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Study Into Genetic Influence on Cholesterol Response to Dietary Fat

Apolipoprotein E Genotype as a Determinant of LDL-cholesterol Response to Dietary Fat Manipulation

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01384032
Acronym
Satgene
Enrollment
88
Registered
2011-06-28
Start date
2009-01-31
Completion date
2011-05-31
Last updated
2011-06-28

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

Conditions

Cardiovascular Diseases

Keywords

CVD, LDL-C, apoE, SFA, DHA

Brief summary

Cardiovascular disease (CVD) is recognised as one of the main causes of death in the western world. LDL- cholesterol ('bad' cholesterol) and other lipids (fats) are important CVD risk factors. Apolipoprotein E (apoE) is an important transporter of fats in the blood. ApoE comes in E2, E3 and E4 forms, depending on your genetic make up. Approximately 60% of the UK population are E3/E3, 25% E4 carriers and 15% E2 carriers. There is some evidence to suggest that an E4 genotype may put you at modestly higher risk of CVD. Furthermore although very inconclusive previous studies have suggested that E4 individuals are slightly more sensitive to the LDL-cholesterol modifying effects of dietary fats (saturated fat, total fat, fish oil) showing slightly, greater reductions when low levels of these fat are consumed, and greater increases when high levels of these fat are consumed. Therefore, the aims of the Satgene study is to examine the impact of modifications in dietary total fat and saturated fat intakes, alone and in combination with fish oil supplement on LDL-cholesterol and other blood lipids, in individuals with an E3 and E4 genotype. The levels of total fat and saturated fat used in the current study are within the range observed in a typical UK population.

Interventions

DIETARY_SUPPLEMENTLow fat diet

Subjects were asked to consume a low fat diet for 8 weeks. Composition: 28% energy from fat, 8% energy from saturated fat, 55% energy from carbohydrate. Subjects were provided with low fat spread, cooking oil and snacks and asked to consume these in place of normally eaten equivalent foods. Subjects were asked to consume two extra portions of carbohydrate per day (e.g. two slices of bread, equivalent to 35g carbohydrate) and to consume low fat dairy products. Subjects also consumed 2g control oil per day during this period. Control oil comprised palm olein and soybean oil.

DIETARY_SUPPLEMENTHgih saturated fat diet

Subjects were asked to consume a high saturated fat diet for 8 weeks. Composition: 38% energy from fat, 18% energy from saturated fat, 45% energy from carbohydrate. Subjects were provided with spread, cooking oil and snacks and asked to consume these in place of normally eaten equivalent foods. Subjects were asked to consume one less portion of carbohydrate per day (e.g. one slice of bread and to consume full fat dairy products. Subjects also consumed 2g control oil per day during this period. Control oil comprised palm olein and soybean oil.

DIETARY_SUPPLEMENTHigh saturated fat diet

Subjects were asked to consume a high saturated fat diet for 8 weeks. Composition: 38% energy from fat, 18% energy from saturated fat, 45% energy from carbohydrate. Subjects were provided with spread, cooking oil and snacks and asked to consume these in place of normally eaten equivalent foods. Subjects were asked to consume one less portion of carbohydrate per day (e.g. one slice of bread and to consume full fat dairy products. Subjects also consumed 6g DHA-rich oil per day during this period providing 3g DHA.

Sponsors

Wellcome Trust
CollaboratorOTHER
University of Reading
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

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

Inclusion criteria

Men & women 35-70 years BMI 20-32 kg/m2 Haemoglobin (anaemia): 12.5-18.0g/l (men) and \> 11.5-16g/l (women) Gamma GT (liver function) (\< 80 IU/l), Triglyceride (between 1-4 mmol/l), Plasma total cholesterol (4.5-8 mmol/l) Glucose (World Health organisation recommend \<7 mmol/L).

Exclusion criteria

* Females who are breast feeding, may be pregnant, or if child-bearing potential are not taking effective contraceptive precautions * Likely to alter oral contraceptive or HRT usage during the course of the study * Blood Pressure \> 160/100 mm Hg (UK guidelines for stage 2 hypertension) * Had suffered a myocardial infarction or stroke in the previous 12 months * Hypertensive medication * Diabetics type I and II * Any volunteers on a weight reducing diet, or vegan/vegetarians as study requires consumption of dairy products and fish oils * On high dose fish oil supplements (\> 1g EPA + DHA per day) * Elevated lipids requiring medication such as statins, fibrates, gall bladder problems or other abnormalities of fat metabolism * Subjects not willing to make the necessary dietary changes during the study * Subjects drinking excessive alcohol (UK recommendations/wk currently for men are, no more than 21 units of alcohol per week or more than four units in any one day. For women, no more than 14 units of alcohol per week or more than three units per day). * Subjects who train at a high level, or attend more than 3 hours organised exercise classes per week

Design outcomes

Primary

MeasureTime frame
Change in low density lipoprotein cholesterol (LDL-C)0, 8, 16, and 24 weeks

Secondary

MeasureTime frameDescription
Change in fasting glucose0, 8, 16, 24 weeks
Change in fasting insulin0, 8, 16, 24 weeks
Change in fasting triglycerides (TAG)0, 8, 16, 24 weeks
Change in C-reactive protein (CRP)0, 8, 16, 24 weeks
Change in blood pressure0, 8, 16, 24 weeks
Change in body weight0, 8, 16, 24 weeks
Change in arterial stiffness0, 8, 16, 24 weeksArterial stiffness is a measure of vascular reactivity. This was assessed by Digital Volume Pulse using Pulse Trace PCA2 Machine (Micromedical, UK)
Change in total cholesterol0, 8, 16, 24 weeks
Change in high-density lipoprotein cholesterol (HDL)0, 8, 16, 24 weeks
Change in apolipoproteins B, CIII and E0, 8, 16, 24 weeks
Change in very low density lipoprotein (VLDL)0, 8, 16, 24 weeks
Change in chylomicrons (CM)0, 8, 16, 24 weeks
Change in inflammatory cytokine production9, 8, 16, 24 weeks
Change in plasma phospholipid fatty acids0, 8, 16, 24 weeks

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 19, 2026