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Pilot Study Lp299v Supplementation in Chronic Heart Failure

Primary Purpose

Heart Failure, Heart Failure With Reduced Ejection Fraction, Heart Failure, Systolic

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Lactobacillus Plantarum 299v Freeze Dried Capsule
Freeze Dried Potato Starch Capsule
Sponsored by
Medical College of Wisconsin
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Heart Failure focused on measuring Endothelial Function, Microbiome, Heart Failure, Ejection Fraction

Eligibility Criteria

21 Years - 89 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Age between 21-89 years old Clinical diagnosis of Congestive Heart Failure (CHF) in the six months prior to enrollment along with an echocardiogram documenting systolic dysfunction with ejection fraction ≤40% Clinical diagnosis of CHF in the six months prior to enrollment along with an echocardiogram documenting diastolic dysfunction with an ejection fraction ≥50%, and a H2FpEFF score of ≥6 New York Heart Association (NYHA) Class II-IIID heart failure symptoms with either ischemic or non-ischemic etiology OR similar diagnosis with congestive heart failure (CHF) along with an echocardiogram documenting an LV ejection fraction of 50% or more with similar NYHA classification as those with LVEF of 40% or less Evidence of systemic inflammation at baseline (C-reactive protein ≥ 2 mg/L at the time of screening) Exclusion Criteria: Heart failure due to severe valve disease such as Aortic Stenosis, Mitral Regurgitation, or Mitral Stenosis Cancer besides non-melanoma skin carcinomas or localized prostate and breast cancer at the time of enrollment with life expectancy <1 year Lung disease such as Chronic Obstructive Pulmonary Disease (COPD), emphysema, or Pulmonary fibrosis Active inflammatory disease or infectious disease at the time of enrollment Current treatment (or use within the past 14 days) of steroids or anti-inflammatory treatments (excluding non-steroidal anti-inflammatory medications or steroids used solely for IV contrast dye allergy) Chronic Kidney Disease with eGFR ≤ 30 mL/min Hepatic Failure (Child's Class B or C) Patients with Gastrointestinal (GI) tract illness such as short gut syndrome, inflammatory bowel disease, or an ileostomy, such that probiotic absorption would be altered Anticipated need for cardiac surgery during the projected study period for the subject Pregnancy Patients who are receiving Vitamin K antagonists such as Coumadin or Warfarin Neutropenia (Absolute Neutrophil Count (ANC) < 1800/mm3) Inability to give informed consent or follow the study protocol On antibiotics at the time of enrollment or within one month of enrollment Currently taking a Lactobacillus based probiotic as an outpatient at the time of enrollment Patients who are unable to walk on treadmill or use a bicycle to participate in exercise testing Allergy to Lp299v probiotic supplement

Sites / Locations

  • Medical College of WisconsinRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Lp299v

Placebo Control

Arm Description

Subjects will consume 20 billion colony forming units of Lp299v (2 capsules) once daily for 12 weeks.

Subjects will consume potato starch (2 capsules) once daily for 12 weeks.

Outcomes

Primary Outcome Measures

Maximal Oxygen Consumption (VO2Max)
This is a measurement of exercise capacity
Brachial Artery Flow Mediated Dilation (FMD%)
This is a measurement of endothelial function in the brachial artery
Carotid-Femoral Pulse Wave Velocity (cfPWV)
Measurement of vascular stiffness

Secondary Outcome Measures

Brachial Artery Absolute Flow Mediated Dilation (FMDmm)
This is a measurement of endothelial function in the brachial artery
Resting shear stress of brachial artery
This is a measurement of vascular stiffness
Resting velocity
This is a measurement of vascular stiffness
Change in serum Soluble Suppression Tumorigenesis (SST2)
This measures cardiac fibrosis
Peak flow velocity
This is a measurement of vascular stiffness
Peak Hyperemic Shear Stress of Brachial Artery
This is a measurement of vascular stiffness
Change in Galectin-3
This measures cardiac fibrosis

Full Information

First Posted
February 21, 2023
Last Updated
August 18, 2023
Sponsor
Medical College of Wisconsin
Collaborators
Advancing a Healthier Wisconsin
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1. Study Identification

Unique Protocol Identification Number
NCT05752760
Brief Title
Pilot Study Lp299v Supplementation in Chronic Heart Failure
Official Title
Impact of Lactobacillus Plantarum 299v Probiotic Supplementation on Vascular Function and Exercise Capacity in Chronic Heart Failure With Reduced and Preserved Ejection Fraction.
Study Type
Interventional

2. Study Status

Record Verification Date
August 2023
Overall Recruitment Status
Recruiting
Study Start Date
February 20, 2023 (Actual)
Primary Completion Date
January 1, 2024 (Anticipated)
Study Completion Date
January 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Medical College of Wisconsin
Collaborators
Advancing a Healthier Wisconsin

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal of this study is to determine the impact of 12 weeks of Lp299v supplementation (20 million cfu/day vs. placebo) on exercise capacity, circulating biomarkers of cardiac remodeling, quality of life, and vascular endothelial function in humans with heart failure and reduced ejection fraction (HFrEF) and heart failure with preserved ejection fraction (HFpEF) who have evidence of residual inflammation based on an elevated C-reactive protein level. This will be done in the setting of a randomized, double-blind, placebo-controlled trial.
Detailed Description
Heart failure (HF) has significant morbidity and mortality and is one of the leading causes of hospital admissions in the United States. In 2017, almost 1 million people were affected and responsible for 1.2 million hospitalizations in the United States alone. Prognosis is poor for patients with HF despite significant medical therapy regimens and device therapy. Worldwide, mortality is as high as 17% during initial hospitalization, as high as 45% within one year of admission, and greater than 50% within five years. According to the Wisconsin Department of Health Services, mortality rates for HF have been increasing in the state since 1980. Wisconsin also consistently had higher rates of HF compared to the remaining states. Emerging data suggest targeting the gut microbiota in HF could be a safe and effective alternative for mitigating inflammation. HF patients have increased systemic circulating endotoxins and lipopolysaccharides due to impaired gut-barrier function, secondary to gut congestion and reduced cardiac output, which drives systemic inflammation. The gut flora of patients with HF also includes more pathogenic bacteria species (candida, campylobacter, shigella, and yersinia) compared to patients with normal heart function. Previous studies by the lab showed that supplementation of 20 billion cfu/day of Lactobacillus plantarum 299v (Lp299v) probiotic decreases systemic inflammation in men with stable coronary artery disease (CAD), and also improves vascular endothelial function (measured by endothelium-dependent vasodilation in the brachial artery and by nitric-oxide dependent vasodilation of resistance arterioles from CAD patients). The investigators have shown that there are significantly decreased levels of IL-8, IL-12 and Leptin in Lp299v-supplemented patients with CAD. Leptin is known to increase IL-6 (which drives increased C-reactive protein expression), IL-8, IL-12 and TNF-α levels, all which activate pro-inflammatory immune responses leading to vasoconstriction and vascular stiffness. Further, our data suggests Lp299v has a significant, favorable anti-inflammatory effect on signaling pathways (NLRP3, IL-6, IL-1β) shown to be important to chronic inflammation in heart failure. Therefore, the investigators plan to perform a pilot study targeting the gut microbiota of patients with HF with oral supplementation with 20 billion cfu/day of Lp299 and determine if Lp299v improves peak oxygen consumption (measured by VO2 max testing), endothelial function (measured by brachial artery flow-mediated dilation), and vascular stiffness (measured by peak wave velocity). We plan to test the hypothesis that Lp299v will improve these measures in the setting of a randomized, double-blind, placebo-controlled clinical trial of 20 subjects. The investigators will additionally test if Lp299v supplementation improves circulating biomarkers of inflammation and cardiac remodeling in chronic heart failure, as well as if it improves the quality of life in patients using the Minnesota Living with Heart Failure Questionnaire and the Kansas City Cardiomyopathy Questionnaire.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Heart Failure, Heart Failure With Reduced Ejection Fraction, Heart Failure, Systolic, Heart Failure With Preserved Ejection Fraction, Heart Failure, Diastolic
Keywords
Endothelial Function, Microbiome, Heart Failure, Ejection Fraction

7. Study Design

Primary Purpose
Basic Science
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
20 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Lp299v
Arm Type
Experimental
Arm Description
Subjects will consume 20 billion colony forming units of Lp299v (2 capsules) once daily for 12 weeks.
Arm Title
Placebo Control
Arm Type
Placebo Comparator
Arm Description
Subjects will consume potato starch (2 capsules) once daily for 12 weeks.
Intervention Type
Other
Intervention Name(s)
Lactobacillus Plantarum 299v Freeze Dried Capsule
Intervention Description
The intervention is a probiotic lactobacillus that is contained in food products in the US
Intervention Type
Other
Intervention Name(s)
Freeze Dried Potato Starch Capsule
Intervention Description
The intervention is potato starch that is freeze dried designed to mimic the lp299v capsule.
Primary Outcome Measure Information:
Title
Maximal Oxygen Consumption (VO2Max)
Description
This is a measurement of exercise capacity
Time Frame
12 weeks
Title
Brachial Artery Flow Mediated Dilation (FMD%)
Description
This is a measurement of endothelial function in the brachial artery
Time Frame
12 weeks
Title
Carotid-Femoral Pulse Wave Velocity (cfPWV)
Description
Measurement of vascular stiffness
Time Frame
12 weeks
Secondary Outcome Measure Information:
Title
Brachial Artery Absolute Flow Mediated Dilation (FMDmm)
Description
This is a measurement of endothelial function in the brachial artery
Time Frame
12 weeks
Title
Resting shear stress of brachial artery
Description
This is a measurement of vascular stiffness
Time Frame
12 weeks
Title
Resting velocity
Description
This is a measurement of vascular stiffness
Time Frame
12 weeks
Title
Change in serum Soluble Suppression Tumorigenesis (SST2)
Description
This measures cardiac fibrosis
Time Frame
12 weeks
Title
Peak flow velocity
Description
This is a measurement of vascular stiffness
Time Frame
12 weeks
Title
Peak Hyperemic Shear Stress of Brachial Artery
Description
This is a measurement of vascular stiffness
Time Frame
12 weeks
Title
Change in Galectin-3
Description
This measures cardiac fibrosis
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
89 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age between 21-89 years old Clinical diagnosis of Congestive Heart Failure (CHF) in the six months prior to enrollment along with an echocardiogram documenting systolic dysfunction with ejection fraction ≤40% Clinical diagnosis of CHF in the six months prior to enrollment along with an echocardiogram documenting diastolic dysfunction with an ejection fraction ≥50%, and a H2FpEFF score of ≥6 New York Heart Association (NYHA) Class II-IIID heart failure symptoms with either ischemic or non-ischemic etiology OR similar diagnosis with congestive heart failure (CHF) along with an echocardiogram documenting an LV ejection fraction of 50% or more with similar NYHA classification as those with LVEF of 40% or less Evidence of systemic inflammation at baseline (C-reactive protein ≥ 2 mg/L at the time of screening) Exclusion Criteria: Heart failure due to severe valve disease such as Aortic Stenosis, Mitral Regurgitation, or Mitral Stenosis Cancer besides non-melanoma skin carcinomas or localized prostate and breast cancer at the time of enrollment with life expectancy <1 year Lung disease such as Chronic Obstructive Pulmonary Disease (COPD), emphysema, or Pulmonary fibrosis Active inflammatory disease or infectious disease at the time of enrollment Current treatment (or use within the past 14 days) of steroids or anti-inflammatory treatments (excluding non-steroidal anti-inflammatory medications or steroids used solely for IV contrast dye allergy) Chronic Kidney Disease with eGFR ≤ 30 mL/min Hepatic Failure (Child's Class B or C) Patients with Gastrointestinal (GI) tract illness such as short gut syndrome, inflammatory bowel disease, or an ileostomy, such that probiotic absorption would be altered Anticipated need for cardiac surgery during the projected study period for the subject Pregnancy Patients who are receiving Vitamin K antagonists such as Coumadin or Warfarin Neutropenia (Absolute Neutrophil Count (ANC) < 1800/mm3) Inability to give informed consent or follow the study protocol On antibiotics at the time of enrollment or within one month of enrollment Currently taking a Lactobacillus based probiotic as an outpatient at the time of enrollment Patients who are unable to walk on treadmill or use a bicycle to participate in exercise testing Allergy to Lp299v probiotic supplement
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Michael E Widlansky, MD
Phone
414-955-6759
Email
mwidlans@mcw.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Michael M Aljadah, MD
Phone
414-955-6982
Email
maljadah@mcw.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Michael E Widlansky, MD
Organizational Affiliation
Medical College of Wisconsin
Official's Role
Principal Investigator
Facility Information:
Facility Name
Medical College of Wisconsin
City
Milwaukee
State/Province
Wisconsin
ZIP/Postal Code
53226
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Michael E Widlansky, MD
Phone
414-955-6759
Email
mwidlans@mcw.edu
First Name & Middle Initial & Last Name & Degree
Michael M Aljadah, MD
Phone
414-955-6982
Email
maljadah@mcw.edu

12. IPD Sharing Statement

Plan to Share IPD
Yes
IPD Sharing Time Frame
Within 1 year of completion of all studies procedures
Citations:
PubMed Identifier
33566058
Citation
Agarwal MA, Fonarow GC, Ziaeian B. National Trends in Heart Failure Hospitalizations and Readmissions From 2010 to 2017. JAMA Cardiol. 2021 Aug 1;6(8):952-956. doi: 10.1001/jamacardio.2020.7472.
Results Reference
background
PubMed Identifier
27340274
Citation
Dick SA, Epelman S. Chronic Heart Failure and Inflammation: What Do We Really Know? Circ Res. 2016 Jun 24;119(1):159-76. doi: 10.1161/CIRCRESAHA.116.308030.
Results Reference
background
Citation
Wisconsin Heart Disease and Stroke Prevention Program, February 2010. www.dhs.wisconsin.gov/publications/p0/p00146.pdf
Results Reference
background
PubMed Identifier
26682791
Citation
Pasini E, Aquilani R, Testa C, Baiardi P, Angioletti S, Boschi F, Verri M, Dioguardi F. Pathogenic Gut Flora in Patients With Chronic Heart Failure. JACC Heart Fail. 2016 Mar;4(3):220-7. doi: 10.1016/j.jchf.2015.10.009. Epub 2015 Dec 9.
Results Reference
background
PubMed Identifier
33597583
Citation
Hofeld BC, Puppala VK, Tyagi S, Ahn KW, Anger A, Jia S, Salzman NH, Hessner MJ, Widlansky ME. Lactobacillus plantarum 299v probiotic supplementation in men with stable coronary artery disease suppresses systemic inflammation. Sci Rep. 2021 Feb 17;11(1):3972. doi: 10.1038/s41598-021-83252-7.
Results Reference
background
PubMed Identifier
20198122
Citation
Iikuni N, Lam QL, Lu L, Matarese G, La Cava A. Leptin and Inflammation. Curr Immunol Rev. 2008 May 1;4(2):70-79. doi: 10.2174/157339508784325046.
Results Reference
background
PubMed Identifier
10357875
Citation
Santos-Alvarez J, Goberna R, Sanchez-Margalet V. Human leptin stimulates proliferation and activation of human circulating monocytes. Cell Immunol. 1999 May 25;194(1):6-11. doi: 10.1006/cimm.1999.1490.
Results Reference
background
Citation
Spertus, J., Kansas City Cardiomyopathy Questionnaire MDDT decision summary. <fda.gov>
Results Reference
background
Citation
Thomas, R, Cohn, J., Minnesota Living with Heart Failure Questionnaire <license.umn.edu/product/minnesota-living-with-heart-fialure-questionnaire-mlhfq>
Results Reference
background

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Pilot Study Lp299v Supplementation in Chronic Heart Failure

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