A novel permutation testing method implicates sixteen nicotinic acetylcholine receptor genes as risk factors for smoking in schizophrenia families

被引:40
作者
Faraone, SV
Su, J
Taylor, L
Wilcox, M
机构
[1] Harvard Univ, Massachusetts Gen Hosp, Sch Med, Dept Psychiat, Boston, MA USA
[2] Harvard Univ, Sch Publ Hlth, Dept Epidemiol, Boston, MA 02115 USA
[3] Harvard Univ, Sch Med, Massachusetts Mental Hlth Ctr, Dept Psychiat, Boston, MA USA
[4] Univ Calif San Diego, Dept Psychiat, San Diego, CA 92103 USA
[5] Genom Therapeut Corp, Waltham, MA USA
关键词
acetylcholine; linkage; nicotinic receptor; genetics; permutation testing; candidate genes;
D O I
10.1159/000077543
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Smoking is a common correlate of schizophrenia, which leads to medical morbidity. Although twin and adoption studies have consistently implicated genes in the etiology of both smoking and schizophrenia, finding genes has been difficult. Several authors have suggested that clinical or neurobiological features associated with schizophrenia, such as smoking, might improve the ability to detect schizophrenia susceptibility genes by identifying genes related to the etiology of that feature. The objective of this study is to assess evidence for linkage of sixteen nicotinic acetylcholine receptor genes and smoking in schizophrenia families, using data from the NIMH Genetics Initiative for schizophrenia. Sixteen nicotinic acetylcholine receptor genes were selected prior to analysis. We used a multipoint sibling pair linkage analysis program, SIBPAL2, with a smoking trait in schizophrenia families. The significance of the group of candidate genes, in addition to each individual candidate gene, was assessed using permutation testing, which adjusted for multiple comparisons. The group of genes showed significant linkage to the smoking trait after adjusting for multiple comparisons through permutation testing (p = 0.039). In addition, two of the individual candidate genes were significant (CHRNA2, p = 0.044) and (CHRNB2, p = 0.015) and two genes were marginally significant (CHRNA7, p = 0.095; CHRNA1, p = 0.076). The significance of the complex hypothesis, involving sixteen genes, implicates the nicotinic system in smoking for schizophrenic families. Individual gene analysis suggests that CHRNA2 and CHRNB2 may play a particular role in this involvement. Such findings help prioritize genes for future case control studies. In addition, we provide a novel permutation method that is useful in future analyses involving a single hypothesis, with multiple candidate genes. Copyright (C) 2004 S. Karger AG, Basel.
引用
收藏
页码:59 / 68
页数:10
相关论文
共 103 条
[1]   Schizophrenia, sensory gating, and nicotinic receptors [J].
Adler, LE ;
Olincy, A ;
Waldo, M ;
Harris, JG ;
Griffith, J ;
Stevens, K ;
Flach, K ;
Nagamoto, H ;
Bickford, P ;
Leonard, S ;
Freedman, R .
SCHIZOPHRENIA BULLETIN, 1998, 24 (02) :189-202
[2]   NORMALIZATION BY NICOTINE OF DEFICIENT AUDITORY SENSORY GATING IN THE RELATIVES OF SCHIZOPHRENICS [J].
ADLER, LE ;
HOFFER, LJ ;
GRIFFITH, J ;
WALDO, MC ;
FREEDMAN, R .
BIOLOGICAL PSYCHIATRY, 1992, 32 (07) :607-616
[3]  
ADLER LE, 1993, AM J PSYCHIAT, V150, P1856
[4]   Meta-analysis of whole-genome linkage scans of bipolar disorder and schizophrenia [J].
Badner, JA ;
Gershon, ES .
MOLECULAR PSYCHIATRY, 2002, 7 (04) :405-411
[5]  
Bergen AW, 1999, GENET EPIDEMIOL, V17, pS55
[6]   Smoking behaviour and biological maturation in males and females: a 20-year longitudinal study. Analysis of data from the Amsterdam Growth and Health Longitudinal Study [J].
Bernaards, CM ;
Kemper, HCG ;
Twisk, JWR ;
van Mechelen, W ;
Snel, J .
ANNALS OF HUMAN BIOLOGY, 2001, 28 (06) :634-648
[7]   Genetic association studies of schizophrenia using the 8p21-22 genes: prepronociceptin (PNOC), neuronal nicotinic cholinergic receptor alpha polypeptide 2 (CHRNA2) and arylamine N-acetyltransferase 1 (NAT1) [J].
Blaveri, E ;
Kalsi, G ;
Lawrence, J ;
Quested, D ;
Moorey, H ;
Lamb, G ;
Kohen, D ;
Shiwach, R ;
Chowdhury, U ;
Curtis, D ;
McQuillin, A ;
Gramoustianou, ES ;
Gurling, HMD .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2001, 9 (06) :469-472
[8]   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
[9]   Location of a major susceptibility locus for familiar schizophrenia on chromosome 1q21-q22 [J].
Brzustowicz, LM ;
Hodgkinson, KA ;
Chow, EWC ;
Honer, WG ;
Bassett, AS .
SCIENCE, 2000, 288 (5466) :678-682
[10]  
Brzustowicz LM, 1999, AM J HUM GENET, V65, P1096, DOI 10.1086/302579