Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis

Objectives: To determine factors influencing the age at onset of rheumatoid arthritis (RA). Methods: A sample of 152 Colombian patients was investigated. Hazard ratios (HRs) that measured the effect size of risk factors on the age at RA onset were computed by using Cox regression models. Results: Po...

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Autores:
Tipo de recurso:
Fecha de publicación:
2011
Institución:
Universidad del Rosario
Repositorio:
Repositorio EdocUR - U. Rosario
Idioma:
eng
OAI Identifier:
oai:repository.urosario.edu.co:10336/22210
Acceso en línea:
https://doi.org/10.1016/j.jbspin.2010.07.014
https://repository.urosario.edu.co/handle/10336/22210
Palabra clave:
Cyclic citrullinated peptide antibody
Article
Disease association
Female
Gene sequence
Human
Major clinical study
Male
Onset age
Rheumatoid arthritis
Risk factor
Adult
Age of onset
Colombia
Female
Hla-dr antigens
Humans
Male
Middle aged
Regression analysis
Retrospective studies
Risk factors
Age
Anti-ccp antibodies
Hla-drb1
Rheumatoid arthritis
Rheumatoid factor
Smoking
Tnf-308 a allele
single nucleotide
rheumatoid
cyclic
anti-idiotypic
Antibodies
Arthritis
Peptides
Polymorphism
Rights
License
Abierto (Texto Completo)
id EDOCUR2_355285894fa09b971d52c9e3cab3747a
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network_name_str Repositorio EdocUR - U. Rosario
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spelling ed11b616-10f3-4c5b-b04a-e85a87536de18aa08ddc-3b0d-4a49-a320-6a8b48a80d500b8abdc7-1887-4fea-accc-c1e36ef0bc53622bc730-0aa3-4b18-84e3-a45eca5909c14cb87ea6-3016-4296-b85f-fadfa37a9554194747786002020-05-25T23:55:46Z2020-05-25T23:55:46Z2011Objectives: To determine factors influencing the age at onset of rheumatoid arthritis (RA). Methods: A sample of 152 Colombian patients was investigated. Hazard ratios (HRs) that measured the effect size of risk factors on the age at RA onset were computed by using Cox regression models. Results: Positive anti-CCP antibodies were associated with an increased risk of early RA onset (HR=1.60; 95% confidence interval, [1.06, 2.4]), whereas the presence of the protective 70DERAA74 sequence was associated with a delayed onset (HR=0.55; [0.33, 0.92]). After controlling for both anti-CCP antibodies and the 70DERAA74 sequence, the following variables did not influence significantly the age at RA onset: gender, ever cigarette smoking, family RA history, the TNF-308 A polymorphism, HLA shared epitope, and the presence of rheumatoid factor. Conclusion: Anti-CCP antibodies and the HLA-DRB1 70DERAA74 sequence influence the age at onset of RA. © 2010 Société française de rhumatologie.application/pdfhttps://doi.org/10.1016/j.jbspin.2010.07.0141297319Xhttps://repository.urosario.edu.co/handle/10336/22210eng178No. 2175Joint Bone SpineVol. 78Joint Bone Spine, ISSN:1297319X, Vol.78, No.2 (2011); pp. 175-178https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952250830&doi=10.1016%2fj.jbspin.2010.07.014&partnerID=40&md5=bcdc9eb7e8ff2fc45bd3b3bf855bd9beAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURCyclic citrullinated peptide antibodyArticleDisease associationFemaleGene sequenceHumanMajor clinical studyMaleOnset ageRheumatoid arthritisRisk factorAdultAge of onsetColombiaFemaleHla-dr antigensHumansMaleMiddle agedRegression analysisRetrospective studiesRisk factorsAgeAnti-ccp antibodiesHla-drb1Rheumatoid arthritisRheumatoid factorSmokingTnf-308 a allelesingle nucleotiderheumatoidcyclicanti-idiotypicAntibodiesArthritisPeptidesPolymorphismAnti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritisarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Diaz F.J.Rojas-Villarraga A.Salazar J.C.Iglesias-Gamarra A.Mantilla R.D.Anaya, Juan-ManuelORIGINAL1-s2-0-S1297319X10002083-main.pdfapplication/pdf162191https://repository.urosario.edu.co/bitstreams/fde1930d-6a55-49c1-9235-bb94e93c2907/downloadd581d04f870408ea01cdcc5685335fe0MD51TEXT1-s2-0-S1297319X10002083-main.pdf.txt1-s2-0-S1297319X10002083-main.pdf.txtExtracted texttext/plain20614https://repository.urosario.edu.co/bitstreams/0b18f721-1230-4df8-ae81-b97666bf1a8e/download3fa56aa36579f4e324050e2593473173MD52THUMBNAIL1-s2-0-S1297319X10002083-main.pdf.jpg1-s2-0-S1297319X10002083-main.pdf.jpgGenerated Thumbnailimage/jpeg4646https://repository.urosario.edu.co/bitstreams/6049aedc-9684-4abf-b7c9-1f9fb836c7da/download748c0fb6ec14d0339404b8c6f7586ab8MD5310336/22210oai:repository.urosario.edu.co:10336/222102022-05-02 07:37:13.081216https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co
dc.title.spa.fl_str_mv Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
title Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
spellingShingle Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
Cyclic citrullinated peptide antibody
Article
Disease association
Female
Gene sequence
Human
Major clinical study
Male
Onset age
Rheumatoid arthritis
Risk factor
Adult
Age of onset
Colombia
Female
Hla-dr antigens
Humans
Male
Middle aged
Regression analysis
Retrospective studies
Risk factors
Age
Anti-ccp antibodies
Hla-drb1
Rheumatoid arthritis
Rheumatoid factor
Smoking
Tnf-308 a allele
single nucleotide
rheumatoid
cyclic
anti-idiotypic
Antibodies
Arthritis
Peptides
Polymorphism
title_short Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
title_full Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
title_fullStr Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
title_full_unstemmed Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
title_sort Anti-CCP antibodies are associated with early age at onset in patients with rheumatoid arthritis
dc.subject.keyword.spa.fl_str_mv Cyclic citrullinated peptide antibody
Article
Disease association
Female
Gene sequence
Human
Major clinical study
Male
Onset age
Rheumatoid arthritis
Risk factor
Adult
Age of onset
Colombia
Female
Hla-dr antigens
Humans
Male
Middle aged
Regression analysis
Retrospective studies
Risk factors
Age
Anti-ccp antibodies
Hla-drb1
Rheumatoid arthritis
Rheumatoid factor
Smoking
Tnf-308 a allele
topic Cyclic citrullinated peptide antibody
Article
Disease association
Female
Gene sequence
Human
Major clinical study
Male
Onset age
Rheumatoid arthritis
Risk factor
Adult
Age of onset
Colombia
Female
Hla-dr antigens
Humans
Male
Middle aged
Regression analysis
Retrospective studies
Risk factors
Age
Anti-ccp antibodies
Hla-drb1
Rheumatoid arthritis
Rheumatoid factor
Smoking
Tnf-308 a allele
single nucleotide
rheumatoid
cyclic
anti-idiotypic
Antibodies
Arthritis
Peptides
Polymorphism
dc.subject.keyword.eng.fl_str_mv single nucleotide
rheumatoid
cyclic
anti-idiotypic
Antibodies
Arthritis
Peptides
Polymorphism
description Objectives: To determine factors influencing the age at onset of rheumatoid arthritis (RA). Methods: A sample of 152 Colombian patients was investigated. Hazard ratios (HRs) that measured the effect size of risk factors on the age at RA onset were computed by using Cox regression models. Results: Positive anti-CCP antibodies were associated with an increased risk of early RA onset (HR=1.60; 95% confidence interval, [1.06, 2.4]), whereas the presence of the protective 70DERAA74 sequence was associated with a delayed onset (HR=0.55; [0.33, 0.92]). After controlling for both anti-CCP antibodies and the 70DERAA74 sequence, the following variables did not influence significantly the age at RA onset: gender, ever cigarette smoking, family RA history, the TNF-308 A polymorphism, HLA shared epitope, and the presence of rheumatoid factor. Conclusion: Anti-CCP antibodies and the HLA-DRB1 70DERAA74 sequence influence the age at onset of RA. © 2010 Société française de rhumatologie.
publishDate 2011
dc.date.created.spa.fl_str_mv 2011
dc.date.accessioned.none.fl_str_mv 2020-05-25T23:55:46Z
dc.date.available.none.fl_str_mv 2020-05-25T23:55:46Z
dc.type.eng.fl_str_mv article
dc.type.coarversion.fl_str_mv http://purl.org/coar/version/c_970fb48d4fbd8a85
dc.type.coar.fl_str_mv http://purl.org/coar/resource_type/c_6501
dc.type.spa.spa.fl_str_mv Artículo
dc.identifier.doi.none.fl_str_mv https://doi.org/10.1016/j.jbspin.2010.07.014
dc.identifier.issn.none.fl_str_mv 1297319X
dc.identifier.uri.none.fl_str_mv https://repository.urosario.edu.co/handle/10336/22210
url https://doi.org/10.1016/j.jbspin.2010.07.014
https://repository.urosario.edu.co/handle/10336/22210
identifier_str_mv 1297319X
dc.language.iso.spa.fl_str_mv eng
language eng
dc.relation.citationEndPage.none.fl_str_mv 178
dc.relation.citationIssue.none.fl_str_mv No. 2
dc.relation.citationStartPage.none.fl_str_mv 175
dc.relation.citationTitle.none.fl_str_mv Joint Bone Spine
dc.relation.citationVolume.none.fl_str_mv Vol. 78
dc.relation.ispartof.spa.fl_str_mv Joint Bone Spine, ISSN:1297319X, Vol.78, No.2 (2011); pp. 175-178
dc.relation.uri.spa.fl_str_mv https://www.scopus.com/inward/record.uri?eid=2-s2.0-79952250830&doi=10.1016%2fj.jbspin.2010.07.014&partnerID=40&md5=bcdc9eb7e8ff2fc45bd3b3bf855bd9be
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