Altered brain activity and functional connectivity in migraine without aura during and outside attack

References

• Headache Classification Committee of the International Headache, S. The international classification of headache disorders, 3rd edition (beta version). Cephalalgia. 2013;33(9):629–808.
   PubMed Web of Science ®Google Scholar
• Global Burden of Disease Study, C. Global, regional, and national incidence, prevalence, and years lived with disability for 301 acute and chronic diseases and injuries in 188 countries, 1990-2013: a systematic analysis for the global burden of disease study 2013. Lancet. 2015;386(9995):743–800.
   PubMed Web of Science ®Google Scholar
• Charles AC, Baca SM. Cortical spreading depression and migraine. Nat Rev Neurol. 2013;9(11):637–644.
   PubMed Web of Science ®Google Scholar
• Edvinsson L, Haanes KA, Warfvinge K. Does inflammation have a role in migraine? Nat Rev Neurol. 2019;15(8):483–490.
   PubMed Web of Science ®Google Scholar
• Akerman S, Holland PR, Goadsby PJ. Diencephalic and brainstem mechanisms in migraine. Nat Rev Neurosci. 2011;12(10):570–584.
   PubMed Web of Science ®Google Scholar
• Cortese F, Coppola G, Di Lenola D, et al. Excitability of the motor cortex in patients with migraine changes with the time elapsed from the last attack. J Headache Pain. 2017;18(1):2. DOI:10.1186/s10194-016-0712-z
   PubMed Web of Science ®Google Scholar
• Cosentino G, Fierro B, Vigneri S, et al. Cyclical changes of cortical excitability and metaplasticity in migraine: evidence from a repetitive transcranial magnetic stimulation study. Pain. 2014;155(6):1070–1078. DOI:10.1016/j.pain.2014.02.024
   PubMed Web of Science ®Google Scholar
• Lv H, Wang Z, Tong E, et al. Resting-state functional MRI: everything that nonexperts have always wanted to know. AJNR Am J Neuroradiol. 2018;39(8):1390–1399. DOI:10.3174/ajnr.A5527
   PubMed Web of Science ®Google Scholar
• Zang YF, Yong H, Chao-Zhe Z, et al. Altered baseline brain activity in children with ADHD revealed by resting-state functional MRI. Brain Dev. 2007;29(2):83–91. DOI:10.1016/j.braindev.2006.07.002
   PubMed Web of Science ®Google Scholar
• Buchel C, Friston K. Assessing interactions among neuronal systems using functional neuroimaging. Neural Netw. 2000;13(8–9):871–882.
   PubMed Web of Science ®Google Scholar
• Yan CG, Wang X-D, Zuo X-N, et al. DPABI: data processing & analysis for (resting-state) brain imaging. Neuroinformatics. 2016;14(3):339–351. DOI:10.1007/s12021-016-9299-4
   PubMed Web of Science ®Google Scholar
• Cao Z, Yu W, Zhang Z, et al. Decreased gray matter volume in the frontal cortex of migraine patients with associated functional connectivity alterations: a VBM and rs-FC study. Pain Res Manag. 2022;2022:2115956.
   PubMed Web of Science ®Google Scholar
• Zhang L, Yu W, Xu M, et al. The hypothalamus may mediate migraine and ictal photophobia: evidence from Granger causality analysis. Neurol Sci. 2022;43:6021–6030.
   PubMed Web of Science ®Google Scholar
• Pietrobon D, Moskowitz MA. Pathophysiology of migraine. Annu Rev Physiol. 2013;75:365–391.
   PubMed Web of Science ®Google Scholar
• Akerman S, Romero-Reyes M, Holland PR. Current and novel insights into the neurophysiology of migraine and its implications for therapeutics. Pharmacol Ther. 2017;172:151–170.
   PubMed Web of Science ®Google Scholar
• DaSilva AF, Becerra L, Makris N, et al. Somatotopic activation in the human trigeminal pain pathway. J Neurosci. 2002;22(18):8183–8192. DOI:10.1523/JNEUROSCI.22-18-08183.2002
   PubMed Web of Science ®Google Scholar
• Stankewitz A, Voit HL, Bingel U, et al. A new trigemino-nociceptive stimulation model for event-related fMRI. Cephalalgia. 2010;30(4):475–485. DOI:10.1111/j.1468-2982.2009.01968.x
   PubMed Web of Science ®Google Scholar
• Schulte LH, Sprenger C, May A. Physiological brainstem mechanisms of trigeminal nociception: an fMRI study at 3T. Neuroimage. 2016;124(Pt A):518–525.
   PubMed Web of Science ®Google Scholar
• Friebel U, Eickhoff SB, Lotze M. Coordinate-based meta-analysis of experimentally induced and chronic persistent neuropathic pain. Neuroimage. 2011;58(4):1070–1080.
   PubMed Web of Science ®Google Scholar
• Goadsby PJ, Holland PR, Martins-Oliveira M, et al. Pathophysiology of migraine: a disorder of sensory processing. Physiol Rev. 2017;97(2):553–622. DOI:10.1152/physrev.00034.2015
   PubMed Web of Science ®Google Scholar
• Starr CJ, Sawaki L, Wittenberg GF, et al. The contribution of the putamen to sensory aspects of pain: insights from structural connectivity and brain lesions. Brain. 2011;134(7):1987–2004. DOI:10.1093/brain/awr117
   PubMed Web of Science ®Google Scholar
• Oertel BG, Preibisch C, Martin T, et al. Separating brain processing of pain from that of stimulus intensity. Hum Brain Mapp. 2012;33(4):883–894. DOI:10.1002/hbm.21256
   PubMed Web of Science ®Google Scholar
• Annak O, Heidegger T, Walter C, et al. Effects of continuous theta-burst stimulation of the primary motor and secondary somatosensory areas on the central processing and the perception of trigeminal nociceptive input in healthy volunteers. Pain. 2019;160(1):172–186. DOI:10.1097/j.pain.0000000000001393
   PubMed Web of Science ®Google Scholar
• Lotsch J, Oertel BG, Felden L, et al. Central encoding of the strength of intranasal chemosensory trigeminal stimuli in a human experimental pain setting. Hum Brain Mapp. 2020;41(18):5240–5254. DOI:10.1002/hbm.25190
   PubMed Web of Science ®Google Scholar
• Valmunen T, Pertovaara A, Taiminen T, et al. Modulation of facial sensitivity by navigated rTMS in healthy subjects. Pain. 2009;142(1):149–158. DOI:10.1016/j.pain.2008.12.031
   PubMed Web of Science ®Google Scholar
• Cao J, Tu Y, Orr SP, et al. Analgesic effects evoked by real and imagined acupuncture: a neuroimaging study. Cereb Cortex. 2019;29(8):3220–3231. DOI:10.1093/cercor/bhy190
   PubMed Web of Science ®Google Scholar
• Li Z, Zeng F, Yin T, et al. Acupuncture modulates the abnormal brainstem activity in migraine without aura patients. NeuroImage Clin. 2017;15:367–375.
   PubMed Web of Science ®Google Scholar
• Price DD. Psychological and neural mechanisms of the affective dimension of pain. Science. 2000;288(5472):1769–1772.
   PubMed Web of Science ®Google Scholar
• Martel M, Harvey M-P, Houde F, et al. Unravelling the effect of experimental pain on the corticomotor system using transcranial magnetic stimulation and electroencephalography. Exp Brain Res. 2017;235(4):1223–1231. DOI:10.1007/s00221-017-4880-0
   PubMed Web of Science ®Google Scholar
• Yang FC, Chou K-H, Fuh J-L, et al. Altered hypothalamic functional connectivity in cluster headache: a longitudinal resting-state functional MRI study. J Neurol Neurosurg Psychiatry. 2015;86(4):437–445. DOI:10.1136/jnnp-2014-308122
   PubMed Web of Science ®Google Scholar
• Woodbury A, Krishnamurthy LC, Bohsali A, et al. Percutaneous electric nerve field stimulation alters cortical thickness in a pilot study of veterans with fibromyalgia. Neurobiol Pain. 2022;12:100093.
   PubMedGoogle Scholar
• Parise M, Kubo TTA, Doring TM, et al. Cuneus and fusiform cortices thickness is reduced in trigeminal neuralgia. J Headache Pain. 2014;15:17.
   PubMed Web of Science ®Google Scholar
• Magon S, May A, Stankewitz A, et al. Cortical abnormalities in episodic migraine: a multi-center 3T MRI study. Cephalalgia. 2019;39(5):665–673. DOI:10.1177/0333102418795163
   PubMed Web of Science ®Google Scholar
• Lei M, Zhang J. Brain function state in different phases and its relationship with clinical symptoms of migraine: an fMRI study based on regional homogeneity (ReHo). Ann Transl Med. 2021;9(11):928.
   PubMed Web of Science ®Google Scholar
• Wang JJ, Chen X, Sah SK, et al. Amplitude of low-frequency fluctuation (ALFF) and fractional ALFF in migraine patients: a resting-state functional MRI study. Clin Radiol. 2016;71(6):558–564. DOI:10.1016/j.crad.2016.03.004
   PubMed Web of Science ®Google Scholar