CMPF does not associate with impaired glucose metabolism in individuals with features of metabolic syndrome

Maria A Lankinen, Kati Hanhineva, Marjukka Kolehmainen, Marko Lehtonen, Seppo Auriola, Hannu Mykkänen, Kaisa Poutanen, Ursula Schwab, Matti Uusitupa, Maria A Lankinen, Kati Hanhineva, Marjukka Kolehmainen, Marko Lehtonen, Seppo Auriola, Hannu Mykkänen, Kaisa Poutanen, Ursula Schwab, Matti Uusitupa

Abstract

Objective: 3-carboxy-4-methyl-5-propyl-2-furanpropanoic acid (CMPF) is a metabolite produced endogenously from dietary sources of furan fatty acids. The richest source of furan fatty acids in human diet is fish. CMPF was recently shown to be elevated in fasting plasma in individuals with gestational diabetes and type 2 diabetes, and mechanistically high level of CMPF was linked to β cell dysfunction. Here we aimed to study the association between plasma CMPF level and glucose metabolism in persons with impaired glucose metabolism.

Methods: Plasma CMPF concentration was measured from plasma samples of the study participants in an earlier controlled dietary intervention. All of them had impaired glucose metabolism and two other characteristics of the metabolic syndrome. Altogether 106 men and women were randomized into three groups for 12 weeks with different fish consumption (either three fatty fish meals per week, habitual fish consumption or maximum of one fish meal per week). Associations between concentration of CMPF and various glucose metabolism parameters at an oral glucose tolerance test at baseline and at the end of the study were studied.

Results: Fasting plasma CMPF concentration was significantly increased after a 12-week consumption of fatty fish three times per week, but the concentration remained much lower compared to concentrations reported in diabetic patients. Increases of plasma CMPF concentrations mostly due to increased fish consumption were not associated with impaired glucose metabolism in this study. Instead, elevated plasma CMPF concentration was associated with decreased 2-hour insulin concentration in OGTT.

Conclusions: Moderately elevated concentration of CMPF in plasma resulting from increased intake of fish is not harmful to glucose metabolism. Further studies are needed to fully explore the role of CMPF in the pathogenesis of impaired glucose metabolism.

Trial registration: ClinicalTrials.gov NCT00573781.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Fig 1. CMPF concentrations before and after…
Fig 1. CMPF concentrations before and after the intervention (0wk and 12 wk) in the Healthy Diet, WGED and Control groups.
Changes between the groups were tested using ANOVA and Bonferroni’s post-hoc tests.

References

    1. Rhee EP, Cheng S, Larson MG, Walford GA, Lewis GD, McCabe E, et al. Lipid profiling identifies a triacylglycerol signature of insulin resistance and improves diabetes prediction in humans. J Clin Invest. 2011;121: 1402–1411. 10.1172/JCI44442
    1. Wong G, Barlow CK, Weir JM, Jowett JB, Magliano DJ, Zimmet P, et al. Inclusion of Plasma Lipid Species Improves Classification of Individuals at Risk of Type 2 Diabetes. PLoS One. 2013;8: e76577 10.1371/journal.pone.0076577
    1. Prentice KJ, Luu L, Allister EM, Liu Y, Jun LS, Sloop KW, et al. The furan fatty acid metabolite CMPF is elevated in diabetes and induces beta cell dysfunction. Cell Metab. 2014;19: 653–666. 10.1016/j.cmet.2014.03.008
    1. Spiteller G. Furan fatty acids: occurrence, synthesis, and reactions. Are furan fatty acids responsible for the cardioprotective effects of a fish diet? Lipids. 2005;40: 755–771.
    1. Vetter W, Wendlinger C. Furan fatty acids—valuable minor fatty acids in food. Lipid Technology. 2013;25: 7–10.
    1. Wahl HG, Tetschner B, Liebich HM. The effect of dietary fish oil supplementation on the concentration of 3-carboxy-4-methyl-5-propyl-2-furanpropionic acid in human blood and urine. J. High Resolut. Chromatogr. 1992;15: 815–818.
    1. Hanhineva K, Lankinen M, Pedret A, Schwab U, Kolehmainen M, Paananen J, et al. Nontargeted Metabolite Profiling Discriminates Diet-Specific Biomarkers for Concumption of Whole Grains, Fatty Fish, and Bilberries in a Randomized Controlled Trial. Journal of Nutrition. 2015;145: 1–12. 10.3945/jn.114.194324
    1. Patel PS, Sharp SJ, Luben RN, Khaw KT, Bingham SA, Wareham NJ, et al. Association between type of dietary fish and seafood intake and the risk of incident type 2 diabetes: the European prospective investigation of cancer (EPIC)-Norfolk cohort study. Diabetes Care. 2009;32: 1857–1863. 10.2337/dc09-0116
    1. Nkondjock A, Receveur O. Fish-seafood consumption, obesity, and risk of type 2 diabetes: an ecological study. Diabetes Metab. 2003;29: 635–642.
    1. Rylander C, Sandanger TM, Engeset D, Lund E. Consumption of lean fish reduces the risk of type 2 diabetes mellitus: a prospective population based cohort study of norwegian women. PLoS One. 2014;9: e89845 10.1371/journal.pone.0089845
    1. Kaushik M, Mozaffarian D, Spiegelman D, Manson JE, Willett WC, Hu FB. Long-chain omega-3 fatty acids, fish intake, and the risk of type 2 diabetes mellitus. Am J Clin Nutr. 2009;90: 613–620. 10.3945/ajcn.2008.27424
    1. van Woudenbergh GJ, van Ballegooijen AJ, Kuijsten A, Sijbrands EJ, van Rooij FJ, Geleijnse JM, et al. Eating fish and risk of type 2 diabetes: A population-based, prospective follow-up study. Diabetes Care. 2009;32: 2021–2026. 10.2337/dc09-1042
    1. Zhang M, Picard-Deland E, Marette A. Fish and Marine Omega-3 Polyunsatured Fatty Acid Consumption and Incidence of Type 2 Diabetes: A Systematic Review and Meta-Analysis. Int J Endocrinol. 2013;2013: 501015 10.1155/2013/501015
    1. de Mello VD, Schwab U, Kolehmainen M, Koenig W, Siloaho M, Poutanen K, et al. A diet high in fatty fish, bilberries and wholegrain products improves markers of endothelial function and inflammation in individuals with impaired glucose metabolism in a randomised controlled trial: the Sysdimet study. Diabetologia. 2011;54: 2755–2767. 10.1007/s00125-011-2285-3
    1. Boelaert J, Lynen F, Glorieux G, Eloot S, Van Landschoot M, Waterloos MA, et al. A novel UPLC-MS-MS method for simultaneous determination of seven uremic retention toxins with cardiovascular relevance in chronic kidney disease patients. Anal Bioanal Chem. 2013;405: 1937–1947. 10.1007/s00216-012-6636-9
    1. Lankinen M, Schwab U, Kolehmainen M, Paananen J, Poutanen K, Mykkänen H, et al. Whole Grain Products, Fish and Bilberries Alter Glucose and Lipid Metabolism in a Randomized, Controlled Trial: The Sysdimet Study. PLoS ONE. 2011;6: e22646 10.1371/journal.pone.0022646
    1. Niwa T. Removal of protein-bound uraemic toxins by haemodialysis. Blood Purif. 2013;35 Suppl 2: 20–25. 10.1159/000350843

Source: PubMed

3
Sottoscrivi