4.3 Article

Self-reported dietary omega-3 polyunsaturated fatty acids are associated with adipose tissue markers and glucose metabolism in apparently healthy subjects

Journal

ANNALS OF HUMAN BIOLOGY
Volume 49, Issue 7-8, Pages 291-298

Publisher

TAYLOR & FRANCIS LTD
DOI: 10.1080/03014460.2022.2144945

Keywords

Eicosapentaenoic fatty acid; docosahexaenoic fatty acid; resistin; plasminogen activator inhibitor 1; adipose tissue

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This study investigated the association of EPA and DHA with PAI-1 and resistin, as well as their impact on glucose metabolism in apparently healthy individuals. The results showed that EPA and DHA can modulate glucose metabolism across different functional states of adipose tissue, and this association is independent of other metabolic risk factors.
Background: Plasminogen activator inhibitor 1 (PAI-1) and resistin are associated with dysfunctional adipose tissue (AT)-related metabolic complications. The role of dietary eicosapentaenoic (EPA) and docosahexaenoic (DHA) fatty acids in this relationship is unknown. Aim: To investigate the association of EPA and DHA with PAI-1 and resistin, as well as the role of this association on the glucose metabolism of apparently healthy subjects. Subjects and methods: Thirty-six healthy individuals were included. Validated food frequency questionnaires were used to analyse dietary habits. Inflammatory and glucose metabolism markers were quantified. Subcutaneous AT samples were obtained, and adipocyte number, area, and macrophage content were assessed. Results: In 36 subjects aged 56 +/- 8 years and with a body mass index of 26 +/- 4 kg/m(2), (log)EPA, and (log)DHA showed significant association with (log)resistin and a marginal association with PAI-1. Adipocyte number, area, and (log)number of macrophages per adipocyte significantly correlated with PAI-1 but not with (log)resistin. Although (log)EPA and (log)DHA were independently associated with (log)insulin, (log)insulin resistance, and C-Peptide, the addition of (log)resistin, but not of PAI-1, into the multivariable model, abolished the associations. Conclusions: EPA and DHA could modulate glucose metabolism across AT functional states. Our data indicate that this association is independent of other metabolic risk factors.

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