Methods for detection of parent-of-origin effects in genetic studies of case-parents triads

被引:201
作者
Weinberg, CR [1 ]
机构
[1] NIEHS, Biostat Branch, Res Triangle Pk, NC 27709 USA
关键词
D O I
10.1086/302466
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
When affected probands and their biological parents are genotyped at a candidate gene or a marker, the resulting case-parents-triad data enable powerful tests for linkage in the presence of association. When linkage disequilibrium has been detected in such a study, the investigator may wish to look further for possible parent-of-origin effects. If, for example, the transmission/disequilibrium test restricted to fathers is statistically significant, whereas that restricted to mothers is not, the investigator might interpret this as evidence for nonexpression of the maternally derived disease gene-that is, imprinting. This report reviews existing methods for detection of parent-of-origin effects, showing that each can be invalid under certain scenarios. Two new methods are proposed, based on application of likelihood-based inference after stratification on both the parental mating type and the inherited number of copies of the allele under study. If there are no maternal genetic effects expressed prenatally during gestation, the parental-asymmetry test is powerful and provides valid estimation of a parent-of-origin parameter. For diseases for which there could be maternal effects on risk, the parent-of-origin likelihood-ratio test provides a robust alternative. Simulations based on an admired population demonstrate good operating characteristics for these procedures, under diverse scenarios.
引用
收藏
页码:229 / 235
页数:7
相关论文
共 10 条
[1]   HAPLOTYPE RELATIVE RISKS - AN EASY RELIABLE WAY TO CONSTRUCT A PROPER CONTROL SAMPLE FOR RISK CALCULATIONS [J].
FALK, CT ;
RUBINSTEIN, P .
ANNALS OF HUMAN GENETICS, 1987, 51 :227-233
[2]  
SCHAID DJ, 1993, AM J HUM GENET, V53, P1114
[3]  
Schaid DJ, 1999, GENET EPIDEMIOL, V16, P250, DOI 10.1002/(SICI)1098-2272(1999)16:3<250::AID-GEPI2>3.0.CO
[4]  
2-T
[5]   ON ESTIMATING HLA/DISEASE ASSOCIATION WITH APPLICATION TO A STUDY OF APLASTIC-ANEMIA [J].
SELF, SG ;
LONGTON, G ;
KOPECKY, KJ ;
LIANG, KY .
BIOMETRICS, 1991, 47 (01) :53-61
[6]  
Spielman RS, 1996, AM J HUM GENET, V59, P983
[7]  
SPIELMAN RS, 1993, AM J HUM GENET, V52, P506
[8]   A log-linear approach to case-parent-triad data: Assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting [J].
Weinberg, CR ;
Wilcox, AJ ;
Lie, RT .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 62 (04) :969-978
[9]   Allowing for missing parents in genetic studies of case-parent triads [J].
Weinberg, CR .
AMERICAN JOURNAL OF HUMAN GENETICS, 1999, 64 (04) :1186-1193
[10]  
Wilcox AJ, 1998, AM J EPIDEMIOL, V148, P893