Association of monoamine oxidase (MAO) activity with alcoholism and alcoholic subtypes
โ Scribed by Devor, Eric J. ;Cloninger, C. Robert ;Hoffman, Paula L. ;Tabakoff, Boris
- Publisher
- John Wiley and Sons
- Year
- 1993
- Tongue
- English
- Weight
- 576 KB
- Volume
- 48
- Category
- Article
- ISSN
- 0148-7299
No coin nor oath required. For personal study only.
โฆ Synopsis
A familial/genetic study of platelet monoamine oxidase (MAO) activity in alcoholics was carried out. M A 0 activities were determined using phenylethylamine (PEA) as substrate at K, concentration (1.2 pM) and at saturating concentration (12.0 pM). Complex segregation analysis of familial data indicated a single major gene mode of transmission of activity at both substrate concentrations. In addition, the present sample size (13 families, 108 members) proved sufficient to allow correlation analysis of enzyme activity with affection status and clinical subtypes of affecteds. M A 0 activity was significantly correlated with alcoholism at both K, and saturating substrate concentrations and a significant correlation between low M A 0 activity and Cloninger Type I1 alcoholism was seen at K, substrate concentration. These results confirm a hierarchical cosegregation of platelet M A 0 activity and alcoholism suggesting that MA0 activity warrants continued status as a marker in alcoholism.
๐ SIMILAR VOLUMES
## Abstract Variation in the personality trait of neuroticism is known to be affected by genetic influences, but despite a number of association studies, the genes involved have not yet been characterized. In a recent study of platelet monoamine oxidase in 1,551 twin subjects, we found a significan
Monoamine oxidase B (MAO-B) is implicated in the cause of Parkinson's disease (PD) because of its role in metabolizing the neurotoxin l-methyl-4-phenyl-l,2,3,6-tetrahydropyridine, and forming H,02 during dopamine metabolism. Altered MAO-B activity has been observed in PD platelets. Polymerase chain
## Monoamine oxidase B (MAO -B ) is an enzyme that has relevance for Parkinson disease (PD) because of its roles in catabolizing dopamine and potentially activating exogenous neurotoxicants. A polymorphism of the gene encoding MAO-B has been identified as a single base change (A or G) in intron