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A short-term increase in dietary cholesterol and fat intake affects high-density lipoprotein composition in healthy subjects.

Nutrition, metabolism, and cardiovascular diseases : NMCD
June 1, 2018
C Morgantini et al. (8 authors)
Comparative StudyJournal ArticleRandomized Controlled TrialResearch Support, N.I.H., ExtramuralResearch Support, Non-U.S. Gov'tHuman StudyClinical
Study Details

Study Goal

The researchers aimed to determine whether a short-term high-cholesterol/high-fat diet alters HDL composition and function in healthy humans.

Results Summary

The study found that a high-cholesterol/high-fat diet significantly increased HDL lipid hydroperoxide content (15-HETE, 5-HETE, 13-HODE) and SAA levels, markers of dysfunctional HDL, while PON-1 activity remained unaffected.

Population

14 healthy young volunteers

Effective Dosage

Not specified

Duration

14 days per diet (low-cholesterol/low-fat and high-cholesterol/high-fat)

Interactions

None mentioned

Extracted Claims (9)
InterventionDirectionEndpointPopulationDosageImpactClaim #
high-cholesterol/high-fat diet (HChF)
increase
HDL concentrations of 15-HETE
healthy young volunteers
+254%
significantly higher
#1
high-cholesterol/high-fat diet (HChF)
increase
HDL concentrations of 5-HETE
healthy young volunteers
+116%
significantly higher
#2
high-cholesterol/high-fat diet (HChF)
increase
HDL concentrations of 13-HODE
healthy young volunteers
+102%
significantly higher
#3
high-cholesterol/high-fat diet (HChF)
increase
SAA levels
healthy young volunteers
+75%
significantly higher
#4
high-cholesterol/high-fat diet (HChF)
increase
haptoglobin
healthy young volunteers
+32%
marginally increased
#5
high-cholesterol/high-fat diet (HChF)
no change
PON-1 activity
healthy young volunteers
-16%
unaffected
#6
short-term elevation in dietary cholesterol and fat intake
increase
HDL lipid hydroperoxide content (15-HETE, 5-HETE, 13-HODE)
healthy subjects
-
increases
#7
short-term elevation in dietary cholesterol and fat intake
increase
SAA levels
healthy subjects
-
increases
#8
physiologic manipulation of dietary cholesterol and fat intake
neutral
HDL lipidome and proteome
healthy subjects
-
affects
#9
Abstract

BACKGROUND AND AIMS: High-cholesterol and high-fat diets alter biochemical composition and anti-oxidant properties of high-density lipoproteins (HDL) in animals. Whether this occurs in humans is unknown. Therefore, we examined the effect of a short-term elevation in dietary cholesterol and fat intake on HDL composition in healthy subjects. METHODS AND RESULTS: In a randomized, crossover clinical trial, 14 healthy young volunteers followed a 14-day low-cholesterol/low-fat diet (LChF) and a 14-day isocaloric high-cholesterol/high-fat diet (HChF) in a random order. After each diet, we measured HDL concentrations of hydroxyeicosatetraenoic acids (HETE), hydroxyoctadecadienoic acids (HODE), and haptoglobin, as well as serum amyloid A (SAA) and paroxonase-1 activity (PON-1). HDL concentrations of 15-HETE (+254%, p = 0.002), 5-HETE (+116%, p = 0.004), 13-HODE (+102%, p = 0.049), and SAA levels (+75%, p = 0.007) were significantly higher after the HChF than after the LChF. Furthermore, haptoglobin was marginally increased (+32%, p = 0.091) while PON-1 activity was unaffected (-16%, p = 0.366) by the HChF. CONCLUSION: In healthy subjects, a short-term elevation in dietary cholesterol and fat intake increases HDL lipid hydroperoxide content (15-HETE, 5-HETE, 13-HODE) and SAA levels, which are key features of dysfunctional HDL. This is the first study showing that a physiologic manipulation of dietary cholesterol and fat intake affects HDL lipidome and proteome in healthy subjects independently of weight changes. CLINICAL TRIAL REGISTRATION: NCT02549144.

Medical Subject Headings (MeSH)
AdultBiomarkersCholesterol, DietaryCross-Over StudiesDiet, High-FatFemaleHealthy VolunteersHumansHydroxyeicosatetraenoic AcidsItalyLinoleic AcidsLipid PeroxidesLipoproteins, HDLMalePostprandial PeriodProspective StudiesSerum Amyloid A ProteinTime FactorsYoung Adult
Study Links
Quality Scores
SafetyNot Assessed
Efficacy75/10
Quality85/10
Citation Metrics
Total Citations11
Citations/Year1.6
Relative Citation Ratio0.53
NIH Percentile28.5%
Research Impact Scores
APT Score0.75
Weight Score2.11
Normalized Score0.67
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