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Migraine genetics: current findings and future lines of research

机译:偏头痛遗传学:当前发现和未来研究方向

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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.
机译:在过去的二十年中,偏头痛研究极大地提高了我们目前对这种常见且使人衰弱的疾病的遗传贡献和病理生理学的认识。尽管如此,这种知识仍需要进一步发展并转化为更有效的治疗方法。迄今为止,已经鉴定出与偏头痛的症状性和单基因形式有关的几种基因,从而允许产生动物模型,这些动物模型极大地促进了对这些罕见形式的偏头痛的潜在机制的当前了解。相反,偏头痛的常见形式正面临更大的挑战,因为它们通常最可能源于多种常见遗传变异与环境触发因素之间的复杂相互作用。本文回顾了我们目前对偏头痛遗传学的理解,从综合征和单基因偏头痛转变为寡聚/多基因偏头痛,最近通过全基因组关联研究取得了一些成功。研究设计中的方法学问题以及生物标志物研究带来的未来前景也将得到简要解决。

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