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N/A N=24 Randomized Triple-blind Basic Science

Effect of Lactose on Blood Lipids

Cardiovascular Risk Factor · Lipaemia · Metabolic Disease

Enrolled (actual)
24
Serious AEs
0.0%
Results posted
Sep 2024
Primary outcome: Primary: Postprandial Changes in Plasma Triglyceride Concentrations — 51; 90; 98 mmol/L x 360 min

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Maltodextrin (Dietary_supplement); Sucrose (Dietary_supplement); Lactose (Dietary_supplement)
Age
Adult · 18+ yrs
Sex
All
Sponsor
University of Bath
Primary completion
Jul 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Postprandial Changes in Plasma Triglyceride Concentrations
51; 90; 98
SECONDARY
Postprandial de Novo Lipogenesis (DNL)
SECONDARY
Dietary Fat Oxidation
SECONDARY
Postprandial Changes in Plasma Insulin Concentrations
SECONDARY
Postprandial Changes in Plasma Glucose Concentrations
SECONDARY
Postprandial Changes in Plasma Galactose Concentrations
SECONDARY
Postprandial Changes in Plasma Fructose Concentrations
SECONDARY
Postprandial Changes in Plasma VLDL-rich Triglyceride [Svedberg Flotation Rate (Sf): 20-400] Concentrations
SECONDARY
Postprandial Changes in Plasma Chylomicron-rich Triglyceride (Sf: >400) Concentrations
SECONDARY
Postprandial Changes in Plasma Lactate Concentrations
SECONDARY
Postprandial Changes in Plasma Non-esterified Fatty Acid Concentrations
SECONDARY
Postprandial Changes in Plasma Beta-hydroxybutyrate Concentrations
SECONDARY
Postprandial Changes in Plasma Uric Acid Concentrations

Summary

This study aims to determine to what extent ingestion of free sugars influence postprandial triglyceridaemia in men and women.

Eligibility Criteria

Inclusion Criteria

  • Age: 18-50 years and premenopausal (for women)

Exclusion criteria

  • Weight instability (>5 kg change in body mass within last 6 months)
  • Diagnosis of any form of diabetes
  • Intolerances or allergies to any of the study procedures (e.g. lactose intolerance)
  • Galactose disorders (e.g. galactokinase deficiency, UDPgalactose-4-epimerase deficiency, galactose-1-phosphate uridyl transferase deficiency)
  • Fructose malabsorption
  • Inborn errors of fructose metabolism (e.g. fructokinase deficiency, aldolase B deficiency, fructose-1,6-bisphosphatase deficiency)
  • Pregnant or lactating
  • Any condition that could introduce bias to the study (e.g. diagnoses of lipid disorders, including cardiovascular disease, or therapies that alter lipid or glucose metabolism, such as statins or niacin).
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT04924530). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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