Association between MCP-1 2518 A>G gene polymorphism and chronic kidney disease

Song Mao1, Liangxia Wu2

  • 1Department of Pediatrics, Shanghai Jiao Tong University Affiliated Sixth People's Hospital, Shanghai, China. edjh123456@sina.com.

Insights

The MCP-1 2518 A>G gene polymorphism was analyzed for chronic kidney disease (CKD) risk. AA genotype showed a protective effect in Caucasians, while AG genotype indicated an increased risk.

Area of Science:

  • Genetics and Molecular Biology
  • Nephrology
  • Immunology

Background:

  • Monocyte chemoattractant protein-1 (MCP-1) plays a role in chronic kidney disease (CKD) pathogenesis.
  • The MCP-1 2518 A>G gene polymorphism influences MCP-1 levels and may impact CKD susceptibility.

Purpose of the Study:

  • To evaluate the association between the MCP-1 2518 A>G gene polymorphism and the risk of developing CKD.
  • To synthesize evidence from existing studies using a meta-analysis approach.

Main Methods:

  • A comprehensive search of electronic databases was conducted to identify relevant studies.
  • Meta-analysis was performed using fixed-effects or random-effects models to calculate pooled odds ratios (ORs) and 95% confidence intervals (CIs).
  • The analysis included a total of 2415 cases and 2011 controls across various populations.

Main Results:

  • No significant association was found between the A allele/GG genotype and CKD risk in overall populations, Asians, Caucasians, or Africans.
  • Similarly, the AA/AG genotype showed no association with CKD risk across these populations.
  • However, the AA genotype was associated with a reduced risk of CKD in Caucasians (OR 0.816, 95% CI 0.703-0.947).
  • Conversely, the AG genotype was linked to an increased risk of CKD in Caucasians (OR 1.230, 95% CI 1.042-1.452).
  • No significant publication bias was detected.

Conclusions:

  • The AA genotype of the MCP-1 2518 A>G polymorphism may confer a protective effect against CKD in Caucasian populations.
  • The AG genotype may represent a risk factor for CKD development in Caucasians.
  • Further research is warranted to confirm these findings and explore underlying mechanisms.

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