Monoamine oxidase (MAO) play a critical role in the degradation of endogeno
us and exogenous amines throughout the body. There are two distinct MAO iso
forms, MAO-A and MAO-B, which both are encoded in genes on the X chromosome
. Alterations in MAO-B activity have previously been connected with several
neurological disorders. Platelet MAO (trbc-MAO) is exclusively of the B-ty
pe and the catalytic activity of this enzyme is under strong, yet unknown,
genetic control. Specific trbc-MAO activity has been reported to be increas
ed in certain neurodegenerative diseases and to correlate with personality
traits such as sensation seeking and impulsiveness. In the present study, w
e investigated if trbc-MAO activity is associated with genotype at a variab
le region (A/G dimorphism) in intron 13 of the human gene encoding MAO-B. T
he MAOB intron 13 allele status and levels of trbc-MAO were determined for
55 Caucasian non-smoking males.
Individuals with the "A-allele" displayed significantly lower enzyme activi
ty than individuals with the "G-allele" displayed significantly lower enzym
e activity than individuals with the "G-allele" i.e. 11.4 +/- 0.6 nmol/10(1
0) platelets/min compared with 13.5 +/- 0.6 (mean +/- SEM, p = 0.019).
The present results suggest that the MAOB genotype may be involved in deter
mining trbc-MAO activity.