Preferential transmission of interleukin-1 receptor antagonist alleles in attention deficit hyperactivity disorder

被引:52
作者
Segman, RH [1 ]
Meltzer, A
Gross-Tsur, V
Kosov, A
Frisch, A
Inbar, E
Darvasi, A
Levy, S
Goltser, T
Weizman, A
Galili-Weisstub, E
机构
[1] Hebrew Univ Jerusalem, Hadassah Med Ctr, Dept Psychiat, IL-91240 Jerusalem, Israel
[2] Hebrew Univ Jerusalem, Hadassah Med Ctr, Child & Adolescent Psychiat Unit, IL-91240 Jerusalem, Israel
[3] Shaare Zedek Med Ctr, Neuropediat Unit, Jerusalem, Israel
[4] Tel Aviv Univ, Sackler Fac Med, Felsenstein Med Res Ctr, IL-69978 Tel Aviv, Israel
[5] Geha Psychiat Hosp, Petah Tiqwa, Israel
[6] Hebrew Univ Jerusalem, Inst Life Sci, IL-91904 Jerusalem, Israel
关键词
attention deficit hyperactivity disorder; ADHD; interleukin-1 receptor antagonist gene; transmission disequilibrium test;
D O I
10.1038/sj/mp/4000919
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
Attention deficit hyperactivity disorder (ADHD) is a common neurodevelopmental disorder, where family data support substantial heritability.(1) To date, association studies focussed mainly on genes regulating dopaminergic neurotransmission.(2) Interleukin-1 (IL-1) activity in the brain has been implicated with differentiation of doparninergic neurons(3,4) and modulation of central monoaminergic reactivity.(5) We investigated the role of interieukin-1 receptor antagonist (IL-1Ra) gene variable number tandem repeat (VNTR) polymorphism,(6) in a sample of 86 children with DSM-IV ADHD and their parents. Transmission disequilibrium analysis showed increased transmission of the IL-1 Ra 4-repeat allele (x(2) = 4.07, P = 0.04) and decreased transmission of the 2-repeat allele (x(2) = 4.59, P = 0.03) to affected children. The 4-repeat allele was associated with a significantly increased risk for ADHD (x(2) = 4.46, df 1, P = 0.035, RR = 1.292, 95% Cl 1.01-1.66). The IL-1Ra 2-repeat allele was associated with a significantly decreased risk for ADHD (x(2) = 4.65, df 1, P= 0.03, RR = 0.763, 95% Cl 0.59-0.98). If replicated, this finding may point to a role for brain cytokine activity in the etiopathogenesis of ADHD.
引用
收藏
页码:72 / 74
页数:3
相关论文
共 24 条
[1]   Mission: Not impossible? Candidate gene studies in child psychiatric disorders [J].
Collier, DA ;
Curran, S ;
Asherson, P .
MOLECULAR PSYCHIATRY, 2000, 5 (05) :457-460
[2]  
CONNERS CK, 1985, PSYCHOPHARMACOL BULL, V21, P809
[3]  
Grimaldi LME, 2000, ANN NEUROL, V47, P361, DOI 10.1002/1531-8249(200003)47:3<361::AID-ANA12>3.0.CO
[4]  
2-N
[5]  
Hurme M, 1998, EUR J IMMUNOL, V28, P2598, DOI 10.1002/(SICI)1521-4141(199808)28:08<2598::AID-IMMU2598>3.3.CO
[6]  
2-B
[7]   Association of two variants in IL-1β and IL-1 receptor antagonist genes with multiple sclerosis [J].
Kantarci, OH ;
Atkinson, EJ ;
Hebrink, DD ;
McMurray, CT ;
Weinshenker, BG .
JOURNAL OF NEUROIMMUNOLOGY, 2000, 106 (1-2) :220-227
[8]   Polymorphisms of the interleukin-1 gene complex in schizophrenia [J].
Katila, H ;
Hänninen, K ;
Hurme, M .
MOLECULAR PSYCHIATRY, 1999, 4 (02) :179-181
[9]   Schedule for Affective Disorders and Schizophrenia for School-Age Children Present and Lifetime version (K-SADS-PL): Initial reliability and validity data [J].
Kaufman, J ;
Birmaher, B ;
Brent, D ;
Rao, U ;
Flynn, C ;
Moreci, P ;
Williamson, D ;
Ryan, N .
JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 1997, 36 (07) :980-988
[10]   Influence of interleukin-1β on exploratory behaviors, plasma ACTH, corticosterone, and central biogenic amines in mice [J].
Lacosta, S ;
Merali, Z ;
Anisman, H .
PSYCHOPHARMACOLOGY, 1998, 137 (04) :351-361