Genes for normal sleep and sleep disorders

被引:46
作者
Tafti, M [1 ]
Maret, S
Dauvilliers, Y
机构
[1] Univ Lausanne, CIG, BEP, CH-1015 Lausanne, Switzerland
[2] Hop Gui de Chauliac, Serv Neurol B, Montpellier, France
[3] INSERM, E0361, Montpellier, France
关键词
apnea; association; circadian; human leucocyte antigen; insomnia; Kleine-Levin syndrome; linkage; narcolepsy; prion protein; sleepwalking; twin;
D O I
10.1080/07853890500372047
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Sleep and wakefulness are complex behaviors that are influenced by many genetic and environmental factors, which are beginning to be discovered. The contribution of genetic. components to sleep disorders is also increasingly recognized as important. Point mutations in the prion protein, period 2, and the prepro-hypocretin/orexin gene have been found as the cause of a few sleep disorders but the possibility that other gene defects may contribute to the pathophysiology of major sleep disorders is worth in-depth investigations. However, single gene disorders are rare and most common disorders are complex in terms of their genetic susceptibility, environmental effects, gene-gene, and gene-environment interactions. We review here the current progress in the genetics of normal and pathological sleep.
引用
收藏
页码:580 / 589
页数:10
相关论文
共 110 条
[1]  
ABE K, 1966, PSYCHIAT NEUROL, V152, P306
[2]   Restless legs syndrome: diagnostic criteria, special considerations, and epidemiology - A report from the restless legs syndrome diagnosis and epidemiology workshop at the National Institutes of Health [J].
Allen, RP ;
Picchietti, D ;
Hening, WA ;
Trenkwalder, C ;
Walters, AS ;
Montplaisi, J .
SLEEP MEDICINE, 2003, 4 (02) :101-119
[3]   Restless legs syndrome - A review of clinical and pathophysiologic features [J].
Allen, RP ;
Earley, CJ .
JOURNAL OF CLINICAL NEUROPHYSIOLOGY, 2001, 18 (02) :128-147
[4]   Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome [J].
Amiel, J ;
Laudier, B ;
Attié-Bitach, T ;
Trang, H ;
de Pontual, L ;
Gener, B ;
Trochet, D ;
Etchevers, H ;
Ray, P ;
Simonneau, M ;
Vekemans, M ;
Munnich, A ;
Gaultier, C ;
Lyonnet, S .
NATURE GENETICS, 2003, 33 (04) :459-461
[5]   A length polymorphism in the circadian clock gene Per3 is linked to delayed sleep phase syndrome and extreme diurnal preference [J].
Archer, SN ;
Robilliard, DL ;
Skene, DJ ;
Smits, M ;
Williams, A ;
Arendt, J ;
von Schantz, M .
SLEEP, 2003, 26 (04) :413-415
[6]  
BAKWIN H, 1970, Lancet, V2, P446, DOI 10.1016/S0140-6736(70)90058-9
[7]   ENURESIS IN TWINS [J].
BAKWIN, H .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1971, 121 (03) :222-&
[8]   Familial incidence of insomnia [J].
Bastien, CH ;
Morin, C .
JOURNAL OF SLEEP RESEARCH, 2000, 9 (01) :49-54
[9]  
BOEYE BF, 1998, NEUROLOGY, V51, P363
[10]   Autosomal dominant restless legs syndrome maps on chromosome 14q [J].
Bonati, MT ;
Ferini-Strambi, L ;
Aridon, P ;
Oldani, A ;
Zucconi, M ;
Casari, G .
BRAIN, 2003, 126 :1485-1492