Microbiome Clinical Trial
Official title:
Effect of Strawberry Consumption on the Microbiome in Healthy Subjects: A Pilot Study
This pilot study will assess the ability of daily consumption of two servings of California strawberries to alter gut microbiome composition, leading to increased bile secretion and decreased plasma cholesterol in a free-living population.
This will be a randomized, double-blinded, placebo controlled, parallel design. Thirty
subjects will be randomized to consume two servings of standardized freeze-dried strawberry
powder (2 x 13g) daily or placebo for 4 weeks, followed by 2 weeks of follow up with beige
diet only to observe whether the effect can be sustained for 2 weeks. Blood will be collected
at baseline (week 0), weeks 4 and week 6 after strawberry consumption. On the day prior to
the study visits participants will collect a stool and a 24-hr urine sample and bring to the
lab. In addition, body weight and composition will be determined and questionnaires and 3-day
food record will be completed. Twenty-four hour urine content of pelargonidin glucuronide
will be measured for compliance. Plasma and fecal cholesterol and bile acids will be
determined at baseline (week 0) and weeks 4 and 6.
Subjects will be assigned an enrollment number after signing the informed consent form
approved by the UCLA Medical Internal Review Board. Subjects will undergo a physical exam,
complete medical history, and blood draw. A standard chem. panel will be performed at the
UCLA clinical laboratory. Eligible subjects will be enrolled into the study upon completion
of screening evaluations and will be randomized to the strawberry or placebo arm at their
baseline visit.
The study will be conducted in healthy free-living subjects (18-55 years). Subjects consume
13 grams standard strawberry powder in the morning and afternoon/evening or placebo powder
for 4 weeks. Subjects will be instructed to eat a beige diet (low fiber<10g and low
polyphenols <3 servings of polyphenol rich fruit/vegetables per day) during the entire study
period. 24 hr urine pelargonidin glucuronide will be measured at weeks 2 (baseline), 6 and 8
for compliance. In addition, pelargondin, ellagic acid, dimethylellagic acid glucuronide and
urolithin glucuronide will be measured in plasma and urine to determine strawberry
phytochemical bioavailability and intestinal/microbiome metabolic capacity. Participants will
meet with the dietitian for assessment of habitual dietary pattern and instructions on
maintain on a beige diet. A list of foods with high fiber and phenolic compounds will be
provided and subjects are instructed to follow the diet during the entirety of the study.
A standardized freeze-dried strawberry powder and a strawberry placebo powder provided by the
California Strawberry Commission will be used. Ten grams of freeze dried powder is equivalent
to about 110 g fresh fruit. One serving of fresh strawberry (one cup) is estimated to weigh
144 g and therefore is equivalent to 13 g of freeze dried powder. Subjects will consume two
packages of 13 g of strawberry powder per day. The powder can be mixed into beverages and
consumed with breakfast and dinner.
Strawberry powder ingredients include Individually Quick Frozen (IQF) strawberries. Placebo
powder ingredients include fructose, sucrose, dextrose, tapioca maltodextrin, modified food
starch, erythritol, cellulose gum, citric acid (anhydrous), N-C Strawberry Flavor Natual
WONF, xanthan gum, malic acid, sugar beet fiber, silicon dioxide, nat. strawberry-type
flavor, FD&C Red #40, FD&C Yellow 6, FD&C Blue 2.
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