A length polymorphism in the circadian clock gene Per3 is linked to delayed sleep phase syndrome and extreme diurnal preference

被引:466
作者
Archer, SN
Robilliard, DL
Skene, DJ
Smits, M
Williams, A
Arendt, J
von Schantz, M [1 ]
机构
[1] Univ Surrey, Ctr Chronobiol, Sch Biomed & Life Sci, Guildford GU2 7XH, Surrey, England
[2] Hosp Gelderse Vallei, Dept Neurol & Sleep Wake Disorders, NL-6710 BA Ede, Netherlands
[3] St Thomas Hosp, Lane Fox Unit, London SE1 7EH, England
关键词
circadian rhythms; phosphorylation; polymorphism (genetics); protein kinases; sleep disorder; circadian rhythm;
D O I
10.1093/sleep/26.4.413
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Study Objectives: To investigate the link between extreme diurnal preference, delayed sleep phase syndrome, and a length polymorphism in Per3. Design: Subjects were genotyped using polymerase chain reaction. Patients or Participants: Subjects with defined diurnal preference as determined by the Horne-Ostberg questionnaire and patients with delayed sleep phase syndrome. Measurements and Results: The Per3 polymorphism correlated significantly with extreme diurnal preference, the longer allele associating with morningness and the shorter allele with eveningness. The shorter allele was strongly associated with the delayed sleep phase syndrome patients, 75% of whom were homozygous. Conclusion: The length of the Per3 repeat region identifies a potential genetic marker for extreme diurnal preference.
引用
收藏
页码:413 / 415
页数:3
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