Literature DB >> 32511788

Power loss due to testing association between covariate-adjusted traits and genetic variants.

Pranav Yajnik1, Michael Boehnke1.   

Abstract

Multiple linear regression is commonly used to test for association between genetic variants and continuous traits and estimate genetic effect sizes. Confounding variables are controlled for by including them as additional covariates. An alternative technique that is increasingly used is to regress out covariates from the raw trait and then perform regression analysis with only the genetic variants included as predictors. In the case of single-variant analysis, this adjusted trait regression (ATR) technique is known to be less powerful than the traditional technique when the genetic variant is correlated with the covariates We extend previous results for single-variant tests by deriving exact relationships between the single-variant score, Wald, likelihood-ratio, and F test statistics and their ATR analogs. We also derive the asymptotic power of ATR analogs of the multiple-variant score and burden tests. We show that the maximum power loss of the ATR analog of the multiple-variant score test is completely characterized by the canonical correlations between the set of genetic variants and the set of covariates. Further, we show that for both single- and multiple-variant tests, the power loss for ATR analogs increases with increasing stringency of Type 1 error control ( α ) and increasing correlation (or canonical correlations) between the genetic variant (or multiple variants) and covariates. We recommend using ATR only when maximum canonical correlation between variants and covariates is low, as is typically true.
© 2020 Wiley Periodicals LLC.

Entities:  

Keywords:  adjusted outcome; covariates; genome-wide association study; linear regression; power loss

Year:  2020        PMID: 32511788      PMCID: PMC7610149          DOI: 10.1002/gepi.22325

Source DB:  PubMed          Journal:  Genet Epidemiol        ISSN: 0741-0395            Impact factor:   2.135


  18 in total

1.  Adjusting for heritable covariates can bias effect estimates in genome-wide association studies.

Authors:  Hugues Aschard; Bjarni J Vilhjálmsson; Amit D Joshi; Alkes L Price; Peter Kraft
Journal:  Am J Hum Genet       Date:  2015-01-29       Impact factor: 11.025

Review 2.  Rare-variant association analysis: study designs and statistical tests.

Authors:  Seunggeung Lee; Gonçalo R Abecasis; Michael Boehnke; Xihong Lin
Journal:  Am J Hum Genet       Date:  2014-07-03       Impact factor: 11.025

3.  Genome-wide association scans for secondary traits using case-control samples.

Authors:  Genevieve M Monsees; Rulla M Tamimi; Peter Kraft
Journal:  Genet Epidemiol       Date:  2009-12       Impact factor: 2.135

4.  A fully adjusted two-stage procedure for rank-normalization in genetic association studies.

Authors:  Tamar Sofer; Xiuwen Zheng; Stephanie M Gogarten; Cecelia A Laurie; Kelsey Grinde; John R Shaffer; Dmitry Shungin; Jeffrey R O'Connell; Ramon A Durazo-Arvizo; Laura Raffield; Leslie Lange; Solomon Musani; Ramachandran S Vasan; L Adrienne Cupples; Alexander P Reiner; Cathy C Laurie; Kenneth M Rice
Journal:  Genet Epidemiol       Date:  2019-01-17       Impact factor: 2.344

5.  A global reference for human genetic variation.

Authors:  Adam Auton; Lisa D Brooks; Richard M Durbin; Erik P Garrison; Hyun Min Kang; Jan O Korbel; Jonathan L Marchini; Shane McCarthy; Gil A McVean; Gonçalo R Abecasis
Journal:  Nature       Date:  2015-10-01       Impact factor: 49.962

6.  Collider scope: when selection bias can substantially influence observed associations.

Authors:  Marcus R Munafò; Kate Tilling; Amy E Taylor; David M Evans; George Davey Smith
Journal:  Int J Epidemiol       Date:  2018-02-01       Impact factor: 7.196

7.  Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits.

Authors:  Ioanna Tachmazidou; Dániel Süveges; Josine L Min; Graham R S Ritchie; Julia Steinberg; Klaudia Walter; Valentina Iotchkova; Jeremy Schwartzentruber; Jie Huang; Yasin Memari; Shane McCarthy; Andrew A Crawford; Cristina Bombieri; Massimiliano Cocca; Aliki-Eleni Farmaki; Tom R Gaunt; Pekka Jousilahti; Marjolein N Kooijman; Benjamin Lehne; Giovanni Malerba; Satu Männistö; Angela Matchan; Carolina Medina-Gomez; Sarah J Metrustry; Abhishek Nag; Ioanna Ntalla; Lavinia Paternoster; Nigel W Rayner; Cinzia Sala; William R Scott; Hashem A Shihab; Lorraine Southam; Beate St Pourcain; Michela Traglia; Katerina Trajanoska; Gialuigi Zaza; Weihua Zhang; María S Artigas; Narinder Bansal; Marianne Benn; Zhongsheng Chen; Petr Danecek; Wei-Yu Lin; Adam Locke; Jian'an Luan; Alisa K Manning; Antonella Mulas; Carlo Sidore; Anne Tybjaerg-Hansen; Anette Varbo; Magdalena Zoledziewska; Chris Finan; Konstantinos Hatzikotoulas; Audrey E Hendricks; John P Kemp; Alireza Moayyeri; Kalliope Panoutsopoulou; Michal Szpak; Scott G Wilson; Michael Boehnke; Francesco Cucca; Emanuele Di Angelantonio; Claudia Langenberg; Cecilia Lindgren; Mark I McCarthy; Andrew P Morris; Børge G Nordestgaard; Robert A Scott; Martin D Tobin; Nicholas J Wareham; Paul Burton; John C Chambers; George Davey Smith; George Dedoussis; Janine F Felix; Oscar H Franco; Giovanni Gambaro; Paolo Gasparini; Christopher J Hammond; Albert Hofman; Vincent W V Jaddoe; Marcus Kleber; Jaspal S Kooner; Markus Perola; Caroline Relton; Susan M Ring; Fernando Rivadeneira; Veikko Salomaa; Timothy D Spector; Oliver Stegle; Daniela Toniolo; André G Uitterlinden; Inês Barroso; Celia M T Greenwood; John R B Perry; Brian R Walker; Adam S Butterworth; Yali Xue; Richard Durbin; Kerrin S Small; Nicole Soranzo; Nicholas J Timpson; Eleftheria Zeggini
Journal:  Am J Hum Genet       Date:  2017-05-25       Impact factor: 11.025

8.  Sex-stratified genome-wide association studies including 270,000 individuals show sexual dimorphism in genetic loci for anthropometric traits.

Authors:  Joshua C Randall; Thomas W Winkler; Zoltán Kutalik; Sonja I Berndt; Anne U Jackson; Keri L Monda; Tuomas O Kilpeläinen; Tõnu Esko; Reedik Mägi; Shengxu Li; Tsegaselassie Workalemahu; Mary F Feitosa; Damien C Croteau-Chonka; Felix R Day; Tove Fall; Teresa Ferreira; Stefan Gustafsson; Adam E Locke; Iain Mathieson; Andre Scherag; Sailaja Vedantam; Andrew R Wood; Liming Liang; Valgerdur Steinthorsdottir; Gudmar Thorleifsson; Emmanouil T Dermitzakis; Antigone S Dimas; Fredrik Karpe; Josine L Min; George Nicholson; Deborah J Clegg; Thomas Person; Jon P Krohn; Sabrina Bauer; Christa Buechler; Kristina Eisinger; Amélie Bonnefond; Philippe Froguel; Jouke-Jan Hottenga; Inga Prokopenko; Lindsay L Waite; Tamara B Harris; Albert Vernon Smith; Alan R Shuldiner; Wendy L McArdle; Mark J Caulfield; Patricia B Munroe; Henrik Grönberg; Yii-Der Ida Chen; Guo Li; Jacques S Beckmann; Toby Johnson; Unnur Thorsteinsdottir; Maris Teder-Laving; Kay-Tee Khaw; Nicholas J Wareham; Jing Hua Zhao; Najaf Amin; Ben A Oostra; Aldi T Kraja; Michael A Province; L Adrienne Cupples; Nancy L Heard-Costa; Jaakko Kaprio; Samuli Ripatti; Ida Surakka; Francis S Collins; Jouko Saramies; Jaakko Tuomilehto; Antti Jula; Veikko Salomaa; Jeanette Erdmann; Christian Hengstenberg; Christina Loley; Heribert Schunkert; Claudia Lamina; H Erich Wichmann; Eva Albrecht; Christian Gieger; Andrew A Hicks; Asa Johansson; Peter P Pramstaller; Sekar Kathiresan; Elizabeth K Speliotes; Brenda Penninx; Anna-Liisa Hartikainen; Marjo-Riitta Jarvelin; Ulf Gyllensten; Dorret I Boomsma; Harry Campbell; James F Wilson; Stephen J Chanock; Martin Farrall; Anuj Goel; Carolina Medina-Gomez; Fernando Rivadeneira; Karol Estrada; André G Uitterlinden; Albert Hofman; M Carola Zillikens; Martin den Heijer; Lambertus A Kiemeney; Andrea Maschio; Per Hall; Jonathan Tyrer; Alexander Teumer; Henry Völzke; Peter Kovacs; Anke Tönjes; Massimo Mangino; Tim D Spector; Caroline Hayward; Igor Rudan; Alistair S Hall; Nilesh J Samani; Antony Paul Attwood; Jennifer G Sambrook; Joseph Hung; Lyle J Palmer; Marja-Liisa Lokki; Juha Sinisalo; Gabrielle Boucher; Heikki Huikuri; Mattias Lorentzon; Claes Ohlsson; Niina Eklund; Johan G Eriksson; Cristina Barlassina; Carlo Rivolta; Ilja M Nolte; Harold Snieder; Melanie M Van der Klauw; Jana V Van Vliet-Ostaptchouk; Pablo V Gejman; Jianxin Shi; Kevin B Jacobs; Zhaoming Wang; Stephan J L Bakker; Irene Mateo Leach; Gerjan Navis; Pim van der Harst; Nicholas G Martin; Sarah E Medland; Grant W Montgomery; Jian Yang; Daniel I Chasman; Paul M Ridker; Lynda M Rose; Terho Lehtimäki; Olli Raitakari; Devin Absher; Carlos Iribarren; Hanneke Basart; Kees G Hovingh; Elina Hyppönen; Chris Power; Denise Anderson; John P Beilby; Jennie Hui; Jennifer Jolley; Hendrik Sager; Stefan R Bornstein; Peter E H Schwarz; Kati Kristiansson; Markus Perola; Jaana Lindström; Amy J Swift; Matti Uusitupa; Mustafa Atalay; Timo A Lakka; Rainer Rauramaa; Jennifer L Bolton; Gerry Fowkes; Ross M Fraser; Jackie F Price; Krista Fischer; Kaarel Krjutå Kov; Andres Metspalu; Evelin Mihailov; Claudia Langenberg; Jian'an Luan; Ken K Ong; Peter S Chines; Sirkka M Keinanen-Kiukaanniemi; Timo E Saaristo; Sarah Edkins; Paul W Franks; Göran Hallmans; Dmitry Shungin; Andrew David Morris; Colin N A Palmer; Raimund Erbel; Susanne Moebus; Markus M Nöthen; Sonali Pechlivanis; Kristian Hveem; Narisu Narisu; Anders Hamsten; Steve E Humphries; Rona J Strawbridge; Elena Tremoli; Harald Grallert; Barbara Thorand; Thomas Illig; Wolfgang Koenig; Martina Müller-Nurasyid; Annette Peters; Bernhard O Boehm; Marcus E Kleber; Winfried März; Bernhard R Winkelmann; Johanna Kuusisto; Markku Laakso; Dominique Arveiler; Giancarlo Cesana; Kari Kuulasmaa; Jarmo Virtamo; John W G Yarnell; Diana Kuh; Andrew Wong; Lars Lind; Ulf de Faire; Bruna Gigante; Patrik K E Magnusson; Nancy L Pedersen; George Dedoussis; Maria Dimitriou; Genovefa Kolovou; Stavroula Kanoni; Kathleen Stirrups; Lori L Bonnycastle; Inger Njølstad; Tom Wilsgaard; Andrea Ganna; Emil Rehnberg; Aroon Hingorani; Mika Kivimaki; Meena Kumari; Themistocles L Assimes; Inês Barroso; Michael Boehnke; Ingrid B Borecki; Panos Deloukas; Caroline S Fox; Timothy Frayling; Leif C Groop; Talin Haritunians; David Hunter; Erik Ingelsson; Robert Kaplan; Karen L Mohlke; Jeffrey R O'Connell; David Schlessinger; David P Strachan; Kari Stefansson; Cornelia M van Duijn; Gonçalo R Abecasis; Mark I McCarthy; Joel N Hirschhorn; Lu Qi; Ruth J F Loos; Cecilia M Lindgren; Kari E North; Iris M Heid
Journal:  PLoS Genet       Date:  2013-06-06       Impact factor: 5.917

9.  The UK10K project identifies rare variants in health and disease.

Authors:  Klaudia Walter; Josine L Min; Jie Huang; Lucy Crooks; Yasin Memari; Shane McCarthy; John R B Perry; ChangJiang Xu; Marta Futema; Daniel Lawson; Valentina Iotchkova; Stephan Schiffels; Audrey E Hendricks; Petr Danecek; Rui Li; James Floyd; Louise V Wain; Inês Barroso; Steve E Humphries; Matthew E Hurles; Eleftheria Zeggini; Jeffrey C Barrett; Vincent Plagnol; J Brent Richards; Celia M T Greenwood; Nicholas J Timpson; Richard Durbin; Nicole Soranzo
Journal:  Nature       Date:  2015-09-14       Impact factor: 49.962

10.  Genome-wide association study of dietary intake in the UK biobank study and its associations with schizophrenia and other traits.

Authors:  Maria Niarchou; Enda M Byrne; Maciej Trzaskowski; Julia Sidorenko; Kathryn E Kemper; John J McGrath; Michael C O' Donovan; Michael J Owen; Naomi R Wray
Journal:  Transl Psychiatry       Date:  2020-02-03       Impact factor: 6.222

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