C9orf72 repeat expansions that cause frontotemporal dementia are detectable among patients with psychosis

被引:20
|
作者
Watson, Annie [1 ]
Pribadi, Mochtar [2 ,3 ]
Chowdari, Kodavali [1 ]
Clifton, Sue [1 ]
Wood, Joel [1 ]
Miller, Bruce L. [4 ]
Coppola, Giovanni [2 ,3 ]
Nimgaonkar, Vishwajit [1 ,5 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Psychiat, Pittsburgh, PA 15213 USA
[2] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Human Behav, Dept Psychiat, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, David Geffen Sch Med, Semel Inst Neurosci & Human Behav, Dept Neurol, Los Angeles, CA 90095 USA
[4] Univ Calif San Francisco, Memory & Aging Ctr, Sandler Neurosci Ctr, San Francisco, CA 94143 USA
[5] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Human Genet, Pittsburgh, PA 15213 USA
关键词
Schizophrenia; Schizoaffective disorder; Dementia; HEXANUCLEOTIDE REPEAT; SCHIZOPHRENIA;
D O I
10.1016/j.psychres.2015.12.007
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
A pathologic hexanucleotide repeat expansion in C9orf72 causes frontotemporal dementia (FTD) or amyotrophic lateral sclerosis (ALS). Behavioral abnormalities can also occur among mutation carriers with FTD, but it is uncertain whether such mutations occur among persons with psychoses per se. Among participants in a genetic study of psychoses (N=739), two pairs of related individuals had C9orf72 expansions, of whom three were diagnosed with schizophrenia (SZ) schizoaffective disorder (SZA), but their clinical features did not suggest dementia or ALS. A few patients with SZ/SZA carry C9orf72 repeat expansions; such individuals are highly likely to develop FTD/ALS. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:200 / 202
页数:3
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