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Effects of Pea Proteins With Different Degrees of Processing on Postprandial Metabolism in Healthy Adults

U

University of Bonn

Status

Completed

Conditions

Postprandial Metabolic Events
Plasma Amino Acid Appearance and Disappearance

Treatments

Other: Pea protein extrudate
Other: Pea protein isolate
Other: Pea protein concentrate
Other: Whey protein

Study type

Interventional

Funder types

Other

Identifiers

NCT06155656
AlProPlant-HS1

Details and patient eligibility

About

The aim of this study is to investigate the postprandial metabolic responses to plant-based protein ingredients of different degrees of processing (pea protein concentrate, isolate, and extrudate) and in comparison to whey protein in healthy adults. Therefore, young healthy subjects consume 4 test meals with 25 g of protein from pea protein concentrate, pea protein isolate, pea protein extrudate or whey protein in a randomized order. In a postprandial period of 6 hours, parameters of protein and glucose metabolism (i.a. plasma amino acids), gastric emptying and hunger/satiety are analysed. It is assumed that the plasma amino acid profile after plant protein ingestion differs depending on processing level of the protein ingredients and in comparison to whey protein.

Full description

In a randomized crossover-design, 20 healthy women and men consume 4 test meals containing either 25 g of protein from plant protein ingredients (pea protein concentrate, isolate, or extrudate) or whey protein together with 1 g paracetamol, which is used as a marker for gastric emptying.

During a postprandial period of 6 hours parameters of protein metabolism (e.g. amino acids in plasma and urine), glucose metabolism (plasma glucose, serum insulin) and gastric emptying rate (based on plasma paracetamol) are analysed. Furthermore, subjective hunger/satiety and acceptance of the meals are assed using visual analogue scales. Each intervention arm will be separated by a washout period of at least 7 days.

Enrollment

20 patients

Sex

All

Ages

20 to 40 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • non-smoking
  • metabolically healthy
  • normal weight (BMI: 18,5 - 24,9 kg/m2)
  • written informed consent

Exclusion criteria

  • pregnancy, lactation
  • hypo- or hypertension
  • underweight or overweight/obesity
  • food intolerances and allergies (especially milk protein, pea, celery)
  • malabsorption syndromes
  • gastrointestinal diseases
  • thyroid diseases
  • diabetes mellitus type 1 and type 2
  • impaired kidney or liver function
  • anaemia
  • blood coagulation disorders
  • irregular menstrual cycle
  • endometriosis, severe menstrual problems
  • hormonal contraception
  • regular use of medications (especially habitual use of paracetamol or medications that may interact with paracetamol)
  • hypersensitivity to paracetamol
  • body weight below 50 kg
  • alcohol abuse
  • glucose-6-phosphate dehydrogenase deficiency
  • Gilbert's syndrome
  • vegan diet
  • eating disorders (especially anorexia nervosa, bulimia nervosa)
  • smoking
  • participation in another study

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Single Blind

20 participants in 4 patient groups

Pea concentrate
Experimental group
Description:
Participants randomized to receive a soup containing 25 g of protein from pea protein concentrate
Treatment:
Other: Pea protein concentrate
Pea isolate
Experimental group
Description:
Participants randomized to receive a soup containing 25 g of protein from pea protein isolate
Treatment:
Other: Pea protein isolate
Pea extrudate
Experimental group
Description:
Participants randomized to receive a soup containing 25 g of protein from pea protein extrudate
Treatment:
Other: Pea protein extrudate
Whey
Active Comparator group
Description:
Participants randomized to receive a soup containing 25 g of protein from whey protein
Treatment:
Other: Whey protein

Trial contacts and locations

1

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Central trial contact

Sarah Egert, Prof PhD

Data sourced from clinicaltrials.gov

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