Migraine genetics: current findings and future lines of research

被引:13
作者
Persico, A. M. [1 ,2 ,3 ]
Verdecchia, M. [1 ,2 ]
Pinzone, V. [1 ,2 ]
Guidetti, V. [4 ]
机构
[1] Univ Campus Biomed, Child & Adolescent Neuropsychiat Unit, I-00128 Rome, Italy
[2] Univ Campus Biomed, Lab Mol Psychiat & Neurogenet, I-00128 Rome, Italy
[3] Mafalda Luce Ctr Pervas Dev Disorders, Milan, Italy
[4] Univ Roma La Sapienza, Dept Pediat & Child Neuropsychiat, Rome, Italy
关键词
Aura; CADASIL; Cortical spreading depression; Headache; Migraine; Trigeminovascular; FAMILIAL HEMIPLEGIC MIGRAINE; GENOME-WIDE ASSOCIATION; METHYLENETETRAHYDROFOLATE REDUCTASE GENE; MTHFR C677T POLYMORPHISM; SCAN PROVIDES EVIDENCE; NECROSIS-FACTOR-ALPHA; SODIUM-CHANNEL SCN1A; SUSCEPTIBILITY LOCI; SIGNIFICANT LINKAGE; TYPICAL MIGRAINE;
D O I
10.1007/s10048-014-0433-x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
In the last two decades, migraine research has greatly advanced our current knowledge of the genetic contributions and the pathophysiology of this common and debilitating disorder. Nonetheless, this knowledge still needs to grow further and to translate into more effective treatments. To date, several genes involved in syndromic and monogenic forms of migraine have been identified, allowing the generation of animal models which have significantly contributed to current knowledge of the mechanisms underlying these rare forms of migraine. Common forms of migraine are instead posing a greater challenge, as they may most often stem from complex interactions between multiple common genetic variants, with environmental triggers. This paper reviews our current understanding of migraine genetics, moving from syndromic and monogenic forms to oligogenic/polygenic migraines most recently addressed with some success through genome-wide association studies. Methodological issues in study design and future perspectives opened by biomarker research will also be briefly addressed.
引用
收藏
页码:77 / 95
页数:19
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