Related Experiment Video
Updated: Apr 21, 2026

Phenotypic Characterization of Macrophages from Rat Kidney by Flow Cytometry
Published on: October 18, 2016
Macrophage migration inhibitory factor -173G/C gene polymorphism increases the risk of renal disease: a meta-analysis
Xiang Tong1, Jie He, Sitong Liu
1West China School of Medicine/West China Hospital, Sichuan University, Chengdu, China.
Aim:
Macrophage migration inhibitory factor (MIF) -173G/C (rs755622) gene polymorphism has been associated with renal disease risk. However, lots of studies have reported inconclusive results. Therefore, we performed a meta-analysis to investigate the relationship between MIF -173G/C gene polymorphism and renal disease susceptibility.
Methods:
We conducted a search in PubMed, Embase (OvidSP), Wanfang databases and China National Knowledge Internet (CNKI) up to 20 June 2014. Odds ratio (OR) and 95% confidence interval (95% CI) were used to test the association. Statistical analyses were performed with STATA version 11.0 software.
Results:
In total, 2755 participants from eight case-control studies were included in this meta-analysis. The pooled results indicated the significant association between MIF -173G/C polymorphism and renal disease risk (CC + CG vs GG, OR = 1.77, P < 0.01; C vs G, OR = 3.94, P < 0.01). In the subgroup analysis, a significant relationship of MIF -173G/C gene polymorphism and renal disease risk in Asians and Caucasians were observed. Additionally, we found that the heterozygote (CG) may strongly increase renal disease risk in children, while the homozygote (CC) may increase the renal disease susceptibility more significantly in adults. Surprisingly, the results found a significant association between MIF -173G/C polymorphism and glucocorticoid resistance in child patients with idiopathic nephrotic syndrome (INS) (C vs G, OR: 3.83, P < 0.01).
Conclusion:
This study suggested that MIF -173G/C gene polymorphism may increase risk of renal disease, especially in children. Furthermore, the meta-analysis also indicated that this gene polymorphism may increase risk of glucocorticoid resistance in child patients with INS.
Insights
The macrophage migration inhibitory factor (MIF) -173G/C gene variant is linked to increased renal disease risk, particularly in children. This polymorphism also correlates with glucocorticoid resistance in pediatric idiopathic nephrotic syndrome.
Area of Science:
- Genetics and Molecular Biology
- Nephrology
- Immunology
Background:
- The macrophage migration inhibitory factor (MIF) -173G/C (rs755622) gene polymorphism has been implicated in renal disease susceptibility.
- Previous studies on this association have yielded inconclusive results, necessitating further investigation.
Purpose of the Study:
- To conduct a meta-analysis to clarify the relationship between the MIF -173G/C gene polymorphism and the risk of developing renal diseases.
- To explore potential associations with specific populations and clinical outcomes such as glucocorticoid resistance.
Main Methods:
- A comprehensive literature search was performed across major databases (PubMed, Embase, Wanfang, CNKI) up to June 2014.
- Meta-analysis was employed using Odds Ratios (OR) and 95% Confidence Intervals (95% CI) to assess the association.
- Statistical analyses were conducted using STATA version 11.0 software.
Main Results:
- The meta-analysis included eight case-control studies with 2755 participants.
- A significant association was found between the MIF -173G/C polymorphism and increased renal disease risk (CC+CG vs GG, OR=1.77; C vs G, OR=3.94).
- Subgroup analyses revealed significant associations in both Asian and Caucasian populations, with varying risk profiles for heterozygotes (CG) in children and homozygotes (CC) in adults. A notable link to glucocorticoid resistance in pediatric idiopathic nephrotic syndrome was also identified (C vs G, OR: 3.83).
Conclusions:
- The MIF -173G/C gene polymorphism appears to elevate the risk of renal disease, with a pronounced effect observed in children.
- This genetic variation is also associated with an increased risk of glucocorticoid resistance in pediatric patients diagnosed with idiopathic nephrotic syndrome.
Related Concept Videos
Pharmacogenetic Phenotypes: Alterations in Pharmacokinetics, Drug Targets and Biologic Milieu
Diabetic Nephropathy

