What makes a good case-control study? Design issues for complex traits such as endometriosis

被引:223
作者
Zondervan, KT [1 ]
Cardon, LR
Kennedy, SH
机构
[1] Univ Oxford, Wellcome Trust Ctr Human Genet, Oxford OX3 6BN, England
[2] Univ Oxford, Nuffield Dept Obstet & Gynaecol, Oxford OX3 9DU, England
关键词
case-control study; complex trait; endometriosis; risk-factor; study design;
D O I
10.1093/humrep/17.6.1415
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
The combined investigation of environmental and genetic risk-factors in complex traits will refocus attention on the case-control study. Endometriosis is an example of a complex trait for which most case-control studies have not followed the basic criteria of epidemiological study design. Appropriate control selection has been a particular problem. This article reviews the principles underlying the design of case-control studies, and their application to the study of endometriosis. Only if it is designed well is the case-control study a suitable alternative to the prospective cohort study. Use of newly diagnosed over prevalent cases is preferable, as the latter may alter risk estimates and complicate the interpretation of findings. Controls should be selected from the source population from which cases arose. Potential confounding should be addressed both in studies of environmental and genetic factors. For endometriosis, a possible design would be to: (i) use newly diagnosed cases with `endometriotic' disease; (ii) collect information predating symptom onset; and (iii) use at least one population-based female control group matched on unadjustable confounders and screened for pelvic symptoms. In conclusion, future studies of complex traits such as endometriosis will have to incorporate both environmental and genetic factors. Only adequately designed studies will allow reliable results to be obtained and any true aetiologic heterogeneity expected to underlie a complex trait to be detected.
引用
收藏
页码:1415 / 1423
页数:9
相关论文
共 64 条
  • [1] *AM FERT SOC, 1985, FERTIL STERIL, V43, P351
  • [2] Counter-matching in studies of gene-environment interaction: Efficiency and feasibility
    Andrieu, N
    Goldstein, AM
    Thomas, DC
    Langholz, B
    [J]. AMERICAN JOURNAL OF EPIDEMIOLOGY, 2001, 153 (03) : 265 - 274
  • [3] [Anonymous], 1998, Modern Epidemiology
  • [4] The power of genomic control
    Bacanu, SA
    Devlin, B
    Roeder, K
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2000, 66 (06) : 1933 - 1944
  • [5] Proportion of the GSTM1 0/0 genotype in some Slavic populations and its correlation with cystic fibrosis and some multifactorial diseases
    Baranov, VS
    Ivaschenko, T
    Bakay, B
    Aseev, M
    Belotserkovskaya, R
    Baranova, H
    Malet, P
    Perriot, J
    Mouraire, P
    Baskakov, VN
    Savitskyi, GA
    Gorbushin, S
    Deyneka, SI
    Michnin, E
    Barchuck, A
    Vakharlovsky, V
    Pavlov, G
    Shilko, VI
    Guembitzkaya, T
    Kovaleva, L
    [J]. HUMAN GENETICS, 1996, 97 (04) : 516 - 520
  • [6] Glutathione S-transferase M1 gene polymorphism and susceptibility to endometriosis in a French population
    Baranova, H
    Bothorishvilli, R
    Canis, M
    Albuisson, E
    Perriot, S
    Glowaczower, E
    Bruhat, MA
    Baranov, V
    Malet, P
    [J]. MOLECULAR HUMAN REPRODUCTION, 1997, 3 (09) : 775 - 780
  • [7] Possible involvement of arylamine N-acetyltransferase 2, glutathione S-transferases M1 and T1 genes in the development of endometriosis
    Baranova, H
    Canis, M
    Ivaschenko, T
    Albuisson, E
    Bothorishvilli, R
    Baranov, V
    Malet, P
    Bruhat, MA
    [J]. MOLECULAR HUMAN REPRODUCTION, 1999, 5 (07) : 636 - 641
  • [8] GSTM1 null polymorphism and susceptibility to endometriosis and ovarian cancer
    Baxter, SW
    Thomas, EJ
    Campbell, IG
    [J]. CARCINOGENESIS, 2001, 22 (01) : 63 - 65
  • [9] Heritability and molecular genetic studies of endometriosis
    Bischoff, FZ
    Simpson, JL
    [J]. HUMAN REPRODUCTION UPDATE, 2000, 6 (01) : 37 - 44
  • [10] CANDIANI GB, 1991, FERTIL STERIL, V56, P230