TY - JOUR
T1 - A review and re-evaluation of an association between the NOTCH4 locus and schizophrenia
AU - Wang, Zhenqi
AU - Wei, Jun
AU - Zhang, Xuan
AU - Guo, Yingjun
AU - Xu, Qi
AU - Liu, Shuzheng
AU - Shi, Jieping
AU - Yu, Yaqin
AU - Ju, Guizhi
AU - Li, Yulin
AU - Shen, Yan
N1 - (c) 2006 Wiley-Liss, Inc.
PY - 2006/12/5
Y1 - 2006/12/5
N2 - This work reviewed all the reports on the NOTCH4 gene in schizophrenia, which have been published since the gene was found to be associated with illness among a British population in 2000. The results from independent studies were inconsistent. Allelic heterogeneity, clinical diagnosis, ethnical backgrounds, and linkage disequilibrium (LD) structures in the human genome may be major reasons for poor replication. A couple of studies suggested that the NOTCH4 gene could play a role in a subgroup of the disease, such as early-onset schizophrenia and negative symptoms. A single study revealed a weak association of the NOTCH4 gene with frontal lobe brain volumes and a strong association with frontal lobe cognitive performance. A meta-analysis showed stronger evidence of the NOTCH4 association in family-based studies than in case-control studies. In a previous study, we found that rs520692, a single nucleotide polymorphism (SNP) at the NOTCH4 locus, was associated with schizophrenia in a Chinese population. In the present study, we applied a large sample size to re-evaluate our initial findings and then confirmed the rs520692 association with illness. The pairwise measures did not show strong LD between paired SNPs although the SNPs tested are located within a 34-kb region, suggesting that LD within the NOTCH4 gene has been broken rapidly by historical recombination in the Chinese population. Taken together, the NOTCH4 gene may be associated with schizophrenia but how the gene contributes to the etiology of the illness needs a further investigation.
AB - This work reviewed all the reports on the NOTCH4 gene in schizophrenia, which have been published since the gene was found to be associated with illness among a British population in 2000. The results from independent studies were inconsistent. Allelic heterogeneity, clinical diagnosis, ethnical backgrounds, and linkage disequilibrium (LD) structures in the human genome may be major reasons for poor replication. A couple of studies suggested that the NOTCH4 gene could play a role in a subgroup of the disease, such as early-onset schizophrenia and negative symptoms. A single study revealed a weak association of the NOTCH4 gene with frontal lobe brain volumes and a strong association with frontal lobe cognitive performance. A meta-analysis showed stronger evidence of the NOTCH4 association in family-based studies than in case-control studies. In a previous study, we found that rs520692, a single nucleotide polymorphism (SNP) at the NOTCH4 locus, was associated with schizophrenia in a Chinese population. In the present study, we applied a large sample size to re-evaluate our initial findings and then confirmed the rs520692 association with illness. The pairwise measures did not show strong LD between paired SNPs although the SNPs tested are located within a 34-kb region, suggesting that LD within the NOTCH4 gene has been broken rapidly by historical recombination in the Chinese population. Taken together, the NOTCH4 gene may be associated with schizophrenia but how the gene contributes to the etiology of the illness needs a further investigation.
KW - Asian Continental Ancestry Group
KW - Cognition
KW - Female
KW - Frontal Lobe
KW - Genetic Predisposition to Disease
KW - Genetics, Population
KW - Humans
KW - Linkage Disequilibrium
KW - Male
KW - Polymorphism, Restriction Fragment Length
KW - Polymorphism, Single Nucleotide
KW - Proto-Oncogene Proteins
KW - Receptors, Notch
KW - Schizophrenia
U2 - 10.1002/ajmg.b.30383
DO - 10.1002/ajmg.b.30383
M3 - Article
C2 - 16894623
SN - 1552-4841
VL - 141B
SP - 902
EP - 906
JO - American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
JF - American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics
IS - 8
ER -