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Completed

NCT Number: NCT04717726

Exercise, Milk Thistle, and Lactobacillus to Influence Plasma Bilirubin

The proposed clinical trial will test our hypothesis that, during exercise, red blood cell (RBC) release of heme and catabolism to bilirubin is an essential process that mediates gene responses that reduce body fat. We will evaluate whether Milk Thistle extract or Lactobacillus Gasseri extends bilirubin circulating times to decrease body fat further. Thus we will perform a 12-week, 6-armed trial with one group performing aerobic exercise 5 times per week (EX) one group receiving a Milk Thistle extract (MT), one group receiving a lactobacillus gasseri supplement (LAC), a group receiving only a placebo (CON), and groups both exercising and receiving the MT (MT + EX) and lactobacillus and exercise (LAC + EX).

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Key information

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

University of Kentucky- Nutrition Assessment Lab

Lexington, Kentucky, 40506, United States

About this study

The investigative team's previous work has shown that BR binds to the PPARalpha protein in fat and liver tissues to activate genes that improve fatty acid oxidation via a hormone known as fibroblast growth factor-21 (FGF21). The investigators recently showed that in high capacity running rats (HCR) compared to low capacity running (LCR), in which the latter are obese, BR levels and PPARalpha-FGF21 were significantly raised in the high-capacity runners. New investigations have shown that Milk Thistle (MT) herbal supplement contains polyphenols that activate pathways that suppress the glucuronyl enzyme UGT1A1 that removes BR from the blood, improving liver function and moderately increasing BR blood levels by ~2-fold. Similar findings have been demonstrated with Lactobacillus Gasseri supplementation. Hence, there is a bilirubin-PPARalpha-FGF21 axis that can be driven by exercise and dietary supplementation. We will test whether exercise and milk thistle or exercise and lactobacillus gasseri synergistically increase bilirubin-PPARalpha-FGF21, further reducing body fat in patients with obesity.

Participants in the EX, EX + MT, and EX + LAC groups will complete five weekly exercise sessions on their own, expending roughly 600 kcal per session. Participants will be provided a Polar A-300 heart rate monitor programmed for their individual attributes (height, weight, age, training status, gender), which gives a real-time estimate of energy expenditure during exercise. Participants will report to the lab once per week to download the exercise sessions and verify compliance. If participants are not compliant (defined as completing 85% of their assigned exercise sessions per month), they will be disqualified. This intervention has been successfully used by the investigators in multiple studies to produce significant weight loss without dietary intervention in this population with a retention rate of over 90% Participants in the MT and EX + MT groups will be provided 900 mg of standardized milk thistle extract daily (300 mg three times per day before meals) over the 12-week regimen. The investigators will use the standardized Jarrow Formulas Milk Thistle Veggie Caps containing 30:1 extract that is standardized to contain 80% total Milk Thistle seed flavonoids (polyphenols), including the critical Silymarin fractions isosilybinins A and B, silybinins A and B, silychristin and silydianin that is active against suppressing the UGT1A1 enzyme increasing plasma bilirubin. The capsules are free of wheat, gluten, soybeans, dairy, egg, fish/shellfish, peanuts/tree nuts, and GMOs. Rationale for using this brand: There have been inconsistencies with previous studies that did not use a standardized silymarin extract, which may have contained low levels of the active polyphenolic flavonoids in the milk thistle plant, which varies in the plant's stems, leaves, roots, and flowers.

Participants in the LAC and LAC + EX groups will receive two doses of 3 billion CFU of lactobacillus gasseri per day for a total of 6 billion CFU, the recommended upper level for supplementation of probiotic cultures. The Swanson brand Lactobacillus gasseri will be used, as these capsules are also free of wheat, gluten, soybeans, dairy, egg, fish/shellfish, peanuts/tree nuts, and GMOs. Importantly, this brand uses acid-resistant designed release capsules to improve the viability of the lactobacillus in the human stomach.

Participants in the CON and EX group will receive a placebo (maltodextrin) made to look identical to the MT capsules.

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

  • Classified as obese (BMI 30-45)
  • Sedentary (do not currently exercise)
  • Aged 18-50 years
  • Without contraindications to exercise

Exclusion criteria

  • Dieting for weight control
  • Tobacco users
  • Have a ragweed allergy
  • Taking antibiotics, hypoglycemic agents, anticoagulants, statins, or NSAIDs
  • Nursing, pregnant, or planning on becoming pregnant
  • Supplementing with a probiotic

Treatment and study plan

Milk Thistle (MT)

Dietary Supplement

Participants in the MT and EX + MT groups will be provided 900 mg of standardized milk thistle extract daily (300 mg three times per day before meals) over the 12-week regimen. We will use the standardized Jarrow Formulas Milk Thistle Veggie Caps containing 30:1 extract that is standardized to contain 80% total Milk Thistle seed flavonoids (polyphenols), including the critical Silymarin fractions isosilybinins A and B, silybinins A and B, silychristin and silydianin that is active against suppressing the UGT1A1 enzyme increasing plasma bilirubin. The capsules are free of wheat, gluten, soybeans, dairy, egg, fish/shellfish, peanuts/tree nuts, and GMOs. Rationale for using this brand: There have been inconsistencies with previous studies that did not use a standardized silymarin extract, which may have contained low levels of the active polyphenolic flavonoids in the milk thistle plant, which varies in the plant's stems, leaves, roots, and flowers.

Lactobacillus Gasseri (LAC)

Dietary Supplement

Participants in the LAC and LAC + EX groups will receive two doses of 3 billion CFU of lactobacillus gasseri per day for a total of 6 billion CFU, the recommended upper level for supplementation of probiotic cultures. We will use Swanson brand Lactobacillus gasseri, whose capsules are also free of wheat, gluten, soybeans, dairy, egg, fish/shellfish, peanuts/tree nuts, and GMOs. Importantly, this brand uses acid-resistant designed release capsules to improve the viability of the lactobacillus in the human stomach.

Exercise (EX)

Behavioral

Participants in the EX, EX + MT, and EX + LAC groups will complete five weekly exercise sessions on their own, expending roughly 600 kcal per session. Participants will be provided a Polar A-300 heart rate monitor programmed for their individual attributes (height, weight, age, training status, gender), which gives a real-time estimate of energy expenditure during exercise. Participants will report to the lab once per week to download the exercise sessions and verify compliance. If participants are not compliant (defined as completing 85% of their assigned exercise sessions per month), they will be disqualified. This intervention has been successfully used by Dr. Flack in multiple studies to produce significant weight loss without dietary intervention in this population with a retention rate of over 90%

Control (CON)

Dietary Supplement

Participants in the CON and EX group will receive a placebo (maltodextrin) made to look identical to the MT and LAC capsules.

Primary outcomes

  1. Lean mass

    Time frame: baseline (prior to initiation of study)

    kg of lean mass will be assessed by air displacement plethysmography (BodPod, Cosmed USA)

  2. Lean mass

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    kg of lean mass will be assessed by air displacement plethysmography (BodPod, Cosmed USA)

  3. Fat mass

    Time frame: baseline (prior to initiation of study)

    kg of fat mass will be assessed by air displacement plethysmography (BodPod, Cosmed USA)

  4. Fat mass

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    kg of fat mass will be assessed by air displacement plethysmography (BodPod, Cosmed USA)

  5. Plasma bilirubin

    Time frame: baseline (prior to initiation of study)

    Plasma bilirubin will be assessed in the fasted state

  6. Plasma bilirubin

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    Plasma bilirubin will be assessed in the fasted state

  7. Plasma FGF21

    Time frame: baseline (prior to initiation of study)

    fibroblast growth factor-21 will be assessed in the fasted state

  8. Plasma FGF21

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    fibroblast growth factor-21 will be assessed in the fasted state

  9. Red blood cell count

    Time frame: baseline (prior to initiation of study)

    Red blood cell count will be assessed in the fasted state

  10. Red blood cell count

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    Red blood cell count will be assessed in the fasted state

  11. Urobilin

    Time frame: baseline (prior to initiation of study)

    Plasma Urobilin will be assessed in the fasted state

  12. Urobilin

    Time frame: 2 weeks (immediately after 12 week exercise and/or supplement intervention)

    Plasma Urobilin will be assessed in the fasted state

Secondary outcomes

  1. Liver function

    Time frame: baseline (prior to initiation of study)

    AST and ALT enzymes will be assessed in the fasted state to demonstrate liver health

  2. Liver function

    Time frame: 12 weeks (immediately after 12 week exercise and/or supplement intervention)

    AST and ALT enzymes will be assessed in the fasted state to demonstrate liver health

Sponsors and collaborators

Lead sponsor

Kyle Flack

Other

Registry information

Official study title

Milk Thistle and Lactobacillus Supplementation to Improve Exercise Outcomes in Obese Patients

Important dates

Study start
2021
Primary completion
2023
Study completion
2023
First posted
Jan 22, 2021
Registry last updated
Jul 28, 2023

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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