Skip to search boxSkip to navigationSkip to main content

Association of DAOA polymorphisms with schizophrenia and clinical symptoms or therapeutic effects

  • Weihua Yue
    ,
  • Guolian Kang
    ,
  • Yanbo Zhang
    ,
  • Mei Qu
    ,
  • Fulei Tang
    ,
  • Yonghua Han
*Corresponding author for this work
  • Peking University
    ,
  • CAS - Academy of Mathematics and System Sciences
    ,
  • Michigan State University
Scholary Output:
Contribution to journal
Article
Peer-review

Abstract

The present study examined the correlation between variants in the d-amino acid oxidase activator (DAOA) locus and clinical symptoms and response to antipsychotics in schizophrenia. Case-control analysis and the family-based association test (FBAT) were performed to investigate whether four single nucleotide polymorphisms (SNPs) at DAOA gene are associated with schizophrenia. The association between the DAOA risk haplotype and clinical symptoms were examined by the positive and negative syndrome scale (PANSS) and the brief psychiatric rating scale (BPRS). Our findings showed that the SNP rs947267 was significantly associated with schizophrenia in both case control and familial trio samples (A > C, χ2 = 8.36, p = 0.004; Z = 2.335, p = 0.019), as well as with specific haplotypes, in particular those formed by the A allele of rs947267. In addition, the risk haplotype AAG was significantly correlated with negative, depression and cognitive impairment factors of PANSS, even with the BPRS change scores after 6-week treatment of atypical antipsychotic drugs (p < 0.05). These results support the hypothesis that variations in DAOA may play a role in schizophrenia and clinical characteristics.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 96-100 (5 pages)

Journal (Volume, Issue Number)

Neuroscience Letters (Volume 416, Issue 1)

Publication milestones

  • Published - 04/06/2007

Publication status

Published - 04/06/2007

ISSN

0304-3940

Publication IDs

  • Scopus: 33947251327
  • PubMed: 17293043

Publication metrics

Metrics

Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1
SciVal
citations
32
SciVal
FWCI
1.60
SciVal
Author count
10
SciVal
Paper percentile
81
Scopus
citations

PlumX, opens in new tab

Captures
36
Citation count
34

Funding Details

This work was supported by grants from the National Natural Science Foundation of China (Nos. 30400149, 30530290, 60274021, and 60334040), and the National Key Project grant (No. 2002BA711A07-06).
FundersFunding numbers
National Key Research and Development Project of China
2002BA711A07-06
NSFC
30400149, 60274021, 30530290, 60334040