Association of autism severity with a monoamine oxidase A functional polymorphism

被引:110
|
作者
Cohen, IL
Liu, X
Schutz, C
White, BN
Jenkins, EC
Brown, WT
Holden, JJA
机构
[1] New York State Inst Basic Res Dev Disabil, Dept Psychol, Staten Isl, NY 10314 USA
[2] New York State Inst Basic Res Dev Disabil, Dept Cytogenet, Staten Isl, NY 10314 USA
[3] New York State Inst Basic Res Dev Disabil, Dept Human Genet, Staten Isl, NY 10314 USA
[4] Queens Univ, Dept Psychiat, Kingston, ON K7L 3N6, Canada
[5] Queens Univ, Dept Physiol, Kingston, ON K7L 3N6, Canada
[6] Queens Univ, Dept Cytogenet, Kingston, ON, Canada
[7] Queens Univ, DNA Res Lab, Kingston, ON, Canada
[8] Trent Univ, Dept Biol, Peterborough, ON K9J 7B8, Canada
关键词
autism; autism severity; genetic heterogeneity; IQ; MAOA; uVNTR;
D O I
10.1034/j.1399-0004.2003.00115.x
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A functional polymorphism (the upstream variable-number tandem repeat region, or uVNTR) in the monoamine oxidase A (MAOA) promoter region has been reported to be associated with behavioral abnormalities as well as increased serotonergic responsivity. We examined the relation between MAOA-uVNTR alleles and the phenotypic expression of autism in 41 males younger than 12.6 years of age. Children with the low-activity MAOA allele had both lower intelligence quotients (IQ) and more severe autistic behavior than children with the high-activity allele. In follow-up testing of 34 of the males at the 1-year time-point, those with the low-activity allele showed a worsening in IQ but no change in the severity of their autistic behavior. We conclude that functional MAOA-uVNTR alleles may act as a genetic modifier of the severity of autism in males.
引用
收藏
页码:190 / 197
页数:8
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