DTNBP1 genotype influences cognitive decline in schizophrenia

被引:93
作者
Burdick, Katherine E.
Goldberg, Terry E.
Funke, Birgit
Bates, John A.
Lencz, Todd
Kucherlapati, Raju
Malhotra, Anil K.
机构
[1] N Shore Long Isl Jewish Hlth Syst, Zucker Hillside Hosp, Div Psychiat Res, Glen Oaks, NY 11004 USA
[2] Harvard Univ, Partners Ctr Genet & Genom, Boston, MA USA
关键词
dysbindin; schizophrenia; cognitive decline; genetics; GENETIC-VARIATION; DYSBINDIN; RISK; PERFORMANCE; DISORDER;
D O I
10.1016/j.schres.2006.09.008
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Intellectual decline is common in schizophrenia and predicts functional outcome. While many patients undergo intellectual decline that typically predates the onset of symptoms, few studies have investigated the underlying mechanism through which this occurs. The current study assessed the relationship between intellectual decline in schizophrenia and genetic variation in dysbindin-1 (DTNBP1). Methods: We assessed cognitive decline in 183 Caucasian patients with schizophrenia using a proxy measure of premorbid IQ with which current general cognitive ability (g) was compared. We then tested for a relationship between the risk haplotype identified in previous work (CTCTAC) and intellectual decline. Results: We found that carriers of the CTCTAC haplotype, demonstrated a significantly greater decline in IQ as compared with non-carriers (p=0.05). Conclusions: These data Suggest that DTNBP1 influences the severity of intellectual decline in schizophrenia and may represent one underlying cause for heterogeneity in cognitive course. (c) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 172
页数:4
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