Mendelian randomization analysis with survival outcomes

被引:9
作者
Cho, Youngjoo [1 ]
Rau, Andrea [2 ,3 ]
Reiner, Alex [4 ]
Auer, Paul L. [2 ]
机构
[1] Univ Texas El Paso, Dept Math Sci, El Paso, TX 79968 USA
[2] Univ Wisconsin, Zilber Sch Publ Hlth, POB 413, Milwaukee, WI 53205 USA
[3] Univ Paris Saclay, GABI, AgroParisTech, INRAE, Essonne, France
[4] Univ Washington, Dept Epidemiol, Seattle, WA 98195 USA
基金
美国国家卫生研究院;
关键词
mendelian randomization; survival data; BIAS;
D O I
10.1002/gepi.22354
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Mendelian randomization (MR) is an established approach for assessing the causal effects of heritable exposures on outcomes. Outcomes of interest often include binary clinical endpoints, but may also include censored survival times. We explore the implications of both the Cox proportional hazard model and the additive hazard model in the context of MR, with a specific emphasis on two-stage methods. We show that naive application of standard MR approaches to censored survival times may induce significant bias. Through simulations and analysis of data from the Women's Health Initiative, we provide practical advice on modeling survival outcomes in MRs.
引用
收藏
页码:16 / 23
页数:8
相关论文
共 15 条
  • [1] Anderson G, 1998, CONTROL CLIN TRIALS, V19, P61
  • [2] Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression
    Bowden, Jack
    Smith, George Davey
    Burgess, Stephen
    [J]. INTERNATIONAL JOURNAL OF EPIDEMIOLOGY, 2015, 44 (02) : 512 - 525
  • [3] Burgess S, 2017, EUR J EPIDEMIOL, V32, P377, DOI 10.1007/s10654-017-0255-x
  • [4] Bias due to participant overlap in two-sample Mendelian randomization
    Burgess, Stephen
    Davies, Neil M.
    Thompson, Simon G.
    [J]. GENETIC EPIDEMIOLOGY, 2016, 40 (07) : 597 - 608
  • [5] Mendelian Randomization Analysis With Multiple Genetic Variants Using Summarized Data
    Burgess, Stephen
    Butterworth, Adam
    Thompson, Simon G.
    [J]. GENETIC EPIDEMIOLOGY, 2013, 37 (07) : 658 - 665
  • [6] Use of Mendelian randomisation to assess potential benefit of clinical intervention
    Burgess, Stephen
    Butterworth, Adam
    Malarstig, Anders
    Thompson, Simon G.
    [J]. BMJ-BRITISH MEDICAL JOURNAL, 2012, 345
  • [7] COX DR, 1972, J R STAT SOC B, V34, P187
  • [8] Mendelian randomization: genetic anchors for causal inference in epidemiological studies
    Davey Smith, George
    Hemani, Gibran
    [J]. HUMAN MOLECULAR GENETICS, 2014, 23 : R89 - R98
  • [9] Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair
    Day, Felix R.
    Ruth, Katherine S.
    Thompson, Deborah J.
    Lunetta, Kathryn L.
    Pervjakova, Natalia
    Chasman, Daniel I.
    Stolk, Lisette
    Finucane, Hilary K.
    Sulem, Patrick
    Bulik-Sullivan, Brendan
    Esko, Tonu
    Johnson, Andrew D.
    Elks, Cathy E.
    Franceschini, Nora
    He, Chunyan
    Altmaier, Elisabeth
    Brody, Jennifer A.
    Franke, Lude L.
    Huffman, Jennifer E.
    Keller, Margaux F.
    McArdle, Patrick F.
    Nutile, Teresa
    Porcu, Eleonora
    Robino, Antonietta
    Rose, Lynda M.
    Schick, Ursula M.
    Smith, Jennifer A.
    Teumer, Alexander
    Traglia, Michela
    Vuckovic, Dragana
    Yao, Jie
    Zhao, Wei
    Albrecht, Eva
    Amin, Najaf
    Corre, Tanguy
    Hottenga, Jouke-Jan
    Mangino, Massimo
    Smith, Albert V.
    Tanaka, Toshiko
    Abecasis, Goncalo R.
    Andrulis, Irene L.
    Anton-Culver, Hoda
    Antoniou, Antonis C.
    Arndt, Volker
    Arnold, Alice M.
    Barbieri, Caterina
    Beckmann, Matthias W.
    Beeghly-Fadiel, Alicia
    Benitez, Javier
    Bernstein, Leslie
    [J]. NATURE GENETICS, 2015, 47 (11) : 1294 - +
  • [10] GRAMBSCH PM, 1994, BIOMETRIKA, V81, P515