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

被引:31
作者
Yue, Weihua
Kang, Guolian
Zhang, Yanbo
Qu, Mei
Tang, Fulei
Han, Yonghua
Ruan, Yan
Lu, Tianlan
Zhang, Jifeng
Zhang, Dai
机构
[1] Peking Univ, Inst Mental Hlth, Beijing 100083, Peoples R China
[2] Chinese Acad Sci, Acad Math & Syst Sci, Beijing, Peoples R China
[3] Michigan State Univ, Dept Probabil & Stat, E Lansing, MI 48824 USA
基金
中国国家自然科学基金;
关键词
schizophrenia; DAOA; association study; clinical symptom; therapeutic effect;
D O I
10.1016/j.neulet.2007.01.056
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
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, x(2) = 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. (c) 2007 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:96 / 100
页数:5
相关论文
共 29 条
[1]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[2]   Association between the polymorphic GRM3 gene and negative symptom improvement during olanzapine treatment [J].
Bishop, JR ;
Ellingrod, VL ;
Moline, J ;
Miller, D .
SCHIZOPHRENIA RESEARCH, 2005, 77 (2-3) :253-260
[3]   Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21 [J].
Blouin, JL ;
Dombroski, BA ;
Nath, SK ;
Lasseter, VK ;
Wolyniec, PS ;
Nestadt, G ;
Thornquist, M ;
Ullrich, G ;
McGrath, J ;
Kasch, L ;
Lamacz, M ;
Thomas, MG ;
Gehrig, C ;
Radhakrishna, U ;
Snyder, SE ;
Balk, KG ;
Neufeld, K ;
Swartz, KL ;
DeMarchi, N ;
Papadimitriou, GN ;
Dikeos, DG ;
Stefanis, CN ;
Chakravarti, A ;
Childs, B ;
Housman, DE ;
Kazazian, HH ;
Antonarakis, SE ;
Pulver, AE .
NATURE GENETICS, 1998, 20 (01) :70-73
[4]  
Brzustowicz LM, 1999, AM J HUM GENET, V65, P1096, DOI 10.1086/302579
[5]   Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method [J].
Camp, NJ ;
Neuhausen, SL ;
Tiobech, J ;
Polloi, A ;
Coon, H ;
Myles-Worsley, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) :1278-1289
[6]   A genomewide linkage study of age at onset in schizophrenia [J].
Cardno, AG ;
Holmans, PA ;
Rees, MI ;
Jones, LA ;
McCarthy, GM ;
Hamshere, ML ;
Williams, NM ;
Norton, N ;
Williams, HJ ;
Fenton, I ;
Murphy, KC ;
Sanders, RD ;
Gray, MY ;
O'Donovan, MC ;
McGuffin, P ;
Owen, MJ .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2001, 105 (05) :439-445
[7]   Genetic and physiological data implicating the new human gene G72 and the gene for D-amino acid oxidase in schizophrenia [J].
Chumakov, I ;
Blumenfeld, M ;
Guerassimenko, O ;
Cavarec, L ;
Palicio, M ;
Abderrahim, H ;
Bougueleret, L ;
Barry, C ;
Tanaka, H ;
La Rosa, P ;
Puech, A ;
Tahri, N ;
Cohen-Akenine, A ;
Delabrosse, S ;
Lissarrague, S ;
Picard, FP ;
Maurice, K ;
Essioux, L ;
Millasseau, P ;
Grel, P ;
Debailleul, V ;
Simon, AM ;
Caterina, D ;
Dufaure, I ;
Malekzadeh, K ;
Belova, M ;
Luan, JJ ;
Bouillot, M ;
Sambucy, JL ;
Primas, G ;
Saumier, M ;
Boubkiri, N ;
Martin-Saumier, S ;
Nasroune, M ;
Peixoto, H ;
Delaye, A ;
Pinchot, V ;
Bastucci, M ;
Guillou, S ;
Chevillon, M ;
Sainz-Fuertes, R ;
Meguenni, S ;
Aurich-Costa, J ;
Cherif, D ;
Gimalac, A ;
Van Duijn, C ;
Gauvreau, D ;
Quelette, G ;
Fortier, I ;
Realson, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (21) :13675-13680
[8]   Dysbindin genotype and negative symptoms in schizophrenia [J].
DeRosse, P ;
Funke, B ;
Burdick, KE ;
Lencz, T ;
Ekholm, JM ;
Kane, JM ;
Kucherlapati, R ;
Malhotra, AK .
AMERICAN JOURNAL OF PSYCHIATRY, 2006, 163 (03) :532-U1
[9]   G72/G30 in schizophrenia and bipolar disorder: Review and meta-analysis [J].
Detera-Wadleigh, Sevilla D. ;
McMahon, Francis J. .
BIOLOGICAL PSYCHIATRY, 2006, 60 (02) :106-114
[10]   Linkage of chromosome 13q32 to schizophrenia in a large veterans affairs cooperative study sample [J].
Faraone, SV ;
Skol, AD ;
Tsuang, DW ;
Bingham, S ;
Young, KA ;
Prabhudesai, S ;
Haverstock, SL ;
Mena, F ;
Menon, ASK ;
Bisset, D ;
Pepple, J ;
Sautter, F ;
Baldwin, C ;
Weiss, D ;
Collins, J ;
Keith, T ;
Boehnke, M ;
Tsuang, MT ;
Schellenberg, GD .
AMERICAN JOURNAL OF MEDICAL GENETICS, 2002, 114 (06) :598-604