Lithium: a key to the genetics of bipolar disorder

被引:26
作者
Cruceanu, Cristiana [1 ]
Alda, Martin [2 ]
Turecki, Gustavo [1 ]
机构
[1] McGill Univ, Douglas Hosp, McGill Grp Suicide Studies, Montreal, PQ H4H 1R3, Canada
[2] Dalhousie Univ, Dept Psychiat, Halifax, NS B3H 4R2, Canada
来源
GENOME MEDICINE | 2009年 / 1卷
关键词
Lithium; Bipolar Disorder; Lithium Treatment; Nephrogenic Diabetes Insipidus; Wellcome Trust Case Control Consortium;
D O I
10.1186/gm79
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Since the 1950s, lithium salts have been the main line of treatment for bipolar disorder (BD), both as a prophylactic and as an episodic treatment agent. Like many psychiatric conditions, BD is genetically and phenotypically heterogeneous, but evidence suggests that individuals who respond well to lithium treatment have more homogeneous clinical and molecular profiles. Response to lithium seems to cluster in families and can be used as a predictor for recurrence of BD symptoms. While molecular studies have provided important information about possible genes involved in BD predisposition or in lithium response, neither the mechanism of action of this drug nor the genetic profile of bipolar disorder is, as yet, completely understood.
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页数:7
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共 99 条
[1]   Response to lithium augmentation in depression is associated with the glycogen synthase kinase 3-beta - 50T/C single nucleotide polymorphism [J].
Adli, Mazda ;
Hollinde, Dorothea L. ;
Stamm, Thomas ;
Wiethoff, Katja ;
Tsahuridu, Martina ;
Kirchheiner, Julia ;
Heinz, Andreas ;
Bauer, Michael .
BIOLOGICAL PSYCHIATRY, 2007, 62 (11) :1295-1302
[2]   A comprehensive linkage analysis of chromosome 21q22 supports prior evidence for a putative bipolar affective disorder locus [J].
Aita, VM ;
Liu, JJ ;
Knowles, JA ;
Terwilliger, JD ;
Baltazar, R ;
Grunn, A ;
Loth, JE ;
Kanyas, K ;
Lerer, B ;
Endicott, J ;
Wang, ZY ;
Penchaszadeh, G ;
Gilliam, TC ;
Baron, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (01) :210-217
[3]   Autosomal recessive inheritance of affective disorders in families of responders to lithium prophylaxis? [J].
Alda, M ;
Grof, E ;
Cavazzoni, P ;
Duffy, A ;
Martin, R ;
Ravindran, L ;
Grof, P .
JOURNAL OF AFFECTIVE DISORDERS, 1997, 44 (2-3) :153-157
[4]   Bipolar disorder: From families to genes [J].
Alda, M .
CANADIAN JOURNAL OF PSYCHIATRY-REVUE CANADIENNE DE PSYCHIATRIE, 1997, 42 (04) :378-387
[5]   MODE OF INHERITANCE IN FAMILIES OF PATIENTS WITH LITHIUM-RESPONSIVE AFFECTIVE-DISORDERS [J].
ALDA, M ;
GROF, P ;
GROF, E ;
ZVOLSKY, P ;
WALSH, M .
ACTA PSYCHIATRICA SCANDINAVICA, 1994, 90 (04) :304-310
[6]   MN blood groups and bipolar disorder: Evidence of genotypic association and Hardy-Weinberg disequilibrium [J].
Alda, M ;
Grof, P ;
Grof, E .
BIOLOGICAL PSYCHIATRY, 1998, 44 (05) :361-363
[7]   Pathways-based analyses of whole-genome association study data in bipolar disorder reveal genes mediating ion channel activity and synaptic neurotransmission [J].
Askland, Kathleen ;
Read, Cynthia ;
Moore, Jason .
HUMAN GENETICS, 2009, 125 (01) :63-79
[8]   A genome screen of a large bipolar affective disorder pedigree supports evidence for a susceptibility locus on chromosome 13q [J].
Badenhop, RF ;
Moses, MJ ;
Scimone, A ;
Mitchell, PB ;
Ewen, KR ;
Rosso, A ;
Donald, JA ;
Adams, LJ ;
Schofield, PR .
MOLECULAR PSYCHIATRY, 2001, 6 (04) :396-403
[9]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[10]   Does lithium treatment still work?: Evidence of stable responses over three decades [J].
Baldessarini, RJ ;
Tondo, L .
ARCHIVES OF GENERAL PSYCHIATRY, 2000, 57 (02) :187-190