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dc.contributor.authorFisher, Benjamin A
dc.contributor.authorCartwright, Alison J
dc.contributor.authorQuirke, Anne-Marie
dc.contributor.authorde Pablo, Paola
dc.contributor.authorRomaguera, Dora
dc.contributor.authorPanico, Salvatore
dc.contributor.authorMattiello, Amalia
dc.contributor.authorGavrila, Diana
dc.contributor.authorNavarro, Carmen
dc.contributor.authorSacerdote, Carlotta
dc.contributor.authorVineis, Paolo
dc.contributor.authorTumino, Rosario
dc.contributor.authorLappin, David F
dc.contributor.authorApazidou, Danae
dc.contributor.authorCulshaw, Shauna
dc.contributor.authorPotempa, Jan
dc.contributor.authorMichaud, Dominique S
dc.contributor.authorRiboli, Elio
dc.contributor.authorVenables, Patrick J
dc.date.accessioned2024-07-04T12:56:33Z
dc.date.available2024-07-04T12:56:33Z
dc.date.issued2015-11-04
dc.identifier.citationFisher Benjamin A, Cartwright AJ, Quirke AM, De Pablo P, Romaguera D, Panico S, et al. Smoking, Porphyromonas gingivalis and the immune response to citrullinated autoantigens before the clinical onset of rheumatoid arthritis in a Southern European nested case-control study. BMC Musculoskelet Disord. 2015 Nov 04;16:331.en
dc.identifier.issn1471-2474
dc.identifier.otherhttp://hdl.handle.net/20.500.13003/10617
dc.identifier.urihttp://hdl.handle.net/20.500.12105/20158
dc.description.abstractBackground: Antibodies to citrullinated proteins (ACPA) occur years before RA diagnosis. Porphyromonas gingivalis expresses its own peptidylarginine deiminase (PPAD), and is a proposed aetiological factor for the ACPA response. Smoking is a risk factor for both ACPA-positive RA and periodontitis. We aimed to study the relation of these factors to the risk of RA in a prospective cohort. Methods: We performed a nested case-control study by identifying pre-RA cases in four populations from the European Prospective Investigation into Cancer and nutrition, matched with three controls. Data on smoking and other covariates were obtained from baseline questionnaires. Antibodies to CCP2 and citrullinated peptides from a-enolase, fibrinogen, vimentin and PPAD were measured. Antibodies to arginine gingipain (RgpB) were used as a marker for P. gingivalis infection and validated in a separate cohort of healthy controls and subjects with periodontitis. Results: We studied 103 pre-RA cases. RA development was associated with several ACPA specificities, but not with antibodies to citrullinated PPAD peptides. Antibody levels to RgpB and PPAD peptides were higher in smokers but were not associated with risk of RA or with pre-RA autoimmunity. Former but not current smoking was associated with antibodies to a-enolase (OR 4.06; 95 % CI 1.02, 16.2 versus 0.54; 0.09-3.73) and fibrinogen peptides (OR 4.24; 95 % CI 1.2-14.96 versus 0.58; 0.13-2.70), and later development of RA (OR 2.48; 95 % CI 1.27-4.84 versus 1.57; 0.85-2.93), independent of smoking intensity. Conclusions: Smoking remains a risk factor for RA well before the clinical onset of disease. In this cohort, P. gingivalis is not associated with pre-RA autoimmunity or risk of RA in an early phase before disease-onset. Antibodies to PPAD peptides are not an early feature of ACPA ontogeny.en
dc.description.sponsorshipFunding was received from the Imperial College London National Institute of Health Research (NIHR) Biomedical Research Centre, and from the European Union funded IMI project 'BeTheCure' (contract number 115142-2) and FP7 grant 'Gums & Joints' (HEALTH-F2-2010-261460). JP acknowledges support by grant DE 022597 from NIH/NIDCR.es_ES
dc.language.isoengen
dc.publisherBioMed Central (BMC) en
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.subjectSmokingen
dc.subjectRheumatoid arthritis (RA)en
dc.subjectAnti-citrullinated protein antibodies (ACPA)en
dc.subjectPorphyromonas gingivalisen
dc.subjectCitrullinationen
dc.subject.meshAutoantigens *
dc.subject.meshCase-Control Studies *
dc.subject.meshCysteine Endopeptidases *
dc.subject.meshAdult *
dc.subject.meshPeriodontitis *
dc.subject.meshHumans *
dc.subject.meshHydrolases *
dc.subject.meshSmoking *
dc.subject.meshMiddle Aged *
dc.subject.meshProtein-Arginine Deiminases *
dc.subject.meshAdhesins, Bacterial *
dc.subject.meshMale *
dc.subject.meshPeptides, Cyclic *
dc.subject.meshProspective Studies *
dc.subject.meshArthritis, Rheumatoid *
dc.subject.meshEurope *
dc.subject.meshPorphyromonas gingivalis *
dc.subject.meshFemale *
dc.titleSmoking, Porphyromonas gingivalis and the immune response to citrullinated autoantigens before the clinical onset of rheumatoid arthritis in a Southern European nested case-control studyen
dc.typeresearch articleen
dc.rights.licenseAttribution 4.0 International*
dc.identifier.pubmedID26537917es_ES
dc.format.volume16es_ES
dc.format.page331es_ES
dc.identifier.doi10.1186/s12891-015-0792-y
dc.relation.publisherversionhttps://dx.doi.org/10.1186/s12891-015-0792-yen
dc.identifier.journalBMC Musculoskeletal Disorderses_ES
dc.rights.accessRightsopen accessen
dc.subject.decsPorphyromonas gingivalis*
dc.subject.decsAdhesinas Bacterianas*
dc.subject.decsFemenino*
dc.subject.decsEuropa (Continente)*
dc.subject.decsArtritis Reumatoide*
dc.subject.decsMasculino*
dc.subject.decsPeriodontitis*
dc.subject.decsFumar*
dc.subject.decsCisteína Endopeptidasas*
dc.subject.decsHumanos*
dc.subject.decsHidrolasas*
dc.subject.decsPersona de Mediana Edad*
dc.subject.decsAutoantígenos*
dc.subject.decsPéptidos Cíclicos*
dc.subject.decsEstudios Prospectivos*
dc.subject.decsAdulto*
dc.subject.decsDesiminasas de la Arginina Proteica*
dc.subject.decsEstudios de Casos y Controles*
dc.identifier.scopus2-s2.0-84946232867
dc.identifier.wos364118000001
dc.identifier.puiL606719034


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