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Associations between circulating macrophage migration inhibitory factor (MIF) levels and rheumatoid arthritis, and between MIF gene polymorphisms and disease susceptibility: a meta-analysis

Authors
Bae, Sang-CheolLee, Young Ho
Issue Date
Feb-2018
Publisher
BMJ PUBLISHING GROUP
Keywords
MIF level; polymorphism; rheumatoid arthritis
Citation
POSTGRADUATE MEDICAL JOURNAL, v.94, no.1108, pp.109 - 115
Indexed
SCIE
SCOPUS
Journal Title
POSTGRADUATE MEDICAL JOURNAL
Volume
94
Number
1108
Start Page
109
End Page
115
URI
https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/2422
DOI
10.1136/postgradmedj-2017-134934
ISSN
0032-5473
Abstract
Aim To systematically review evidence regarding the relationship between circulating macrophage migration inhibitory factor (MIF) levels and rheumatoid arthritis (RA), and the association between MIF gene polymorphisms and RA susceptibility. Design We performed a meta-analysis on data of serum/plasma MIF levels in patients with RA and in controls, and on associations between the MIF−173 C/G and −794CATT₅₋₈ polymorphisms and RA susceptibility. Patients Twelve studies, comprising a total of 362 RA cases and 531 controls evaluated for MIF levels, and 2367 RA cases and 2395 controls evaluated for MIF polymorphisms, were included. Results MIF levels were significantly higher in the RA group than in the control group (standardised mean difference (95% CI) 0.923 (0.766 to 1.080), p<0.001). Stratification by ethnicity revealed significantly higher MIF levels in the RA group in Caucasian, Asian and Latin American populations. MIF levels were significantly higher in patients with RA, regardless of adjustment, sample size or data type evaluated. RA was identified to be significantly associated with the MIF−173 C allele (OR (95% CI) 1.271 (1.141 to 1.416), p<0.001), as well as with the −794CATT₇ allele (OR (95% CI) 1.229 (1.084 to 1.415), p=0.002) and the −794CATT₇-MIF-173C haplotype RA (OR (95% CI) 1.433 (1.138 to 1.805), p=0.002). Conclusions Our meta-analyses revealed significantly higher circulating MIF levels in patients with RA, and found evidence of associations between the MIF−173 C/G and −794CATT₅₋₈ polymorphisms and RA susceptibility.
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