4.2 Article

Effects of a healthy Nordic diet on gene expression changes in peripheral blood mononuclear cells in response to an oral glucose tolerance test in subjects with metabolic syndrome: a SYSDIET sub-study

Journal

GENES AND NUTRITION
Volume 11, Issue -, Pages -

Publisher

BIOMED CENTRAL LTD
DOI: 10.1186/s12263-016-0521-4

Keywords

mRNA gene expression; Metabolic syndrome; PBMCs; Nordic diet; OGTT

Funding

  1. NordForsk Nordic Centre of Excellence in Food, Nutrition and Health [070014]
  2. Akershus University College of Applied Sciences (Norway)
  3. Academy of Finland [131593]
  4. University of Oslo (Norway)
  5. Swedish Research council
  6. Svenska Diabetesforbundet
  7. SRP Diabetes
  8. Finnish Diabetes Research Foundation
  9. Finnish Foundation for Cardiovascular Research
  10. Sigrid Juselius Foundation
  11. Kuopio University Hospital (Finland)
  12. Druvan Foundation
  13. Skane University Hospital
  14. Heart-Lung Foundation
  15. Diabetesfonden
  16. Foundation Cerealia (Sweden)
  17. Danish Obesity Research Centre (DanORC)
  18. Danish Council for Strategic Research (DairyHealth, BioFunCarb) (Denmark)
  19. Agricultural Productivity Fund
  20. University of Iceland (Iceland)

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Background: Diet has a great impact on the risk of developing features of metabolic syndrome (MetS), type 2 diabetes mellitus (T2DM), and cardiovascular diseases (CVD). We evaluated whether a long-term healthy Nordic diet (ND) can modify the expression of inflammation and lipid metabolism-related genes in peripheral blood mononuclear cells (PBMCs) during a 2-h oral glucose tolerance test (OGTT) in individuals with MetS. Methods: A Nordic multicenter randomized dietary study included subjects (n = 213) with MetS, randomized to a ND group or a control diet (CD) group applying an isocaloric study protocol. In this sub-study, we included subjects (n = 89) from three Nordic centers: Kuopio (n = 26), Lund (n = 30), and Oulu (n = 33) with a maximum weight change of +/- 4 kg, high-sensitivity C-reactive protein concentration <= 10 mg L-1, and baseline body mass index <39 kg m(-2). PBMCs were isolated, and the mRNA gene expression analysis was measured by quantitative real-time polymerase chain reaction (qPCR). We analyzed the mRNA expression changes of 44 genes before and after a 2hOGTT at the beginning and the end of the intervention. Results: The healthy ND significantly down-regulated the expression of toll-like receptor 4 (TLR4), interleukin 18 (IL18), and thrombospondin receptor (CD36) mRNA transcripts and significantly up-regulated the expression of peroxisome proliferator-activated receptor delta (PPARD) mRNA transcript after the 2hOGTT compared to the CD. Conclusions: A healthy ND is able to modify the gene expression in PBMCs after a 2hOGTT. However, more studies are needed to clarify the biological and clinical relevance of these findings.

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