Association of IL-6 -174G > C and -572G > C Polymorphisms with Risk of Legg-Calve-Perthes Disease in Iranian Children

Fetal Pediatr Pathol. 2021 Jun;40(3):206-213. doi: 10.1080/15513815.2019.1693671. Epub 2019 Nov 22.

Abstract

Legg-Calve-Perthes disease (LCPD) is an idiopathic avascular necrosis of the capital femoral epiphysis of the femoral head with multifactorial etiology. The aim of this study was to analyze the association of IL-6 polymorphisms with LCPD risk in Iranian children. Methods: The study comprised of 45 children diagnosed with LCPD and 60 healthy subjects. The IL-6 -174 G > C and -597 G > C polymorphisms were genotyped by PCR-RFLP assay. Odds ratios (OR) and 95% confidence intervals (CI) were calculated on the risk genotypes and alleles. Results: The mutant homozygote genotype (CC) of IL-6 -174 G > C polymorphism was associated with increased risk of LCPD (OR 3.554; 95% CI: 0.1.578-8.004; p = 0.002). There was no significant association between IL-6 -597 G > C polymorphism and an increased risk of LCPD. Conclusions: Our results suggest that the IL-6 -174 G > C but not the IL-6 -597 G > C polymorphism may increase LCPD susceptibility in Iranian children.

Keywords: IL-6; Legg-Calve-Perthes disease; association; interleukin; polymorphism.

MeSH terms

  • Child
  • Humans
  • Interleukin-6* / genetics
  • Iran
  • Legg-Calve-Perthes Disease* / genetics
  • Odds Ratio
  • Polymorphism, Genetic

Substances

  • IL6 protein, human
  • Interleukin-6