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Completed

NCT Number: NCT03719794

Probiotics for Vascular Inflammation in Metabolic Syndrome

Subjects with metabolic syndrome are known to possess chronic low-level inflammation. Furthermore, such individuals are at risk of developing atherosclerosis in coronary and other vascular beds. In particular, subjects with metabolic syndrome, prediabetes and type II diabetes mellitus were shown to possess vascular inflammation in carotid atherosclerosis as demonstrated using FDG-PET. In the current pilot proposal, the investigators wish to study the impact of 3-month probiotic supplementation on vascular and systemic inflammation in subjects with metabolic syndrome in the context of a randomized, placebo-controlled, pilot trial.

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Key information

Age range

50 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Cardiovascular Prevention and Rehabilitation Center

Montreal, Quebec, H1T 1N6, Canada

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male and female age > 50 years
  • Presence of MetS as defined according to recent updated criteria (13): Presence of at least three of five criteria, namely abdominal obesity (waist circumference cut-off) depending on the recently published ethnic-based variations (14), triglycerides > 1.70 mmol/l, decreased HDL-cholesterol (< 1.0 mmol/l in men and < 1.3 mmol/l in women), systolic blood pressure > 130 mmHg or diastolic blood pressure > 85 mmHg, and FPG > 5.6 mmol/l.
  • Willingness to complete questionnaires, records, and diaries associated with the study and to complete all clinic visits.
  • Willingness to discontinue consumption of fermented foods or probiotics (e.g. yoghourts, with live, active cultures or supplements).
  • Able to provide informed consent.

Exclusion criteria

  • Concurrent consumption of fermented foods or probiotics (e.g. yoghourts, with live, active cultures or supplements). Subjects will be eligible for participation, however, after a two-week washout period
  • Overt or documented vascular disease (coronary heart disease, cerebrovascular disease, or peripheral vascular disease).
  • Participants suffering from dementia (mini mental state examination) or depression (geriatric depression scale).
  • Concurrent statin therapy. (Statins have been shown to reduce vascular inflammation as measured by FDG-PET-see section 9.1).
  • Color blind
  • Concurrent antibiotic therapy. However, screened participants would be eligible to participate two weeks after completing their course of antibiotics (wash-out period).
  • Known to be pregnant or breast-feeding or planning on becoming pregnant in the next 18 months.
  • Women of childbearing potential not using effective contraception. Acceptable methods of birth control includes:
  • Hormonal contraceptives including combined oral contraceptives, hormone birth control patch, vaginal contraceptive ring, injectable contraceptives, or hormonal implants;
  • Intrauterine devices (IUD) or Intrauterine system (IUS);
  • Tubal ligation;
  • Vasectomy of partner;
  • Double barrier method (use of physical barrier by both partners, e.g. male condom and diaphragm, male condom and cervical cap).
  • Positive pregnancy test in women of childbearing potential.
  • Allergy to milk, soy, or yeast.
  • Use of another investigational product within 3 months of the screening visit.
  • Claustrophobia
  • Patient with pacemaker
  • Patient with BMI greater than 40 kg/m2
  • Immune disorder.
  • Drug and alcohol abuse
  • Current use of NSAIDs
  • Liver and kidney disorders
  • Bleeding/blood disorder

Treatment and study plan

Probiotic supplement

Dietary Supplement

Probiotic supplement once daily (xyz) for 12 weeks

Placebo supplement

Dietary Supplement

Placebo supplement once daily for 12 weeks

Primary outcomes

  1. The primary outcome is to evaluate the change on vascular inflammation (measured by FDG-PET), so as to test the hypothesis that probiotic treatment reduces vascular inflammation in comparison to placebo.

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    PET-CT scan of the carotid arteries and ascending thoracic aorta will be performed 2 hours post I.V. The participant will be injected with 18F-FDG.

Secondary outcomes

  1. Mesure of High-sensitivity C-reactive protein (hs-CRP) a systemic inflammatory marker.

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Change with hs-CRP

  2. Mesure of Tumor necrosis factor alpha (TNF-α) a systemic inflammatory marker.

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Change with TNF-α

  3. Mesure of Matrix metallopeptidase 9 (MMP-9)

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Change with MMP-9

  4. Cognitive function at rest by a standard pen-paper battery test.

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Cognitive functions will be measured at rest with a pen-paper battery test by a neuropsychologist. The investigators will measure change of score to the cognitive tests.

  5. Intestinal microbiota community composition

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    To evaluate the impact on intestinal microbiota community composition

Other outcomes

  1. Mesure of blood fasting glucose

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Change in fasting glucose

  2. Mesure of blood Serum lipids

    Time frame: At baseline and following 12 weeks of probiotic supplementation or placebo.

    Change in serum lipids

Sponsors and collaborators

Lead sponsor

Montreal Heart Institute

Other

Collaborators

  • Lallemand Health Solutions

Registry information

Official study title

Probiotics for Vascular Inflammation in Metabolic Syndrome (PROMISE): a 12-Week Pilot Study, Randomized,Double-Blinded, Placebo-Controlled Trial

Acronym: PROMISE

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Oct 25, 2018
Registry last updated
Jan 14, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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