TY - JOUR
T1 - A genetic variation in the dysbindin gene (DTNBP1) is associated with memory performance in healthy controls
AU - Hashimoto, Ryota
AU - Noguchi, Hiroko
AU - Hori, Hiroaki
AU - Nakabayashi, Tetsuo
AU - Suzuki, Tatsuyo
AU - Iwata, Nakao
AU - Ozaki, Norio
AU - Kosuga, Asako
AU - Tatsumi, Masahiko
AU - Kamijima, Kunitoshi
AU - Harada, Seiichi
AU - Takeda, Masatoshi
AU - Saitoh, Osamu
AU - Kunugi, Hiroshi
N1 - Funding Information:
This work was supported in part by Grants-in-Aid from the Japanese Ministry of Health, Labor and Welfare (H19-kokoro-002 and H18-kokoro-005), the Japanese Ministry of Education, Culture, Sports, Science and Technology, CREST (Core research for Evolutional Science and Technology) of JST (Japan Science and Technology Agency), Grant-in-Aid for Scientific Research on Priority Areas · Research on Pathomechanisms of Brain Disorders · from the Ministry of Education, Culture, Sports, Science and Technology of Japan (18023045) and Japan Foundation for Neuroscience and Mental Health.
PY - 2010
Y1 - 2010
N2 - Schizophrenia is a common psychiatric disorder characterized by disturbances of cognition, emotion and social functioning. There are few studies investigating a possible genetic basis for the underlying mechanism of cognitive dysfunctions. A genetic variation in the dysbindin gene (DTNBP1: dystrobrevin binding protein 1), a susceptibility gene for schizophrenia, has been reported to be associated with general cognitive ability and cognitive decline in patients with schizophrenia. Although profound disturbances of memory performance are observed in schizophrenia, only one study has reported a relationship between this gene and spatial working memory in a Caucasian population. We examined a possible association between a protective haplotype of DTNBP1 for developing schizophrenia and memory performance measured by the Wechsler Memory Scale-Revised (WMS-R) and the Wechsler Adult Intelligence Scale-Revised (WAIS-R) in 165 healthy volunteers and 70 patients with schizophrenia in a Japanese population. Healthy controls that carry the protective haplotype showed higher performance in several memory domains measured by the WMS-R than those who did not. Genotype effect on memory performance was not observed in patients with schizophrenia. This haplotype did not affect IQ and its sub-scores as measured by the Wechsler Adult Intelligence Scale-Revised in both groups. These data suggest that DTNBP1 may have impact on parts of memory functions.
AB - Schizophrenia is a common psychiatric disorder characterized by disturbances of cognition, emotion and social functioning. There are few studies investigating a possible genetic basis for the underlying mechanism of cognitive dysfunctions. A genetic variation in the dysbindin gene (DTNBP1: dystrobrevin binding protein 1), a susceptibility gene for schizophrenia, has been reported to be associated with general cognitive ability and cognitive decline in patients with schizophrenia. Although profound disturbances of memory performance are observed in schizophrenia, only one study has reported a relationship between this gene and spatial working memory in a Caucasian population. We examined a possible association between a protective haplotype of DTNBP1 for developing schizophrenia and memory performance measured by the Wechsler Memory Scale-Revised (WMS-R) and the Wechsler Adult Intelligence Scale-Revised (WAIS-R) in 165 healthy volunteers and 70 patients with schizophrenia in a Japanese population. Healthy controls that carry the protective haplotype showed higher performance in several memory domains measured by the WMS-R than those who did not. Genotype effect on memory performance was not observed in patients with schizophrenia. This haplotype did not affect IQ and its sub-scores as measured by the Wechsler Adult Intelligence Scale-Revised in both groups. These data suggest that DTNBP1 may have impact on parts of memory functions.
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U2 - 10.3109/15622970902736503
DO - 10.3109/15622970902736503
M3 - Article
C2 - 19353385
AN - SCOPUS:77950841062
SN - 1562-2975
VL - 11
SP - 431
EP - 438
JO - World Journal of Biological Psychiatry
JF - World Journal of Biological Psychiatry
IS - 2 PART 2
ER -