Lo Castro Flavia, Bonini Niccolò, Iannone Luigi Francesco, Boccalini Alberto, Brovia Daria, Pani Luca, Boriani Giuseppe, Guerzoni Simona
Digital and Predictive Medicine, Pharmacology and Clinical Metabolic Toxicology-Headache Center and Drug Abuse-Laboratory of Clinical Pharmacology and Pharmacogenomics, AOU Policlinico di Modena, Modena, Italy.
Cardiology Division, AOU Policlinico di Modena, Modena, Italy.
Eur J Neurol. 2025 Sep;32(9):e70351. doi: 10.1111/ene.70351.
Migraine is associated with an increased cardiovascular risk, including hypertension. Anti-calcitonin gene related peptide (CGRP) monoclonal antibodies (mAbs) are effective preventive treatments, but concerns have been raised about their potential hypertensive effects. Herein, we assess the early changes in blood pressure (BP) during anti-CGRP mAbs treatment in patients with migraine using 24-h Holter monitoring.
We conducted a prospective, real-world study including 20 patients with episodic migraine (EM) during the early treatment with anti-CGRP mAbs. Participants underwent 24-h Holter BP monitoring before treatment and 4 weeks after the first injection. The primary outcome was the change in mean systolic BP (SBP). Secondary outcomes included changes in diastolic BP (DBP), differential BP, diurnal/nocturnal values, heart rate (HR), and dipping patterns.
Mean 24-h SBP and DBP showed non-significant differences after treatment (-2.4 mmHg and -1.8 mmHg, p = 0.075). No significant changes were observed in diurnal BP, but a significant reduction in nocturnal DBP was detected (-2.6 mmHg, p = 0.026). Consistently, the proportion of patients with a physiological dipping profile increased from 45.0% to 85.0% post-treatment (p = 0.008). HR remained unchanged, and no patients had mean PAD ≥ 130/80. No adverse events were reported.
Anti-CGRP mAbs did not induce clinically relevant BP increases in the early treatment phase and were associated with improved nocturnal DBP and a favorable shift in dipping profile in patients with EM. These findings suggest the short-term cardiovascular safety of anti-CGRP mAbs, though further studies with larger cohorts and longer follow-up are warranted.
偏头痛与包括高血压在内的心血管风险增加有关。抗降钙素基因相关肽(CGRP)单克隆抗体(mAbs)是有效的预防性治疗药物,但人们对其潜在的高血压作用表示担忧。在此,我们使用24小时动态心电图监测评估偏头痛患者在抗CGRP mAbs治疗期间血压(BP)的早期变化。
我们进行了一项前瞻性的真实世界研究,纳入20例发作性偏头痛(EM)患者,在其接受抗CGRP mAbs早期治疗期间进行观察。参与者在治疗前和首次注射后4周接受24小时动态血压监测。主要结局是平均收缩压(SBP)的变化。次要结局包括舒张压(DBP)变化、血压差值、昼夜/夜间血压值、心率(HR)和血压波动模式。
治疗后24小时平均SBP和DBP无显著差异(分别为-2.4 mmHg和-1.8 mmHg,p = 0.075)。日间血压无显著变化,但夜间DBP显著降低(-2.6 mmHg,p = 0.026)。一致的是,生理性血压波动模式的患者比例从治疗前的45.0%增加到治疗后的85.0%(p = 0.008)。HR保持不变,且没有患者的平均血压差值≥130/80。未报告不良事件。
抗CGRP mAbs在早期治疗阶段未引起临床上相关的血压升高,且与EM患者夜间DBP改善及血压波动模式的有利变化相关。这些发现提示抗CGRP mAbs的短期心血管安全性,不过仍需要更大样本量和更长随访时间的进一步研究。