THE AFFECTED SIB-PAIR METHOD IN THE CONTEXT OF AN EPIDEMIOLOGIC-STUDY DESIGN - COMMENTARY

被引:18
作者
KHOURY, MJ
FLANDERS, WD
LIPTON, RB
DORMAN, JS
机构
[1] EMORY UNIV,SCH PUBL HLTH,DIV EPIDEMIOL,ATLANTA,GA 30322
[2] LOYOLA UNIV,MED CTR,DEPT PREVENT MED & EPIDEMIOL,MAYWOOD,IL 60153
[3] UNIV PITTSBURGH,GRAD SCH PUBL HLTH,DEPT EPIDEMIOL,PITTSBURGH,PA 15260
关键词
EPIDEMIOLOGIC METHODS; FAMILIAL GENETIC; SIB-PAIR METHOD;
D O I
10.1002/gepi.1370080408
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
The purpose of this commentary is to provide a framework for using the well-known sib-pair methodology in the context of epidemiologic study designs. Using examples from the Pittsburgh family studies of insulin-dependent diabetes mellitus, we illustrate that the sib-pair method can be used in family-based epidemiologic studies. In a cohort study, unaffected relatives of probands ascertained from well-defined populations are followed for disease development. Disease risks are then stratified according to the number of alleles at one or more loci (0, 1, 2) that are identical by descent (ibd) with the proband. In the absence of linkage between the marker locus and the disease locus, disease risks are expected to be identical in the three groups. Measures of relative risk can be computed (with share-0 as baseline group). In a case-control study, relatives of probands that become affected (cases) are compared to a sample of relatives of probands that stay unaffected (controls) with respect to the number of alleles ibd with the proband. Measures of odds ratio can be computed (with share-0 as baseline group). In both cohort and case-control approaches, covariates including other genetic markers and environmental exposures can be evaluated in relation to disease risk and also for evidence of interaction with the specific marker of interest using stratified and multivariate analyses. Family-based epidemiologic studies allow investigators to study, in a single design, the role of environmental factors and specific gene loci in the etiology of diseases.
引用
收藏
页码:277 / 282
页数:6
相关论文
共 28 条
[1]   A MORE POWERFUL ROBUST SIB-PAIR TEST OF LINKAGE FOR QUANTITATIVE TRAITS [J].
AMOS, CI ;
ELSTON, RC ;
WILSON, AF ;
BAILEYWILSON, JE .
GENETIC EPIDEMIOLOGY, 1989, 6 (03) :435-449
[2]  
BLACKWELDER W C, 1985, Genetic Epidemiology, V2, P85, DOI 10.1002/gepi.1370020109
[3]   LOGISTIC-REGRESSION ANALYSIS AND EFFICIENT DESIGN FOR 2-STAGE STUDIES [J].
CAIN, KC ;
BRESLOW, NE .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1988, 128 (06) :1198-1206
[4]  
DAVENDER DE, 1984, J CHRON DIS, V37, P555
[5]  
DAY NE, 1976, TISSUE ANTIGENS, V8, P109
[6]   FAMILY STUDIES - THE KEY TO UNDERSTANDING THE GENETIC AND ENVIRONMENTAL ETIOLOGY OF CHRONIC DISEASE [J].
DORMAN, JS ;
TRUCCO, M ;
LAPORTE, RE ;
KULLER, LH .
GENETIC EPIDEMIOLOGY, 1988, 5 (05) :305-310
[7]   THE EXPOSURE ODDS RATIO IN NESTED CASE-CONTROL STUDIES WITH COMPETING RISKS [J].
FLANDERS, WD ;
LOUV, WC .
AMERICAN JOURNAL OF EPIDEMIOLOGY, 1986, 124 (04) :684-692
[8]   ESTIMATION OF RISK RATIOS IN CASE-BASE STUDIES WITH COMPETING RISKS [J].
FLANDERS, WD ;
DERSIMONIAN, R ;
RHODES, P .
STATISTICS IN MEDICINE, 1990, 9 (04) :423-435
[9]   INVESTIGATION OF LINKAGE BETWEEN A QUANTITATIVE TRAIT AND A MARKER LOCUS [J].
HASEMAN, JK ;
ELSTON, RC .
BEHAVIOR GENETICS, 1972, 2 (01) :3-19
[10]   LIKELIHOOD ANALYSIS OF MULTI-STATE MODELS FOR DISEASE INCIDENCE AND MORTALITY [J].
KALBFLEISCH, JD ;
LAWLESS, JF .
STATISTICS IN MEDICINE, 1988, 7 (1-2) :149-160