Meta-analysis of functional MBL polymorphisms Associations with rheumatoid arthritis and primary Sjogren's syndrome
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Song, G. G. | - |
dc.contributor.author | Bae, S-C. | - |
dc.contributor.author | Seo, Y. H. | - |
dc.contributor.author | Kim, J-H. | - |
dc.contributor.author | Choi, S. J. | - |
dc.contributor.author | Ji, J. D. | - |
dc.contributor.author | Lee, Y. H. | - |
dc.date.accessioned | 2021-08-02T18:29:34Z | - |
dc.date.available | 2021-08-02T18:29:34Z | - |
dc.date.created | 2021-05-12 | - |
dc.date.issued | 2014-09 | - |
dc.identifier.issn | 0340-1855 | - |
dc.identifier.uri | https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/25787 | - |
dc.description.abstract | Objective The aim of this study was to determine whether functional mannose-binding lectin gene (MBL) polymorphisms are associated with the susceptibility to rheumatoid arthritis (RA) or primary Sjögren’s syndrome (pSS). Methods A meta-analysis was conducted to investigate the potential association of RA or pSS with MBL polymorphisms, including the codon 54 (allele B), codon 57 (allele C), and codon 52 (allele D) variants of exon 1, and the − 550 (allele L) and − 221 (allele X) promoter variants. Results A total of 12 comparative studies, including eight RA (1623 patients and 1671 controls) and four pSS (280 patients and 516 controls) studies, were included in the meta-analysis. The meta-analysis revealed no association between the MBL B allele and RA in the overall study population (odds ratio [OR] 0.991, 95 % confidence interval [CI] 0.726–1.355, p = 0.957). However, the meta-analysis showed significant associations between the MBL D, H, and X alleles and RA in the overall population (OR 1.708, 95 % CI 1.077–2.707, p = 0.023; OR 1.936, 95 % CI 1.218–3.078, p = 0.005; OR 1.582, 95 % CI 1.216–2.057, p = 0.001, respectively). An association was found between the MBL B allele and pSS in the overall study population (OR 0.691, 95 % CI 0.541–0.917, p = 0.010). Stratification by ethnicity indicated a trend toward an association between the B allele and pSS in European populations, but no association in Asian populations (OR 0.689, 95 % CI 0.465–1.021, p = 0.063; OR 0.896, 95 % CI 0.311–2.562, p = 0.838, respectively). Conclusion This meta-analysis demonstrated an association between the MBL D, L, and X alleles and the risk of RA. It also demonstrated an association between the MBL B allele and the susceptibility to pSS, suggesting a protective role of the MBL B allele against the development of pSS. | - |
dc.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | SPRINGER HEIDELBERG | - |
dc.title | Meta-analysis of functional MBL polymorphisms Associations with rheumatoid arthritis and primary Sjogren's syndrome | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Bae, S-C. | - |
dc.identifier.doi | 10.1007/s00393-014-1408-x | - |
dc.identifier.scopusid | 2-s2.0-84929519336 | - |
dc.identifier.wosid | 000341506800012 | - |
dc.identifier.bibliographicCitation | ZEITSCHRIFT FUR RHEUMATOLOGIE, v.73, no.7, pp.657 - 664 | - |
dc.relation.isPartOf | ZEITSCHRIFT FUR RHEUMATOLOGIE | - |
dc.citation.title | ZEITSCHRIFT FUR RHEUMATOLOGIE | - |
dc.citation.volume | 73 | - |
dc.citation.number | 7 | - |
dc.citation.startPage | 657 | - |
dc.citation.endPage | 664 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | N | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Rheumatology | - |
dc.relation.journalWebOfScienceCategory | Rheumatology | - |
dc.subject.keywordPlus | MANNOSE-BINDING LECTIN | - |
dc.subject.keywordPlus | SYSTEMIC-LUPUS-ERYTHEMATOSUS | - |
dc.subject.keywordPlus | TRIPLET REPEAT POLYMORPHISM | - |
dc.subject.keywordPlus | MICA GENE | - |
dc.subject.keywordPlus | ANKYLOSING-SPONDYLITIS | - |
dc.subject.keywordPlus | JAPANESE PATIENTS | - |
dc.subject.keywordPlus | INNATE IMMUNITY | - |
dc.subject.keywordPlus | SUSCEPTIBILITY | - |
dc.subject.keywordPlus | INFECTION | - |
dc.subject.keywordPlus | PROTEIN | - |
dc.subject.keywordAuthor | Variant alleles | - |
dc.subject.keywordAuthor | Autoimmunity | - |
dc.subject.keywordAuthor | Mannose-binding lectin gene | - |
dc.subject.keywordAuthor | Promoter regions, genetic | - |
dc.subject.keywordAuthor | Complement system proteins | - |
dc.identifier.url | https://link.springer.com/article/10.1007%2Fs00393-014-1408-x | - |
Items in ScholarWorks are protected by copyright, with all rights reserved, unless otherwise indicated.
222, Wangsimni-ro, Seongdong-gu, Seoul, 04763, Korea+82-2-2220-1365
COPYRIGHT © 2021 HANYANG UNIVERSITY.
Certain data included herein are derived from the © Web of Science of Clarivate Analytics. All rights reserved.
You may not copy or re-distribute this material in whole or in part without the prior written consent of Clarivate Analytics.