Key result
The MAOA-LPR polymorphism showed no association with auditory evoked potential components in 234 normal young Chinese females.
Why the study?
Is the MAOA-LPR polymorphism associated with long-latency auditory evoked potentials in healthy young females?
Observational (n=234)
Is the MAOA-LPR polymorphism associated with long-latency auditory evoked potentials in healthy young females?
The MAOA-LPR polymorphism does not appear to play a major role in modulating auditory evoked potentials in normal young females.
Answers are grounded in this paper and cite their sources.
No clinical role for MAOA-LPR testing in auditory evoked potentials; leaves open its relevance in other populations or phenotypes.
The components of auditory evoked potentials (AEPs) have been demonstrated to be heritable and to be influenced by different neurotransmitter activities such as serotonin or dopamine. Monoamine oxidase A (MAOA) is a mitochondrial enzyme involved in the degradation of dopamine, serotonin and norepinephrine. We examined the potential association of the functional 30-bp repeat MAOA gene-linked polymorphism region (MAOA-LPR) in 234 normal young Chinese females. The results demonstrated that there is no association for MAOA-LPR polymorphism and AEP components. Our negative findings suggested that this genetic polymorphism does not play a major role in the modulation of AEPs in normal young females, but we could not exclude that other polymorphisms of the MAOA gene affect AEP components. Further exploration of the other polymorphisms of the MAOA gene and multiple interactions of the polymorphisms in various neurotransmitter systems may be needed in future studies.
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Yu et al. (2004) conducted an observational in Healthy (n=234). MAOA-LPR polymorphism was evaluated on Auditory evoked potentials (AEPs) components. The MAOA-LPR polymorphism showed no association with auditory evoked potential components in 234 normal young Chinese females.
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