Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis
Rheumatoid arthritis (RA) progresses more rapidly in some patients than in others and diverse factors influence radiographic progression in a specific population. Thus, we searched for variables that are associated with an early appearance of substantial joint damage in patients with RA by using rad...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2009
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22249
- Acceso en línea:
- https://doi.org/10.1016/j.jaut.2008.11.004
https://repository.urosario.edu.co/handle/10336/22249
- Palabra clave:
- Epitope
Hla dr antigen
Adult
Article
Child
Clinical feature
Controlled study
Disease duration
Family history
Female
Human
Joint injury
Major clinical study
Male
Preschool child
Priority journal
Rheumatoid arthritis
Risk factor
Single nucleotide polymorphism
Survival time
Adult
Age of onset
Aged
Autoantibodies
Colombia
Female
Follow-up studies
Foot joints
Hand joints
Hla-dr antigens
Humans
Joints
Male
Middle aged
Proportional hazards models
Sex factors
Steroids
Time factors
Tumor necrosis factor-alpha
Wrist joint
Anti-ccp antibodies
Extra-articular manifestations
Family relations
Genetics
Hla-drb1
Polymorphisms
Radiography
Rheumatoid arthritis
Rheumatoid factor
Tumor necrosis factor
cyclic
rheumatoid
Arthritis
Peptides
- Rights
- License
- Abierto (Texto Completo)
id |
EDOCUR2_39263882245386c228cbf3fbc9c4d5e4 |
---|---|
oai_identifier_str |
oai:repository.urosario.edu.co:10336/22249 |
network_acronym_str |
EDOCUR2 |
network_name_str |
Repositorio EdocUR - U. Rosario |
repository_id_str |
|
dc.title.spa.fl_str_mv |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
title |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
spellingShingle |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis Epitope Hla dr antigen Adult Article Child Clinical feature Controlled study Disease duration Family history Female Human Joint injury Major clinical study Male Preschool child Priority journal Rheumatoid arthritis Risk factor Single nucleotide polymorphism Survival time Adult Age of onset Aged Autoantibodies Colombia Female Follow-up studies Foot joints Hand joints Hla-dr antigens Humans Joints Male Middle aged Proportional hazards models Sex factors Steroids Time factors Tumor necrosis factor-alpha Wrist joint Anti-ccp antibodies Extra-articular manifestations Family relations Genetics Hla-drb1 Polymorphisms Radiography Rheumatoid arthritis Rheumatoid factor Tumor necrosis factor cyclic rheumatoid Arthritis Peptides |
title_short |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
title_full |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
title_fullStr |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
title_full_unstemmed |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
title_sort |
Familial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritis |
dc.subject.keyword.spa.fl_str_mv |
Epitope Hla dr antigen Adult Article Child Clinical feature Controlled study Disease duration Family history Female Human Joint injury Major clinical study Male Preschool child Priority journal Rheumatoid arthritis Risk factor Single nucleotide polymorphism Survival time Adult Age of onset Aged Autoantibodies Colombia Female Follow-up studies Foot joints Hand joints Hla-dr antigens Humans Joints Male Middle aged Proportional hazards models Sex factors Steroids Time factors Tumor necrosis factor-alpha Wrist joint Anti-ccp antibodies Extra-articular manifestations Family relations Genetics Hla-drb1 Polymorphisms Radiography Rheumatoid arthritis Rheumatoid factor Tumor necrosis factor |
topic |
Epitope Hla dr antigen Adult Article Child Clinical feature Controlled study Disease duration Family history Female Human Joint injury Major clinical study Male Preschool child Priority journal Rheumatoid arthritis Risk factor Single nucleotide polymorphism Survival time Adult Age of onset Aged Autoantibodies Colombia Female Follow-up studies Foot joints Hand joints Hla-dr antigens Humans Joints Male Middle aged Proportional hazards models Sex factors Steroids Time factors Tumor necrosis factor-alpha Wrist joint Anti-ccp antibodies Extra-articular manifestations Family relations Genetics Hla-drb1 Polymorphisms Radiography Rheumatoid arthritis Rheumatoid factor Tumor necrosis factor cyclic rheumatoid Arthritis Peptides |
dc.subject.keyword.eng.fl_str_mv |
cyclic rheumatoid Arthritis Peptides |
description |
Rheumatoid arthritis (RA) progresses more rapidly in some patients than in others and diverse factors influence radiographic progression in a specific population. Thus, we searched for variables that are associated with an early appearance of substantial joint damage in patients with RA by using radiographic assessments. A cohort of 157 consecutively enrolled Colombian RA patients was followed for an average of 3.2 ± 3.1 years. Information on patient demographics and cumulative clinical and laboratory manifestations over the course of the disease was registered, including family history of RA in first-degree relatives, extra-articular manifestations, rheumatoid factor, anti-CCP3 antibodies, TNF single nucleotide polymorphism at -308 position, and HLA-DRB1 status. Radiographs were scored according to the Sharp-van der Heijde method. Survival analyses of the time at appearance of substantial joint damage were performed by using Weibull models. A review of literature about the influence of familial RA on the progression of disease was done. Our results show that family history of RA is consistently associated with joint damage (i.e. erosive and joint narrowing disease). This effect was not found in all the populations reviewed. In addition, we confirm the effect of HLA-DRB1 shared epitope and anti-CCP seropositivity on erosive disease. Family history of RA is a key risk factor for joint damage and depends on the investigated population because variations in both additive and non-additive genetic factors and the environmental variance are specific to the population. Our results emphasize the usefulness of assessing familial disease, testing anti-CCP antibodies and genotyping HLA-DRB1 gene in patients with RA because these factors may be used to predict clinical outcomes and guide therapeutic interventions. © 2008 Elsevier Ltd. All rights reserved. |
publishDate |
2009 |
dc.date.created.spa.fl_str_mv |
2009 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:55:53Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:55:53Z |
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.jaut.2008.11.004 |
dc.identifier.issn.none.fl_str_mv |
10959157 08968411 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22249 |
url |
https://doi.org/10.1016/j.jaut.2008.11.004 https://repository.urosario.edu.co/handle/10336/22249 |
identifier_str_mv |
10959157 08968411 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
69 |
dc.relation.citationIssue.none.fl_str_mv |
No. 1 |
dc.relation.citationStartPage.none.fl_str_mv |
64 |
dc.relation.citationTitle.none.fl_str_mv |
Journal of Autoimmunity |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 32 |
dc.relation.ispartof.spa.fl_str_mv |
Journal of Autoimmunity, ISSN:10959157, 08968411, Vol.32, No.1 (2009); pp. 64-69 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-58849141572&doi=10.1016%2fj.jaut.2008.11.004&partnerID=40&md5=575d08d44cf525bc32af5a4076ee2629 |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
institution |
Universidad del Rosario |
dc.source.instname.spa.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
bitstream.url.fl_str_mv |
https://repository.urosario.edu.co/bitstreams/c2993238-03b8-42e4-b616-aa56760894a9/download https://repository.urosario.edu.co/bitstreams/04141d00-14fd-44ea-9156-ae9085a6d79e/download https://repository.urosario.edu.co/bitstreams/1eff04d6-e348-48b1-ab98-5ee529cc3dd6/download |
bitstream.checksum.fl_str_mv |
8c6b6f2a31503a6fc334957b55453a45 65d251a08daec595507a391333c8486d f42ba7e9a0e29756f87c6c91fdba6d38 |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositorio institucional EdocUR |
repository.mail.fl_str_mv |
edocur@urosario.edu.co |
_version_ |
1814167430390349824 |
spelling |
522497016005eca3af5-1738-4c18-97a2-253457e3ab800e639382-bc74-4099-a388-e247ddabf2a6d214c293-69dd-45fc-93da-ca521a8a1b1f55e9af6d-30cd-435d-88af-c069a9fcaabccb44c18d-c693-4ba5-ba89-8993a5634ee0194747786002020-05-25T23:55:53Z2020-05-25T23:55:53Z2009Rheumatoid arthritis (RA) progresses more rapidly in some patients than in others and diverse factors influence radiographic progression in a specific population. Thus, we searched for variables that are associated with an early appearance of substantial joint damage in patients with RA by using radiographic assessments. A cohort of 157 consecutively enrolled Colombian RA patients was followed for an average of 3.2 ± 3.1 years. Information on patient demographics and cumulative clinical and laboratory manifestations over the course of the disease was registered, including family history of RA in first-degree relatives, extra-articular manifestations, rheumatoid factor, anti-CCP3 antibodies, TNF single nucleotide polymorphism at -308 position, and HLA-DRB1 status. Radiographs were scored according to the Sharp-van der Heijde method. Survival analyses of the time at appearance of substantial joint damage were performed by using Weibull models. A review of literature about the influence of familial RA on the progression of disease was done. Our results show that family history of RA is consistently associated with joint damage (i.e. erosive and joint narrowing disease). This effect was not found in all the populations reviewed. In addition, we confirm the effect of HLA-DRB1 shared epitope and anti-CCP seropositivity on erosive disease. Family history of RA is a key risk factor for joint damage and depends on the investigated population because variations in both additive and non-additive genetic factors and the environmental variance are specific to the population. Our results emphasize the usefulness of assessing familial disease, testing anti-CCP antibodies and genotyping HLA-DRB1 gene in patients with RA because these factors may be used to predict clinical outcomes and guide therapeutic interventions. © 2008 Elsevier Ltd. All rights reserved.application/pdfhttps://doi.org/10.1016/j.jaut.2008.11.0041095915708968411https://repository.urosario.edu.co/handle/10336/22249eng69No. 164Journal of AutoimmunityVol. 32Journal of Autoimmunity, ISSN:10959157, 08968411, Vol.32, No.1 (2009); pp. 64-69https://www.scopus.com/inward/record.uri?eid=2-s2.0-58849141572&doi=10.1016%2fj.jaut.2008.11.004&partnerID=40&md5=575d08d44cf525bc32af5a4076ee2629Abierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocUREpitopeHla dr antigenAdultArticleChildClinical featureControlled studyDisease durationFamily historyFemaleHumanJoint injuryMajor clinical studyMalePreschool childPriority journalRheumatoid arthritisRisk factorSingle nucleotide polymorphismSurvival timeAdultAge of onsetAgedAutoantibodiesColombiaFemaleFollow-up studiesFoot jointsHand jointsHla-dr antigensHumansJointsMaleMiddle agedProportional hazards modelsSex factorsSteroidsTime factorsTumor necrosis factor-alphaWrist jointAnti-ccp antibodiesExtra-articular manifestationsFamily relationsGeneticsHla-drb1PolymorphismsRadiographyRheumatoid arthritisRheumatoid factorTumor necrosis factorcyclicrheumatoidArthritisPeptidesFamilial disease, the HLA-DRB1 shared epitope and anti-CCP antibodies influence time at appearance of substantial joint damage in rheumatoid arthritisarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Rojas-Villarraga, AdrianaDiaz, Francisco J.Calvo-Páramo, EnriqueSalazar, Juan C.Iglesias-Gamarra, AntonioMantilla, Ruben D.Anaya, Juan-ManuelORIGINAL1-s2-0-S0896841108001364-main.pdfapplication/pdf164337https://repository.urosario.edu.co/bitstreams/c2993238-03b8-42e4-b616-aa56760894a9/download8c6b6f2a31503a6fc334957b55453a45MD51TEXT1-s2-0-S0896841108001364-main.pdf.txt1-s2-0-S0896841108001364-main.pdf.txtExtracted texttext/plain41016https://repository.urosario.edu.co/bitstreams/04141d00-14fd-44ea-9156-ae9085a6d79e/download65d251a08daec595507a391333c8486dMD52THUMBNAIL1-s2-0-S0896841108001364-main.pdf.jpg1-s2-0-S0896841108001364-main.pdf.jpgGenerated Thumbnailimage/jpeg4760https://repository.urosario.edu.co/bitstreams/1eff04d6-e348-48b1-ab98-5ee529cc3dd6/downloadf42ba7e9a0e29756f87c6c91fdba6d38MD5310336/22249oai:repository.urosario.edu.co:10336/222492022-05-02 07:37:13.585857https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |