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Confirmation of CCR6 as a risk factor for anti-topoisomerase I antibodies in systemic sclerosis.
Ochoa, Eguzkine; Martin, José-Ezequiel; Assasi, Shervin; Beretta, Lorenzo; Carreira, Patricia; Guillén, Alfredo; Simeón, Carmen Pilar; Koumakis, Eugénie; Dieude, Philippe; Allanore, Yannick; García-Hernández, Francisco J; Espinosa, Gerard; Castellví, Ivan; Trapiella, Jose Luis; Rodriguez, Luis; González-Gay, Miguel Ángel; Egurbide, María Victoria; Sáez, Luis; Callejas-Rubio, Jose Luis; Vargas-Hitos, Jose Antonio; Hunzelmann, Nicolas; Riemekasten, Gabriela; Witte, Torsten; Distler, Jörg H W; Kreuter, Alexander; Lunardi, Claudio; Santaniello, Alessandro; Tan, Filemon K; Shiels, Paul G; Herrick, Ariane; Worthington, Jane; Vonk, Madelon C; Koeleman, Bobby P; Radstake, Timothy R D J; Mayes, Maureen D; Martin, Javier.
Afiliação
  • Ochoa E; Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain. eguzki8A@gmail.com.
  • Martin JE; Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain.
  • Assasi S; The University of Texas Health Science Center-Houston, Houston, TX, USA.
  • Beretta L; Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca' Granda Ospedale Maggioire Policlinico di Milano, Milan, Italy.
  • Carreira P; Department of Rheumatology, Hospital 12 de Octubre, Madrid, Spain.
  • Guillén A; Department of Internal Medicine, Hospital Valle de Hebrón, Barcelona, Spain.
  • Simeón CP; Department of Internal Medicine, Hospital Valle de Hebrón, Barcelona, Spain.
  • Koumakis E; INSERM, Institut Cochin, Cochin Hospital, AP-HP, INSERM U1016, Sorbonne Paris Cité, and Paris Descartes University, Paris, France.
  • Dieude P; Paris Diderot University, INSERM U699, and Hôpital Bichat Claude Bernard, AP-HP, Paris, France.
  • Allanore Y; INSERM, Institut Cochin, Cochin Hospital, AP-HP, INSERM U1016, Sorbonne Paris Cité, and Paris Descartes University, Paris, France.
  • García-Hernández FJ; Department of Internal Medicine, Hospital Virgen del Rocío, Sevilla, Spain.
  • Espinosa G; Department of Internal Medicine, Autoimmune Diseases Unit, Hospital Clínico, Barcelona, Spain.
  • Castellví I; Department of Rheumatology, Hospital Universitario de la Santa Creu y Sant Pau, Barcelona, Spain.
  • Trapiella JL; Department of Internal Medicine, Hospital Universitario Central de Asturias, Oviedo, Spain.
  • Rodriguez L; Department of Rheumatology, Hospital Clínico Universitario San Carlos, Madrid, Spain.
  • González-Gay MÁ; Department of Rheumatology, Hospital Universitario Marqués de Valdecilla, IFIMAV, Santander, Spain.
  • Egurbide MV; Department of Internal Medicine, Hospital Universitario Cruces, Barakaldo, Spain.
  • Sáez L; Department of Internal Medicine, Systemic Autoimmune Diseases Unit, Hospital Universitario Miguel Servet, Zaragoza, Spain.
  • Callejas-Rubio JL; Department of Systemic Autoimmune Diseases, Hospital Clínico Universitario San Cecilio, Granada, Spain.
  • Vargas-Hitos JA; Department of Internal Medicine, Hospital Virgen de las Nieves, Granada, Spain.
  • Hunzelmann N; Department of Dermatology, University of Cologne, Cologne, Germany.
  • Riemekasten G; Department of Rheumatology and Clinical Immunology, Charité University Hospital, Berlin, Germany.
  • Witte T; Department of Clinical Immunology, Hannover Medical School, Hannover, Germany.
  • Distler JH; Department of Internal Medicine, Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany.
  • Kreuter A; Department of Dermatology, Venereology, and Allergology, Ruhr-University Bochum, Bochum, Germany.
  • Lunardi C; Department of Medicine, Università degli Studi di Verona, Verona, Italy.
  • Santaniello A; Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca' Granda Ospedale Maggioire Policlinico di Milano, Milan, Italy.
  • Tan FK; The University of Texas Health Science Center-Houston, Houston, TX, USA.
  • Shiels PG; Section of Epigenetics, Institute of Cancer Sciences, MVLS, University of Glasgow, Glasgow, UK.
  • Herrick A; Arthritis Research UK Epidemiology Unit and NIHR Manchester Musculoskeletal Biomedical Research Unit, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
  • Worthington J; Arthritis Research UK Epidemiology Unit and NIHR Manchester Musculoskeletal Biomedical Research Unit, University of Manchester, Manchester Academic Health Science Centre, Manchester, UK.
  • Vonk MC; Department of Rheumatology, Radboud University, Nijmegen Medical Centre, Nijmegen HC, The Netherlands.
  • Koeleman BP; Section Complex Genetics, Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Radstake TR; Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, The Netherlands.
  • Mayes MD; The University of Texas Health Science Center-Houston, Houston, TX, USA.
  • Martin J; Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Granada, Spain.
Clin Exp Rheumatol ; 33(4 Suppl 91): S31-5, 2015.
Article em En | MEDLINE | ID: mdl-26314374
OBJECTIVES: The current knowledge of the influence of systemic sclerosis (SSc) risk loci in the clinical sub-phenotypes is still limited. The main limitation lies in the low frequency of some sub-phenotypes which could be solved by replication studies in independent cohorts and meta-analysis between studies. In this regard, CCR6 gene variants have been recently associated with anti-topoisomerase I positive (ATA+) production in SSc patients in a candidate gene study. This gene has been proposed to have a critical role in IL-17-driven autoimmunity in human diseases. METHODS: In order to confirm the association between CCR6 and ATA+ SSc patients, we performed an independent replication study in populations of European ancestry. We studied two CCR6 genetic variants (rs968334 and rs3093024) in a total of 901 ATA+ SSc cases, 3,258 ATA- SSc cases and 7,865 healthy controls and compared allelic frequencies for those SNPs in ATA+ SSc with healthy controls and also with ATA- SSc patients. RESULTS: The comparison performed between ATA+ SSc patients and healthy controls showed significant association with SNP rs968334 (p=4.88x10(-2), OR=1.11). When we compared ATA+ SSc cases with ATA- SSc, both SNPs, rs3093024 and rs968334, showed significant associations (p=2.89x10(-2), OR=1.13; p=1.69x10(-2), OR=1.15). Finally, in order to increase even more sample size and statistical power, we meta-analysed our study with the previous reported and found a significant association between SNP rs3093024 and ATA+ SSc patients (p=1.00x10(-4), OR=1.16) comparing with healthy controls. CONCLUSIONS: Our work confirms the association of CCR6 gene and ATA+ SSc patients.
Assuntos
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Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Autoanticorpos / DNA Topoisomerases Tipo I / Polimorfismo de Nucleotídeo Único / Receptores CCR6 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans País/Região como assunto: America do norte / Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Escleroderma Sistêmico / Autoanticorpos / DNA Topoisomerases Tipo I / Polimorfismo de Nucleotídeo Único / Receptores CCR6 Tipo de estudo: Diagnostic_studies / Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies / Systematic_reviews Limite: Humans País/Região como assunto: America do norte / Europa Idioma: En Ano de publicação: 2015 Tipo de documento: Article