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Exercise Training Influences Gut Microbiota and Cardiovascular Health Through Inflammation Control in Adult Hypertensive Population: the MicroFit Study

Primary Purpose

Hypertension, Microbiota

Status
Recruiting
Phase
Not Applicable
Locations
Italy
Study Type
Interventional
Intervention
exercise training
Probiotics
Placebo
Sponsored by
University of Bologna
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Hypertension focused on measuring hypertension, gut microbiota, exercise training, physical activity, central hemodynamics, arterial stiffness, pulse wave velocity

Eligibility Criteria

40 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Arterial hypertension*; Stable antihypertensive therapy in the last 2 months, with controlled blood pressure values; Age 40-65 years; Willing to sign the written informed consent; Written and spoken Italian language comprehension. Exclusion Criteria: Atrial fibrillation; Diabetes mellitus either type I or II; Active cancer; Inflammatory bowel disease; Heart failure NYHA class III to IV; Recent antibiotic or probiotic treatment in the previous month for any reason; Recent myocardial infarction or hospital admission for any other reason in the previous 6 months; Any other condition that the medical doctor (MD) considers to contraindicate the participation in an exercise program of High intensity; Pulmonary disease requiring oxygen therapy; Relevant neurological condition impairing motor or cognitive function; Severe depressive disorder; Pregnancy.

Sites / Locations

  • University of BolognaRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Active Comparator

Placebo Comparator

Arm Label

Exercise training

Probiotics

Placebo

Arm Description

high intensity interval training: thrice a week

VSL#3# probiotic: twice daily

Comparator of the Probiotics arm

Outcomes

Primary Outcome Measures

To describe the modification of the gut microbiota composition and function after the exercise training compared to probiotic supplements and to placebo.
Changes in measures of gut microbiota composition and function from time 0 to 3 months (alpha diversity, beta diversity, taxonomy, relative abundance of microbial genes and pathways)

Secondary Outcome Measures

To describe the association between gut microbiota patterns with impaired central hemodynamics
To measure the association of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, with central hemodynamics parameters (central blood pressure, aortic stiffness, pulse pressure amplification, augmentation index).
To test the association of the systemic inflammation with the modification of gut microbiota composition/functionality.
To test the association between inflammatory markers (alpha-1-acid glycoprotein, high-sensitive c-reactive protein) and gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways.
To test the modification of endothelial function after the exercise training in comparison to probiotic supplements and placebo.
To measure variation in endothelial glycocalyx thickness before and after 3-mo intervention
To identify the variation of the gut microbiota composition and function in the long term follow up after the intervention
Measures of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways at the end of the intervention (3 months) and after the 9-mo follow up.
To describe the association between gut microbiota patterns with impaired central hemodynamics in the long term follow up 6 months after the intervention
To measure the association of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, with central hemodynamics parameters (central blood pressure, aortic stiffness, pulse pressure amplification, augmentation index)
To test the association of the systemic inflammation with the modification of gut microbiota composition/functionality, after the long term follow up 6 months after the intervention.
To test the association between inflammatory markers (alpha-1-acid glycoprotein, high-sensitive c-reactive protein) and gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, at 9-mo follow up.
To test the modification of endothelial function after the exercise training in comparison to probiotic supplements and placebo, after the long term follow up 6 months after the intervention
To measure variation in endothelial glycocalyx thickness at 9-mo follow up

Full Information

First Posted
June 16, 2023
Last Updated
July 21, 2023
Sponsor
University of Bologna
Collaborators
Actial Farmaceutica S.r.l.
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1. Study Identification

Unique Protocol Identification Number
NCT05967715
Brief Title
Exercise Training Influences Gut Microbiota and Cardiovascular Health Through Inflammation Control in Adult Hypertensive Population: the MicroFit Study
Official Title
Exercise Training Influences Gut Microbiota and Cardiovascular Health Through Inflammation Control in Adult Hypertensive Population: the MicroFit Study
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 3, 2023 (Actual)
Primary Completion Date
April 2, 2026 (Anticipated)
Study Completion Date
April 2, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Bologna
Collaborators
Actial Farmaceutica S.r.l.

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Cardiovascular diseases are the number 1 cause of death globally, taking an estimated 17.9 million lives each year (31% of deaths worldwide). Hypertension, with 1.13 billion people affected worldwide, is the leading risk factor for global mortality. Physical inactivity is among the modifiable cardiovascular risk factors. While the beneficial effects of physical activity on cardiovascular system are widely known, the mechanisms involved are not completely understood. Both exercise training and hypertension are linked to inflammation. Furthermore, there is evidence that gut microbiota regulates inflammatory patterns. Recent investigations showed a relationship between exercise training and the composition/functionality of the gut microbiota. Anyway, the modification of the composition and functionality of the gut microbiota in hypertension due to the exercise training and the relative involvement of oxidative stress and inflammation are not completely understood. In literature an association between gut microbiota composition and arterial stiffness is described, in particular, the investigators observed both a direct correlation between arterial stiffness and abundances of bacteria associated with altered gut permeability and inflammation; and an inverse relationship between arterial stiffness, microbiota diversity, and abundances of bacteria associated with most fit microbiota composition. Anyway, while these association were stable in animal studies, in human studies none of the identified interventional trials was able to demonstrate this relationship. Of note, only half of human studies measured BP, and very few adjusted the vascular analyses for BP variation, which is a major determinant of arterial stiffness. This is a non-profit, monocentric, non-pharmacological interventional study, a randomized controlled trial with three intervention arms, partial double-blind, aiming to verify the hypothesis that, in hypertensive patients in primary prevention with cardiovascular risk factors, physical exercise favorably modifies the intestinal bacterial flora compared to the probiotic, with a positive impact on cardiovascular health, and to demonstrate that this involves inflammation modulation. There will be 3 intervention arms, with 1:1:1 stratified randomization by gender: 1. Administration of controlled physical activity training; 2. Administration of probiotic; 3. Administration of placebo. Arms 2 and 3 will be double-blind. The intervention will last for three months, followed by a 6-month follow-up period. Afterwards, the medical team may be contacted for further tests/assessments or simply for information about the participant's health status, for a total duration of 24 months. The investigators hypothesize that hypertensive patients in cardiovascular primary prevention have a dysbiotic gut microbial signatures, that could be a new marker of early vascular aging. Secondly, the investigators anticipate that exercise training will modify both gut microbiota and hemodynamic profile, and that a relationship exists between gut microbiota and hemodynamic modifications. Thirdly, the investigators expect that the beneficial effects of exercise training are driven by positive changes in the inflammatory modulators.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hypertension, Microbiota
Keywords
hypertension, gut microbiota, exercise training, physical activity, central hemodynamics, arterial stiffness, pulse wave velocity

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
Only for the "probiotics" and "placebo" arms
Allocation
Randomized
Enrollment
75 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Exercise training
Arm Type
Experimental
Arm Description
high intensity interval training: thrice a week
Arm Title
Probiotics
Arm Type
Active Comparator
Arm Description
VSL#3# probiotic: twice daily
Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Comparator of the Probiotics arm
Intervention Type
Behavioral
Intervention Name(s)
exercise training
Intervention Description
high intensity interval training
Intervention Type
Other
Intervention Name(s)
Probiotics
Intervention Description
VSL#3# Probiotic
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Probiotic Placebo
Primary Outcome Measure Information:
Title
To describe the modification of the gut microbiota composition and function after the exercise training compared to probiotic supplements and to placebo.
Description
Changes in measures of gut microbiota composition and function from time 0 to 3 months (alpha diversity, beta diversity, taxonomy, relative abundance of microbial genes and pathways)
Time Frame
time 0 and 3 months
Secondary Outcome Measure Information:
Title
To describe the association between gut microbiota patterns with impaired central hemodynamics
Description
To measure the association of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, with central hemodynamics parameters (central blood pressure, aortic stiffness, pulse pressure amplification, augmentation index).
Time Frame
time 0 and 3 months
Title
To test the association of the systemic inflammation with the modification of gut microbiota composition/functionality.
Description
To test the association between inflammatory markers (alpha-1-acid glycoprotein, high-sensitive c-reactive protein) and gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways.
Time Frame
time 0 and 3 months
Title
To test the modification of endothelial function after the exercise training in comparison to probiotic supplements and placebo.
Description
To measure variation in endothelial glycocalyx thickness before and after 3-mo intervention
Time Frame
time 0, and 3 months
Title
To identify the variation of the gut microbiota composition and function in the long term follow up after the intervention
Description
Measures of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways at the end of the intervention (3 months) and after the 9-mo follow up.
Time Frame
from 3 to 9 months.
Title
To describe the association between gut microbiota patterns with impaired central hemodynamics in the long term follow up 6 months after the intervention
Description
To measure the association of gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, with central hemodynamics parameters (central blood pressure, aortic stiffness, pulse pressure amplification, augmentation index)
Time Frame
at 9-mo follow up
Title
To test the association of the systemic inflammation with the modification of gut microbiota composition/functionality, after the long term follow up 6 months after the intervention.
Description
To test the association between inflammatory markers (alpha-1-acid glycoprotein, high-sensitive c-reactive protein) and gut microbiota diversity indexes, taxonomy, relative abundance of microbial genes and pathways, at 9-mo follow up.
Time Frame
at 9-mo follow up
Title
To test the modification of endothelial function after the exercise training in comparison to probiotic supplements and placebo, after the long term follow up 6 months after the intervention
Description
To measure variation in endothelial glycocalyx thickness at 9-mo follow up
Time Frame
at 9-mo follow up

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Arterial hypertension*; Stable antihypertensive therapy in the last 2 months, with controlled blood pressure values; Age 40-65 years; Willing to sign the written informed consent; Written and spoken Italian language comprehension. Exclusion Criteria: Atrial fibrillation; Diabetes mellitus either type I or II; Active cancer; Inflammatory bowel disease; Heart failure NYHA class III to IV; Recent antibiotic or probiotic treatment in the previous month for any reason; Recent myocardial infarction or hospital admission for any other reason in the previous 6 months; Any other condition that the medical doctor (MD) considers to contraindicate the participation in an exercise program of High intensity; Pulmonary disease requiring oxygen therapy; Relevant neurological condition impairing motor or cognitive function; Severe depressive disorder; Pregnancy.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Davide Agnoletti, PhD
Phone
00390512145597
Email
davide.agnoletti2@unibo.it
Facility Information:
Facility Name
University of Bologna
City
Bologna
ZIP/Postal Code
40138
Country
Italy
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Davide Agnoletti, PhD
Phone
00390512145579
Email
davide.agnoletti2@unibo.it

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Exercise Training Influences Gut Microbiota and Cardiovascular Health Through Inflammation Control in Adult Hypertensive Population: the MicroFit Study

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