Blood pressure elevation in erenumab-treated patients with migraine: A retrospective real-world experience

被引:10
|
作者
Chhabra, Nikita [1 ]
Mead-Harvey, Carolyn [2 ]
Dodoo, Christopher A. [2 ]
Iser, Courtney [3 ]
Taylor, Hallie [1 ]
Chaudhary, Hira [1 ]
Vanood, Aimen [1 ]
Dodick, David W. [1 ]
机构
[1] Mayo Clin, Dept Neurol, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Dept Quantitat Hlth Sci, Scottsdale, AZ USA
[3] Mercy Clin, Dept Neurol, Oklahoma City, OK USA
来源
HEADACHE | 2024年 / 64卷 / 03期
关键词
calcitonin gene-related peptide; hypertension; migraine; SAFETY; CGRP;
D O I
10.1111/head.14679
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
BackgroundErenumab is a monoclonal antibody that targets the calcitonin gene-related peptide (CGRP) receptor and is approved for the preventative treatment of migraine in adults. CGRP is involved in the regulation of vasomotor tone under physiologic and pathologic conditions, including hypertension. While there has not been evidence of hypertension in preclinical models or clinical trials, post-marketing data suggest erenumab may be associated with hypertension. This led to a warning in the United States Food and Drug Administration prescribing information for erenumab.ObjectiveTo determine the frequency of worsening blood pressure (BP) after initiation of erenumab in patients with migraine and how this is associated with hypertension.MethodsThis is an observational retrospective cohort study evaluating patients at a tertiary headache or neurology department. Systolic and diastolic BPs were compared between the initial visit prior to initiation of erenumab, and follow-up visit while on erenumab. Worsening BP was defined as moving from a lower stage to a higher stage of BP, as defined by the American Heart Association. Serious adverse vascular events were also recorded.ResultsA total of 335 patients were included in the final analysis (mean [SD] age of 45.7 [14.40] years, 83.9% [281/335] female). At baseline, 20.9% (70/335) of patients had a prior diagnosis of hypertension. The median (interquartile range) time to follow-up appointment from initial appointment was 20.5 (13.3-35.3) weeks. The mean (SD) BP at baseline was systolic 124.7 (15) mmHg and diastolic 77 (11) mmHg, and at follow-up was systolic 124.0 (15) mmHg and diastolic 77.8 (9) mmHg. Overall, 23.3% (78/335) of all patients had worsening BP, whereas 13/225 (3.9%) patients had improvement in their BP. Patients with atrial fibrillation were more likely to develop worsening BP (odds ratio, 4.9, 95% confidence interval 1.12-21.4; p = 0.035). There was no association between worsening BP and pre-existing hypertension, sex, body mass index, or age. One patient had non-ST elevation myocardial infarction attributed to a hypertensive emergency while on erenumab.ConclusionWe found that 23.3% of patients initiated on erenumab may have developed worsening BP, suggesting the need for BP monitoring in patients initiated on erenumab. This study aimed to determine how often blood pressure (BP) increases in patients with migraine after initiation of erenumab, a migraine preventative treatment. We compared patients' BP before starting erenumab versus while on erenumab. We found that nearly a quarter of patients developed higher BP, suggesting the need for BP monitoring in patients taking erenumab.
引用
收藏
页码:233 / 242
页数:10
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