IDEAS home Printed from https://ideas.repec.org/a/plo/pgen00/1009713.html
   My bibliography  Save this article

Multitrait GWAS to connect disease variants and biological mechanisms

Author

Listed:
  • Hanna Julienne
  • Vincent Laville
  • Zachary R McCaw
  • Zihuai He
  • Vincent Guillemot
  • Carla Lasry
  • Andrey Ziyatdinov
  • Cyril Nerin
  • Amaury Vaysse
  • Pierre Lechat
  • Hervé Ménager
  • Wilfried Le Goff
  • Marie-Pierre Dube
  • Peter Kraft
  • Iuliana Ionita-Laza
  • Bjarni J Vilhjálmsson
  • Hugues Aschard

Abstract

Genome-wide association studies (GWASs) have uncovered a wealth of associations between common variants and human phenotypes. Here, we present an integrative analysis of GWAS summary statistics from 36 phenotypes to decipher multitrait genetic architecture and its link with biological mechanisms. Our framework incorporates multitrait association mapping along with an investigation of the breakdown of genetic associations into clusters of variants harboring similar multitrait association profiles. Focusing on two subsets of immunity and metabolism phenotypes, we then demonstrate how genetic variants within clusters can be mapped to biological pathways and disease mechanisms. Finally, for the metabolism set, we investigate the link between gene cluster assignment and the success of drug targets in randomized controlled trials.Author summary: Genome-wide association studies (GWAS) established numerous associations between genetic variants and human traits. The anonymized summary of GWAS results is generally made publicly available to the scientific community and can be explored further. Amongst the many possible secondary analyses, one is to study the effect of a genetic variant on several traits (multi-trait GWAS) rather than a unique trait. We compared several tests to conduct multi-trait GWAS on simulated and real data. We detected 322 new associations that were not previously reported by standard GWAS. We then detected clusters of genetic variants having a similar effect across several traits. Focusing on two subsets of immunity and metabolism traits, we demonstrate how genetic variants within clusters can be mapped to biological pathways and disease mechanisms. Finally, for the metabolism set, we investigate the link between gene cluster and success of drug targets in random control trials. We propose this method for improving the functional interpretation of GWAS results.

Suggested Citation

  • Hanna Julienne & Vincent Laville & Zachary R McCaw & Zihuai He & Vincent Guillemot & Carla Lasry & Andrey Ziyatdinov & Cyril Nerin & Amaury Vaysse & Pierre Lechat & Hervé Ménager & Wilfried Le Goff & , 2021. "Multitrait GWAS to connect disease variants and biological mechanisms," PLOS Genetics, Public Library of Science, vol. 17(8), pages 1-36, August.
  • Handle: RePEc:plo:pgen00:1009713
    DOI: 10.1371/journal.pgen.1009713
    as

    Download full text from publisher

    File URL: https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1009713
    Download Restriction: no

    File URL: https://journals.plos.org/plosgenetics/article/file?id=10.1371/journal.pgen.1009713&type=printable
    Download Restriction: no

    File URL: https://libkey.io/10.1371/journal.pgen.1009713?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:plo:pgen00:1009713. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    We have no bibliographic references for this item. You can help adding them by using this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: plosgenetics (email available below). General contact details of provider: https://journals.plos.org/plosgenetics/ .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.