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CompletedNCT01571622WheyGLP-1Updated Mar 31, 2014

Whey Protein on Posprandial Glucose, Insulin GLP-1, GIP and DPP4 in Type 2 Diabetes

An interventional study of Whey before Breakfast and Water before breakfast in Type 2 Diabetes Mellitus, sponsored by Tel Aviv University. Completed at 1 site in Israel. Open to participants aged 40 Years to 70 Years. Per ClinicalTrials.gov, last updated 2014-03-31.

Sponsored by Tel Aviv University · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
19
Allocation
Randomized
Ages
40 Years to 70 Years
Sex
All
01

Study summary

The aim of the present study is to examine the therapeutic effect of whey protein concentrate (WPC 80) in adult subjects with in type 2 diabetes. Whey protein will be administered before breakfast and its effects on posprandial glucose, insulin, c-peptide, intact and total GIP and GLP-1, and DPP-4 plasma levels will be assessed.

Read the detailed description

Milk and dairy product consumption has been associated with lower risk of metabolic disorders and cardiovascular diseases (1). A population-based prospective study (CARDIA) revealed that dairy consumption was inversely associated with the prevalence of all components of the insulin resistance syndrome (IRS) in overweight individuals (2).

Whey accounts for about 20% of whole milk protein, while casein accounts for the rest. Whey protein is a source of bioactive components and branch chained amino acids (BCAAs) which could play a further role in the control of food intake and management of glucose metabolism, obesity and diabetes (1,3,4).

Whey protein appears to have insulinotropic and glucose lowering properties in healthy adults (6-9), and also in individuals with type 2 diabetes (10,11). The magnitude of postprandial blood glucose reduction following ingestion of whey protein is comparable to that observed with pharmaceutical interventions such as sulfonylureas (12) or nateglinide (13). These findings imply an important role for whey protein in the management of type 2 diabetes (10).

Whey protein seems to induce insulinotropic/β-cell-stimulating and glucose lowering effects via bioactive peptides generated during gastrointestinal digestion of BCAAs contained in β-lactoglobulin, the major whey protein (14).

These bioactive peptides stimulate the release of several gut hormones, especially the incretins, glucose-dependent insulinotropic polypeptide (GIP) and glucagon-like peptide-1 (GLP-1), which potentiate insulin secretion from β-cells and are also associated with the control of food intake (9, 15-17). Increased plasma levels of GIP and GLP-1 have been reported following whey ingestion in patients with type 2 diabetes (10). The stimulatory effect of whey protein on GLP-1 is especially important since it has been shown that postprandial GLP-1 secretion is reduced in type 2 diabetes (18).

The bioactive peptides generated from whey protein may also serve as endogenous inhibitors of dipeptidyl peptidase-4 (DPP-4) in the proximal gut, preventing incretin (GIP and GLP-1) degradation (19, 20). Indeed, recently DPP-4 inhibitors have been found and identified in Whey protein (21). All these may reduce postprandial blood glucose levels.

Incretin action is enhanced by whey protein ingestion, possibly through incretin degradation via inhibition of DPP-4 (19,20). This is important in light of several incretin-based therapies such as continuous administration of GLP-1 (19), treatment with degradation-resistant GLP-1R agonists (Exendin-4) (15,23-25), and therapy with DPP-4 inhibitors (Sitagliptin, Liraglutide and others gliptines ) (15,23-27) all of which have lead to substantial improvements in glucose control and β-cell function in subjects with type 2 diabetes.

Whey protein stimulates GLP-1 secretion and prevents its inactivation by DPP 4. Thus, by potentiating GLP-1 secretion and enhancing its action, (15), whey protein may represent a valuable tool for treating type 2 diabetes.

02

Conditions studied

  • Type 2 Diabetes Mellitus

Keywords

  • Whey protein
  • type 2 diabetes
03

In context

Diabetes Mellitus, Type 2

9,359 studies on the registry are indexed under Diabetes Mellitus, Type 2; 1,318 are open to participants now.

This study's enrollment of 19 is below the median of 80 across 7,525 interventional studies indexed under Diabetes Mellitus, Type 2.

Browse Diabetes Mellitus, Type 2 studies →

Lead sponsor

Tel Aviv University is the lead sponsor of 100 studies on the registry; 26 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
40 Years to 70 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  1. Type 2 diabetic patients
  2. Duration of diabetes: 1-10 years
  3. Subjects ≥ 40 and ≤70 years of age
  4. Metformin therapy and all oral antidiabetic medication will be allowed
  5. Overweight or obese (BMI: 25 to 35 kg/m2)
  6. Normal liver and kidney function
  7. Normal thyroid function
  8. Read and understood the informed consent form and signed it voluntarily

Exclusion criteria

Exclusion Criteria:

  1. Liver, heart, kidney, lung, infectious, neurological, psychiatric, immunological or neoplastic diseases.
  2. Type 1 or insulin treated diabetes.
  3. Pregnancy or lactation
  4. Illicit drug abuse or alcoholism
  5. Subject treated with insulin or treatment with degradation-resistant GLP-1R agonists (Exendin-4) or similar and DPP4 inhibitors (Januvia)
  6. Subjects taking anoretic drugs
  7. Subjects on steroid treatment
  8. Subjects known by the principal investigator to be unable to cooperate for any reason.
  9. Known hypersensitivity to milk components
  10. Subjects after bariatric surgery.

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05

Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
19 participants (actual)

Study arms

  • Placebo comparator
    Water before breakfast

    Each patient will consume a high-GI breakfast (white bread). Each subject will be pretreated 30 min before breakfast with 250 ml of water

    Dietary Supplement: Whey before Breakfast · Dietary Supplement: Water before breakfast

  • Experimental
    Whey before breakfast

    Each patient will consume a high-GI breakfast (white bread). Each subject will be pretreated 30 min before breakfast with Whey Protein Concentrate (WPC 80 %) 45 gr dissolved in 250 ml of water\\

    Dietary Supplement: Whey before Breakfast · Dietary Supplement: Water before breakfast

Interventions

  • Dietary supplementWhey before Breakfast

    After consumption of whey before breakfast samples will be taken every 30 minutes for quantification of glucose, insulin, GlP-1 and GIP

  • Dietary supplementWater before breakfast

    After water before breakfast the blood samples will be taken every 30 min for quantification of glucose, insulin, GLP-1 and GIP,

06

What researchers measure

Primary outcomes

  1. Glucose response

    In all 25 subjects, the effects of whey protein ingestion posprandial glucose, will be measured. Thirty minutes prior to breakfast, subjects will preloaded with one of 2 alternatives: 1. (250 ml) water 2. Whey Protein Concentrate (WPC 80 %), 45 gr dissolved in 250 ml of water

    Time frame: During 4 hours meal challenge

Secondary outcomes

  1. Insulin GLP-1, GIP and DPP4

    In all 25 subjects, the effects of whey protein on posprandial insulin, C- peptide, GIP, GLP-1, and dipeptil dipeptidase-4 (DPP-4) after standardized breakfast will be measured. Thirty minutes prior to breakfast, subjects will preloaded with one of 2 alternatives: 1. (250 ml) water 2. Whey Protein Concentrate (WPC 80 %), 45 gr dissolved in 250 ml of water

    Time frame: During 4 hours after meal challange

07

Study locations

1 site
  • Diabetes Unit E. Wolfson Hospital
    Holon, Tel Aviv 58100, Israel
08

References and documents

Publications

  • Jakubowicz D, Froy O, Ahren B, Boaz M, Landau Z, Bar-Dayan Y, Ganz T, Barnea M, Wainstein J. Incretin, insulinotropic and glucose-lowering effects of whey protein pre-load in type 2 diabetes: a randomised clinical trial. Diabetologia. 2014 Sep;57(9):1807-11. doi: 10.1007/s00125-014-3305-x. Epub 2014 Jul 10. PubMed 25005331 ↗
09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 31, 2014, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT01571622
Lead sponsor
Tel Aviv University
Responsible party
Daniela Jakubowicz (Professor Daniela Jakubowicz MD, Tel Aviv University) — Principal investigator
First posted
Apr 5, 2012
Start date
Apr 2012
Primary completion
Jan 2013
Completion
Sep 2013
Last update
Mar 31, 2014

Study contacts

Daniela Jakubowicz, MD
principal investigator · Diabetes Unit E. Wolfson Medical Center Tel Aviv University

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Mar 2014. You cannot join it, but the record below documents what was studied.

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