AI Article Synopsis

  • The study investigates the link between two genetic polymorphisms, CCR2-V64I and MCP-1-2518A/G, and generalised aggressive periodontitis (GAgP) in a Chinese population.
  • Researchers analyzed blood samples from 124 GAgP patients and 94 healthy individuals to assess these gene variations using PCR-RFLP methods.
  • Results indicate that specific genotypes of CCR2 and MCP-1 may reduce the risk of GAgP in females, while in males, a potential interaction between these genotypes and smoking increases susceptibility to the disease.

Article Abstract

Objective: to examine the possible association of CCR2-V64I and MCP-1-2518A/G polymorphisms with generalised aggressive periodontitis (GAgP) in the Chinese population.

Methods: one hundred and twenty-four GAgP patients and 94 healthy subjects were included in the study. A peripheral blood sample was obtained from each subject and genomic DNA was isolated. Gene polymorphisms of CCR2-V64I and MCP-1-2518A/G were analysed by standard polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) assay.

Results: a possible combined effect of CCR2-V64I and MCP-1-2518A/G was observed in the female GAgP patients, as the odds ratio for VV genotype (CCR2) and G+ genotype ( MCP-1) was 0.2 (P = 0.023). Individuals carrying VV genotype and G+ genotype were at reduced risk for GAgP. A possible combined effect of genotype and smoking was observed in the male GAgP patients, as the odds ratio for VV genotype (CCR2) and smoking, or G+ genotype (MCP-1) and smoking were 7.4 (P = 0.022) and 4.9 (P = 0.030), respectively.

Conclusion: the combined association of CCR2-V64I and MCP-1-2518A/G polymorphisms may play an important role in determining GAgP susceptibility in Chinese females. A possible combined effect of genotype and smoking on GAgP susceptibility was suggested in males.

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Article Synopsis
  • The study investigates the link between two genetic polymorphisms, CCR2-V64I and MCP-1-2518A/G, and generalised aggressive periodontitis (GAgP) in a Chinese population.
  • Researchers analyzed blood samples from 124 GAgP patients and 94 healthy individuals to assess these gene variations using PCR-RFLP methods.
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