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Research Article| Volume 42, ISSUE 1, P130-134, January 1993

The role of fatty acid saturation on plasma lipids, lipoproteins, and apolipoproteins: II. The plasma total and low-density lipoprotein cholesterol response of individual fatty acids

  • Janice Derr
    Affiliations
    Department of Statistics, The Pennsylvania State University, University Park, PA USA.

    Department of Nutrition, The Pennsylvania State University, University Park, PA USA.

    the Mary Imogene Bassett Research Insitute, Columbia University, Cooperstown, NY USA.

    the American Cocoa Research Institute, McLean, VA USA.
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  • P.M. Kris-Etherton
    Correspondence
    Address reprint requests to P.M. Kris-Etherton, PhD, Nutrition Department, The Pennsylvania State University, S-126 Henderson Bldg, University Park, PA 16802.
    Affiliations
    Department of Statistics, The Pennsylvania State University, University Park, PA USA.

    Department of Nutrition, The Pennsylvania State University, University Park, PA USA.

    the Mary Imogene Bassett Research Insitute, Columbia University, Cooperstown, NY USA.

    the American Cocoa Research Institute, McLean, VA USA.
    Search for articles by this author
  • Thomas A. Pearson
    Affiliations
    Department of Statistics, The Pennsylvania State University, University Park, PA USA.

    Department of Nutrition, The Pennsylvania State University, University Park, PA USA.

    the Mary Imogene Bassett Research Insitute, Columbia University, Cooperstown, NY USA.

    the American Cocoa Research Institute, McLean, VA USA.
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  • Frances H. Seligson
    Affiliations
    Department of Statistics, The Pennsylvania State University, University Park, PA USA.

    Department of Nutrition, The Pennsylvania State University, University Park, PA USA.

    the Mary Imogene Bassett Research Insitute, Columbia University, Cooperstown, NY USA.

    the American Cocoa Research Institute, McLean, VA USA.
    Search for articles by this author
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      Abstract

      Regression analyses were performed on individual data from our two previous clinical investigations to establish the cholesterolemic effects of individual fatty acids. Our principal objective was to determine the effects of stearic acid on plasma total cholesterol (TC) and low-density lipoprotein (LDL) cholesterol levels. Our second objective was to determine the variation in the cholesterolemic response of individuals to changes (Δ) in the major dietary fatty acids. The best-fitting linear regression equations relating ΔTC and ΔLDL (mg/dL) were as follows: ΔTC = 2.3 ΔC14:0 + 3.0 ΔC16:0 − 0.8 ΔC18:0 − 1.0Δpolyunsaturated fatty acids (PUFA) and ΔLDL = 2.6 ΔC14:0 + 2.9 ΔC16:0 − 0.5 ΔC18:0 − 0.7 ΔPUFA, where Δ fatty acid = change in intake expressed as percent of calories. Based on these equations, in which stearic acid has a significant, negative regression coefficient, and the other regression models analyzed, it appears that stearic acid has an independent cholesterol-lowering effect. Using the equation we developed, 75% of the actual cholesterolemic responses were within ± 10 mg/dL of the predicted response. In summary, we have developed a predictive equation (similar to those developed by both Keys and Hegsted) to estimate changes in plasma TC and LDL cholesterol levels of young men in response to changes in dietary fatty acids. However, our predictive equation separates stearic acid from the other long-chain saturated fatty acids (SFA) and indicates that it has an independent cholesterol-lowering effect. Thus, stearic acid is a unique long-chain SFA because of its effect on plasma cholesterol level.
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