Genotype-based association test for general pedigrees: The genotype-PDT

被引:96
作者
Martin, ER
Bass, MP
Gilbert, JR
Pericak-Vance, MA
Hauser, ER
机构
[1] Duke Univ, Ctr Med, Durham, NC 27710 USA
[2] Duke Univ, Ctr Human Genet, Durham, NC 27710 USA
关键词
linkage disequilibrium; family-based tests of association; Alzheimer disease;
D O I
10.1002/gepi.10258
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Many family-based tests of linkage disequilibrium (LD) are based on counts of alleles rather than genotypes. However, allele-based tests may not. detect interactions among alleles at a single locus that are apparent when examining associations with genotypes. Family-based tests of LD based on genotypes have been developed, but they are typically valid as tests of association only in families with a single affected individual. To take advantage of families with multiple affected individuals, we propose the genotype-pedigree disequilibrium test (geno-PDT) to test for LD between marker locus genotypes and disease. Unlike previous tests for genotypic association, the geno-PDT is valid in general pedigrees. Simulations to compare the power of the allele-based PDT and geno-PDT reveal that under an additive model, the allele-based PDT is more powerful, but that the geno-PDT can have greater power when the genetic model is recessive or dominant. Perhaps the most important property of the geno-PDT is the ability to test for association with particular genotypes, which can reveal underlying patterns of association at the genotypic level. These genotype-specific tests can be used to suggest possible underlying genetic models that are consistent with the pattern of genotypic association. This is illustrated through an application to a candidate gene analysis of the MLLT3 gene in families with Alzheimer disease. The geno-PDT approach for testing genotypes in general family data provides a useful tool for identifying genes in complex disease, and partitioning individual genotype contributions will help to dissect the influence of genotype on risk. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:203 / 213
页数:11
相关论文
共 24 条
[1]  
Bass MP, 2002, AM J HUM GENET, V71, P569
[2]   The number of trait loci in late-onset Alzheimer disease [J].
Daw, EW ;
Payami, H ;
Nemens, EJ ;
Nochlin, D ;
Bird, TD ;
Schellenberg, GD ;
Wijsman, EM .
AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (01) :196-204
[3]   Probability of detection of genotyping errors and mutations as inheritance inconsistencies in nuclear-family data [J].
Douglas, JA ;
Skol, AD ;
Boehnke, M .
AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (02) :487-495
[4]   FLUORESCENCE-BASED OLIGONUCLEOTIDE LIGATION ASSAY FOR ANALYSIS OF CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR GENE-MUTATIONS [J].
EGGERDING, FA ;
IOVANNISCI, DM ;
BRINSON, E ;
GROSSMAN, P ;
WINNDEEN, ES .
HUMAN MUTATION, 1995, 5 (02) :153-165
[5]  
Farrer LA, 2001, AM J HUM GENET, V69, P200
[6]   A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data [J].
Gordon, D ;
Heath, SC ;
Liu, X ;
Ott, J .
AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (02) :371-380
[7]   Epidemiology of dementia and Alzheimer's disease [J].
Hendrie, HC .
AMERICAN JOURNAL OF GERIATRIC PSYCHIATRY, 1998, 6 (02) :S3-S18
[8]   Power calculations for a general class of tests of linkage and association that use nuclear families with affected and unaffected sibs [J].
Kaplan, NL ;
Martin, ER .
THEORETICAL POPULATION BIOLOGY, 2001, 60 (03) :193-201
[9]  
Kaplan NL, 1997, AM J HUM GENET, V60, P691
[10]   Association of single-nucleotide polymorphisms of the tau gene with late-onset Parkinson disease [J].
Martin, ER ;
Scott, WK ;
Nance, MA ;
Watts, RL ;
Hubble, JP ;
Koller, WC ;
Lyons, K ;
Pahwa, R ;
Stern, MB ;
Colcher, A ;
Hiner, BC ;
Jankovic, J ;
Ondo, WG ;
Allen, FH ;
Goetz, CG ;
Small, GW ;
Masterman, D ;
Mastaglia, F ;
Laing, NG ;
Stajich, JM ;
Ribble, RC ;
Booze, MW ;
Rogala, A ;
Hauser, MA ;
Zhang, FY ;
Gibson, RA ;
Middleton, LT ;
Roses, AD ;
Haines, JL ;
Scott, BL ;
Pericak-Vance, MA ;
Vance, JM .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2001, 286 (18) :2245-2250