Cited by 41Fatty Acid Research and HealthNutritional Studies and DietDiet, Metabolism, and Disease

Poly is more effective than monounsaturated fat for dietary management in the metabolic syndrome: The muffin study

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Miller, Michael, Sorkin, John D., Mastella, Laura, Sutherland, Aimee, Rhyne, Jeffrey, Donnelly, Patrick, Simpson, Kathy, Goldberg, Andrew P.·2016·Journal of clinical lipidology

Abstract

Background The metabolic syndrome (MetS) is highly prevalent and associated with an increased risk for type 2 diabetes mellitus (T2DM) and cardiovascular disease (CVD). Lifestyle recommendations to treat MetS often include the replacement of saturated fats (SFAs) and monosaccharides with unsaturated fat. However, it is unclear whether metabolic parameters will improve more when the saturated fat in American Heart Association (AHA) diets is replaced with higher concentrations of monounsaturated or polyunsaturated fatty acids (MUFA or PUFA).Objective To test the hypothesis that an AHA diet enriched in MUFA improves lipoprotein lipids, insulin resistance, inflammation, and endothelial function to a greater extent than a diet enriched in PUFA in middle-aged men and women with MetS.Methods A prospective, open-label, parallel group design with randomization to a hypocaloric MUFA or PUFA-enriched diet after weight stabilization on an AHA step I diet. Participants consumed 3 MUFA-enriched or PUFA-enriched muffins daily with additional supplementation as required to ensure 25%-50% increases in dietary fat intake from these sources at the expense of SFA and the opposing unsaturated fat. Changes in MetS components were measured at baseline and after 6 months of dietary intervention.Results Thirty-nine participants (mean age, 60.8 years; 79% African-American, 60% women) with MetS completed the 6-month study. Compared to baseline, assignment to either MUFA (n = 23) or PUFA (n = 16) both were associated with weight loss (MUFA: -2.3 ± 1 kg, P = .06; PUFA: -4.6 ± 2 kg; P = .002), but PUFA was also associated with reductions in triglycerides (TG) (-30 ± 18 mg/dL, P = .02), systolic blood pressure (BP) (-7 ± 3 mm Hg, P = .01), diastolic BP (DBP) (-4 ± 2 mm Hg, P = .01) and improved flow mediated dilation (FMD) (7.1% ± 1.8% vs 13.6% ± 2%, absolute increase; P = .0001). When compared to MUFA treatment, PUFA intervention was associated with reduced TG (P = .04) and DBP (P = .07) as well as increased FMD (P = .04) even after adjustment for changes in weight. There was no effect on total cholesterol, low-density lipoprotein cholesterol, glucose, high-sensitivity C-reactive protein (hs-CRP), or other inflammatory proteins. Overall, 25% (4 of 16) assigned to PUFA and 13% (3 of 23) to MUFA converted to non-MetS status.Conclusion Substitution of SFA with PUFA in patients with MetS is associated with greater reductions in TG and improvement in endothelial function than MUFA that is independent of weight loss. These preliminary findings raise the possibility that PUFA may be the unsaturated fat of choice to reduce cardiometabolic risk in patients with MetS.

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  • The prevalence of metabolic syndrome is increasing globally, driven by rising obesity rates and sedentary lifestyles.

    “The prevalence of MetS is increasing globally, driven by rising obesity rates and sedentary lifestyles [1].”

    From Marine-Based Omega-3 Fatty Acids and Metabolic Syndrome: A Systematic Review and Meta-Analysis of Randomized Controlled Trials (2025) · cites this paper as [1]

    The Abstract Background calls metabolic syndrome “highly prevalent,” and the Introduction describes it as common. Neither passage says its prevalence is increasing globally or attributes an increase to rising obesity rates and sedentary lifestyles. (LLM, conf=0.84)

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  1. [29]Jakobsen MU O'Reilly EJ Heitmann BL Major types of dietary fat and risk of coronary heart disease: a pooled analysis of 11 cohort studies. Am J Clin Nutr 2009 89 1425 1432 19211817 PMC2676998

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Authors
Miller, M., Sorkin, J. D., Mastella, L., Sutherland, A., Rhyne, J., Donnelly, P., Simpson, K., & Goldberg, A. P.
Affiliations
University of Maryland, Baltimore (US)
Corresponding author
Miller, Michael
Venue
Journal of clinical lipidology
Publisher
Elsevier BV
Published
2016-07
Volume
10
Issue
4
Pages
996-1003
ISSN
  • 1876-4789 (ISSN-L)
  • 1933-2874
OpenAlex
W2346312442
Cited by
41
References
43
Citations by year
2026: 2 · 2025: 3 · 2024: 1 · 2023: 4 · 2022: 4 · 2021: 4 · 2020: 7 · 2019: 7 · 2018: 4 · 2017: 5
FWCI
5.57
Type
journal article
Language
en
Open access
Locations
  • Journal of clinical lipidology (acceptedVersion)
  • PubMed (publishedVersion)
  • PubMed Central (acceptedVersion)
Funders
  • VA Merit (I01CX000147)
  • Baltimore VA Geriatric Research, Education and Clinical Center
  • NHLBI
  • Nutrition Obesity Research Center (NORC) (DK072488-4)
Topics
  • Health Sciences › Nursing › Nutrition and Dietetics › Fatty Acid Research and Health
  • Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Nutritional Studies and Diet
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diet, Metabolism, and Disease
Keywords
metabolic syndrome, polyunsaturated fatty acids, monounsaturated fatty acids, fat replacement, saturated fat, weight loss, triglycerides, blood pressure, flow-mediated dilation, endothelial function, insulin resistance, inflammation, lipoprotein lipids, type 2 diabetes risk, cardiovascular risk, middle-aged adults, African Americans
MeSH terms
Adult, Aged, Dietary Fats, Unsaturated, Endothelium, Vascular, Fatty Acids, Monounsaturated, Fatty Acids, Unsaturated, Female, Humans, Insulin Resistance, Lipoproteins, Male, Middle Aged, Metabolic Syndrome, Overweight

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