4.6 Article

Circulating Levels of Fatty Acid-Binding Protein Family and Metabolic Phenotype in the General Population

Journal

PLOS ONE
Volume 8, Issue 11, Pages -

Publisher

PUBLIC LIBRARY SCIENCE
DOI: 10.1371/journal.pone.0081318

Keywords

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Funding

  1. Ministry of Education, Culture, Sports, Science and Technology
  2. Uehara Memorial Foundation
  3. Mitsubishi Pharma Research Foundation
  4. Naito Foundation Natural Science Scholarship
  5. Takeda Science Foundation
  6. Mochida Memorial Foundation for Medical and Pharmaceutical Research
  7. Kanae Foundation for the Promotion of Medical Science
  8. Cardiovascular Research Foundation
  9. Suzuken Memorial Foundation
  10. Sumitomo Foundation
  11. Tokyo Biochemical Research Foundation
  12. Japan Diabetes Foundation
  13. Ono Medical Research Foundation
  14. Novartis Foundation (Japan) for the Promotion of Science
  15. Akiyama Life Science Foundation
  16. Terumo Life Science Foundation
  17. Daiwa Securities Health Foundation
  18. Suhara Memorial Foundation
  19. Takeda Medical Research Foundation
  20. Japan Foundation for Applied Enzymology
  21. Ichiro Kanehara Foundation
  22. Grants-in-Aid for Scientific Research [23591106] Funding Source: KAKEN

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Objective: Fatty acid-binding proteins (FABPs) are a family of 14-15-kDa proteins, and some FABPs have been to be used as biomarkers of tissue injury by leak from cells. However, recent studies have shown that FABPs can be secreted from cells into circulation. Here we examined determinants and roles of circulating FABPs in a general population. Methods: From the database of the Tanno-Sobetsu Study, a study with a population-based cohort design, data in 2011 for 296 subjects on no medication were retrieved, and FABP1 similar to 5 in their serum samples were assayed. Results: Level of FABP4, but not the other isoforms, showed a gender difference, being higher in females than in males. Levels of all FABPs were negatively correlated with estimated glomerular filtration rate (eGFR), but a distinct pattern of correlation with other clinical parameters was observed for each FABP isoform; significant correlates were alanine aminotransferase (ALT), blood pressure (BP), and brain natriuretic peptide (BNP) for FABP1, none besides eGFR for FABP2, age, BP, and BNP for FABP3, age, waist circumference (WC), BP, BNP, lipid variables, high-sensitivity C-reactive protein (hsCRP), and HOMA-R for FABP4, and age, WC, BP, ALT, BNP, and HOMA-R for FABP5. FABP4 is the most strongly related to metabolic markers among FABPs. In a multivariate regression analysis, FABP4 level was an independent predictor of HOMAR after adjustment of age, gender, WC, BP, HDL cholesterol, and hsCRP. Conclusions: Each FABP isoform level showed a distinct pattern of correlation with clinical parameters, although levels of all FABPs were negatively determined by renal function. Circulating FABP4 appears to be a useful biomarker for detecting preclinical stage of metabolic syndrome, especially insulin resistance, in the general population.

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