Literature DB >> 34506852

A genome-wide association meta-analysis identifies new eosinophilic esophagitis loci.

Xiao Chang1, Michael March1, Frank Mentch1, Kenny Nguyen1, Joseph Glessner1, Huiqi Qu1, Yichuan Liu1, Glen Furuta2, Seema Aceves3, Nirmala Gonsalves4, Kari Nadeau5, Antonella Cianferoni6, Jonathan Spergel6, Patrick Sleiman7, Hakon Hakonarson8.   

Abstract

BACKGROUND: Eosinophilic esophagitis (EoE) is a chronic inflammatory disorder of the esophagus marked by eosinophilic infiltration. Cumulative evidence indicates that the risk of EoE involves the complex interplay of both genetic and environmental factors. Because only a few genetic loci have been identified in EoE, the genetic underpinning of EoE remains largely elusive.
OBJECTIVE: We sought to identify genetic loci associated with EoE.
METHODS: Four EoE cohorts were genotyped using the Illumina single nucleotide polymorphism array platform, totaling 1,930 cases and 13,634 controls of European ancestry. Genotype imputation was performed with the Michigan Imputation Server using the Trans-Omics for Precision Medicine reference panel including whole-genome sequencing data from more than 100,000 individuals. Meta-analysis was conducted to identify potential novel genetic loci associated with EoE.
RESULTS: Our study identified 11 new genome-wide significant loci, of which 6 are common variant loci, including 5q31.1 (rs2106984, P = 4.16 × 10-8; odds ratio [OR], 1.26, RAD50), 15q22.2 (rs2279293, P = 1.23 × 10-10; OR, 0.69, RORA), and 15q23 (rs56062135, P = 2.91 × 10-11; OR, 1.29, SMAD3), which have been previously associated with allergic conditions. Interestingly, a low-frequency synonymous mutation within the MATN2 gene was identified as the most significant single nucleotide polymorphism at the 8q22.1 locus. We also identified 5 sex-specific loci in the EoE cases, including an inflammatory bowel disease-associated locus at 9p24.1 (rs62541556, P = 4.4 × 10-8; OR, 1.11, JAK2).
CONCLUSIONS: Our findings demonstrate shared genetic underpinnings between EoE and other immune-mediated diseases and provide novel candidate genes for therapeutic target identification and prioritization.
Copyright © 2021 American Academy of Allergy, Asthma & Immunology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Eosinophilic esophagitis; GWAS; genetic correlation; genetic variants

Mesh:

Year:  2021        PMID: 34506852      PMCID: PMC9579995          DOI: 10.1016/j.jaci.2021.08.018

Source DB:  PubMed          Journal:  J Allergy Clin Immunol        ISSN: 0091-6749            Impact factor:   14.290


  60 in total

1.  Principal components analysis corrects for stratification in genome-wide association studies.

Authors:  Alkes L Price; Nick J Patterson; Robert M Plenge; Michael E Weinblatt; Nancy A Shadick; David Reich
Journal:  Nat Genet       Date:  2006-07-23       Impact factor: 38.330

Review 2.  Timing during translation matters: synonymous mutations in human pathologies influence protein folding and function.

Authors:  Robert Rauscher; Zoya Ignatova
Journal:  Biochem Soc Trans       Date:  2018-07-31       Impact factor: 5.407

3.  Twin and family studies reveal strong environmental and weaker genetic cues explaining heritability of eosinophilic esophagitis.

Authors:  Eileen S Alexander; Lisa J Martin; Margaret H Collins; Leah C Kottyan; Heidi Sucharew; Hua He; Vincent A Mukkada; Paul A Succop; J Pablo Abonia; Heather Foote; Michael D Eby; Tommie M Grotjan; Alexandria J Greenler; Evan S Dellon; Jeffrey G Demain; Glenn T Furuta; Larry E Gurian; John B Harley; Russell J Hopp; Amir Kagalwalla; Ajay Kaul; Kari C Nadeau; Richard J Noel; Philip E Putnam; Karl F von Tiehl; Marc E Rothenberg
Journal:  J Allergy Clin Immunol       Date:  2014-09-22       Impact factor: 10.793

4.  Integrative approaches for large-scale transcriptome-wide association studies.

Authors:  Alexander Gusev; Arthur Ko; Huwenbo Shi; Gaurav Bhatia; Wonil Chung; Brenda W J H Penninx; Rick Jansen; Eco J C de Geus; Dorret I Boomsma; Fred A Wright; Patrick F Sullivan; Elina Nikkola; Marcus Alvarez; Mete Civelek; Aldons J Lusis; Terho Lehtimäki; Emma Raitoharju; Mika Kähönen; Ilkka Seppälä; Olli T Raitakari; Johanna Kuusisto; Markku Laakso; Alkes L Price; Päivi Pajukanta; Bogdan Pasaniuc
Journal:  Nat Genet       Date:  2016-02-08       Impact factor: 38.330

5.  Newly identified genetic risk variants for celiac disease related to the immune response.

Authors:  Karen A Hunt; Alexandra Zhernakova; Graham Turner; Graham A R Heap; Lude Franke; Marcel Bruinenberg; Jihane Romanos; Lotte C Dinesen; Anthony W Ryan; Davinder Panesar; Rhian Gwilliam; Fumihiko Takeuchi; William M McLaren; Geoffrey K T Holmes; Peter D Howdle; Julian R F Walters; David S Sanders; Raymond J Playford; Gosia Trynka; Chris J J Mulder; M Luisa Mearin; Wieke H M Verbeek; Valerie Trimble; Fiona M Stevens; Colm O'Morain; Nicholas P Kennedy; Dermot Kelleher; Daniel J Pennington; David P Strachan; Wendy L McArdle; Charles A Mein; Martin C Wapenaar; Panos Deloukas; Ralph McGinnis; Ross McManus; Cisca Wijmenga; David A van Heel
Journal:  Nat Genet       Date:  2008-03-02       Impact factor: 38.330

6.  Antigen phagocytosis by B cells is required for a potent humoral response.

Authors:  Ana Martínez-Riaño; Elena R Bovolenta; Pilar Mendoza; Clara L Oeste; María Jesús Martín-Bermejo; Paola Bovolenta; Martin Turner; Nuria Martínez-Martín; Balbino Alarcón
Journal:  EMBO Rep       Date:  2018-07-09       Impact factor: 8.807

7.  The NHGRI-EBI GWAS Catalog of published genome-wide association studies, targeted arrays and summary statistics 2019.

Authors:  Annalisa Buniello; Jacqueline A L MacArthur; Maria Cerezo; Laura W Harris; James Hayhurst; Cinzia Malangone; Aoife McMahon; Joannella Morales; Edward Mountjoy; Elliot Sollis; Daniel Suveges; Olga Vrousgou; Patricia L Whetzel; Ridwan Amode; Jose A Guillen; Harpreet S Riat; Stephen J Trevanion; Peggy Hall; Heather Junkins; Paul Flicek; Tony Burdett; Lucia A Hindorff; Fiona Cunningham; Helen Parkinson
Journal:  Nucleic Acids Res       Date:  2019-01-08       Impact factor: 16.971

8.  Use of >100,000 NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium whole genome sequences improves imputation quality and detection of rare variant associations in admixed African and Hispanic/Latino populations.

Authors:  Madeline H Kowalski; Huijun Qian; Ziyi Hou; Jonathan D Rosen; Amanda L Tapia; Yue Shan; Deepti Jain; Maria Argos; Donna K Arnett; Christy Avery; Kathleen C Barnes; Lewis C Becker; Stephanie A Bien; Joshua C Bis; John Blangero; Eric Boerwinkle; Donald W Bowden; Steve Buyske; Jianwen Cai; Michael H Cho; Seung Hoan Choi; Hélène Choquet; L Adrienne Cupples; Mary Cushman; Michelle Daya; Paul S de Vries; Patrick T Ellinor; Nauder Faraday; Myriam Fornage; Stacey Gabriel; Santhi K Ganesh; Misa Graff; Namrata Gupta; Jiang He; Susan R Heckbert; Bertha Hidalgo; Chani J Hodonsky; Marguerite R Irvin; Andrew D Johnson; Eric Jorgenson; Robert Kaplan; Sharon L R Kardia; Tanika N Kelly; Charles Kooperberg; Jessica A Lasky-Su; Ruth J F Loos; Steven A Lubitz; Rasika A Mathias; Caitlin P McHugh; Courtney Montgomery; Jee-Young Moon; Alanna C Morrison; Nicholette D Palmer; Nathan Pankratz; George J Papanicolaou; Juan M Peralta; Patricia A Peyser; Stephen S Rich; Jerome I Rotter; Edwin K Silverman; Jennifer A Smith; Nicholas L Smith; Kent D Taylor; Timothy A Thornton; Hemant K Tiwari; Russell P Tracy; Tao Wang; Scott T Weiss; Lu-Chen Weng; Kerri L Wiggins; James G Wilson; Lisa R Yanek; Sebastian Zöllner; Kari E North; Paul L Auer; Laura M Raffield; Alexander P Reiner; Yun Li
Journal:  PLoS Genet       Date:  2019-12-23       Impact factor: 6.020

9.  Genome-wide association analysis of eosinophilic esophagitis provides insight into the tissue specificity of this allergic disease.

Authors:  Leah C Kottyan; Benjamin P Davis; Joseph D Sherrill; Kan Liu; Mark Rochman; Kenneth Kaufman; Matthew T Weirauch; Samuel Vaughn; Sara Lazaro; Andrew M Rupert; Mojtaba Kohram; Emily M Stucke; Katherine A Kemme; Albert Magnusen; Hua He; Phillip Dexheimer; Mirna Chehade; Robert A Wood; Robbie D Pesek; Brian P Vickery; David M Fleischer; Robert Lindbad; Hugh A Sampson; Vincent A Mukkada; Phil E Putnam; J Pablo Abonia; Lisa J Martin; John B Harley; Marc E Rothenberg
Journal:  Nat Genet       Date:  2014-07-13       Impact factor: 38.330

10.  HaploReg v4: systematic mining of putative causal variants, cell types, regulators and target genes for human complex traits and disease.

Authors:  Lucas D Ward; Manolis Kellis
Journal:  Nucleic Acids Res       Date:  2015-12-10       Impact factor: 16.971

View more
  2 in total

1.  Single-cell RNA-Seq of human esophageal epithelium in homeostasis and allergic inflammation.

Authors:  Mark Rochman; Ting Wen; Michael Kotliar; Phillip J Dexheimer; Netali Ben-Baruch Morgenstern; Julie M Caldwell; Hee-Woong Lim; Marc E Rothenberg
Journal:  JCI Insight       Date:  2022-06-08

Review 2.  Molecular Mechanisms of Eosinophilic Esophagitis.

Authors:  Yury V Zhernov; Sonya O Vysochanskaya; Vitaly A Sukhov; Olga K Zaostrovtseva; Denis S Gorshenin; Ekaterina A Sidorova; Oleg V Mitrokhin
Journal:  Int J Mol Sci       Date:  2021-12-07       Impact factor: 5.923

  2 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.