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Impact of High-fat Meals Varying in Fatty Acid Composition on Adipose and Systemic Metabolic-inflammatory Responses

Impact of High-fat Meals Varying in Fatty Acid Composition on Adipose and Systemic Metabolic-inflammatory Responses: a Randomized Controlled Postprandial Study

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03712579
Enrollment
8
Registered
2018-10-19
Start date
2019-01-21
Completion date
2020-10-15
Last updated
2022-05-17

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

Conditions

Cardiovascular Diseases, Inflammation, Inflammatory Response, Obesity, Overweight

Brief summary

Cardiometabolic disorders are a leading cause of death worldwide. Replacing saturated fatty acids (SFA) with unsaturated fatty acids is recommended as a way of lowering cardiometabolic disease risk. Consuming a diet rich in SFA may lead to a greater metabolic-inflammatory response in white adipose tissue during the fasting state, when compared to eating a diet rich in monounsaturated fatty acids (MUFA). Since individuals spend most of the day in the fed (or postprandial) state, it is important to see how different types of dietary fatty acids affect postprandial white adipose tissue and systemic metabolic-inflammatory responses. This study will investigate the effect of a SFA-rich meal on markers of white adipose tissue and systemic metabolic-inflammation, compared to a MUFA-rich meal in overweight adults. In a randomised, single blind controlled, cross-over manner participants will consume either a SFA- or MUFA-rich meal and sequential blood and white adipose tissue samples will be collected before and until 6 hours postprandially.

Interventions

DIETARY_SUPPLEMENTSFA-Rich Meal

Saturated fatty acid-rich test meal, containing 75g test fat

DIETARY_SUPPLEMENTMUFA-Rich Meal

Monounsaturated fatty acid-rich test meal, containing 75g test fat

Sponsors

Loughborough University
Lead SponsorOTHER

Study design

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

Eligibility

Sex/Gender
ALL
Age
18 Years to 50 Years
Healthy volunteers
Yes

Inclusion criteria

* 18-50 years * BMI = 25-40 kg/m2 * Male or Female * Waist circumference \>94 cm (men) and \>80cm (women)\* * Physically active (\> 3 x 30 min moderate intensity exercise per week) * Systolic blood pressure \< 160 mmHg and diastolic blood pressure \< 100 mmHg * No cardiometabolic (e.g. heart disease, high blood pressure, type 2 diabetes) or inflammatory illness * NOTE: If waist circumference falls below 94 cm for men or 80cm for women but BMI is \>25 kg/m2 volunteers may still be recruited at the PI's discretion.

Exclusion criteria

* Smoker * Previous diagnosis of anaemia * Women who are pregnant or lactating * Taking medication known to interfere with study outcomes (e.g. treatment for hyperlidaemia, hypertension, inflammation or hypercoagulation) or prescribed antibiotics within the last 3 months * Taking nutritional supplements known to interfere with study outcomes (e.g. fish oil or evening primrose oil) * Unstable weight history (\>3 kg loss or gain in the previous 3 months) * An allergy to lidocaine * Those with known or suspected food intolerances, allergies or hypersensitivity to any components of the meal (e.g. lactose/wheat intolerance) * Alcohol consumption \>28 units per week for a man or \>21 units per week for a woman * Any other unusual medical history or diet and lifestyle habits or practices that would preclude volunteers from participating in a dietary intervention or metabolic study * Parallel participation in another intervention study

Design outcomes

Primary

MeasureTime frameDescription
Protein expression (content and phosphorylation) of key markers of metabolic inflammation in white adipose tissue (for example assessment of NFKB/IKBa total protein and phosphorylation by western blot analysis)White adipose tissue samples will be collected at -0.5 (fasted), 1, 4 and 6 hours postprandiallyThis will be assessed following the collection of white adipose tissue samples across the postprandial period

Secondary

MeasureTime frameDescription
Systemic Markers of Inflammation (for example TNFa and IL-6 concentrations, determined using an ELISA)Blood samples will be collected at -0.5 (fasted) until 6 hours postprandiallyThis will be assessed following the collection of blood samples
Gene expression of key markers of metabolic inflammation in white adipose tissueWhite adipose tissue samples will be collected at -0.5 (fasted), 1, 4 and 6 hours postprandiallyThis will be assessed following the collection of white adipose tissue samples
Characterisation of immune cell populations (monocyte subsets) from peripheral blood mononuclear cells (measured using flow cytometry analysis)Blood samples will be collected at -0.5 (fasted) and 4 hours postprandiallyAssessed following the collection of blood samples
Serum Markers of Insulin ResistanceBlood samples will be collected at -0.5 (fasted) until 6 hours postprandiallyAssessed following the collection of blood samples
Serum Lipid Profile (primarily triacylglycerol and non-esterified fatty acid concentrations, measured using a spectrophotometric assay)Blood samples will be collected at -0.5 (fasted) until 6 hours postprandiallyAssessed following the collection of blood samples

Countries

United Kingdom

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026