Serotonin transporter gene and schizophrenia: evidence for association/linkage disequilibrium in families with affected siblings

被引:44
作者
Hranilovic, D
Schwab, SG
Jernej, B
Knapp, M
Lerer, B
Albus, M
Rietschel, M
Kanyas, K
Borrmann, M
Lichtermann, D
Maier, W
Wildenauer, DB
机构
[1] Rudjer Boskovic Inst, Lab Neurochem & Mol Neurobiol, HR-10000 Zagreb, Croatia
[2] Univ Zagreb, Croatian Inst Brain Res, HR-10002 Zagreb, Croatia
[3] Univ Bonn, Dept Psychiat, D-53105 Bonn, Germany
[4] Univ Bonn, Dept Med Stat, D-53105 Bonn, Germany
[5] Hebrew Univ Jerusalem, Hadassah Med Ctr, Biol Psychiat Unit, IL-91120 Jerusalem, Israel
[6] Mental State Hosp, D-85529 Haar, Germany
关键词
5-HTT; polymorphism; schizophrenia; TDT; intron; promoter;
D O I
10.1038/sj.mp.4000599
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The serotonergic (5-HT) system has been implicated in the etiopathogenesis of psychoses. Since the 5-HT transporter plays an important role in regulation of 5-HT transmission, its gene can be considered as a candidate for vulnerability to psychiatric disorders. Two polymorphic sites of the 5-HT transporter gene-5-HTTLPR, a VNTR in the 5' regulatory region, and a VNTR in the second intron-were studied in a sample of 61 families with schizophrenia for transmission disequilibrium. Each family contained at least two siblings affected with schizophrenia or schizoaffective disorder (mainly schizophrenic). One hundred and thirty-nine affected offspring with parental information for genotyping, were available for analysis. No preferential transmission of either short or long alleles of the promoter polymorphism was observed. However, a transmission distortion was detected for alleles of the intronic VNTR polymorphism (chi(TDT max)(2) =14.33; P = 0.0002; corrected P Value = 0.0003) resulting in more frequent than expected transmission of the 12 repeat allele, This finding adds additional evidence to the idea that the serotonergic system may be involved in development of psychoses.
引用
收藏
页码:91 / 95
页数:5
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