Effects of an Organic Plant-rich Diet on Gut Microbiome and Vascular Function (ORGAMIC Pilot Study)

Healthy Men and Women Clinical Trial

Official title:

Effects of an Organic Plant-rich Diet on Gut Microbiome and Vascular Function: the ORGAMIC Pilot Study

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04276974
• Other study ID #: HR-19/20-14
• Status: Completed
• Phase: N/A
• Start date: February 24, 2020
• Est. completion date: July 17, 2021

Study information

• Verified date: March 2022
• Source: King's College London
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Previous work have shown that consumption of foods rich in polyphenols, such as berries and cocoa, led to beneficial changes in the gut microbiota composition, as well as improvements in biomarkers of cardiovascular disease risk in healthy volunteers. In addition, recent studies suggest that pesticide exposure has a detrimental effect on the gut microbiome in human populations and laboratory animals.The aim of this pilot study is to investigate the effects of short-term consumption of an organic and a non-organic plant rich diet on urinary polyphenol and pesticide levels, gut microbiome and selected biomarkers of cardiovascular health in a group of young healthy individuals. Healthy men and women participants (10) will be recruited for a 2-arm randomised crossover controlled trial. Urinary polyphenol and pesticide levels after consumption of an organic and non-organic plant rich diet for 4 days will be analysed. Changes in gut microbiome composition and biomarkers of cardiovascular disease risk (flow-mediated dilation, blood pressure and arterial stiffness) will also be investigated.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 17
• Est. completion date: July 17, 2021
• Est. primary completion date: July 17, 2021
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 40 Years

Eligibility

Inclusion Criteria:

• Healthy men and women aged 20-40 years old.
• Body mass index between 18.5 and 30 kg/m2.
• Non-smokers
• Not already participating in a clinical trial.
• No diagnosed heart attack, stroke, angina, thrombosis, liver or kidney diseases, diabetes, chronic gastrointestinal disorder or cancer.
• Not currently taking any medication
• No history of excess alcohol intake or substance abuse.
• Happy to follow dietary instructions before and during the study and to attend the research centre for breakfast and lunch for a total of 10 days.
• Ability to prepare basic meals from ingredients provided.
• No food intolerances, allergies, hypersensitivity or follow any dietary restriction (e.g. gluten intolerance, coeliac, lactose intolerance) that will prevent your ability to follow the test diets.
• Weight stable (no weight change by more than 3 kg in the last 2 months).
• No travel arrangements outside the United Kingdom (UK) within the period of data collection.
• Able to understand the information sheet and willing to comply with study protocol.
• Able to give informed written consent.

Exclusion Criteria:

• Women who are pregnant, intending to become pregnant, or breastfeeding.
• Participation in another clinical trial - Unable to comply with the study protocol.
• Weight change >3kg in preceding 2 months and body mass index <18.5 or >30 kg/m2
• Current smokers, or reported giving up smoking within the last 6 months History of substance abuse, previous or current high alcohol intake (>28 units/week for males and >21 units/week for females).
• Reported history of Cardiovascular disease, diabetes, cancer, kidney, liver or bowel disease, gastrointestinal disorder or use of drug likely to alter gastrointestinal function)
• Blood pressure =160/100 mmHg
• Travel arrangements outside UK within the period of data collection.

Related Conditions & MeSH terms

• Healthy Men and Women

Intervention

Other:
• Organic diet
Organic plant-rich foods (2000kcal for women, 2500kcal for men)
• Non-organic diet
Likewise Non-organic plant-rich foods (2000kcal for women, 2500kcal for men)

Locations

Country	Name	City	State
United Kingdom	Department of Nutritional Sciences, School of Life Course Sciences, Faculty of Life Sciences and Medicine, King's College London	London

Sponsors (1)

Lead Sponsor	Collaborator
King's College London

Country where clinical trial is conducted

United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Changes in urinary pesticides levels	Determine changes in urinary pesticides levels after consumption of organic plant-rich diet for 4 days measuring by chromatography coupled with mass spectrometry analytical techniques (HPLC-MS)	Baseline & 4 days after
Primary	Changes in urinary polyphenol levels	Determine changes in urinary polyphenol profiles after consumption of organic or non-organic plant-rich diet for 4 days measuring by chromatography coupled with mass spectrometry analytical techniques (HPLC-MS)	Baseline & 4 days after
Primary	Changes in gut microbiome composition	To determine the changes of the composition and diversity of gut microbiome (genus & species) in faecal samples collected from participants via microbiome analysis after consumption of organic or non-organic plant-rich diet for 4 days	Baseline & 4 days after
Secondary	Changes in flow-mediated-dilation (FMD) in the brachial artery	Determine changes in flow mediated dilation (FMD) of the brachial artery using a 12 MHz ultrasound transducer (Vivid I) coupled with a sphygmomanometer cuff after consumption of organic or non-organic plant-rich diet for 4 days	Baseline & 4 days after
Secondary	Changes in blood pressure	Determine changes in systolic and diastolic blood pressure after consumption of organic or non-organic plant-rich diet for 4 days	Baseline & 4 days after
Secondary	Changes in pulse wave velocity (PWV)	Determine changes in arterial stiffness via applanation tonometry after consumption of organic or non-organic plant-rich diet for 4 days. Carotid-femoral pulse wave velocity (cfPWV) will be measured using the SphygmoCor CvMS tonometer to produce PWV readings in m/s	Baseline & 4 days after
Secondary	Change in augmentation Index (AIx)	Determine the changes on augmentation Index (AIx) using a Sphygmocor device, after consumption of organic or non-organic plant-rich diet for 4 days	Baseline & 4 days after