Required sample size and nonreplicability thresholds for heterogeneous genetic associations

被引:86
作者
Moonesinghe, Ramal [3 ]
Khoury, Muin J. [3 ]
Liu, Tiebin [3 ]
Ioannidis, John P. A. [1 ,2 ,4 ]
机构
[1] Univ Ioannina, Sch Med, Dept Hyg & Epidemiol, Clin & Mol Epidemiol Unit, GR-45110 Ioannina, Greece
[2] Fdn Res & Technol Hellas, Biomed Res Inst, Ioannina 45110, Greece
[3] Ctr Dis Control & Prevent, Coordinating Ctr Hlth Promot, Natl Off Publ Hlth Genom, Atlanta, GA 30341 USA
[4] Tufts Univ, Sch Med, Dept Med, Boston, MA 02111 USA
关键词
genome; heterogeneity; metaanalysis; polymorphism;
D O I
10.1073/pnas.0705554105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Many gene-disease associations proposed to date have not been consistently replicated across different populations. Nonreplication often reflects false positives in the original claims. However, occasionally, nonreplication may be due to heterogeneity due to biases or even genuine diversity of the genetic effects in different populations. Here, we propose methods for estimating the required sample size to replicate an association across many studies with different amounts of between-study heterogeneity, when data are summarized through metaanalysis. We demonstrate thresholds of between-study heterogeneity (tau(2)(0)) above which one cannot reach adequate power to replicate a proposed association at a specified level of statistical significance when k studies are performed (regardless of how large these studies are). Based on empirical evidence from 91 proposed gene-disease associations (50 on candidate genes and 41 from genome-wide association efforts), the observed between-study heterogeneity is often close to or even surpasses nonreplicability thresholds. With more modest between-study heterogeneity, the required sample size increases considerably compared with when no between-study heterogeneity exists. Increases are steep as tau(2)(0) is approached. Therefore, some true associations may not be practically possible to replicate with consistency, no matter how large studies are conducted. Efforts should be made to minimize between-study heterogeneity in targeted genetic effects.
引用
收藏
页码:617 / 622
页数:6
相关论文
共 47 条
[11]  
Greenland S, 1983, Stat Med, V2, P243, DOI 10.1002/sim.4780020219
[12]   The power of statistical tests for moderators in meta-analysis [J].
Hedges, LV ;
Pigott, TD .
PSYCHOLOGICAL METHODS, 2004, 9 (04) :426-445
[13]   The power of statistical tests in meta-analysis [J].
Hedges, LV ;
Pigott, TD .
PSYCHOLOGICAL METHODS, 2001, 6 (03) :203-217
[14]   A common variant on chromosome 9p21 affects the risk of myocardial infarction [J].
Helgadottir, Anna ;
Thorleifsson, Gudmar ;
Manolescu, Andrei ;
Gretarsdottir, Solveig ;
Blondal, Thorarinn ;
Jonasdottir, Aslaug ;
Jonasdottir, Adalbjorg ;
Sigurdsson, Asgeir ;
Baker, Adam ;
Palsson, Arnar ;
Masson, Gisli ;
Gudbjartsson, Daniel F. ;
Magnusson, Kristinn P. ;
Andersen, Karl ;
Levey, Allan I. ;
Backman, Valgerdur M. ;
Matthiasdottir, Sigurborg ;
Jonsdottir, Thorbjorg ;
Palsson, Stefan ;
Einarsdottir, Helga ;
Gunnarsdottir, Steinunn ;
Gylfason, Arnaldur ;
Vaccarino, Viola ;
Hooper, W. Craig ;
Reilly, Muredach P. ;
Granger, Christopher B. ;
Austin, Harland ;
Rader, Daniel J. ;
Shah, Svati H. ;
Quyyumi, Arshed A. ;
Gulcher, Jeffrey R. ;
Thorgeirsson, Gudmundur ;
Thorsteinsdottir, Unnur ;
Kong, Augustine ;
Stefansson, Kari .
SCIENCE, 2007, 316 (5830) :1491-1493
[15]   Measuring inconsistency in meta-analyses [J].
Higgins, JPT ;
Thompson, SG ;
Deeks, JJ ;
Altman, DG .
BMJ-BRITISH MEDICAL JOURNAL, 2003, 327 (7414) :557-560
[16]  
Higgins Julian, 2002, J Health Serv Res Policy, V7, P51, DOI 10.1258/1355819021927674
[17]   A comprehensive review of genetic association studies [J].
Hirschhorn, JN ;
Lohmueller, K ;
Byrne, E ;
Hirschhorn, K .
GENETICS IN MEDICINE, 2002, 4 (02) :45-61
[18]   Editorial: Once and again - Issues surrounding replication in genetic association studies [J].
Hirschhorn, JN ;
Altshuler, D .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (10) :4438-4441
[19]   Genome-wide association studies for common diseases and complex traits [J].
Hirschhorn, JN ;
Daly, MJ .
NATURE REVIEWS GENETICS, 2005, 6 (02) :95-108
[20]   Gene-environment interactions in human diseases [J].
Hunter, DJ .
NATURE REVIEWS GENETICS, 2005, 6 (04) :287-298