4.6 Review

Impact of Replacement of Individual Dietary SFAs on Circulating Lipids and Other Biomarkers of Cardiometabolic Health: A Systematic Review and Meta-Analysis of Randomized Controlled Trials in Humans

Journal

ADVANCES IN NUTRITION
Volume 13, Issue 4, Pages 1200-1225

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1093/advances/nmab143

Keywords

palmitic acid; stearic acid; myristic acid; medium-chain fatty acids; saturated fatty acids; unsaturated fatty acids; lipoproteins; fasting lipid profile; glucose; insulin

Funding

  1. Biotechnology and Biological Sciences Research Council (BBSRC) UK Joint Programme Initiative HDHL Biomarkers: Fatty Acid Metabolism-Interlinking Diet with Cardiometabolic Health (FAME) [BB/P028217/1]

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This systematic review assessed the impact of individual saturated fatty acids (SFAs) and their substitutions with other fatty acids on the prevention of cardiometabolic disease (CMD). The results showed that replacing palmitic acid with unsaturated fatty acids can lower LDL-cholesterol concentrations, but no significant effects were observed on other CMD risk markers.
Little is known of the impact of individual SFAs and their isoenergetic substitution with other SFAs or unsaturated fatty acids (UFAs) on the prevention of cardiometabolic disease (CMD). This systematic literature review assessed the impact of such dietary substitutions on a range of fasting CMD risk markers, including lipid profile, markers of glycemic control and inflammation, and metabolic hormone concentrations. Eligible randomized controlled trials (RCTs) investigated the effect of isoenergetic replacements of individual dietary SFAs for >= 14 d on >= 1 CMD risk markers in humans. Searches of the PubMed, Embase, Scopus, and Cochrane CENTRAL databases on 14 February, 2021 identified 44 RCTs conducted in participants with a mean +/- SD age of 39.9 +/- 15.2 y. Studies' risk of bias was assessed using the Cochrane Risk of Bias tool 2.0 for RCTs. Random-effect meta-analyses assessed the effect of >= 3 similar dietary substitutions on the same CMD risk marker. Other dietary interventions were described in qualitative syntheses. We observed reductions in LDL-cholesterol concentrations after the replacement of palmitic acid (16:0) with UFAs (-0.36 mmol/L; 95% CI: -0.50, -0.21 mmol/L; I-2 = 96.0%, n = 18 RCTs) or oleic acid (18:1n-9) (-0.16 mmol/L; 95% CI: -0.28, -0.03 mmol/L; I-2 = 89.6%, n = 9 RCTs), with a similar impact on total cholesterol and apoB concentrations. No effects on other CMD risk markers, including HDL-cholesterol, triacylglycerol, glucose, insulin, or C-reactive protein concentrations, were evident. Similarly, we found no evidence of a benefit from replacing dietary stearic acid (18:0) with UFAs on CMD risk markers (n = 4 RCTs). In conclusion, the impact of replacing dietary palmitic acid with UFAs on lipid biomarkers is aligned with current public health recommendations. However, owing to the high heterogeneity and limited studies, relations between all individual SFAs and biomarkers of cardiometabolic health need further confirmation from RCTs.

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