The Effect of Habitual Fat Intake, IL6 Polymorphism, and Different Diet Strategies on Inflammation in Postmenopausal Women with Central Obesity

Nutrients. 2019 Jul 10;11(7):1557. doi: 10.3390/nu11071557.

Abstract

The hypothesis that habitual fat intake, the IL6 genotype, the Mediterranean diet or the central European diet for 16 weeks affect biomarkers of inflammation in centrally obese postmenopausal women, was tested in a randomized controlled trial. Dietary intake was assessed using a three-day food diary. Lipid parameters were measured using a Beckman Coulter AU analyzer. Transcription of TNF and IL6 genes was analyzed in peripheral blood mononuclear cells using real-time PCR. Concentrations of tumor necrosis factor alpha (TNFα) and interleukin 6 (IL6) were measured with ELISA. rs1800795 polymorphism of IL6 was analyzed using hydrolyzing probes. Higher energy intake from fat was associated with higher IL6 levels (p < 0.05). Significantly (p < 0.01) lower total cholesterol (T-C) and low-density lipoprotein cholesterol (LDL-C) concentrations were observed in the GG IL6 rs1800795 genotype group. Both diets significantly (p < 0.001) decreased TNFα concentrations. Neither IL6 gene transcription levels nor blood IL6 concentrations were affected by them. Our findings confirm that habitual fat intake may affect inflammation. The rs1800795 IL6 polymorphism alone did not significantly affect body weight or body composition in aimed group, but C-allele carriers had higher levels of T-C and LDL-C. This polymorphism did not affect inflammation. Both diets may lead to a decrease in TNFα concentration.

Keywords: IL6; TNFα; dietary fat; dietary intervention; postmenopausal women; single nucleotide polymorphism.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Diet, Mediterranean*
  • Dietary Fats / analysis*
  • Female
  • Humans
  • Inflammation / genetics
  • Interleukin-6 / genetics*
  • Leukocytes, Mononuclear / metabolism
  • Middle Aged
  • Obesity, Abdominal* / diet therapy
  • Obesity, Abdominal* / genetics
  • Polymorphism, Single Nucleotide / genetics
  • Postmenopause*
  • Tumor Necrosis Factor-alpha / genetics

Substances

  • Dietary Fats
  • IL6 protein, human
  • Interleukin-6
  • Tumor Necrosis Factor-alpha