Overcoming the winner's curse:: Estimating penetrance parameters from case-control data

被引:283
作者
Zollner, Sebastian
Pritchard, Jonathan K.
机构
[1] Univ Michigan, Dept Biostat, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Dept Psychiat, Ann Arbor, MI 48109 USA
[3] Univ Michigan, Ctr Stat Genet, Ann Arbor, MI 48109 USA
关键词
D O I
10.1086/512821
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Genomewide association studies are now a widely used approach in the search for loci that affect complex traits. After detection of significant association, estimates of penetrance and allele-frequency parameters for the associated variant indicate the importance of that variant and facilitate the planning of replication studies. However, when these estimates are based on the original data used to detect the variant, the results are affected by an ascertainment bias known as the "winner's curse." The actual genetic effect is typically smaller than its estimate. This overestimation of the genetic effect may cause replication studies to fail because the necessary sample size is underestimated. Here, we present an approach that corrects for the ascertainment bias and generates an estimate of the frequency of a variant and its penetrance parameters. The method produces a point estimate and confidence region for the parameter estimates. We study the performance of this method using simulated data sets and show that it is possible to greatly reduce the bias in the parameter estimates, even when the original association study had low power. The uncertainty of the estimate decreases with increasing sample size, independent of the power of the original test for association. Finally, we show that application of the method to case-control data can improve the design of replication studies considerably.
引用
收藏
页码:605 / 615
页数:11
相关论文
共 21 条
  • [1] Bias in estimates of quantitative-trait-locus effect in genome scans: Demonstration of the phenomenon and a method-of-moments procedure for reducing bias
    Allison, DB
    Fernandez, JR
    Heo, M
    Zhu, SK
    Etzel, C
    Beasley, TM
    Amos, CI
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2002, 70 (03) : 575 - 585
  • [2] The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes
    Altshuler, D
    Hirschhorn, JN
    Klannemark, M
    Lindgren, CM
    Vohl, MC
    Nemesh, J
    Lane, CR
    Schaffner, SF
    Bolk, S
    Brewer, C
    Tuomi, T
    Gaudet, D
    Hudson, TJ
    Daly, M
    Groop, L
    Lander, ES
    [J]. NATURE GENETICS, 2000, 26 (01) : 76 - 80
  • [3] COMPETITIVE BIDDING IN HIGH-RISK SITUATIONS
    CAPEN, EC
    CLAPP, RV
    CAMPBELL, WM
    [J]. JOURNAL OF PETROLEUM TECHNOLOGY, 1971, 23 (JUN): : 641 - &
  • [4] The Pro115Gln and Pro12Ala PPAR gamma gene mutations in obesity and type 2 diabetes
    Clement, K
    Hereberg, S
    Passinge, B
    Galan, P
    Varroud-Vial, M
    Shuldiner, AR
    Beamer, BA
    Charpentier, G
    Guy-Grand, B
    Froguel, P
    Vaisse, C
    [J]. INTERNATIONAL JOURNAL OF OBESITY, 2000, 24 (03) : 391 - 393
  • [5] A Pro12Ala substitution in PPARγ2 associated with decreased receptor activity, lower body mass index and improved insulin sensitivity
    Deeb, SS
    Fajas, L
    Nemoto, M
    Pihlajamäki, J
    Mykkänen, L
    Kuusisto, J
    Laakso, M
    Fujimoto, W
    Auwerx, J
    [J]. NATURE GENETICS, 1998, 20 (03) : 284 - 287
  • [6] Complement factor H polymorphism and age-related macular degeneration
    Edwards, AO
    Ritter, R
    Abel, KJ
    Manning, A
    Panhuysen, C
    Farrer, LA
    [J]. SCIENCE, 2005, 308 (5720) : 421 - 424
  • [7] Large upward bias in estimation of locus-specific effects from genomewide scans
    Göring, HHH
    Terwilliger, JD
    Blangero, J
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (06) : 1357 - 1369
  • [8] The Pro12Ala polymorphism in PPAR γ2 may confer resistance to type 2 diabetes
    Hara, K
    Okada, T
    Tobe, K
    Yasuda, K
    Mori, Y
    Kadowaki, H
    Hagura, R
    Akanuma, Y
    Kimura, S
    Ito, C
    Kadowaki, T
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 271 (01) : 212 - 216
  • [9] A common genetic variant is associated with adult and childhood obesity
    Herbert, A
    Gerry, NP
    McQueen, MB
    Heid, IM
    Pfeufer, A
    Illig, T
    Wichmann, HE
    Meitinger, T
    Hunter, D
    Hu, FB
    Colditz, G
    Hinney, A
    Hebebrand, J
    Koberwitz, K
    Zhu, XF
    Cooper, R
    Ardlie, K
    Lyon, H
    Hirschhorn, JN
    Laird, NM
    Lenburg, ME
    Lange, C
    Christman, MF
    [J]. SCIENCE, 2006, 312 (5771) : 279 - 283
  • [10] A comprehensive review of genetic association studies
    Hirschhorn, JN
    Lohmueller, K
    Byrne, E
    Hirschhorn, K
    [J]. GENETICS IN MEDICINE, 2002, 4 (02) : 45 - 61