Tafti Mehdi
Center for Integrative Genomics, University of Lausanne, Génopode, 1015 Lausanne, Switzerland.
Sleep Med. 2009 Sep;10 Suppl 1:S17-21. doi: 10.1016/j.sleep.2009.07.002. Epub 2009 Aug 5.
Sleep disorders commonly involve genetic susceptibility, environmental effects, and interactions between these factors. The heritability of sleep patterns has been shown in studies of monozygotic twins, and sleep electroencephalogram patterns offer a unique genetic fingerprint which may assist in the identification of genes involved in the regulation of sleep. Genetic factors are also thought to play a role in sleep disorders; narcolepsy is a disabling sleep condition and research has revealed the complexity of underlying genetic and environmental influences in the development of this disorder. An understanding of sleep regulation at the molecular level is essential in the identification of new targets for the treatment of sleep disorders, and genome-wide association studies for both normal sleep and sleep disorders may shed new light on the molecular architecture of mechanisms regulating these behaviours.
睡眠障碍通常涉及遗传易感性、环境影响以及这些因素之间的相互作用。同卵双胞胎研究表明了睡眠模式的遗传性,睡眠脑电图模式提供了一种独特的遗传指纹,可能有助于识别参与睡眠调节的基因。遗传因素也被认为在睡眠障碍中起作用;发作性睡病是一种使人衰弱的睡眠状况,研究揭示了这种疾病发展过程中潜在的遗传和环境影响的复杂性。在分子水平上理解睡眠调节对于确定治疗睡眠障碍的新靶点至关重要,针对正常睡眠和睡眠障碍的全基因组关联研究可能会为调节这些行为的机制的分子结构提供新的线索。