Metabolic Syndrome Clinical Trial
Official title:
Acute Effects of Dietary Fats and Carbohydrate on Insulinaemia, Lipaemia, Inflammatory Responses and Gastrointestinal Peptide Secretion in Subjects With Metabolic Syndrome
There is increasing evidence suggests that elevated levels of postprandial triacylglycerol (TAG)-rich lipoproteins may promote the development of cardiovascular diseases (CVD). A prolonged and elevated postprandial lipemia is associated with increased risk of CVD by a variety of mechanisms such as insulin resistance, inflammation, endothelial dysfunction and oxidative stress. However, current evidence on the acute effects of type of fats on postprandial insulinaemia, gastrointestinal peptide secretion, inflammatory response, as well as satiation are limited and inconsistent, in particular in metabolic syndrome population in Asian. Hence, this study aimed to investigate the postprandial effects of high fat meals enriched with i) palm olein, ii) high oleic sunflower oil, and iii) high linoleic sunflower oil, compared with a low fat/high carbohydrate meal, in 30 subjects with metabolic syndrome.
A randomized, double-blind, crossover design study was conducted to test the acute effects
of high fat meals enriched with (1) saturated fatty acids (SFA); (2) monounsaturated fatty
acids (MUFA); (3) polyunsaturated fatty acids (PUFA) vs. (4) a low fat/high carbohydrate
(CARB) meal on postprandial insulinaemic, lipaemic and inflammatory responses, as well as
gastrointestinal peptide secretion and satiation on 30 metabolic syndrome subjects (15 men
and 15 women). Primary outcome of this study is postprandial changes of C-peptide. Other
measured outcomes including insulin and glucose responses, lipids, cytokines and
gastrointestinal peptides. Subjective appetite measurements were taken as exploratory
outcomes using visual analogue scales.
Subjects were asked to participate in four postprandial challenges, separated by at least
one week. On the day preceding the postprandial intervention, subjects were provided a low
fat meal (< 10 g) to consume as their evening meal. They were required to fast over night
after 10 pm and arrive at the research unit at 7:30 am - 9:00 am the following morning.
Fasting blood samples were collected and subjects were instructed to consume the allocated
test meal within 10 minutes. Further venous blood will be collected at regular intervals for
up to 6 hours postprandially. During the 6 hours of the experimental study, the subjects
were refrained from the consumption of any food or drink except plain water which they will
be asked to consume at regular intervals (up to 750 mL over the 6 hours).
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Allocation: Randomized, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Prevention
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