Imaging the inflammatory phenotype in migraine

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Standard

Imaging the inflammatory phenotype in migraine. / Christensen, Rune Häckert; Gollion, Cédric; Amin, Faisal Mohammad; Moskowitz, Michael A.; Hadjikhani, Nouchine; Ashina, Messoud.

I: Journal of Headache and Pain, Bind 23, Nr. 1, 60, 2022.

Publikation: Bidrag til tidsskriftReviewForskningfagfællebedømt

Harvard

Christensen, RH, Gollion, C, Amin, FM, Moskowitz, MA, Hadjikhani, N & Ashina, M 2022, 'Imaging the inflammatory phenotype in migraine', Journal of Headache and Pain, bind 23, nr. 1, 60. https://doi.org/10.1186/s10194-022-01430-y

APA

Christensen, R. H., Gollion, C., Amin, F. M., Moskowitz, M. A., Hadjikhani, N., & Ashina, M. (2022). Imaging the inflammatory phenotype in migraine. Journal of Headache and Pain, 23(1), [60]. https://doi.org/10.1186/s10194-022-01430-y

Vancouver

Christensen RH, Gollion C, Amin FM, Moskowitz MA, Hadjikhani N, Ashina M. Imaging the inflammatory phenotype in migraine. Journal of Headache and Pain. 2022;23(1). 60. https://doi.org/10.1186/s10194-022-01430-y

Author

Christensen, Rune Häckert ; Gollion, Cédric ; Amin, Faisal Mohammad ; Moskowitz, Michael A. ; Hadjikhani, Nouchine ; Ashina, Messoud. / Imaging the inflammatory phenotype in migraine. I: Journal of Headache and Pain. 2022 ; Bind 23, Nr. 1.

Bibtex

@article{08238920e5d440eaa83cf4149e878a9b,
title = "Imaging the inflammatory phenotype in migraine",
abstract = "Several preclinical and clinical lines of evidence suggest a role of neuroinflammation in migraine. Neuroimaging offers the possibility to investigate and localize neuroinflammation in vivo in patients with migraine, and to characterize specific inflammatory constituents, such as vascular permeability, and macrophage or microglia activity. Despite all imaging data accumulated on neuroinflammation across the past three decades, an overview of the imaging evidence of neuroinflammation in migraine is still missing. We conducted a systematic review in the Pubmed and Embase databases to evaluate existing imaging data on inflammation in migraine, and to identify gaps in the literature. We included 20 studies investigating migraine without aura (N = 4), migraine with aura (N = 8), both migraine with and without aura (N = 3), or hemiplegic migraine (N = 5). In migraine without aura, macrophage activation was not evident. In migraine with aura, imaging evidence suggested microglial and parameningeal inflammatory activity. Increased vascular permeability was mostly found in hemiplegic migraine, and was atypical in migraine with and without aura. Based on the weight of existing and emerging data, we show that most studies have concentrated on demonstrating increased vascular permeability as a marker of neuroinflammation, with tools that may not have been optimal. In the future, novel, more sensitive techniques, as well as imaging tracers delineating specific inflammatory pathways may further bridge the gap between preclinical and clinical findings.",
author = "Christensen, {Rune H{\"a}ckert} and C{\'e}dric Gollion and Amin, {Faisal Mohammad} and Moskowitz, {Michael A.} and Nouchine Hadjikhani and Messoud Ashina",
note = "Publisher Copyright: {\textcopyright} 2022, The Author(s).",
year = "2022",
doi = "10.1186/s10194-022-01430-y",
language = "English",
volume = "23",
journal = "Journal of Headache and Pain",
issn = "1129-2369",
publisher = "SpringerOpen",
number = "1",

}

RIS

TY - JOUR

T1 - Imaging the inflammatory phenotype in migraine

AU - Christensen, Rune Häckert

AU - Gollion, Cédric

AU - Amin, Faisal Mohammad

AU - Moskowitz, Michael A.

AU - Hadjikhani, Nouchine

AU - Ashina, Messoud

N1 - Publisher Copyright: © 2022, The Author(s).

PY - 2022

Y1 - 2022

N2 - Several preclinical and clinical lines of evidence suggest a role of neuroinflammation in migraine. Neuroimaging offers the possibility to investigate and localize neuroinflammation in vivo in patients with migraine, and to characterize specific inflammatory constituents, such as vascular permeability, and macrophage or microglia activity. Despite all imaging data accumulated on neuroinflammation across the past three decades, an overview of the imaging evidence of neuroinflammation in migraine is still missing. We conducted a systematic review in the Pubmed and Embase databases to evaluate existing imaging data on inflammation in migraine, and to identify gaps in the literature. We included 20 studies investigating migraine without aura (N = 4), migraine with aura (N = 8), both migraine with and without aura (N = 3), or hemiplegic migraine (N = 5). In migraine without aura, macrophage activation was not evident. In migraine with aura, imaging evidence suggested microglial and parameningeal inflammatory activity. Increased vascular permeability was mostly found in hemiplegic migraine, and was atypical in migraine with and without aura. Based on the weight of existing and emerging data, we show that most studies have concentrated on demonstrating increased vascular permeability as a marker of neuroinflammation, with tools that may not have been optimal. In the future, novel, more sensitive techniques, as well as imaging tracers delineating specific inflammatory pathways may further bridge the gap between preclinical and clinical findings.

AB - Several preclinical and clinical lines of evidence suggest a role of neuroinflammation in migraine. Neuroimaging offers the possibility to investigate and localize neuroinflammation in vivo in patients with migraine, and to characterize specific inflammatory constituents, such as vascular permeability, and macrophage or microglia activity. Despite all imaging data accumulated on neuroinflammation across the past three decades, an overview of the imaging evidence of neuroinflammation in migraine is still missing. We conducted a systematic review in the Pubmed and Embase databases to evaluate existing imaging data on inflammation in migraine, and to identify gaps in the literature. We included 20 studies investigating migraine without aura (N = 4), migraine with aura (N = 8), both migraine with and without aura (N = 3), or hemiplegic migraine (N = 5). In migraine without aura, macrophage activation was not evident. In migraine with aura, imaging evidence suggested microglial and parameningeal inflammatory activity. Increased vascular permeability was mostly found in hemiplegic migraine, and was atypical in migraine with and without aura. Based on the weight of existing and emerging data, we show that most studies have concentrated on demonstrating increased vascular permeability as a marker of neuroinflammation, with tools that may not have been optimal. In the future, novel, more sensitive techniques, as well as imaging tracers delineating specific inflammatory pathways may further bridge the gap between preclinical and clinical findings.

U2 - 10.1186/s10194-022-01430-y

DO - 10.1186/s10194-022-01430-y

M3 - Review

C2 - 35650524

AN - SCOPUS:85131081559

VL - 23

JO - Journal of Headache and Pain

JF - Journal of Headache and Pain

SN - 1129-2369

IS - 1

M1 - 60

ER -

ID: 345279633