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Impacts of Fermented Pea- and Legume-based Product on Gut Microbiota and Health (HealthFerm)

U

University of Eastern Finland

Status

Active, not recruiting

Conditions

Metabolic Syndrome

Treatments

Other: Unfermented meat alternative
Other: Fermented meat alternative

Study type

Interventional

Funder types

Other

Identifiers

NCT06743828
159/2024 HealthFerm

Details and patient eligibility

About

This study aims to investigate the effects of consuming fermented pea- and legume-based product on gut and overall human health. It is a randomized, single-blinded, controlled, cross-over trial with a dietary intervention.

A total of 100 participants will be enrolled in this study and they will eat both fermented and unfermented pea- and legume-based products for three weeks. Participants will eat their habitual diet between the dietary intervention periods (wash-out).

During the study, participants' perceived health, inflammatory markers, glucose and lipid metabolism, tryptophan metabolites, gastrointestinal symptoms, and gut microbiota will be assessed.

Full description

Plant-based protein sources, such as those derived from peas and legumes, are experiencing high demand due to their role in reducing reliance on animal products and promoting a more sustainable food system. Despite this, there is limited information available regarding the impact of components like fibre in plant-based foods on protein and other nutrients' metabolism. In addition, the evidence of the health effects of meat alternatives is still scarce.

Food fermentation emerges as a potential solution to enhance the absorption of plant-based protein and various nutrients in the small intestine. This is achieved by reducing antinutrients and facilitating the absorption process. Additionally, food fermentation has implications for the composition and metabolic activity of the gut microbiota, influencing metabolism, immune responses, intestinal function, and overall health. The metabolism of tryptophan in the gut, modulated by the gut microbiota and the production of various metabolites, may serve as a key link in these observed health effects.

The fermentation of plant-based foods potentially enhances their beneficial health effects, and investigating this contributes to an increased understanding of the gut-mediated health effects of foods and the mechanisms behind them. This study is part of a European research project HealthFerm.

Detailed objectives are to:

  1. compare fermented and unfermented pea- and legume-based food products on blood lipid and glucose metabolism and gastrointestinal comfort as well as perceived and observed overall well-being.
  2. study the effects of fermented and unfermented pea- and legume-based food consumption on gut permeability and inflammation markers.
  3. study the difference in microbiota composition, diversity, and its contribution to cardiometabolic outcomes after consuming fermented and unfermented pea- and legume-based food products .
  4. study the difference in microbiota-related metabolites, especially tryptophan metabolites, between fermented and unfermented pea- and legume-based food products.

A total of 100 participants will be enrolled in this randomized, single-blinded, controlled, cross-over trial, during which they will eat both fermented and unfermented pea- and legume-based products as part of their habitual diet. The study follows this sequence:

Weeks 1-3: Habitual diet Weeks 4-6: Intervention diet 1 Weeks 7-9: Habitual diet (wash-out) Weeks 10-12: Intervention diet 2

Fasting blood, urinary and faecal samples, as well as food diaries and questionnaires, are collected at the end of each study period to assess participants' diet, perceived health, gastrointestinal symptoms, inflammatory markers, glucose and lipid metabolism, tryptophan metabolites, and gut microbiota composition and their metabolites, such as short-chain fatty acids. In addition, participants' values and attitudes towards fermented foods are assessed. At the end of the study, participants will receive their laboratory results and dietary guidance for their habitual diet from a registered dietitian.

Enrollment

100 estimated patients

Sex

All

Ages

30 to 70 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Waist circumference >90 cm (women) or >100 cm (men) OR BMI 27-35 kg/m2

  • One of the following:

    • raised blood pressure (systolic ≥ 130 mmHg and/or diastolic 85 mmHg)
    • raised fasting plasma glucose (≥ 5.6 mmol/l)
    • raised triglycerides (≥ 1.7 mmol/l)
    • raised total cholesterol (≥ 5 mmol/l)
    • raised LDL (≥ 3 mmol/l)
    • reduced HDL (women < 1.3 mmol/l, men 1.0 mmol/l)
  • Consumption of at least one meal where the main protein source is meat, fish, or meat alternative on most days

  • Willingness to follow intervention diets for the whole study

Exclusion criteria

  • Diagnosed chronic diseases and conditions which could hamper the adherence to the dietary intervention protocol, e.g., type 1 or 2 diabetes, chronic liver, thyroid, kidney, or gastrointestinal diseases
  • Pregnancy and lactation
  • Gluten-free or vegan diet
  • Recent use of antibiotics (within 3 months)
  • Gastrointestinal surgery (within 6 months)
  • Alcohol abuse (AUDIT ≥ 15 p and measures of liver function)
  • regular smoking or use of snus or nicotine bags

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

100 participants in 3 patient groups

Fermented product
Experimental group
Description:
Participants consume a fermented pea- and legume-based product daily for three weeks within their diet.
Treatment:
Other: Fermented meat alternative
Unfermented product
Active Comparator group
Description:
Participants consume an unfermented pea- and legume-based product daily for three weeks within their diet.
Treatment:
Other: Unfermented meat alternative
Habitual diet
No Intervention group
Description:
Participants consume their habitual diet without any intervention products.

Trial contacts and locations

1

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Central trial contact

Marjukka Kolehmainen; Vilma Liikonen

Data sourced from clinicaltrials.gov

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