偏头痛与扩大的血管周围间隙之间的关系
The Relationship between Migraine and Enlarged Perivascular Spaces
DOI: 10.12677/acm.2024.14102727, PDF,    国家自然科学基金支持
作者: 康富丽, 王 怡, 蔡青青, 马璟曦*:重庆医科大学,重庆;重庆市人民医院神经内科,重庆;廖金成:重庆市人民医院神经内科,重庆;薛瑞灵:重庆医科大学,重庆;重庆市人民医院康复医学科,重庆;李佳妮:重庆医科大学附属第二医院神经内科,重庆
关键词: 偏头痛胶质淋巴系统血管周围间隙扩大形成机制Migraine Glymphatic System Enlarged Perivascular Spaces Formation Mechanism
摘要: 偏头痛(Migraine)是一种原发性、终身性神经系统疾病,其反复发作可能与脑小血管病(Cerebral Small Vessel Disease, CSVD)有关。偏头痛缺乏特异影像学特征,由偏头痛引起的脑小血管病的特征在磁共振上可能表现为无症状腔隙性梗死(LIs)、脑白质病变(WMLs)、血管周围间隙扩大(Enlarged Perivascular Spaces, EPVS)和脑微出血(CMBs)。目前已有越来越多的研究探讨了偏头痛与血管周围间隙扩大之间的关系。胶质淋巴系统(Glymphatic System, GS)是近年来神经科学领域的新方向,是脑内代谢废物清除的重要途径,其与偏头痛之间的关系的研究也日渐增多,而血管周围间隙(Perivascular Spaces, PVS)可作为GS发挥作用的重要环节之一。本综述总结了GS、EPVS的形成机制以及二者与偏头痛之间的相关关系,以期临床上对GS、EPVS以及偏头痛有更多的关注及研究,为偏头痛的诊断、预防及治疗提供新思路。
Abstract: Migraine is a primary, lifespan neurological disorder with recurrent attacks that may be associated with Cerebral Small Vessel Disease (CSVD). Migraine lacks specific neuroimaging findings, and CSVD caused by migraine may be characterized by silent Lacunar Infarcts (LIs), White-Matter Lesions (WMLs), Enlarged Perivascular Spaces (EPVS) and Cerebral Microbleeds (CMBs) on magnetic resonance. There is growing evidence to shed light on the relevant relationship between EPVS and migraine. Recently, Glymphatic System (GS), a new direction in neuroscience, is an important pathway for the removal of metabolic wastes from the brain, and a growing number of studies have explored the relationship between GS and migraine. Meanwhile, the Perivascular Spaces (PVS) can be one of the important links in the role of GS. This review summarizes the formation mechanism of GS and EPVS and the potential correlation between them and migraine, aims to have more clinical attention and research on GS, EPVS, and migraine and provide new ideas for the diagnosis, prevention, and treatment of migraine.
文章引用:康富丽, 王怡, 蔡青青, 廖金成, 薛瑞灵, 李佳妮, 马璟曦. 偏头痛与扩大的血管周围间隙之间的关系[J]. 临床医学进展, 2024, 14(10): 782-787. https://doi.org/10.12677/acm.2024.14102727

参考文献

[1] Diseases, G.B.D. and Injuries, C. (2020) Global Burden of 369 Diseases and Injuries in 204 Countries and Territories, 1990-2019: A Systematic Analysis for the Global Burden of Disease Study 2019. The Lancet, 396, 1204-1222.
[2] Stovner, L.J., Hagen, K., Linde, M. and Steiner, T.J. (2022) The Global Prevalence of Headache: An Update, with Analysis of the Influences of Methodological Factors on Prevalence Estimates. The Journal of Headache and Pain, 23, Article No. 34. [Google Scholar] [CrossRef] [PubMed]
[3] Negm, M., Housseini, A.M., Abdelfatah, M. and Asran, A. (2018) Relation between Migraine Pattern and White Matter Hyperintensities in Brain Magnetic Resonance Imaging. The Egyptian Journal of Neurology, Psychiatry and Neurosurgery, 54, Article No. 24. [Google Scholar] [CrossRef] [PubMed]
[4] Schain, A.J., Melo-Carrillo, A., Strassman, A.M. and Burstein, R. (2017) Cortical Spreading Depression Closes Paravascular Space and Impairs Glymphatic Flow: Implications for Migraine Headache. The Journal of Neuroscience, 37, 2904-2915. [Google Scholar] [CrossRef] [PubMed]
[5] Wardlaw, J.M., Smith, E.E., Biessels, G.J., Cordonnier, C., Fazekas, F., Frayne, R., et al. (2013) Neuroimaging Standards for Research into Small Vessel Disease and Its Contribution to Ageing and Neurodegeneration. The Lancet Neurology, 12, 822-838. [Google Scholar] [CrossRef] [PubMed]
[6] Iliff, J.J., Wang, M., Liao, Y., Plogg, B.A., Peng, W., Gundersen, G.A., et al. (2012) A Paravascular Pathway Facilitates CSF Flow through the Brain Parenchyma and the Clearance of Interstitial Solutes, Including Amyloid β. Science Translational Medicine, 4, 147ra111. [Google Scholar] [CrossRef] [PubMed]
[7] Zhang, Y., Zhang, C., He, X., Li, Z., Meng, J., Mao, R., et al. (2023) Interaction between the Glymphatic System and Α-Synuclein in Parkinson’s Disease. Molecular Neurobiology, 60, 2209-2222. [Google Scholar] [CrossRef] [PubMed]
[8] Iliff, J.J., Chen, M.J., Plog, B.A., Zeppenfeld, D.M., Soltero, M., Yang, L., et al. (2014) Impairment of Glymphatic Pathway Function Promotes Tau Pathology after Traumatic Brain Injury. The Journal of Neuroscience, 34, 16180-16193. [Google Scholar] [CrossRef] [PubMed]
[9] Huang, W., Zhang, Y., Zhou, Y., Zong, J., Qiu, T., Hu, L., et al. (2023) Glymphatic Dysfunction in Migraine Mice Model. Neuroscience, 528, 64-74. [Google Scholar] [CrossRef] [PubMed]
[10] Xie, L., Kang, H., Xu, Q., Chen, M.J., Liao, Y., Thiyagarajan, M., et al. (2013) Sleep Drives Metabolite Clearance from the Adult Brain. Science, 342, 373-377. [Google Scholar] [CrossRef] [PubMed]
[11] Iliff, J.J. and Nedergaard, M. (2013) Is There a Cerebral Lymphatic System? Stroke, 44, S93-S95. [Google Scholar] [CrossRef] [PubMed]
[12] Jessen, N.A., Munk, A.S.F., Lundgaard, I. and Nedergaard, M. (2015) The Glymphatic System: A Beginner’s Guide. Neurochemical Research, 40, 2583-2599. [Google Scholar] [CrossRef] [PubMed]
[13] Ma, Q., Ineichen, B.V., Detmar, M. and Proulx, S.T. (2017) Outflow of Cerebrospinal Fluid Is Predominantly through Lymphatic Vessels and Is Reduced in Aged Mice. Nature Communications, 8, Article No. 1434. [Google Scholar] [CrossRef] [PubMed]
[14] Rennels, M., Blaumanis, O. and Grady, P. (1990) Rapid Solute Transport Throughout the Brain via Paravascular Fluid Pathways. Advances in Neurology, 52, 431-439.
[15] Rennels, M.L., Gregory, T.F., Blaumanis, O.R., Fujimoto, K. and Grady, P.A. (1985) Evidence for a ‘Paravascular’ Fluid Circulation in the Mammalian Central Nervous System, Provided by the Rapid Distribution of Tracer Protein Throughout the Brain from the Subarachnoid Space. Brain Research, 326, 47-63. [Google Scholar] [CrossRef] [PubMed]
[16] Pearce, J.M.S. (2002) Rudolf Ludwig Karl Virchow (1821-1902). Journal of Neurology, 249, 492-493. [Google Scholar] [CrossRef] [PubMed]
[17] Brown, R., Benveniste, H., Black, S.E., Charpak, S., Dichgans, M., Joutel, A., et al. (2018) Understanding the Role of the Perivascular Space in Cerebral Small Vessel Disease. Cardiovascular Research, 114, 1462-1473. [Google Scholar] [CrossRef] [PubMed]
[18] 谭鑫, 吴波, 刘鸣. 扩大的血管周围间隙与卒中关系的研究现状及趋势[C]//第十五次中国脑血管病大会2015论文汇编. 南京: 四川大学华西医院神经内科, 2015: 445.
[19] Riba-Llena, I., Jiménez-Balado, J., Castañé, X., Girona, A., López-Rueda, A., Mundet, X., et al. (2018) Arterial Stiffness Is Associated with Basal Ganglia Enlarged Perivascular Spaces and Cerebral Small Vessel Disease Load. Stroke, 49, 1279-1281. [Google Scholar] [CrossRef] [PubMed]
[20] Bown, C.W., Khan, O.A., Liu, D., Remedios, S.W., Pechman, K.R., Terry, J.G., et al. (2023) Enlarged Perivascular Space Burden Associations with Arterial Stiffness and Cognition. Neurobiology of Aging, 124, 85-97. [Google Scholar] [CrossRef] [PubMed]
[21] Charidimou, A., Jaunmuktane, Z., Baron, J., Burnell, M., Varlet, P., Peeters, A., et al. (2014) White Matter Perivascular Spaces: An MRI Marker in Pathology-Proven Cerebral Amyloid Angiopathy? Neurology, 82, 57-62. [Google Scholar] [CrossRef] [PubMed]
[22] Charidimou, A., Hong, Y.T., Jäger, H.R., Fox, Z., Aigbirhio, F.I., Fryer, T.D., et al. (2015) White Matter Perivascular Spaces on Magnetic Resonance Imaging: Marker of Cerebrovascular Amyloid Burden? Stroke, 46, 1707-1709. [Google Scholar] [CrossRef] [PubMed]
[23] Granberg, T., Moridi, T., Brand, J.S., Neumann, S., Hlavica, M., Piehl, F., et al. (2020) Enlarged Perivascular Spaces in Multiple Sclerosis on Magnetic Resonance Imaging: A Systematic Review and Meta-Analysis. Journal of Neurology, 267, 3199-3212. [Google Scholar] [CrossRef] [PubMed]
[24] Miyata, M., Kakeda, S., Iwata, S., Nakayamada, S., Ide, S., Watanabe, K., et al. (2017) Enlarged Perivascular Spaces Are Associated with the Disease Activity in Systemic Lupus Erythematosus. Scientific Reports, 7, Article No. 12566. [Google Scholar] [CrossRef] [PubMed]
[25] Charidimou, A., Boulouis, G., Pasi, M., Auriel, E., van Etten, E.S., Haley, K., et al. (2017) MRI-Visible Perivascular Spaces in Cerebral Amyloid Angiopathy and Hypertensive Arteriopathy. Neurology, 88, 1157-1164. [Google Scholar] [CrossRef] [PubMed]
[26] Hicks, A.J., Sinclair, B., Shultz, S.R., Pham, W., Silbert, L.C., Schwartz, D.L., et al. (2023) Associations of Enlarged Perivascular Spaces with Brain Lesions, Brain Age, and Clinical Outcomes in Chronic Traumatic Brain Injury. Neurology, 101, e63-e73. [Google Scholar] [CrossRef] [PubMed]
[27] Meng, J., Shen, M., Lu, Y., Feng, H., Chen, X., Xu, D., et al. (2023) Correlation of Glymphatic System Abnormalities with Parkinson’s Disease Progression: A Clinical Study Based on Non-Invasive fMRI. Journal of Neurology, 271, 457-471. [Google Scholar] [CrossRef] [PubMed]
[28] Ramirez, J., Berezuk, C., McNeely, A.A., Scott, C.J.M., Gao, F. and Black, S.E. (2014) Visible Virchow-Robin Spaces on Magnetic Resonance Imaging of Alzheimer’s Disease Patients and Normal Elderly from the Sunnybrook Dementia Study. Journal of Alzheimers Disease, 43, 415-424. [Google Scholar] [CrossRef] [PubMed]
[29] Schick, S., Gahleitner, A., Wöber-Bingöl, C., Wöber, C., Ba-Ssalamah, A., Schoder, M., et al. (1999) Virchow-Robin Spaces in Childhood Migraine. Neuroradiology, 41, 283-287. [Google Scholar] [CrossRef] [PubMed]
[30] Samanta, D. (2015) Sporadic Hemiplegic Migraine and Giant Tumefactive Perivascular Space: Is There an Association? Acta Neurologica Belgica, 116, 619-620. [Google Scholar] [CrossRef] [PubMed]
[31] Akar, G., Eser, M., Taşdemir, S.S. and Gözke, E. (2015) Giant Virchow-Robin Spaces in a Patient with Migraine: Case Report. Turkiye Klinikleri Journal of Neurology, 10, 36-38. [Google Scholar] [CrossRef
[32] Yuan, Z., Li, W., Tang, H., Mei, Y., Qiu, D., Zhang, M., et al. (2023) Enlarged Perivascular Spaces in Patients with Migraine: A Case-Control Study Based on 3T MRI. Annals of Clinical and Translational Neurology, 10, 1160-1169. [Google Scholar] [CrossRef] [PubMed]
[33] Husøy, A.K., Indergaard, M.K., Honningsvåg, L., Håberg, A.K., Hagen, K., Linde, M., et al. (2015) Perivascular Spaces and Headache: A Population-Based Imaging Study (HUNT-MRI). Cephalalgia, 36, 232-239. [Google Scholar] [CrossRef] [PubMed]
[34] Mestre, H., Kostrikov, S., Mehta, R.I. and Nedergaard, M. (2017) Perivascular Spaces, Glymphatic Dysfunction, and Small Vessel Disease. Clinical Science, 131, 2257-2274. [Google Scholar] [CrossRef] [PubMed]
[35] Schain, A.J., Melo-Carrillo, A., Strassman, A.M. and Burstein, R. (2017) Cortical Spreading Depression Closes Paravascular Space and Impairs Glymphatic Flow: Implications for Migraine Headache. The Journal of Neuroscience, 37, 2904-2915. [Google Scholar] [CrossRef] [PubMed]
[36] Messlinger, K. (2018) The Big CGRP Flood—Sources, Sinks and Signalling Sites in the Trigeminovascular System. The Journal of Headache and Pain, 19, Article No. 22. [Google Scholar] [CrossRef] [PubMed]
[37] Eftekhari, S., Salvatore, C.A., Calamari, A., Kane, S.A., Tajti, J. and Edvinsson, L. (2010) Differential Distribution of Calcitonin Gene-Related Peptide and Its Receptor Components in the Human Trigeminal Ganglion. Neuroscience, 169, 683-696. [Google Scholar] [CrossRef] [PubMed]
[38] Russo, A.F. (2015) Calcitonin Gene-Related Peptide (CGRP): A New Target for Migraine. Annual Review of Pharmacology and Toxicology, 55, 533-552. [Google Scholar] [CrossRef] [PubMed]
[39] Goadsby, P.J., Edvinsson, L. and Ekman, R. (1990) Vasoactive Peptide Release in the Extracerebral Circulation of Humans during Migraine Headache. Annals of Neurology, 28, 183-187. [Google Scholar] [CrossRef] [PubMed]
[40] Rosic, A.B., Dukefoss, D.B., Åbjørsbråten, K.S., Tang, W., Jensen, V., Ottersen, O.P., et al. (2019) Aquaporin‐4‐Independent Volume Dynamics of Astroglial Endfeet during Cortical Spreading Depression. Glia, 67, 1113-1121. [Google Scholar] [CrossRef] [PubMed]
[41] Shirolapov, I., Zakharov, A., Gochhait, S., Pyatin, V., Sergeeva, M., Romanchuk, N., et al. (2023) Aquaporin-4 as the Main Element of the Glymphatic System for Clearance of Abnormal Proteins and Prevention of Neurodegeneration: A Review. Wseas Transactions on Biology and Biomedicine, 20, 110-118. [Google Scholar] [CrossRef