Pain genetics: past, present and future

被引:230
作者
Mogil, Jeffrey S. [1 ,2 ]
机构
[1] McGill Univ, Dept Psychol, Montreal, PQ H3A 1B1, Canada
[2] McGill Univ, Alan Edwards Ctr Res Pain, Montreal, PQ H3A 1B1, Canada
关键词
GENOME-WIDE ASSOCIATION; QUANTITATIVE TRAIT LOCUS; HEREDITARY SENSORY NEUROPATHY; FAMILIAL HEMIPLEGIC MIGRAINE; CATECHOL-O-METHYLTRANSFERASE; LOW-BACK-PAIN; RISK-FACTORS; INDIVIDUAL-DIFFERENCES; MOLECULAR-BASIS; CONGENITAL INSENSITIVITY;
D O I
10.1016/j.tig.2012.02.004
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Chronic pain is a classic example of gene x environment interaction: inflammatory and/or nerve injuries are known or suspected to be the etiology of most chronic pain syndromes, but only a small minority of those subjected to such injuries actually develop chronic pain. Once chronic pain has developed, pain severity and analgesic response are also highly variable among individuals. Although animal genetics studies have been ongoing for over two decades, only recently have comprehensive human twin studies and large-scale association studies been performed. Here, I review recent and accelerating progress in, and continuing challenges to, the identification of genes contributing to such variability. Success in this endeavor will hopefully lead to both better management of pain using currently available therapies and the development and/or prioritizing of new ones.
引用
收藏
页码:258 / 266
页数:9
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