scholarly journals Macrophage migration inhibitory factor polymorphism and the risk of ulcerative colitis and Crohn's disease in Asian and European populations: a meta-analysis

BMJ Open ◽  
2013 ◽  
Vol 3 (12) ◽  
pp. e003729 ◽  
Author(s):  
Ning-Bo Hao ◽  
Ya Fei He ◽  
Gang Luo ◽  
Xin Yong ◽  
Yao Zhang ◽  
...  
2016 ◽  
Vol 22 ◽  
pp. S57
Author(s):  
Manish Tripathi ◽  
Pankaj Asati ◽  
Jitendra Choudhary ◽  
Arttrika Ranjan ◽  
Sunit Shukla ◽  
...  

Cytokine ◽  
2010 ◽  
Vol 51 (2) ◽  
pp. 173-177 ◽  
Author(s):  
Hisakazu Shiroeda ◽  
Tomomitsu Tahara ◽  
Masakatsu Nakamura ◽  
Tomoyuki Shibata ◽  
Tomoe Nomura ◽  
...  

2018 ◽  
Vol 9 ◽  
Author(s):  
Oscar Illescas ◽  
Juan C. Gomez-Verjan ◽  
Lizbeth García-Velázquez ◽  
Tzipe Govezensky ◽  
Miriam Rodriguez-Sosa

2017 ◽  
Vol 94 (1108) ◽  
pp. 109-115 ◽  
Author(s):  
Sang-Cheol Bae ◽  
Young Ho Lee

AimTo 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.DesignWe 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.PatientsTwelve 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.ResultsMIF 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).ConclusionsOur 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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