Thirty-five alcoholic families have been studied to investigate the relationship between DNA markers at the monoamine oxidase (MAO) loci and 1) platelet activity levels and 2) alcoholism. A quantitative linkage analysis failed to reveal any evidence that the variation in activity levels cosegregates
Monoamine oxidases and alcoholism. I. Studies in unrelated alcoholics and normal controls
β Scribed by Parsian, A. ;Suarez, B. K. ;Tabakoff, B. ;Hoffman, P. ;Ovchinnikova, L. ;Fisher, L. ;Cloninger, C. R.
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 839 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0148-7299
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β¦ Synopsis
Abstract
Low platelet MAO activity has been associated with alcoholism. In order to evaluate the role of MAO genes in susceptibility to alcoholism, we have taken a biochemical and molecular genetic approach. The sample consisted of 133 alcoholic probands who were classified by subtypes of alcoholism and 92 normal controls. For those subjects typed for platelet MAO activity, alcoholics (N = 74) were found not to differ from the nonβalcoholics controls (N = 34). Neither was there a significant difference between type I and type II alcoholics or between either subtype and normal controls. However, we do find significant differences between male and female alcoholics, but not between male and female controls. The allele frequency distribution for the MAOβA and MAOβB dinucleotide repeats is different between the alcoholic sample (N = 133) and the normal control sample (N = 92). In a twoβway analysis of variance of MAOβB activity as a function of the allelic variation of each marker locus and diagnosis, there is no evidence for mean differences in activity levels for the different alleles. Our findings do not rule out a role for the MAOβB gene in controlling the enzyme activity because the dinucleotide repeats are located in introns. Β© 1995 WileyβLiss, Inc.
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