Literature DB >> 34592835

Rare, Damaging DNA Variants in CORIN and Risk of Coronary Artery Disease: Insights From Functional Genomics and Large-Scale Sequencing Analyses.

Minxian Wang1,2,3, Vivian S Lee-Kim2,4, Deepak S Atri2,4, Nadine H Elowe2, John Yu2, Colin W Garvie2, Hong-Hee Won5, Joseph E Hadaya1, Bryan T MacDonald2, Kevin Trindade6, Olle Melander7,8, Daniel J Rader6, Pradeep Natarajan1,2,3,9, Sekar Kathiresan3,9,10, Virendar K Kaushik2, Amit V Khera1,3,9, Rajat M Gupta1,2.   

Abstract

BACKGROUND: Corin is a protease expressed in cardiomyocytes that plays a key role in salt handling and intravascular volume homeostasis via activation of natriuretic peptides. It is unknown if Corin loss-of-function (LOF) is causally associated with risk of coronary artery disease (CAD).
METHODS: We analyzed all coding CORIN variants in an Italian case-control study of CAD. We functionally tested all 64 rare missense mutations in Western Blot and Mass Spectroscopy assays for proatrial natriuretic peptide cleavage. An expanded rare variant association analysis for Corin LOF mutations was conducted in whole exome sequencing data from 37 799 CAD cases and 212 184 controls.
RESULTS: We observed LOF variants in CORIN in 8 of 1803 (0.4%) CAD cases versus 0 of 1725 controls (P, 0.007). Of 64 rare missense variants profiled, 21 (33%) demonstrated <30% of wild-type activity and were deemed damaging in the 2 functional assays for Corin activity. In a rare variant association study that aggregated rare LOF and functionally validated damaging missense variants from the Italian study, we observed no association with CAD-21 of 1803 CAD cases versus 12 of 1725 controls with adjusted odds ratio of 1.61 ([95% CI, 0.79-3.29]; P=0.17). In the expanded sequencing dataset, there was no relationship between rare LOF variants with CAD was also observed (odds ratio, 1.15 [95% CI, 0.89-1.49]; P=0.30). Consistent with the genetic analysis, we observed no relationship between circulating Corin concentrations with incident CAD events among 4744 participants of a prospective cohort study-sex-stratified hazard ratio per SD increment of 0.96 ([95% CI, 0.87-1.07], P=0.48).
CONCLUSIONS: Functional testing of missense mutations improved the accuracy of rare variant association analysis. Despite compelling pathophysiology and a preliminary observation suggesting association, we observed no relationship between rare damaging variants in CORIN or circulating Corin concentrations with risk of CAD.

Entities:  

Keywords:  coronary artery disease; homeostasis; mutation; natriuretic peptides; odds ratio

Mesh:

Substances:

Year:  2021        PMID: 34592835      PMCID: PMC8555653          DOI: 10.1161/CIRCGEN.121.003399

Source DB:  PubMed          Journal:  Circ Genom Precis Med        ISSN: 2574-8300


  58 in total

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2.  Comparison and integration of deleteriousness prediction methods for nonsynonymous SNVs in whole exome sequencing studies.

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Journal:  Circulation       Date:  2020-05-14       Impact factor: 29.690

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Journal:  Nat Genet       Date:  2020-11-23       Impact factor: 38.330

9.  Exome sequencing identifies rare LDLR and APOA5 alleles conferring risk for myocardial infarction.

Authors:  Ron Do; Nathan O Stitziel; Hong-Hee Won; Anders Berg Jørgensen; Stefano Duga; Pier Angelica Merlini; Adam Kiezun; Martin Farrall; Anuj Goel; Or Zuk; Illaria Guella; Rosanna Asselta; Leslie A Lange; Gina M Peloso; Paul L Auer; Domenico Girelli; Nicola Martinelli; Deborah N Farlow; Mark A DePristo; Robert Roberts; Alexander F R Stewart; Danish Saleheen; John Danesh; Stephen E Epstein; Suthesh Sivapalaratnam; G Kees Hovingh; John J Kastelein; Nilesh J Samani; Heribert Schunkert; Jeanette Erdmann; Svati H Shah; William E Kraus; Robert Davies; Majid Nikpay; Christopher T Johansen; Jian Wang; Robert A Hegele; Eliana Hechter; Winfried Marz; Marcus E Kleber; Jie Huang; Andrew D Johnson; Mingyao Li; Greg L Burke; Myron Gross; Yongmei Liu; Themistocles L Assimes; Gerardo Heiss; Ethan M Lange; Aaron R Folsom; Herman A Taylor; Oliviero Olivieri; Anders Hamsten; Robert Clarke; Dermot F Reilly; Wu Yin; Manuel A Rivas; Peter Donnelly; Jacques E Rossouw; Bruce M Psaty; David M Herrington; James G Wilson; Stephen S Rich; Michael J Bamshad; Russell P Tracy; L Adrienne Cupples; Daniel J Rader; Muredach P Reilly; John A Spertus; Sharon Cresci; Jaana Hartiala; W H Wilson Tang; Stanley L Hazen; Hooman Allayee; Alex P Reiner; Christopher S Carlson; Charles Kooperberg; Rebecca D Jackson; Eric Boerwinkle; Eric S Lander; Stephen M Schwartz; David S Siscovick; Ruth McPherson; Anne Tybjaerg-Hansen; Goncalo R Abecasis; Hugh Watkins; Deborah A Nickerson; Diego Ardissino; Shamil R Sunyaev; Christopher J O'Donnell; David Altshuler; Stacey Gabriel; Sekar Kathiresan
Journal:  Nature       Date:  2014-12-10       Impact factor: 49.962

10.  The mutational constraint spectrum quantified from variation in 141,456 humans.

Authors:  Konrad J Karczewski; Laurent C Francioli; Grace Tiao; Beryl B Cummings; Jessica Alföldi; Qingbo Wang; Ryan L Collins; Kristen M Laricchia; Andrea Ganna; Daniel P Birnbaum; Laura D Gauthier; Harrison Brand; Matthew Solomonson; Nicholas A Watts; Daniel Rhodes; Moriel Singer-Berk; Eleina M England; Eleanor G Seaby; Jack A Kosmicki; Raymond K Walters; Katherine Tashman; Yossi Farjoun; Eric Banks; Timothy Poterba; Arcturus Wang; Cotton Seed; Nicola Whiffin; Jessica X Chong; Kaitlin E Samocha; Emma Pierce-Hoffman; Zachary Zappala; Anne H O'Donnell-Luria; Eric Vallabh Minikel; Ben Weisburd; Monkol Lek; James S Ware; Christopher Vittal; Irina M Armean; Louis Bergelson; Kristian Cibulskis; Kristen M Connolly; Miguel Covarrubias; Stacey Donnelly; Steven Ferriera; Stacey Gabriel; Jeff Gentry; Namrata Gupta; Thibault Jeandet; Diane Kaplan; Christopher Llanwarne; Ruchi Munshi; Sam Novod; Nikelle Petrillo; David Roazen; Valentin Ruano-Rubio; Andrea Saltzman; Molly Schleicher; Jose Soto; Kathleen Tibbetts; Charlotte Tolonen; Gordon Wade; Michael E Talkowski; Benjamin M Neale; Mark J Daly; Daniel G MacArthur
Journal:  Nature       Date:  2020-05-27       Impact factor: 69.504

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  3 in total

1.  Corin Missense Variants, Blood Pressure, and Hypertension in 11 322 Black Individuals: Insights From REGARDS and the Jackson Heart Study.

Authors:  Vibhu Parcha; Marguerite R Irvin; Leslie A Lange; Nicole D Armstrong; Akhil Pampana; Mariah Meyer; Suzanne E Judd; Garima Arora; Pankaj Arora
Journal:  J Am Heart Assoc       Date:  2022-06-14       Impact factor: 6.106

Review 2.  Corin: A Key Mediator in Sodium Homeostasis, Vascular Remodeling, and Heart Failure.

Authors:  Xianrui Zhang; Xiabing Gu; Yikai Zhang; Ningzheng Dong; Qingyu Wu
Journal:  Biology (Basel)       Date:  2022-05-07

Review 3.  Genome interpretation using in silico predictors of variant impact.

Authors:  Panagiotis Katsonis; Kevin Wilhelm; Amanda Williams; Olivier Lichtarge
Journal:  Hum Genet       Date:  2022-04-30       Impact factor: 5.881

  3 in total

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