期刊
JPAD-JOURNAL OF PREVENTION OF ALZHEIMERS DISEASE
卷 8, 期 1, 页码 19-28出版社
EDITIONS SERDI
DOI: 10.14283/jpad.2020.53
关键词
Alzheimer's disease; B-hydroxybutyrate; medium chain triglyceride (MCT); pharmacokinetic; body composition; coconut oil
This study found significant inter-individual variability in BHB response to MCT oil intake, influenced by various factors such as visceral fat, BMI, waist/hip ratio, and nutrient content of pre-study meals. This highlights the challenges in interpreting clinical responses to MCT intake across different age groups and health statuses.
OBJECTIVES, DESIGN, SETTING: The ketogenic effect of medium chain triglyceride (MCT) oil offers potential for Alzheimer's disease prevention and treatment. Limited literature suggests a linear B-hyroxybutyrate (BHB) response to increasing MCT doses. This pharmacokinetic study evaluates factors affecting BHB response in three subject groups. PARTICIPANTS: Healthy subjects without cognitive deficits <65years, similarly healthy subjects >=65years, and those with Alzheimer's Disease were assessed. INTERVENTION: Different doses (0g,14g, 28g, 42g) of MCT oil (99.3% C8:0) were administered, followed by fasting during the study period. Measurements BHB measured by finger prick sampling hourly for 5 hours after ingestion. Each subject attended four different days for each ascending dose. Data was also collected on body composition, BMI, waist/hip ratio, grip strength, gait speed, nutrient content of pre-study breakfast and side effects. RESULTS: Twenty-five participants: eight healthy; average age of 44yr (25-61), nine healthy; 79yr (65-90) and eight with AD; 78.6yr (57-86) respectively. Compiled data showed the expected linear dose response relationship. No group differences, with baseline corrected area under the blood vs. time curve (r(2)=0.98) and maximum concentrations (r(2)=0.97). However, there was notable individual variability in maximum BHB response (42g dose: 0.4 -2.1mM), and time to reach maximum BHB response both, within and between individuals. Variability was unrelated to age, sex, sarcopenic or AD status. Visceral fat, BMI, waist/hip ratio and pretest meal CHO and protein content all affected the BHB response (p<0.001). CONCLUSION: There was a large inter-individual variability, with phenotype effects identified. This highlights challenges in interpreting clinical responses to MCT intake.
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