Carter Sarah C, Cucchiara Brett, Reehal Navpreet, Hamilton Katherine, Kaiser Eric A, Favilla Christopher G
Department of Neurology, University of Pennsylvania, Philadelphia, PA, United States.
Front Neurol. 2024 Apr 29;15:1399792. doi: 10.3389/fneur.2024.1399792. eCollection 2024.
Calcitonin gene-related peptide (CGRP) plays an important role in cerebral vasodilation, so here we aim to quantify the impact of CGRP monoclonal antibody (mAb) therapy on cerebral hemodynamics.
In 23 patients with chronic and episodic migraine, cerebral hemodynamic monitoring was performed (1) prior to and (2) 3-months into CGRP-mAb therapy. Transcranial Doppler monitored cerebral blood flow velocity (CBFv) in the middle cerebral artery (MCA) and posterior cerebral artery (PCA), from which cerebrovascular reactivity (CVR) and cerebral autoregulation (CA; ) were calculated.
CA was similar off and on treatment, in the MCA ( = 0.42) and PCA ( = 0.72). CVR was also unaffected by treatment, in the MCA ( = 0.38) and PCA ( = 0.92). CBFv and blood pressure were also unaffected. The subgroup of clinical responders (>50% reduction in migraine frequency) exhibited a small reduction in MCA-CBFv (6.0 cm/s; IQR: 1.1-12.4; = 0.007) and PCA-CBFv (8.9 cm/s; IQR: 6.9-10.3; = 0.04).
Dynamic measures of cerebrovascular physiology were preserved after 3 months of CGRP-mAb therapy, but a small reduction in CBFv was observed in patients who responded to treatment. Subgroup findings should be interpreted cautiously, but further investigation may clarify if CBFv is dependent on the degree of CGRP inhibition or may serve as a biomarker of drug sensitivity.
降钙素基因相关肽(CGRP)在脑血管舒张中起重要作用,因此我们旨在量化CGRP单克隆抗体(mAb)治疗对脑血流动力学的影响。
对23例慢性发作性偏头痛患者进行脑血流动力学监测,(1)在CGRP - mAb治疗前,(2)治疗3个月后。经颅多普勒监测大脑中动脉(MCA)和大脑后动脉(PCA)的脑血流速度(CBFv),并据此计算脑血管反应性(CVR)和脑自动调节功能(CA)。
治疗前后,MCA( = 0.42)和PCA( = 0.72)的CA相似。治疗对CVR也无影响,MCA( = 0.38)和PCA( = 0.92)均如此。CBFv和血压也未受影响。临床有反应的亚组(偏头痛发作频率降低> 50%)的MCA - CBFv有小幅降低(6.0 cm/s;四分位间距:1.1 - 12.4; = 0.007),PCA - CBFv也有小幅降低(8.9 cm/s;四分位间距:6.9 - 10.3; = 0.04)。
CGRP - mAb治疗3个月后,脑血管生理的动态指标得以保留,但在有治疗反应的患者中观察到CBFv有小幅降低。亚组研究结果应谨慎解读,但进一步研究可能会阐明CBFv是否依赖于CGRP抑制程度,或是否可作为药物敏感性的生物标志物。