The migraine-stroke connection: A genetic perspective

被引:19
作者
Malik, Rainer [1 ]
Winsvold, Bendik [2 ,3 ,4 ]
Auffenberg, Eva [1 ,5 ]
Dichgans, Martin [1 ,6 ]
Freilinger, Tobias [5 ]
机构
[1] Inst Stroke & Dementia Res ISD, Munich, Germany
[2] FORMI, Oslo, Norway
[3] Oslo Univ Hosp, Dept Neurol, Oslo, Norway
[4] Univ Oslo, Oslo, Norway
[5] Hertie Inst Clin Brain Res HIH, Dept Neurol & Epileptol, Tubingen, Germany
[6] Munich Cluster Syst Neurol SyNergy, Munich, Germany
关键词
CADASIL; migraine pathophysiology; genetic susceptibility; cortical spreading depression; hemiplegic migraine; mouse model; genomewide association study; GENOME-WIDE ASSOCIATION; FAMILIAL HEMIPLEGIC MIGRAINE; HEREDITARY HEMORRHAGIC TELANGIECTASIA; AUTOSOMAL-DOMINANT ARTERIOPATHY; CERVICAL ARTERY DISSECTION; TRANSFORMING-GROWTH-FACTOR; SUSCEPTIBILITY LOCI; CARDIOVASCULAR-DISEASE; VASCULAR RETINOPATHY; SUBCORTICAL INFARCTS;
D O I
10.1177/0333102415621055
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background A complex relationship between migraine and vascular disease has long been recognized. The pathophysiological basis underlying this correlation is incompletely understood. Aim The aim of this review is to focus on the migraine-vascular disorders connection from a genetic perspective, illustrating potentially shared (molecular) mechanisms. Results We first summarize the clinical presentation and genetic basis of CADASIL and other monogenic vascular syndromes with migraine as a prominent disease manifestation. Based on data from transgenic mouse models for familial hemiplegic migraine, we then discuss cortical spreading depression as a potential mechanistic link between migraine and ischemic stroke. Finally, we review data from genome-wide association studies, with a focus on overlapping findings with cervical artery dissection, ischemic stroke in general and cardiovascular disease. Conclusion A wealth of data supports a genetic link between migraine and vascular disease. Based on growing high-throughput data-sets, new genotyping techniques and in-depth phenotyping, further insights are expected for the future.
引用
收藏
页码:658 / 668
页数:11
相关论文
共 80 条
  • [61] Neurologic symptoms are common during gestation and puerperium in CADASIL
    Roine, S
    Pöyhönen, M
    Timonen, S
    Tuisku, S
    Marttila, R
    Sulkava, R
    Kalimo, H
    Viitanen, M
    [J]. NEUROLOGY, 2005, 64 (08) : 1441 - 1443
  • [62] Association of the C677T polymorphism in the MTHFR gene with migraine: a meta-analysis
    Rubino, E.
    Ferrero, M.
    Rainero, I.
    Binello, E.
    Vaula, G.
    Pinessi, L.
    [J]. CEPHALALGIA, 2009, 29 (08) : 818 - 825
  • [63] Migraine and risk of ischaemic heart disease: a systematic review and meta-analysis of observational studies
    Sacco, S.
    Ornello, R.
    Ripa, P.
    Tiseo, C.
    Degan, D.
    Pistoia, F.
    Carolei, A.
    [J]. EUROPEAN JOURNAL OF NEUROLOGY, 2015, 22 (06) : 1001 - 1011
  • [64] ACE D/I polymorphism, migraine, and cardiovascular disease in women
    Schuerks, M.
    Zee, R. Y. L.
    Buring, J. E.
    Kurth, T.
    [J]. NEUROLOGY, 2009, 72 (07) : 650 - 656
  • [65] Genetic Determinants of Cardiovascular Events among Women with Migraine: A Genome-Wide Association Study
    Schuerks, Markus
    Buring, Julie E.
    Ridker, Paul M.
    Chasman, Daniel I.
    Kurth, Tobias
    [J]. PLOS ONE, 2011, 6 (07):
  • [66] MTHFR 677C>T and ACE D/I Polymorphisms in Migraine: A Systematic Review and Meta-Analysis
    Schuerks, Markus
    Rist, Pamela M.
    Kurth, Tobias
    [J]. HEADACHE, 2010, 50 (04): : 588 - 599
  • [67] Vasoconstrictive neurovascular coupling during focal ischemic depolarizations
    Shin, Hwa Kyoung
    Dunn, Andrew K.
    Jones, Phillip B.
    Boas, David A.
    Moskowitz, Michael A.
    Ayata, Cenk
    [J]. JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2006, 26 (08) : 1018 - 1030
  • [68] Peri-infarct depolarizations lead to loss of perfusion in ischaemic gyrencephalic cerebral cortex
    Strong, Anthony J.
    Anderson, Peter J.
    Watts, Helena R.
    Virley, David J.
    Lloyd, Andrew
    Irving, Elaine A.
    Nagafuji, Toshiaki
    Ninomiya, Mitsuyoshi
    Nakamura, Hajime
    Dunn, Andrew K.
    Graf, Rudolf
    [J]. BRAIN, 2007, 130 : 995 - 1008
  • [69] Clinical and genetic analysis of a large Dutch family with autosomal dominant vascular retinopathy, migraine and Raynaud's phenomenon
    Terwindt, GM
    Haan, J
    Ophoff, RA
    Groenen, SMA
    Storimans, CWJM
    Lanser, JBK
    Roos, RAC
    Bleeker-Wagemakers, EM
    Frants, RR
    Ferrari, MD
    [J]. BRAIN, 1998, 121 : 303 - 316
  • [70] A population-based study of familial hemiplegic migraine suggests revised diagnostic criteria
    Thomsen, LL
    Eriksen, MK
    Roemer, SF
    Andersen, I
    Olesen, J
    Russell, MB
    [J]. BRAIN, 2002, 125 : 1379 - 1391