Literature DB >> 21296850

FCGR3B copy number variation is associated with systemic lupus erythematosus risk in Afro-Caribbeans.

Mariam Molokhia1, Manuela Fanciulli, Enrico Petretto, Alan Leslie Patrick, Paul McKeigue, Amy L Roberts, Tim J Vyse, Tim J Aitman.   

Abstract

OBJECTIVES: To evaluate FCGR3B copy number variation (CNV) in African and European populations and to determine if FCGR3B copy number is associated with SLE and SLE nephritis risk in Afro-Caribbeans, adjusting for African genetic ancestry.
METHODS: We estimated FCGR3B to determine if there were ethnic variations in CNV (unrelated unadmixed Europeans and Africans). We then examined CNV at FCGR3B in relation to SLE and SLE nephritis within a case-control collection of 134 cases of SLE (37 with SLE nephritis) and 589 population controls of mainly Afro-Caribbean descent resident in Trinidad.
RESULTS: We found a significant difference in copy number FCGR3B distribution between unadmixed African and European UK cohorts, with 27 (29%) vs 3 (5%) for those with low (0 or 1) copy FCGR3B, respectively, P = 0.002. In a Trinidadian SLE case-control study, low FCGR3B CNV was associated with SLE risk 1.7 (95% CI 1.1, 2.8), P = 0.02, which remained after adjustment for African genetic ancestry; odds ratios (ORs) 1.7 (95% CI 1.0, 2.8), P = 0.04.
CONCLUSION: Our studies suggest that FCGR3B low copy number is associated with SLE risk in Afro-Caribbean populations independently of CNV due to African ancestry.

Entities:  

Mesh:

Substances:

Year:  2011        PMID: 21296850      PMCID: PMC3670581          DOI: 10.1093/rheumatology/keq456

Source DB:  PubMed          Journal:  Rheumatology (Oxford)        ISSN: 1462-0324            Impact factor:   7.580


  21 in total

1.  Estimation of admixture and detection of linkage in admixed populations by a Bayesian approach: application to African-American populations.

Authors:  P M McKeigue; J R Carpenter; E J Parra; M D Shriver
Journal:  Ann Hum Genet       Date:  2000-03       Impact factor: 1.670

Review 2.  Copy-number variations associated with neuropsychiatric conditions.

Authors:  Edwin H Cook; Stephen W Scherer
Journal:  Nature       Date:  2008-10-16       Impact factor: 49.962

3.  Glutathione S-transferase genotypes and allergic responses to diisocyanate exposure.

Authors:  P Piirilä; H Wikman; R Luukkonen; K Kääriä; C Rosenberg; H Nordman; H Norppa; H Vainio; A Hirvonen
Journal:  Pharmacogenetics       Date:  2001-07

4.  Glutathione- S-transferase micro and theta gene polymorphisms as new risk factors of atopic bronchial asthma.

Authors:  T E Ivaschenko; O G Sideleva; V S Baranov
Journal:  J Mol Med (Berl)       Date:  2001-09-06       Impact factor: 4.599

5.  The influence of CCL3L1 gene-containing segmental duplications on HIV-1/AIDS susceptibility.

Authors:  Enrique Gonzalez; Hemant Kulkarni; Hector Bolivar; Andrea Mangano; Racquel Sanchez; Gabriel Catano; Robert J Nibbs; Barry I Freedman; Marlon P Quinones; Michael J Bamshad; Krishna K Murthy; Brad H Rovin; William Bradley; Robert A Clark; Stephanie A Anderson; Robert J O'connell; Brian K Agan; Seema S Ahuja; Rosa Bologna; Luisa Sen; Matthew J Dolan; Sunil K Ahuja
Journal:  Science       Date:  2005-01-06       Impact factor: 47.728

6.  FCGR3B copy number variation is not associated with lupus nephritis in a Chinese population.

Authors:  J Lv; Y Yang; X Zhou; L Yu; R Li; P Hou; H Zhang
Journal:  Lupus       Date:  2009-11-27       Impact factor: 2.911

7.  Deletion polymorphism upstream of IRGM associated with altered IRGM expression and Crohn's disease.

Authors:  Steven A McCarroll; Alan Huett; Petric Kuballa; Shannon D Chilewski; Aimee Landry; Philippe Goyette; Michael C Zody; Jennifer L Hall; Steven R Brant; Judy H Cho; Richard H Duerr; Mark S Silverberg; Kent D Taylor; John D Rioux; David Altshuler; Mark J Daly; Ramnik J Xavier
Journal:  Nat Genet       Date:  2008-09       Impact factor: 38.330

8.  Psoriasis is associated with increased beta-defensin genomic copy number.

Authors:  Edward J Hollox; Ulrike Huffmeier; Patrick L J M Zeeuwen; Raquel Palla; Jesús Lascorz; Diana Rodijk-Olthuis; Peter C M van de Kerkhof; Heiko Traupe; Gys de Jongh; Martin den Heijer; André Reis; John A L Armour; Joost Schalkwijk
Journal:  Nat Genet       Date:  2007-12-02       Impact factor: 38.330

9.  FCGR3B copy number variation is associated with susceptibility to systemic, but not organ-specific, autoimmunity.

Authors:  Manuela Fanciulli; Penny J Norsworthy; Enrico Petretto; Rong Dong; Lorraine Harper; Lavanya Kamesh; Joanne M Heward; Stephen C L Gough; Adam de Smith; Alexandra I F Blakemore; Philippe Froguel; Catherine J Owen; Simon H S Pearce; Luis Teixeira; Loic Guillevin; Deborah S Cunninghame Graham; Charles D Pusey; H Terence Cook; Timothy J Vyse; Timothy J Aitman
Journal:  Nat Genet       Date:  2007-05-21       Impact factor: 38.330

10.  Copy number polymorphism in Fcgr3 predisposes to glomerulonephritis in rats and humans.

Authors:  Timothy J Aitman; Rong Dong; Timothy J Vyse; Penny J Norsworthy; Michelle D Johnson; Jennifer Smith; Jonathan Mangion; Cheri Roberton-Lowe; Amy J Marshall; Enrico Petretto; Matthew D Hodges; Gurjeet Bhangal; Sheetal G Patel; Kelly Sheehan-Rooney; Mark Duda; Paul R Cook; David J Evans; Jan Domin; Jonathan Flint; Joseph J Boyle; Charles D Pusey; H Terence Cook
Journal:  Nature       Date:  2006-02-16       Impact factor: 49.962

View more
  14 in total

1.  A genome-wide characterization of copy number variations in native populations of Peninsular Malaysia.

Authors:  Ruiqing Fu; Siti Shuhada Mokhtar; Maude Elvira Phipps; Boon-Peng Hoh; Shuhua Xu
Journal:  Eur J Hum Genet       Date:  2018-02-23       Impact factor: 4.246

Review 2.  Association between FCGR3B copy number variations and susceptibility to autoimmune diseases: a meta-analysis.

Authors:  Young Ho Lee; Sang-Cheol Bae; Young Ho Seo; Jae-Hoon Kim; Sung Jae Choi; Jong Dae Ji; Gwan Gyu Song
Journal:  Inflamm Res       Date:  2015-09-25       Impact factor: 4.575

3.  Low copy number of FCGR3B is associated with lupus nephritis in a Chinese population.

Authors:  Zhaohui Zheng; Ruohan Yu; Congcong Gao; Xianan Jian; Songxia Quan; Guolan Xing; Shengyun Liu; Zhangsuo Liu
Journal:  Exp Ther Med       Date:  2017-08-30       Impact factor: 2.447

4.  cnvCapSeq: detecting copy number variation in long-range targeted resequencing data.

Authors:  Evangelos Bellos; Vikrant Kumar; Clarabelle Lin; Jordi Maggi; Zai Yang Phua; Ching-Yu Cheng; Chui Ming Gemmy Cheung; Martin L Hibberd; Tien Yin Wong; Lachlan J M Coin; Sonia Davila
Journal:  Nucleic Acids Res       Date:  2014-09-16       Impact factor: 16.971

Review 5.  Role of cytokines in systemic lupus erythematosus: recent progress from GWAS and sequencing.

Authors:  John J Connolly; Hakon Hakonarson
Journal:  J Biomed Biotechnol       Date:  2012-05-10

Review 6.  Complex and multi-allelic copy number variation in human disease.

Authors:  Christina L Usher; Steven A McCarroll
Journal:  Brief Funct Genomics       Date:  2015-07-09       Impact factor: 4.241

7.  UGT2B17 copy number gain in a large ankylosing spondylitis multiplex family.

Authors:  Mohammed Uddin; Walter P Maksymowych; Robert Inman; Dafna Gladman; Alexandra Munn; Ramin Yazdani; Fawnda Pellett; Sean Hamilton; Darren D O'Rielly; Proton Rahman
Journal:  BMC Genet       Date:  2013-08-08       Impact factor: 2.797

Review 8.  IgE-based immunotherapy of cancer: challenges and chances.

Authors:  J Singer; E Jensen-Jarolim
Journal:  Allergy       Date:  2013-10-14       Impact factor: 13.146

9.  Comparison of Multiple Methods for Determination of FCGR3A/B Genomic Copy Numbers in HapMap Asian Populations with Two Public Databases.

Authors:  Yuan-Yuan Qi; Xu-Jie Zhou; Ding-Fang Bu; Ping Hou; Ji-Cheng Lv; Hong Zhang
Journal:  Front Genet       Date:  2016-12-26       Impact factor: 4.599

10.  Susceptibility for Lupus Nephritis by Low Copy Number of the FCGR3B Gene Is Linked to Increased Levels of Pathogenic Autoantibodies.

Authors:  Johannes C Nossent; Andrea Becker-Merok; Maureen Rischmueller; Sue Lester
Journal:  Autoimmune Dis       Date:  2013-06-20
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.