Related Experiment Video
Updated: Mar 26, 2026

A Plate-Based Assay for the Measurement of Endogenous Monoamine Release in Acute Brain Slices
Published on: August 11, 2021
Monoamine oxidase and agitation in psychiatric patients
Matea Nikolac Perkovic1, Dubravka Svob Strac1, Gordana Nedic Erjavec1
1Rudjer Boskovic Institute, Division of Molecular Medicine, Bijenicka cesta 54, 10000 Zagreb, Croatia.
Abstract:
Subjects with schizophrenia or conduct disorder display a lifelong pattern of antisocial, aggressive and violent behavior and agitation. Monoamine oxidase (MAO) is an enzyme involved in the degradation of various monoamine neurotransmitters and neuromodulators and therefore has a role in various psychiatric and neurodegenerative disorders and pathological behaviors. Platelet MAO-B activity has been associated with psychopathy- and aggression-related personality traits, while variants of the MAOA and MAOB genes have been associated with diverse clinical phenotypes, including aggressiveness, antisocial problems and violent delinquency. The aim of the study was to evaluate the association of platelet MAO-B activity, MAOB rs1799836 polymorphism and MAOA uVNTR polymorphism with severe agitation in 363 subjects with schizophrenia and conduct disorder. The results demonstrated significant association of severe agitation and smoking, but not diagnosis or age, with platelet MAO-B activity. Higher platelet MAO-B activity was found in subjects with severe agitation compared to non-agitated subjects. Platelet MAO-B activity was not associated with MAOB rs1799836 polymorphism. These results suggested the association between increased platelet MAO-B activity and severe agitation. No significant association was found between severe agitation and MAOA uVNTR or MAOB rs1799836 polymorphism, revealing that these individual polymorphisms in MAO genes are not related to severe agitation in subjects with schizophrenia and conduct disorder. As our study included 363 homogenous Caucasian male subjects, our data showing this negative genetic association will be a useful addition to future meta-analyses.
Insights
Increased platelet monoamine oxidase-B (MAO-B) activity is linked to severe agitation in individuals with schizophrenia or conduct disorder. Genetic variations in MAOA and MAOB genes were not associated with agitation in this study group.
Area of Science:
- Neuroscience
- Psychiatry
- Genetics
Background:
- Monoamine oxidase (MAO) enzymes regulate neurotransmitters, impacting psychiatric disorders and behavior.
- Platelet MAO-B activity and MAO gene variants are implicated in aggression and antisocial traits.
Purpose of the Study:
- To investigate the association between platelet MAO-B activity, MAOB rs1799836 polymorphism, and MAOA uVNTR polymorphism with severe agitation.
Main Methods:
- Studied 363 Caucasian males with schizophrenia or conduct disorder.
- Assessed platelet MAO-B activity and specific MAOA/MAOB gene polymorphisms.
- Correlated findings with the presence and severity of agitation.
Main Results:
- Severe agitation showed a significant association with higher platelet MAO-B activity.
- Platelet MAO-B activity was also associated with smoking status.
- No significant association was found between severe agitation and MAOB rs1799836 or MAOA uVNTR polymorphisms.
Conclusions:
- Elevated platelet MAO-B activity may be a biomarker for severe agitation in schizophrenia and conduct disorder.
- Specific MAO gene polymorphisms (MAOA uVNTR, MAOB rs1799836) are not directly related to severe agitation in this population.
Related Concept Videos
Antidepressant Drugs: MAOIs and Other Agents
Mania and Antimanic Drugs: Overview
Parkinson's Disease: Treatment
Parkinson's Disease is primarily a result of the loss of dopaminergic neurons in the substantia nigra pars compacta. The cornerstone of...
Drugs Affecting Neurotransmitter Synthesis
Drugs Affecting Neurotransmitter Release or Uptake
Adrenergic Agonists: Indirect-Acting Agents
One mechanism involves depleting stored catecholamines by displacing them from synaptic vesicles. These agents, known as "displacers," are transported into vesicles at the expense of noradrenaline. Examples include amphetamine and tyramine, which lack a catechol moiety, resulting in prolonged action, improved oral...

