A method for meta-analysis of molecular association studies

被引:576
作者
Thakkinstian, A
McElduff, P
D'Este, C
Duffy, D
Attia, J
机构
[1] Mahidol Univ, Ramathibodi Hosp, Fac Med, Clin Epidemiol Unit, Bangkok 10400, Thailand
[2] Univ Manchester, Sch Med, Manchester M13 9PT, Lancs, England
[3] Univ Newcastle, Fac Med & Hlth Sci, Ctr Clin Epidemiol & Biostat, Newcastle, NSW 2308, Australia
[4] Bancroft Ctr, Queensland Inst Med Res, Herston, Qld, Australia
关键词
case-control studies; cohort studies; gene frequency; model polymorphisin (genetics); regression;
D O I
10.1002/sim.2010
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Although populationation-based molecular association Studies are becoming increasingly popular, methodology for the meta-analysis of these studies has been neglected, particularly with regard to two issues: testing Hardy-Weinberg equilibrium (HWE), and pooling results in a manner that reflects a biological model of gene effect. We propose a process for pooling results from population-based molecular association Studies which consists of the following steps: (1) checking HWE using chi-square goodness of fit: we suggest performing sensitivity analysis with and without Studies that are in HWE. (2) Heterogeneity is then checked, and if present, possible causes are explored. (3) If no heterogeneity is present, regression analysis is used to pool data and to determine the gene effect. (4) If there is a significant gene effect, pairwise group differences are analysed and these data are allowed to 'dictate' the best genetic model. (5) Data may then be pooled using this model. This method is easily performed using standard software, and has the advantage of not assuming an a priori genetic model. Copyright (c) 2004 John Wiley & Soils, Ltd.
引用
收藏
页码:1291 / 1306
页数:16
相关论文
共 60 条
[21]   A DISEQUILIBRIUM COEFFICIENT APPROACH TO HARDY-WEINBERG TESTING [J].
HERNANDEZ, JL ;
WEIR, BS .
BIOMETRICS, 1989, 45 (01) :53-70
[22]  
Hosmer W., 2000, Applied Logistic Regression, VSecond
[23]  
Jorgensen HL, 1996, BRIT MED J, V313, P586, DOI 10.1136/bmj.313.7057.586
[24]   Measured haplotype analysis of the angiotensin-I converting enzyme gene [J].
Keavney, B ;
McKenzie, CA ;
Connell, JMC ;
Julier, C ;
Ratcliffe, PJ ;
Sobel, E ;
Lathrop, M ;
Farrall, M .
HUMAN MOLECULAR GENETICS, 1998, 7 (11) :1745-1751
[25]   The BsmI vitamin D receptor restriction fragment length polymorphism (bb) influences the effect of calcium intake on bone mineral density [J].
Kiel, DP ;
Myers, RH ;
Cupples, LA ;
Kong, XF ;
Zhu, XH ;
Ordovas, J ;
Schaefer, EJ ;
Felson, DT ;
Rush, D ;
Wilson, PWF ;
Eisman, JA ;
Holick, MF .
JOURNAL OF BONE AND MINERAL RESEARCH, 1997, 12 (07) :1049-1057
[26]  
Kleinbaum DG., 1988, APPL REGRESSION ANAL, P369
[27]   Association of vitamin D receptor gene polymorphism with bone mineral density in Slovenian postmenopausal women [J].
Marc, J ;
Prezelj, J ;
Komel, R ;
Kocijancic, A .
GYNECOLOGICAL ENDOCRINOLOGY, 2000, 14 (01) :60-64
[28]  
Marsh D G, 1991, Clin Exp Allergy, V21 Suppl 1, P168, DOI 10.1111/j.1365-2222.1991.tb01722.x
[29]   VITAMIN-D RECEPTOR GENOTYPES IN OSTEOPOROSIS [J].
MELHUS, H ;
KINDMARK, A ;
AMER, S ;
WILEN, B ;
LINDH, E ;
LJUNGHALL, S .
LANCET, 1994, 344 (8927) :949-950
[30]  
Neter J., 1990, APPL STAT MODELS