Effect of Polymorphisms of Three Genes Mediating Monoamine Signalling on Brain Morphometry in Schizophrenia and Healthy Subjects.
- Author:
Anupa A VIJAYAKUMARI
1
;
John P JOHN
;
Harsha N HALAHALLI
;
Pradip PAUL
;
Priyadarshini THIRUNAVUKKARASU
;
Meera PURUSHOTTAM
;
Sanjeev JAIN
Author Information
- Publication Type:Original Article
- Keywords: Magnetic resonance imaging; Gene polymorphism; Catechol-O-methyl transferase; 5-Hydroxy tryptamine 2A; 5-Hydroxy tryptamine transporter linked polymorphic region; Voxel-based morphometry
- MeSH: Alleles; Brain*; Catechol O-Methyltransferase; Humans; India; Magnetic Resonance Imaging; National Institute of Mental Health (U.S.); Negotiating*; Neurosciences; Outpatients; Phenotype; Schizophrenia*
- From:Clinical Psychopharmacology and Neuroscience 2015;13(1):68-82
- CountryRepublic of Korea
- Language:English
- Abstract: OBJECTIVE: We examined the effect of risk alleles of polymorphisms of three schizophrenia risk genes that mediate monoamine signalling in the brain on regional brain volumes of schizophrenia and healthy control subjects. The risk alleles and the gene polymorphisms studied were: Val allele of catechol o-methyltransferase (COMT) rs4680 polymorphism; short allele of 5-hydroxy tryptamine transporter linked polymorphic region (5HTTLPR) polymorphism; and T allele of 5-hydroxy tryptamine 2A (5HT2A) rs6314 polymorphism. METHODS: The study was carried out on patients with recent onset schizophrenia (n=41) recruited from the outpatient department of National Institute of Mental Health and Neurosciences, Bangalore, India and healthy control subjects (n=39), belonging to South Indian Dravidian ethnicity. Individual and additive effects of risk alleles of the above gene polymorphisms on brain morphometry were explored using voxel-based morphometry. RESULTS: Irrespective of phenotypes, individuals with the risk allele T of the rs6314 polymorphism of 5HT2A gene showed greater (at cluster-extent equivalent to family wise error-correction [FWEc] p<0.05) regional brain volumes in the left inferior temporal and left inferior occipital gyri. Those with the risk alleles of the other two polymorphisms showed a trend (at p<0.001, uncorrected) towards lower regional brain volumes. A trend (at p<0.001, uncorrected) towards additive effects of the above 3 risk alleles (subjects with 2 or 3 risk alleles vs. those with 1 or no risk alleles) on brain morphology was also noted. CONCLUSION: The findings of the present study have implications in understanding the role of individual and additive effects of genetic variants in mediating regional brain morphometry in health and disease.
