Literature DB >> 24952213

Association of STAT6 variants with asthma risk: a systematic review and meta-analysis.

Xubo Qian1, Yuan Gao2, Xiaohong Ye3, Meiping Lu4.   

Abstract

A large number of studies have reported that the genetic variants in STAT6 gene may be implicated in susceptibility to asthma, but with inconsistent results. Therefore, the aim of this meta-analysis was to determine the likelihood of developing asthma for the individuals with different STAT6 variants. The database including Pubmed, Embase and CNKI (Chinese National Knowledge Infrastructure) were searched to find the relevant papers. Data were extracted by two independent reviewers and the odds radios (ORs) were pooled with 95% confidence intervals (CIs), using random effect or fixed effect models as appropriate, to indicate the risk of asthma for different STAT6 variants. The heterogeneity and bias were tested for each pooled result. Data from 19 studies were pooled that reported associations of rs324015, rs71802646 and rs324011 in STAT6 gene with asthma risk. The results demonstrated that 13GT and short GT in rs71802646 were both associated with increased risk of asthma in overall analysis (OR = 1.26 for 13GT and 1.30 for short GT). Further, subgroup analysis showed an increased risk of asthma in Asian population with 13GT (OR = 1.21), 14GT (OR = 1.97) and short GT (OR = 1.27). Besides, 13GT, 14GT and short GT all contributed to higher risk of atopic asthma, with OR 1.50, 2.21 and 1.65 respectively. However, rs324015 (G>A) appeared to be associated with decreased risk for atopic asthma (with OR = 0.83, 0.68 and 0.79 for A, AA and AA+AG respectively). Both overall and subgroup analyses indicated no effect of rs324011 on asthma risk. In conclusion, our meta-analyses suggest that short GT repeats of rs71802646 in STAT6 contribute to higher risk for asthma, while rs324015 may have a protective effect on atopic asthma.
Copyright © 2014 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Asthma; Genetic polymorphism; Meta-analysis; STAT6

Mesh:

Substances:

Year:  2014        PMID: 24952213     DOI: 10.1016/j.humimm.2014.06.007

Source DB:  PubMed          Journal:  Hum Immunol        ISSN: 0198-8859            Impact factor:   2.850


  8 in total

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Authors:  Philip Duodu; Geohaira Sosa; Jorge Canar; Olivia Chhugani; Ana M Gamero
Journal:  J Interferon Cytokine Res       Date:  2022-07-25       Impact factor: 3.657

2.  Frequency distribution of cytokine and associated transcription factor single nucleotide polymorphisms in Zimbabweans: Impact on schistosome infection and cytokine levels.

Authors:  Andrew John Hanton; Fiona Scott; Katharina Stenzel; Norman Nausch; Grace Zdesenko; Takafira Mduluza; Francisca Mutapi
Journal:  PLoS Negl Trop Dis       Date:  2022-06-27

3.  Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

Authors:  Florence Demenais; Patricia Margaritte-Jeannin; Kathleen C Barnes; William O C Cookson; Janine Altmüller; Wei Ang; R Graham Barr; Terri H Beaty; Allan B Becker; John Beilby; Hans Bisgaard; Unnur Steina Bjornsdottir; Eugene Bleecker; Klaus Bønnelykke; Dorret I Boomsma; Emmanuelle Bouzigon; Christopher E Brightling; Myriam Brossard; Guy G Brusselle; Esteban Burchard; Kristin M Burkart; Andrew Bush; Moira Chan-Yeung; Kian Fan Chung; Alexessander Couto Alves; John A Curtin; Adnan Custovic; Denise Daley; Johan C de Jongste; Blanca E Del-Rio-Navarro; Kathleen M Donohue; Liesbeth Duijts; Celeste Eng; Johan G Eriksson; Martin Farrall; Yuliya Fedorova; Bjarke Feenstra; Manuel A Ferreira; Maxim B Freidin; Zofia Gajdos; Jim Gauderman; Ulrike Gehring; Frank Geller; Jon Genuneit; Sina A Gharib; Frank Gilliland; Raquel Granell; Penelope E Graves; Daniel F Gudbjartsson; Tari Haahtela; Susan R Heckbert; Dick Heederik; Joachim Heinrich; Markku Heliövaara; John Henderson; Blanca E Himes; Hiroshi Hirose; Joel N Hirschhorn; Albert Hofman; Patrick Holt; Jouke Hottenga; Thomas J Hudson; Jennie Hui; Medea Imboden; Vladimir Ivanov; Vincent W V Jaddoe; Alan James; Christer Janson; Marjo-Riitta Jarvelin; Deborah Jarvis; Graham Jones; Ingileif Jonsdottir; Pekka Jousilahti; Michael Kabesch; Mika Kähönen; David B Kantor; Alexandra S Karunas; Elza Khusnutdinova; Gerard H Koppelman; Anita L Kozyrskyj; Eskil Kreiner; Michiaki Kubo; Rajesh Kumar; Ashish Kumar; Mikko Kuokkanen; Lies Lahousse; Tarja Laitinen; Catherine Laprise; Mark Lathrop; Susanne Lau; Young-Ae Lee; Terho Lehtimäki; Sébastien Letort; Albert M Levin; Guo Li; Liming Liang; Laura R Loehr; Stephanie J London; Daan W Loth; Ani Manichaikul; Ingo Marenholz; Fernando J Martinez; Melanie C Matheson; Rasika A Mathias; Kenji Matsumoto; Hamdi Mbarek; Wendy L McArdle; Mads Melbye; Erik Melén; Deborah Meyers; Sven Michel; Hamida Mohamdi; Arthur W Musk; Rachel A Myers; Maartje A E Nieuwenhuis; Emiko Noguchi; George T O'Connor; Ludmila M Ogorodova; Cameron D Palmer; Aarno Palotie; Julie E Park; Craig E Pennell; Göran Pershagen; Alexey Polonikov; Dirkje S Postma; Nicole Probst-Hensch; Valery P Puzyrev; Benjamin A Raby; Olli T Raitakari; Adaikalavan Ramasamy; Stephen S Rich; Colin F Robertson; Isabelle Romieu; Muhammad T Salam; Veikko Salomaa; Vivi Schlünssen; Robert Scott; Polina A Selivanova; Torben Sigsgaard; Angela Simpson; Valérie Siroux; Lewis J Smith; Maria Solodilova; Marie Standl; Kari Stefansson; David P Strachan; Bruno H Stricker; Atsushi Takahashi; Philip J Thompson; Gudmar Thorleifsson; Unnur Thorsteinsdottir; Carla M T Tiesler; Dara G Torgerson; Tatsuhiko Tsunoda; André G Uitterlinden; Ralf J P van der Valk; Amaury Vaysse; Sailaja Vedantam; Andrea von Berg; Erika von Mutius; Judith M Vonk; Johannes Waage; Nick J Wareham; Scott T Weiss; Wendy B White; Magnus Wickman; Elisabeth Widén; Gonneke Willemsen; L Keoki Williams; Inge M Wouters; James J Yang; Jing Hua Zhao; Miriam F Moffatt; Carole Ober; Dan L Nicolae
Journal:  Nat Genet       Date:  2017-12-22       Impact factor: 38.330

Review 4.  Type 2 Inflammation in Eosinophilic Esophagitis: From Pathophysiology to Therapeutic Targets.

Authors:  Francesca Racca; Gaia Pellegatta; Giuseppe Cataldo; Edoardo Vespa; Elisa Carlani; Corrado Pelaia; Giovanni Paoletti; Maria Rita Messina; Emanuele Nappi; Giorgio Walter Canonica; Alessandro Repici; Enrico Heffler
Journal:  Front Physiol       Date:  2022-01-12       Impact factor: 4.566

5.  Association of NOD1, CXCL16, STAT6 and TLR4 gene polymorphisms with Malaysian patients with Crohn's disease.

Authors:  Kek Heng Chua; Jin Guan Ng; Ching Ching Ng; Ida Hilmi; Khean Lee Goh; Boon Pin Kee
Journal:  PeerJ       Date:  2016-03-31       Impact factor: 2.984

Review 6.  Genetic Mechanisms of Asthma and the Implications for Drug Repositioning.

Authors:  Yue Huo; Hong-Yu Zhang
Journal:  Genes (Basel)       Date:  2018-05-03       Impact factor: 4.096

7.  Association of STAT6 gene variants with food allergy diagnosed by double-blind placebo-controlled food challenges.

Authors:  C D van Ginkel; M E Pettersson; A E J Dubois; G H Koppelman
Journal:  Allergy       Date:  2018-04-06       Impact factor: 13.146

8.  CYP2C19 and STAT6 Variants Influence the Outcome of Proton Pump Inhibitor Therapy in Pediatric Eosinophilic Esophagitis.

Authors:  Edward B Mougey; Andre Williams; Ashlan J Kunz Coyne; Carolina Gutiérrez-Junquera; Sonia Fernández-Fernández; Maria Luz Cilleruelo; Ana Rayo; Luis Echeverría; Enriqueta Román; Carmen González Lois; Montserrat Chao; Hadeel Al-Atrash; John J Lima; James P Franciosi
Journal:  J Pediatr Gastroenterol Nutr       Date:  2019-11       Impact factor: 2.839

  8 in total

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