No association between the dopamine D3 receptor Bal I polymorphism and schizophrenia in a family-based study of a Palestinian Arab population

• Published in: American journal of medical genetics 2000-12, Vol.96 (6), p.778-780
• Main Authors: Kremer, I., Rietschel, M., Dobrusin, M., Mujaheed, M., Murad, I., Blanaru, M., Bannoura, I., Müller, D.J., Schulze, T.G., Reshef, A., Gathas, S., Schwab, S., Wildenauer, D., Bachner-Melman, R., Belmaker, R.H., Maier, W., Ebstein, R.P.
• Format: Article
• Language: English
• Subjects: Alleles; Arabs - genetics; Cohort Studies; dopamine d3 receptor; Family Health; Gene Frequency; genetics; Genotype; haplotype relative risk; Humans; Israel; linkage disequilibrium; polymorphism; Polymorphism, Genetic; Receptors, Dopamine D2 - genetics; Receptors, Dopamine D3; schizophrenia; Schizophrenia - genetics
• ISSN: 0148-7299; 1096-8628
• DOI: 10.1002/1096-8628(20001204)96:6<778::AID-AJMG16>3.0.CO;2-2

Several recent meta‐analyses appear to show a weak but significant effect of both forms of the gly/ser DRD3 polymorphism in conferring risk for schizophrenia. Since most studies have employed the artifact‐prone case‐control design, we thought it worthwhile to examine the role of this polymorphism using a robust family‐based strategy in an ethnic group not previously systematically studied in psychiatric genetics, Palestinian Arabs. We failed to obtain any evidence in 129 Palestinian triads, using the haplotype relative risk (allele frequency: Pearson chi‐square = 0.009, P > 0.1, df = 1, n = 258 alleles) or transmission disequilibrium test design (chi‐square = 0.38, P > 0.1, n = 86 families) for association/linkage (or increased homozygosity) of the DRD3 Bal I polymorphism to schizophrenia in our sample. Am. J. Med. Genet. (Neuropsychiatr. Genet.) 96:778–780, 2000. © 2000 Wiley‐Liss, Inc.