Schizophrenia is a highly heritable condition, as demonstrated in family, twin and adoption studies. Candidate genes from the dopaminergic system have long been hypothesized to be involved in the etiology of this disorder. In the present study, we investigated the genetic association between polymorphisms in the D2 and D3 dopamine receptor (DRD2, DRD3) genes and schizophrenia. We examined 90 trios from Portugal, and negative results were obtained from association studies with both Haplotype Relative Risk (HRR) and Transmission Disequilibrium Test (TDT), as well as TRANSMIT. Therefore, we conclude that neither the DRD2 nor the DRD3 gene polymorphisms investigated are associated with schizophrenia in our sample. (C) 2004 Elsevier Ireland Ltd. All rights reserved.

Family association study between DRD2 and DRD3 gene polymorphisms and schizophrenia in a Portuguese population / A. Ambrosio, J. Kennedy, F. Macciardi, A. Macedo, J. Valente, A. Dourado, C. Oliveira, C. Pato. - In: PSYCHIATRY RESEARCH. - ISSN 0165-1781. - 125:3(2004), pp. 185-191.

Family association study between DRD2 and DRD3 gene polymorphisms and schizophrenia in a Portuguese population

F. Macciardi;
2004

Abstract

Schizophrenia is a highly heritable condition, as demonstrated in family, twin and adoption studies. Candidate genes from the dopaminergic system have long been hypothesized to be involved in the etiology of this disorder. In the present study, we investigated the genetic association between polymorphisms in the D2 and D3 dopamine receptor (DRD2, DRD3) genes and schizophrenia. We examined 90 trios from Portugal, and negative results were obtained from association studies with both Haplotype Relative Risk (HRR) and Transmission Disequilibrium Test (TDT), as well as TRANSMIT. Therefore, we conclude that neither the DRD2 nor the DRD3 gene polymorphisms investigated are associated with schizophrenia in our sample. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
Association study; Candidate genes; Haplotypes; Linkage disequilibrium; Schizophrenia
Settore MED/03 - Genetica Medica
2004
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/201479
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