Correlation of length of VNTR alleles at the X-linked MAOA gene and phenotypic effect in Tourette syndrome and drug abuse

Mol Psychiatry. 1998 Jan;3(1):50-60. doi: 10.1038/


Abnormalities in monoamine oxidase (MAO) levels have been implicated in a wide range of psychiatric disorders. We have examined a VNTR polymorphism at the X-linked MAOA gene to test two hypotheses: (1) Do variants of the MAOA gene play a role in any of the behavioral disorders associated with Tourette syndrome or drug abuse? (2) If so, is there any correlation between the length of the alleles and the phenotypic effect? We examined two independent groups: 375 TS patients, relatives and controls, and 280 substance abusers and controls. The alleles were divided into four groups of increasing size. There was a significant association between the MAOA gene and behavioral phenotypes in both groups, and in both the longest alleles were associated with the greatest phenotypic effect. The strongest effect was for the diagnosis of drug dependence (P=0.00003). The VNTR allele groups were in significant linkage disequilibrium with the Fnu4H1 polymorphism previously shown to be associated with MAO-A activity. While these results are consistent with the possibility that different-sized alleles of the short-repeat polymorphisms themselves may play a role in gene regulation, further studies directly linking these alleles with enzyme levels need to be done.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alleles
  • Analysis of Variance
  • Chromosome Mapping
  • Family
  • Humans
  • Isoenzymes / genetics
  • Linkage Disequilibrium
  • Mental Disorders / classification
  • Mental Disorders / genetics*
  • Minisatellite Repeats*
  • Monoamine Oxidase / genetics*
  • Multivariate Analysis
  • Phenotype
  • Quantitative Trait, Heritable
  • Reference Values
  • Regression Analysis
  • Substance-Related Disorders / genetics*
  • Tourette Syndrome / genetics*
  • X Chromosome*


  • Isoenzymes
  • Monoamine Oxidase