that αCGRP agonists could be a therapeutic option to mediate the cardiovascular protective effects of exercise in clinical setting where exercise is not possible or contraindicated. Of note, FDA has recently approved αCGRP antagonists for migraine prophylaxis therapy, however, the cardiovascular safety of long-term anti-CGRP therapy in individuals with cardiovascular diseases has yet to be established. Current evidence from preclinical models suggests that chronic αCGRP antagonism may abolish the cardiovascular protective effects of exercise in both normotension and chronic hypertension.
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Skaria et al. (2022) conducted a review in Cardiovascular diseases and migraine. α-Calcitonin Gene-Related Peptide (αCGRP) signaling and exercise was evaluated. Preclinical evidence suggests exercise-induced αCGRP signaling mediates cardiovascular protection, raising concerns that chronic αCGRP antagonism for migraine may abolish these benefits.
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