Schizophrenia is not associated with DRD4 48-base-pair-repeat length or individual alleles: Results of a meta-analysis

被引:19
作者
Glatt, SJ
Faraone, SV
Tsuang, MT
机构
[1] Massachusetts Mental Hlth Ctr, Harvard Med Sch, Dept Psychiat, Boston, MA 02115 USA
[2] Massachusetts Gen Hosp, Harvard Inst Psychiat Epidemiol & Genet, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Psychiat Serv, Boston, MA 02114 USA
[4] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
关键词
schizophrenia; gene; association; meta-analysis; dopamine; D4; receptor;
D O I
10.1016/S0006-3223(03)00180-X
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Background: The gene DRD4, coding for dopamine receptor D4, was considered a candidate for association with schizophrenia based on its upregulation in postmortem schizophrenic brain and affinity for clozapine. Many studies sought allelic association of a 48-base-pair repeat in DRD4 exon 3 with schizophrenia, but found no strong evidence for a relationship. The present work sought to determine if this observation reflected the true absence of association or the low power of individual studies. Methods: We performed four meta-analyses, sequentially considering the two-, four-, and seven-repeat alleles as risk alleles., and then considering repeat length of the 48-base-pair segment as a risk factor. Each meta-analysis included at least 2300 cases and 2100 controls from 14-16 studies. Results: The pooled odds ratio from each analysis approximated 1.0, and none were significant. Heterogeneity was not observed, although gender moderated the effects of repeat length and the seven-repeat allele. Conclusions: Despite over 90% power to detect a significant odds ratio of 1.4 or less, none was observed. This polymorphism seems not to influence risk for most schizophrenia cases; however, a sex-dependent relationship, or a role in some clinical features of the disorder, cannot be excluded and should be pursued experimentally.
引用
收藏
页码:629 / 635
页数:7
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