4.5 Article

The FADS1 genotypes modify the effect of linoleic acid-enriched diet on adipose tissue inflammation via pro-inflammatory eicosanoid metabolism

Journal

EUROPEAN JOURNAL OF NUTRITION
Volume 61, Issue 7, Pages 3707-3718

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s00394-022-02922-y

Keywords

Adipose tissue; Arachidonic acid; Eicosanoid; FADS1; Inflammation; Linoleic acid

Funding

  1. University of Eastern Finland (UEF)
  2. Kuopio University Hospital
  3. Finnish Diabetes Research Foundation
  4. Academy of Finland [138006, 309311]
  5. Finnish Cultural Foundation
  6. Northern Savo Regional Fund
  7. University of Eastern Finland Spearhead Funding (Karkihanke)
  8. Juho Vainio Foundation
  9. Matti Uusitupa Foundation (juhlaseminaarirahasto)
  10. Swedish Heart Lung Foundation
  11. Swedish Research Council
  12. Tripartite Immunometabolism Consortium-Novo Nordisk Foundation [NNF15CC0018486]
  13. Academy of Finland (AKA) [309311, 138006, 138006, 309311] Funding Source: Academy of Finland (AKA)

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The study investigated the role of FADS1 variants in regulating dietary linoleic acid-induced effects on adipose tissue inflammation. The results showed that individuals with the TT genotype had increased inflammation in adipose tissue after a LA-enriched diet, while the CC genotype may play a protective role.
Purpose Fatty acid desaturase (FADS) variants associate with fatty acid (FA) and adipose tissue (AT) metabolism and inflammation. Thus, the role of FADS1 variants in the regulation of dietary linoleic acid (LA)-induced effects on AT inflammation was investigated. Methods Subjects homozygotes for the TT and CC genotypes of the FADS1-rs174550 (TT, n = 25 and CC, n = 28) or -rs174547 (TT, n = 42 and CC, n = 28), were either recruited from the METabolic Syndrome In Men cohort to participate in an intervention with LA-enriched diet (FADSDIET) or from the Kuopio Obesity Surgery (KOBS) study. GC and LC-MS for plasma FA proportions and eicosanoid concentrations and AT gene expression for AT inflammatory score (AT-InSc) was determined. Results We observed a diet-genotype interaction between LA-enriched diet and AT-InSc in the FADSDIET. In the KOBS study, interleukin (IL)1 beta mRNA expression in AT was increased in subjects with the TT genotype and highest LA proportion. In the FADSDIET, n-6/LA proportions correlated positively with AT-InSc in those with the TT genotype but not with the CC genotype after LA-enriched diet. Specifically, LA- and AA-derived pro-inflammatory eicosanoids related to CYP450/sEH-pathways correlated positively with AT-InSc in those with the TT genotype, whereas in those with the CC genotype, the negative correlations between pro-inflammatory eicosanoids and AT-InSc related to COX/LOX-pathways. Conclusions LA-enriched diet increases inflammatory AT gene expression in subjects with the TT genotype, while CC genotype could play a protective role against LA-induced AT inflammation. Overall, the FADS1 variant could modify the dietary LA-induced effects on AT inflammation through the differential biosynthesis of AA-derived eicosanoids.

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