Association of MB-COMT polymorphisms with schizophrenia-susceptibility and symptom severity in an African cohort |
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Authors: | Wright Galen E B Niehaus Dana J H van der Merwe Lize Koen Liezl Korkie Lundi J Kinnear Craig J Drögemöller Britt I Warnich Louise |
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Affiliation: | Department of Genetics, Stellenbosch University, Private bag X1, Matieland, 7602, South Africa. |
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Abstract: | The catechol-O-methyltransferase (COMT) gene is an attractive schizophrenia candidate gene, encoding a catabolic dopamine enzyme. The enzyme exists as two distinct isoforms, with the membrane bound enzyme (i.e. MB-COMT) being predominantly expressed in the brain. Since African populations remain underrepresented in genetic/genomic research, we performed an association study to determine whether MB-COMT genetic variants are associated with schizophrenia-susceptibility and symptom severity in the South African Xhosa population. Fourteen candidate polymorphisms were selected by means of a literature search and in silico analyses and were subsequently genotyped in a cohort of 238 Xhosa schizophrenia patients and 240 healthy Xhosa controls. Genetic association was tested with schizophrenia-susceptibility as well as symptom severity within the patient group. Polymorphisms of interest were also analysed using functional assays. Two SNPs, rs2020917 (OR=0.54, 95% CI 0.37-0.79; P=0.0011) and rs737865 (OR=0.52, 95% CI 0.36-0.74; P=0.0002), in the P2 promoter region were significantly associated with schizophrenia as well as an increase (increase=11.2%, 95% CI 3.7%-19.2%; P=0.0031) in reporter gene expression. The minor alleles of these SNPs were underrepresented in the schizophrenia cohort, indicating a possible protective effect. The P2 region also formed part of a haplotype found to be associated with the severity of the negative symptoms of the disorder. The data generated by this study indicate that genetic variation of MB-COMT could be associated with schizophrenia and negative symptom severity in the Xhosa population and may therefore be one of the genomic loci contributing towards the disorder in the South African community. Future large-scale studies in other African schizophrenia populations are required to further elucidate the significance of these findings. |
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Keywords: | 22qDS, 22q11.2 deletion syndrome A, adenine bp, base pairs C, cytosine CI, confidence interval COMT, catechol-O-methyltransferase DNA, deoxyribonucleic acid DSM-IV, diagnostic and statistical manual of mental disorders G, guanine gDNA, genomic DNA HWE, Hardy–Weinberg equilibrium kb, kilobase pairs LD, linkage disequilibrium LQ, lower quartile MB-COMT, membrane-bound catechol-O-methyltransferase Met, methionine n, individuals OCD, obsessive–compulsive disorder OR, odds ratio PCR, polymerase chain reaction S-COMT, soluble catechol-O-methyltransferase SANS, Scale for the Assessment of Negative Symptoms SAPS, Scale for the Assessment of Positive Symptoms SNP, single nucleotide polymorphism T, thymine UQ, upper quartile Val, valine |
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