Genetic Epidemiology 5 - What makes a good genetic association study?

被引:344
作者
Hattersley, AT
McCarthy, MI [1 ]
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX1 2JD, England
[2] Peninsula Med Sch, Inst Biomed & Clin Sci, Exeter, Devon, England
[3] Univ Oxford, Oxford Ctr Diabet Endocrinol & Metab, Oxford OX3 7LJ, England
基金
英国惠康基金;
关键词
D O I
10.1016/S0140-6736(05)67531-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Genetic association studies are central to efforts to identify and characterise genomic variants underlying susceptibility to multifactorial disease. However, obtaining robust replication of initial association findings has proved difficult. Much of this inconsistency can be attributed to inadequacies in study design, implementation, and interpretation-inadequately powered sample groups are a major concern. Several additional factors affect the quality of any given association study, with appropriate sample-recruitment strategy, logical variant selection, minimum genotyping error, relevant data analysis, and valid interpretation all essential to generation of robust findings. Replication has a vital role in showing that associations that are identified reflect interesting biological processes rather than methodological quirks. For an unbiased view of the evidence for and against any particular association, study quality, rather than significance value, needs to play the dominant part.
引用
收藏
页码:1315 / 1323
页数:9
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共 88 条
  • [1] Genomewide scans of complex human diseases:: True linkage is hard to find
    Altmüller, J
    Palmer, LJ
    Fischer, G
    Scherb, H
    Wjst, M
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2001, 69 (05) : 936 - 950
  • [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] The power of genomic control
    Bacanu, SA
    Devlin, B
    Roeder, K
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (06) : 1933 - 1944
  • [4] Human type 1 diabetes and the insulin gene: Principles of mapping polygenes
    Bennett, ST
    Todd, JA
    [J]. ANNUAL REVIEW OF GENETICS, 1996, 30 : 343 - 370
  • [5] MUTATION IN BLOOD-COAGULATION FACTOR-V ASSOCIATED WITH RESISTANCE TO ACTIVATED PROTEIN-C
    BERTINA, RM
    KOELEMAN, BPC
    KOSTER, T
    ROSENDAAL, FR
    DIRVEN, RJ
    DERONDE, H
    VANDERVELDEN, PA
    REITSMA, PH
    [J]. NATURE, 1994, 369 (6475) : 64 - 67
  • [6] Clinical epidemiological quality in molecular genetic research - The need for methodological standards
    Bogardus, ST
    Concato, J
    Feinstein, AR
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1999, 281 (20): : 1919 - 1926
  • [7] A transcription factor regulatory circuit in differentiated pancreatic cells
    Boj, SF
    Párrizas, M
    Maestro, MA
    Ferrer, J
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (25) : 14481 - 14486
  • [8] ESTIMATING SAMPLE SIZES FOR BINARY, ORDERED CATEGORICAL, AND CONTINUOUS OUTCOMES IN 2 GROUP COMPARISONS
    CAMPBELL, MJ
    JULIOUS, SA
    ALTMAN, DG
    [J]. BRITISH MEDICAL JOURNAL, 1995, 311 (7013) : 1145 - 1148
  • [9] Population stratification and spurious allelic association
    Cardon, LR
    Palmer, LJ
    [J]. LANCET, 2003, 361 (9357) : 598 - 604
  • [10] Mapping complex disease loci in whole-genome association studies
    Carlson, CS
    Eberle, MA
    Kruglyak, L
    Nickerson, DA
    [J]. NATURE, 2004, 429 (6990) : 446 - 452