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Effect of Different Fat Enriched Meats on the Hepatic Cholesterol Synthesis

A Randomized Study to Assess the Effect of Different Fat Enriched Meats on the Hepatic Cholesterol Synthesis

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02259153
Enrollment
20
Registered
2014-10-08
Start date
2014-03-31
Completion date
2014-08-31
Last updated
2014-10-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cholesterol, Diet, High-Fat, Fatty Acids, Hyperlipidemias, Lipid Metabolism Disorders, Sterols

Keywords

Lipids, Non Cholesterol Sterols, Oxysterols, Cholesterol Metabolism

Brief summary

The objective of the study is to assess the effect of two diets with different fat composition on cholesterol metabolism. The study was a randomized cross-over trial where volunteers follow two study periods with different types of meat (lean and fat red meat) separately by a ten days wash-out period. At the beginning of the study and after the study periods the following parameters are determined: anthropometric (weight, waist, circumference and body mass index), blood pressure, dietary (72-hours dietary registry) and exercise assessments and biochemical analysis (total cholesterol, triglycerides, HDL cholesterol, LDL cholesterol, apolipoprotein A1, apolipoprotein B, iron, transferring, ferritin, uric acid, glucose, HbA1c and insulin). Serum concentration of non cholesterol sterols (sitosterol, campesterol, stigmasterol, desmosterol and lanosterol) and oxysterols (24S-hydroxycholesterol, 27-hydroxycholesterol and 7α-hydroxycholestenone) were measured by High Performance Liquid Chromatography tandem Mass Spectrometry in these subjects throughout along the study in order to demonstrate the effect of different red meat on the hepatic metabolism of cholesterol.

Interventions

BEHAVIORALChanges in cholesterol metabolism
OTHERLean red meat diet
OTHERFat red meat diet

Sponsors

Instituto Aragones de Ciencias de la Salud
Lead SponsorOTHER_GOV

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

* Normolipemic healthy subjects defined by levels of LDL cholesterol and triglycerides below the 90th percentile adjusted for age and sex. * Diet and stable lifestyle with controllable feeding.

Exclusion criteria

* Pregnancy or intention of pregnancy during the study. * Lipid lowering drugs in the last 3 months.

Design outcomes

Primary

MeasureTime frame
Changes in lipid profileBaseline and after 10 days of intervention
Changes in non cholesterol sterols and oxysterols serum concentrationsBaseline and after 10 days of intervention

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 17, 2026