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NCT Number: NCT03620266

Effects of Bilberry and Oat Intake After Type 2 Diabetes and/or MI

Background:

Bilberries from Sweden, rich in polyphenols, have shown cholesterol-lowering effects in small studies, and the cholesterol-lowering properties of oats, with abundant beta-glucans and potentially bioactive phytochemicals, are well established. Both may provide cardiometabolic benefits for patients with manifest chronic cardiometabolic disease, such as type 2 diabets mellitus (T2DM) and myocardial infarction (MI). However, large studies of adequate statistical power and appropriate duration are needed to confirm clinically relevant treatment effects. No previous study has evaluated the potential additive or synergistic effects of bilberry combined with oats on cardiometabolic risk factors.

Design:

This is a double-blind, randomized, placebo-controlled clinical trial. Our primary objective is to assess cardioprotective effects of diet supplementation with dried bilberry and with bioprocessed oat bran, with a secondary explorative objective of assessing their combination, compared with a neutral isocaloric reference supplement, for patients diagnosed with T2DM and/or MI. Patients will be randomized 1:1:1:1 to a three-month intervention. The primary endpoint is the difference in LDL cholesterol change between the intervention groups after three months. The major secondary endpoint is exercise capacity at three months. Other secondary endpoints include plasma concentrations of biochemical markers of inflammation, glycaemia, and gut microbiota composition after three months.

Implications:

Secondary prevention after cardiometabolic disease, including T2DM and MI, has improved during the last decades but diabetes complications, readmissions and cadiovascular related deaths following these conditions remain large health care challenges. Controlling hyperlipidemia, hyperglycaemia, hypertension and inflammation is critical to preventing (new) cardiovascular events, but novel pharmacological treatments for these conditions are expensive and associated with negative side effects. If bilberry and/or oat, in addition to standard medical therapy, can lower LDL cholesterol and inflammation more than standard therapy alone, this could be a cost-effective and safe dietary strategy for secondary prevention in high-risk patients or risk prevention in subjects with T2DM.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Steno Diabetes center, Aarhus, Denmark

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Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Confirmed T2DM diagnosis (any treatment modality accepted) and/or within 3 years post STEMI or NSTEMI
  • Completed coronary angiography/PCI
  • Male and female subjects ≥18 years
  • Allocated to atorvastatin at a daily dose of 80 mg (only eligible for patients enrolled up to 7 days post MI and not for T2D subjects)
  • Written informed consent

Exclusion criteria

  • Emergency coronary artery bypass grafting
  • <18 years of age
  • LDL cholesterol <2.0 mmol/L
  • Daily intake or the intent to initiate daily intake of bilberry in any form or daily intake of >15 g of oatmeal or equivalent
  • Food allergy/intolerance to gluten, bilberries or legumes
  • Previous randomization in the BioDiaMI trial
  • Inability to provide informed consent

Treatment and study plan

Bilberry

Dietary Supplement

The dietary intervention will continued for three months. After randomization, participants will be given bilberry shakes (active), liquid oat shakes (active), a combination shake with bilberry and oats, or reference shakes (placebo product containing no active bilberry or active oats but with similar taste and texture as both oat and bilberry), for intake two times a day (t.i.d). The formula for the shakes to be used in the intervention will be finalized during the initial project period.

Placebo

Dietary Supplement

The dietary intervention will be continued for three months. After randomization, participants will be given bilberry shakes (active), liquid oat shakes (active), a combination shake with bilberry and oats, or reference shakes (placebo product containing no active bilberry or active oats but with similar taste and texture), for intake two times a day (t.i.d). The formula for the shakes to be used in the intervention will be finalized during the initial project period.

Bioprocessed oat bran

Dietary Supplement

The dietary intervention will be continued for three months. After randomization, participants will be given bilberry shakes (active), liquid oat shakes (active), a combination shake with bilberry and oats, or reference shakes (placebo product containing no active bilberry or active oats but with similar taste and texture), for intake two times a day (t.i.d). The formula for the shakes to be used in the intervention will be finalized during the initial project period.

Combination bilberry/oats

Dietary Supplement

The dietary intervention will be continued for three months. After randomization, participants will be given bilberry shakes (active), liquid oat shakes (active), a combination shake with bilberry and oats, or reference shakes (placebo product containing no active bilberry or active oats but with similar taste and texture), for intake two times a day (t.i.d). The formula for the shakes to be used in the intervention will be finalized during the initial project period.

Primary outcomes

  1. Plasma levels of LDL cholesterol

    Time frame: Three months

    The effect of intervention on difference between the groups of LDL cholesterol after three months

Secondary outcomes

  1. Plasma lipid profile

    Time frame: Three months

    The effect of intervention on differences between the groups of fasting lipid profile including HDL, triglycerides, total cholesterol, small-dense LDL cholesterol, apo A, apo B, Lp(a) and oxidized LDL.

  2. Symptom-limited bicycle ergometer test

    Time frame: Three months

    The effect of intervention on exercise capacity (measured as maximal workload in Watts and as estimated maximal oxygen uptake (VO2 max))

  3. Dynamic unilateral heel-lft and unilateral shoulder flexion tests

    Time frame: Three months

    The effect of intervention on muscle endurance

  4. Self-reported physical activity level

    Time frame: Three months

    The effect of intervention on the Frändin/Grimby activity scale (6 levels of physical activity, min:1 (low activity) max:6 (heavy activity)) and the Haskell physical activity scale ("For how many days were you physically active during the last week for at least 20 minutes?", min:0 max:7)

  5. Plasma Cardiac Troponin Concentration

    Time frame: Three months

    Change in plasma cardiac troponin (high-sensitivity cardiac troponin T or I) concentration from baseline to 3 months to assess myocardial injury.

    The effect of intervention on Troponin levels, Unit of Measure: ng/L

  6. Plasma NT-proBNP Concentration

    Time frame: Three months

    Change in plasma N-terminal pro-B-type natriuretic peptide (NT-proBNP) concentration from baseline to 3 months to assess cardiac stress, pg/mL

  7. Plasma hs-CRP Concentration

    Time frame: Three months

    Change in plasma high-sensitivity C-reactive protein (hs-CRP) concentration from baseline to 3 months to assess systemic inflammation.

    Unit of Measure: mg/L

  8. Plasma IL-6 Concentration

    Time frame: Three months

    Change in plasma interleukin-6 (IL-6) concentration from baseline to 3 months to assess inflammatory response.

    Unit of Measure: pg/mL

  9. Glycosylated Hemoglobin (HbA1c)

    Time frame: Three months

    Change in glycosylated hemoglobin (HbA1c) from baseline to 3 months to assess glycemic control.

    Unit of Measure: %

  10. Fasting Plasma Insulin Concentration

    Time frame: Three months

    Change in fasting plasma insulin concentration from baseline to 3 months to assess insulin sensitivity and metabolic status.

    Unit of Measure: µIU/mL (micro-international units per milliliter)

  11. Fasting Plasma C-Peptide Concentration

    Time frame: Three months

    Change in fasting plasma C-peptide concentration from baseline to 3 months to assess endogenous insulin secretion and beta-cell function.

    Unit of Measure: ng/mL

  12. Serum Creatinine Concentration

    Time frame: Three months

    Change in serum creatinine concentration from baseline to 3 months to assess renal function.

    Unit of Measure: mg/dL

  13. Fasting Plasma Glucose Concentration

    Time frame: Three months

    Change in fasting plasma glucose concentration from baseline to 3 months to assess glycemic control.

    Unit of Measure: mg/dL

    Unit of Measure: mg/dL

  14. Serum Cystatin C Concentration

    Time frame: Three months

    Change in serum cystatin C concentration from baseline to 3 months to assess renal function and estimate glomerular filtration independent of muscle mass.

    Unit of Measure: mg/L

    Unit of Measure: mg/dL

    Unit of Measure: mg/dL

  15. Untargeted plasma metabolome

    Time frame: Three months

    Untargeted plasma metabolomics will be employed to exploratively assess alterations in endogenous and exposome-related metabolites and to identify metabolites that may differ with treatment.

  16. Fecal samples of gut microbiota composition

    Time frame: Three months

    These exploratory analyses of will allow to investigate the extent to which gut microbiota composition and activity differs between responders and non-responders to the interventions.

  17. Left ventricular systolic function

    Time frame: Three months

    The effect of intervention on left ventricular function. Baseline left ventricular systolic function, expressed as global ejection fraction in percent according to the biplane Simpson method, will be evaluated by echocardiography by the discharging physician. The procedure will be repeated after three months by an experienced echocardiography technician blinded to results of the initial examinations

  18. Resting heart rate

    Time frame: Three months

    The effect of intervention on resting heart rate

  19. Systolic and diastolic blood pressure

    Time frame: Three months

    The effect of intervention on blood pressure (mmHg)

  20. Urine albumin-creatinine ratio

    Time frame: Three months

    Urine albumin-creatinine ratio will be measured for for T2DM only

  21. Continuous glucose monitoring with Continuous Glucose Monitors (CGM) - FreeStyle model 2

    Time frame: Three months

    Continuous glucose monitoring (in a subset of T2DM only, n=100 in total)

  22. Body composition with multi-frequency bioimpedance

    Time frame: Three months

    The effect of intervention on body composition measured with multi-frequency bioimpedance (for T2DM only)

  23. Diabetic retinal changes

    Time frame: Three months

    The effect of intervention on diabetic retinal changes (eye fundus examination) (in a subset of T2DM only, n=100 in total)

  24. Platelet aggregation (Primary hemostasis)

    Time frame: Three months

    Ex vivo platelet aggregation in whole blood measured with impedance aggregometry (Multiplate®, Roche, Switzerland) after stimulation with adenosine diphosphate (ADP), arachidonic acid and thrombin-related activation peptide (TRAP-6). Unit of measure: Aggregation units x min. (in a subset of T2DM only, n=100 in total)

  25. P-selectin levels (Primary hemostasis)

    Time frame: Three months

    Plasma concentration of P-selectin measured with commercial ELISA (CD62P Quantikine, Biotechne, Dublin, Ireland). Unit of measure: ng/mL. (in a subset of T2DM only, n=100 in total)

  26. Ex vivo thrombin generation (Secondary hemostasis)

    Time frame: Three months

    Ex vivo thrombin generation (endogenous thrombin potential) in platelet-poor plasma measured using Calibrated Automated Thrombogram (BV Thrombinoscope, Maastricht, the Netherlands) after stimulation with tissue factor. Unit of measure: nM x min. (in a subset of T2DM only, n=100 in total)

  27. Prothrombin fragment 1+2 (Secondary hemostasis)

    Time frame: Three months

    Plasma concentration of prothrombin fragment 1+2, measured with commercial ELISA (EnzygnostTM, Siemens Healthineers, Ballerup, Denmark). Unit of measure: pmol/L. (in a subset of T2DM only, n=100 in total)

  28. Fibrinolysis speed

    Time frame: Three months

    Ex vivo fibrinolytic capacity (fibrinolysis speed) in whole blood measured with in-house modified rotational thromboelastometry after stimulation with tissue factor and tissue plasminogen activator. Unit of measure: mm/min. (in a subset of T2DM only, n=100 in total)

  29. Fibrinolytic capacity

    Time frame: Three months

    Ex vivo fibrinolytic capacity (time from peak fibrin to 50% lysis) in platelet-poor plasma measured with in-house turbidimetric fibrin formation and lysis assay. Unit of measure: seconds. (in a subset of T2DM only, n=100 in total)

  30. Fibrinolytic markers

    Time frame: Three months

    Plasma concentrations of plasminogen activity, tissue plasminogen activator (unit of measure: ng/mL) and plasminogen activator inhibitor-1 (unit of measure: ng/mL) measured with ELISA (Technozym®, Technoclone, Vienna, Austria). (in a subset of T2DM only, n=100 in total)

  31. Endothelial activation

    Time frame: Three months

    Plasma concentrations of syndecan-1 (unit of measure: ng/mL) and thrombomodulin (unit of measure: ng/mL) measured with commercial ELISA kits (CD138 kit and CD141 kit, Diaclone, Medix Biochemica, Espoo, Finland). (in a subset of T2DM only, n=100 in total)

  32. Inflammation

    Time frame: Three months

    The effect of intervention on inflammatory markers (Olink panel) (in a subset of T2DM only, n=100 in total)

  33. Oxidative stress

    Time frame: Three months

    The effect of intervention on 8-Oxo-2'-deoxyguanosine levels (in a subset of T2DM only, n=100 in total)

Sponsors and collaborators

Lead sponsor

Ole Frobert, MD, PhD

Other

Collaborators

  • Aarhus University Hospital
  • Chalmers University of Technology
  • Falu Hospital
  • Odense University Hospital
  • Region Skane
  • Region Västmanland
  • Vastra Gotaland Region
  • Värmland County Council, Sweden

Registry information

Official study title

Effects of Bilberry and Oat Intake on Plasma Lipid Profile, Inflammation, and Exercise Capacity in Patients With Type 2 Diabetes and/or Myocardial Infarction (BioDiaMI): a Randomized, Double-blind, Placebo-controlled Trial

Acronym: BioDiaMI

Important dates

Study start
2021
Primary completion
2026
Study completion
2026
First posted
Aug 8, 2018
Registry last updated
Mar 23, 2026

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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