The Role of Gut Microbiota in Heart Failure and Pre-Heart Failure With Preserved Ejection Fraction

Sponsor
University of Florida (Other)
Overall Status
Recruiting
CT.gov ID
NCT02728154
Collaborator
National Heart, Lung, and Blood Institute (NHLBI) (NIH)
220
1
104.2
2.1

Study Details

Study Description

Brief Summary

Gut microbiota play an important role in normal cardiovascular function and pathophysiology of cardiovascular diseases. Patients with heart failure (HF) have substantial hemodynamic changes which lead to intestinal hypoperfusion and congestion and eventually change gut morphology, permeability, function and composition of gut microbiota and cause translocation of microbial and endotoxins into the blood stream. Additionally, metabolites derived from gut microbiota modulate the pathophysiology of HF. Patients with HF have intestinal overgrowth of pathogenic bacteria and increased gut permeability. Accumulating evidence demonstrates that antibiotic treatment benefits patients with acute coronary syndromes and reduces the incidence of ischemic cardiovascular events. Taking the strong association of gut microbiota with HF into account, it is reasonable to speculate that gut microbiota could contribute to the progression of pre-HF with preserved ejection fraction (pre-HFpEF) to HF with preserved ejection fraction (HFpEF). Pre-HFpEF remains poorly understood, yet has high prevalence and a significantly high risk for death in comparison to patient without pre-HFpEF. We hypothesize that altered gut microbiota is involved in the initiation and establishment of HF and pre-HFpEF.

Condition or Disease Intervention/Treatment Phase
  • Other: Blood Sample
  • Other: Stool Sample

Detailed Description

The research study will initially enroll 50 subjects without HF as normal controls,120 subjects with history of HF and 50 subjects with pre-HFpEF to characterize gut microbiota. The subjects will provide blood samples and a stool sample.

Study Design

Study Type:
Observational
Anticipated Enrollment :
220 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Characterize the Gut Microbiota in Subjects With Heart Failure and Pre-heart Failure With Preserved Ejection Fraction
Actual Study Start Date :
Oct 1, 2016
Anticipated Primary Completion Date :
Jun 8, 2025
Anticipated Study Completion Date :
Jun 8, 2025

Arms and Interventions

Arm Intervention/Treatment
Normal control

The subjects in the normal heart function group will provide a blood sample and stool sample.

Other: Blood Sample
One tablespoon of blood will be drawn once during the study.

Other: Stool Sample
One stool sample will be collected.

heart failure

The subjects in history of heart failure group will provide a blood sample and stool sample.

Other: Blood Sample
One tablespoon of blood will be drawn once during the study.

Other: Stool Sample
One stool sample will be collected.

pre-HFpEF

The subjects in history of diastolic dysfunction but not had heart failure clinical presentations group will provide a blood sample and stool sample.

Other: Blood Sample
One tablespoon of blood will be drawn once during the study.

Other: Stool Sample
One stool sample will be collected.

Outcome Measures

Primary Outcome Measures

  1. Stool sample for fecal microbiota between the groups [Day 1]

    Stool samples will be collected to compare the fecal microbiota of subjects with normal, diastolic heart dysfunction before heart failure developed and heart failure.

Secondary Outcome Measures

  1. Blood samples for inflammatory cytokines between the groups [Day 1]

    Blood samples will be used to compare difference in inflammatory cytokines including Interleukin-1 (IL-1), 6, 17 between groups using ELISA kits.

  2. Blood samples for SAA between the groups [Day 1]

    Blood samples will be used to compare difference in serum amyloid (SAA) a between groups using ELISA kits.

  3. Blood samples for inflammatory cells between the groups [Day 1]

    Blood samples will be used for difference in progenitor/inflammatory cells between the groups.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Competent and willing to provide consent

  • Control subjects with normal heart function

  • Subjects with history of HF

  • Subjects with impaired ventricular relaxation and/or elevated left ventricular end diastolic pressure measured by echocardiography and/or catheterization, yet has not had HF clinical presentations

Exclusion Criteria:
  • intestinal surgery,

  • inflammatory bowel disease,

  • celiac disease,

  • lactose intolerance,

  • chronic pancreatitis or

  • other malabsorption disorder

Contacts and Locations

Locations

Site City State Country Postal Code
1 Cardiovascular Clinic at UF Health Gainesville Florida United States 32610

Sponsors and Collaborators

  • University of Florida
  • National Heart, Lung, and Blood Institute (NHLBI)

Investigators

  • Principal Investigator: Carl J Pepine, MD, University of Florida

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
University of Florida
ClinicalTrials.gov Identifier:
NCT02728154
Other Study ID Numbers:
  • IRB201600380 - N
  • 5R01HL132448
First Posted:
Apr 5, 2016
Last Update Posted:
Jul 7, 2022
Last Verified:
Jul 1, 2022
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Keywords provided by University of Florida
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 7, 2022