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ADuLT: An efficient and robust time-to-event GWAS

Author

Listed:
  • Emil M. Pedersen

    (Aarhus University
    Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH)

  • Esben Agerbo

    (Aarhus University
    Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH
    Centre for Integrated Register-based Research at Aarhus University)

  • Oleguer Plana-Ripoll

    (Aarhus University
    Aarhus University and Aarhus University Hospital)

  • Jette Steinbach

    (Aarhus University)

  • Morten D. Krebs

    (Copenhagen University Hospital - Mental Health Services CPH)

  • David M. Hougaard

    (Statens Serum Institut)

  • Thomas Werge

    (Copenhagen University Hospital - Mental Health Services CPH
    Copenhagen University
    Copenhagen University)

  • Merete Nordentoft

    (Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH
    Copenhagen University Hospital - Mental Health Services CPH)

  • Anders D. Børglum

    (Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH
    Aarhus University
    Aarhus University)

  • Katherine L. Musliner

    (Aarhus University
    Aarhus University Hospital-Psychiatry
    Aarhus University)

  • Andrea Ganna

    (University of Helsinki)

  • Andrew J. Schork

    (Copenhagen University Hospital - Mental Health Services CPH
    Copenhagen University
    The Translational Genomics Research Institute (TGEN))

  • Preben B. Mortensen

    (Aarhus University
    Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH)

  • John J. McGrath

    (Aarhus University
    University of Queensland
    The Park Centre for Mental Health)

  • Florian Privé

    (Aarhus University
    Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH)

  • Bjarni J. Vilhjálmsson

    (Aarhus University
    Lundbeck Foundation Initiative for Integrative Psychiatric Research, iPSYCH
    Aarhus University
    the Broad Institute of MIT and Harvard)

Abstract

Proportional hazards models have been proposed to analyse time-to-event phenotypes in genome-wide association studies (GWAS). However, little is known about the ability of proportional hazards models to identify genetic associations under different generative models and when ascertainment is present. Here we propose the age-dependent liability threshold (ADuLT) model as an alternative to a Cox regression based GWAS, here represented by SPACox. We compare ADuLT, SPACox, and standard case-control GWAS in simulations under two generative models and with varying degrees of ascertainment as well as in the iPSYCH cohort. We find Cox regression GWAS to be underpowered when cases are strongly ascertained (cases are oversampled by a factor 5), regardless of the generative model used. ADuLT is robust to ascertainment in all simulated scenarios. Then, we analyse four psychiatric disorders in iPSYCH, ADHD, Autism, Depression, and Schizophrenia, with a strong case-ascertainment. Across these psychiatric disorders, ADuLT identifies 20 independent genome-wide significant associations, case-control GWAS finds 17, and SPACox finds 8, which is consistent with simulation results. As more genetic data are being linked to electronic health records, robust GWAS methods that can make use of age-of-onset information will help increase power in analyses for common health outcomes.

Suggested Citation

  • Emil M. Pedersen & Esben Agerbo & Oleguer Plana-Ripoll & Jette Steinbach & Morten D. Krebs & David M. Hougaard & Thomas Werge & Merete Nordentoft & Anders D. Børglum & Katherine L. Musliner & Andrea G, 2023. "ADuLT: An efficient and robust time-to-event GWAS," Nature Communications, Nature, vol. 14(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-023-41210-z
    DOI: 10.1038/s41467-023-41210-z
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    References listed on IDEAS

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    1. Zachary R. McCaw & Jacqueline M. Lane & Richa Saxena & Susan Redline & Xihong Lin, 2020. "Operating characteristics of the rank‐based inverse normal transformation for quantitative trait analysis in genome‐wide association studies," Biometrics, The International Biometric Society, vol. 76(4), pages 1262-1272, December.
    2. Hon-Cheong So & Pak C Sham, 2010. "A Unifying Framework for Evaluating the Predictive Power of Genetic Variants Based on the Level of Heritability Explained," PLOS Genetics, Public Library of Science, vol. 6(12), pages 1-13, December.
    3. Clare Bycroft & Colin Freeman & Desislava Petkova & Gavin Band & Lloyd T. Elliott & Kevin Sharp & Allan Motyer & Damjan Vukcevic & Olivier Delaneau & Jared O’Connell & Adrian Cortes & Samantha Welsh &, 2018. "The UK Biobank resource with deep phenotyping and genomic data," Nature, Nature, vol. 562(7726), pages 203-209, October.
    4. Aysu Okbay & Jonathan P. Beauchamp & Mark Alan Fontana & James J. Lee & Tune H. Pers & Cornelius A. Rietveld & Patrick Turley & Guo-Bo Chen & Valur Emilsson & S. Fleur W. Meddens & Sven Oskarsson & Jo, 2016. "Genome-wide association study identifies 74 loci associated with educational attainment," Nature, Nature, vol. 533(7604), pages 539-542, May.
    5. Noah Zaitlen & Sara Lindström & Bogdan Pasaniuc & Marilyn Cornelis & Giulio Genovese & Samuela Pollack & Anne Barton & Heike Bickeböller & Donald W Bowden & Steve Eyre & Barry I Freedman & David J Fri, 2012. "Informed Conditioning on Clinical Covariates Increases Power in Case-Control Association Studies," PLOS Genetics, Public Library of Science, vol. 8(11), pages 1-13, November.
    6. Vassily Trubetskoy & Antonio F. Pardiñas & Ting Qi & Georgia Panagiotaropoulou & Swapnil Awasthi & Tim B. Bigdeli & Julien Bryois & Chia-Yen Chen & Charlotte A. Dennison & Lynsey S. Hall & Max Lam & K, 2022. "Mapping genomic loci implicates genes and synaptic biology in schizophrenia," Nature, Nature, vol. 604(7906), pages 502-508, April.
    7. Rounak Dey & Wei Zhou & Tuomo Kiiskinen & Aki Havulinna & Amanda Elliott & Juha Karjalainen & Mitja Kurki & Ashley Qin & Seunggeun Lee & Aarno Palotie & Benjamin Neale & Mark Daly & Xihong Lin, 2022. "Efficient and accurate frailty model approach for genome-wide survival association analysis in large-scale biobanks," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
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