4.8 Article

Hepatic saturated fatty acid fraction is associated with de novo lipogenesis and hepatic insulin resistance

Journal

NATURE COMMUNICATIONS
Volume 11, Issue 1, Pages -

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41467-020-15684-0

Keywords

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Funding

  1. Ministry of Economic Affairs and Climate Policy
  2. Unilever RD Wageningen
  3. Netherlands Cardiovascular Research Initiative
  4. Dutch Heart Foundation [CVON2014-02 ENERGISE]
  5. ZonMW [016.veni.188.036]
  6. Diabetes Fonds (Dutch Diabetes Research Foundation) [2017.81.004]
  7. Advanced ERC Grant [694717]
  8. ERC [759161]
  9. European Research Council (ERC) [759161] Funding Source: European Research Council (ERC)

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Hepatic steatosis is associated with poor cardiometabolic health, with de novo lipogenesis (DNL) contributing to hepatic steatosis and subsequent insulin resistance. Hepatic saturated fatty acids (SFA) may be a marker of DNL and are suggested to be most detrimental in contributing to insulin resistance. Here, we show in a cross-sectional study design (ClinicalTrials.gov ID: NCT03211299) that we are able to distinguish the fractions of hepatic SFA, mono- and polyunsaturated fatty acids in healthy and metabolically compromised volunteers using proton magnetic resonance spectroscopy (H-1-MRS). DNL is positively associated with SFA fraction and is elevated in patients with non-alcoholic fatty liver and type 2 diabetes. Intriguingly, SFA fraction shows a strong, negative correlation with hepatic insulin sensitivity. Our results show that the hepatic lipid composition, as determined by our H-1-MRS methodology, is a measure of DNL and suggest that specifically the SFA fraction may hamper hepatic insulin sensitivity. Hepatic steatosis is associated with poor cardiometabolic health, with de novo lipogenesis (DNL) contributing to hepatic steatosis and subsequent insulin resistance. Here, the authors use H-1-MRS methodology to show hepatic SFA fraction is a measure of DNL and specifically may hamper hepatic insulin sensitivity.

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