Longitudinal differences in iron deposition in periaqueductal gray matter and anterior cingulate cortex are associated with response to erenumab in migraine

被引:10
作者
Nikolova, Simona [1 ]
Chong, Catherine Daniela [1 ,2 ,3 ]
Dumkrieger, Gina M. [1 ]
Li, Jing [4 ]
Wu, Teresa [3 ,5 ]
Schwedt, Todd J. [1 ,3 ,6 ]
机构
[1] Mayo Clin, Dept Neurol, Phoenix, AZ USA
[2] Mayo Clin, Dept Physiol & Biomed Engn, Phoenix, AZ USA
[3] ASU Mayo Ctr Innovat Imaging, Tempe, AZ USA
[4] Georgia Tech, Sch Ind & Syst Engn, Atlanta, GA USA
[5] Arizona State Univ, Sch Comp Informat Decis Syst Engn, Tempe, AZ USA
[6] Mayo Clin, Dept Neurol, 5777 E Mayo Blvd, Phoenix, AZ 85054 USA
基金
美国国家卫生研究院;
关键词
Migraine; iron; magnetic resonance imaging; T2*; erenumab; calcitonin gene-related peptide; STATE FUNCTIONAL CONNECTIVITY; DEEP BRAIN NUCLEI; EPISODIC MIGRAINE; DESCENDING PAIN; DOUBLE-BLIND; MRI; HEADACHE; ABNORMALITIES; ACCUMULATION; RELAXATION;
D O I
10.1177/03331024221144783
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
ObjectivesThe objective of this longitudinal study was to determine whether brain iron accumulation, measured using magnetic resonance imaging magnetic transverse relaxation rates (T2*), is associated with response to erenumab for the treatment of migraine. MethodsParticipants (n = 28) with migraine, diagnosed using international classification of headache disorders 3rd edition criteria, were eligible if they had six to 25 migraine days during a four-week headache diary run-in phase. Participants received two treatments with 140 mg erenumab, one immediately following the pre-treatment run-in phase and a second treatment four weeks later. T2* data were collected immediately following the pre-treatment phase, and at two weeks and eight weeks following the first erenumab treatment. Patients were classified as erenumab responders if their migraine-day frequency at five-to-eight weeks post-initial treatment was reduced by at least 50% compared to the pre-treatment run-in phase. A longitudinal Sandwich estimator approach was used to compare longitudinal group differences (responders vs non-responders) in T2* values, associated with iron accumulation. Group visit effects were calculated with a significance threshold of p = 0.005 and cluster forming threshold of 250 voxels. T2* values of 19 healthy controls were used for a reference. The average of each significant region was compared between groups and visits with Bonferroni corrections for multiple comparisons with significance defined as p < 0.05. ResultsPre- and post-treatment longitudinal imaging data were available from 28 participants with migraine for a total of 79 quantitative T2* images. Average subject age was 42 +/- 13 years (25 female, three male). Of the 28 subjects studied, 53.6% were erenumab responders. Comparing longitudinal T2* between erenumab responders vs non-responders yielded two comparisons which survived the significance threshold of p < 0.05 after correction for multiple comparisons: the difference at eight weeks between the erenumab-responders and non-responders in the periaqueductal gray (mean +/- standard error; responders 43 +/- 1 ms vs non-responders 32.5 +/- 1 ms, p = 0.002) and the anterior cingulate cortex (mean +/- standard error; responders 50 +/- 1 ms vs non-responders 40 +/- 1 ms, p = 0.01). ConclusionsErenumab response is associated with higher T2* in the periaqueductal gray and anterior cingulate cortex, regions that participate in pain processing and modulation. T2* differences between erenumab responders vs non-responders, a measure of brain iron accumulation, are seen at eight weeks post-treatment. Less iron accumulation in the periaqueductal gray and anterior cingulate cortex might play a role in the therapeutic mechanisms of migraine reduction associated with erenumab.
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