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| Name | Class |
|---|---|
| Mars, Inc. | INDUSTRY |
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Cocoa flavanols form part of the family of chemicals (also found in red wine and tea) which have aroused interest due to population studies suggesting that diets high in these substances might reduce risks of heart disease. In the laboratory, these flavanols have been shown to cause blood vessels to widen and blood flow to increase. As dysfunction in this ability of blood vessels to widen is now thought to play a central role in the complications of diabetes, novel ways to mitigate this are constantly being sought.
The present study aims to use non-invasive magnetic resonance imaging (MRI) to measure foot and brain blood flow before and after 7 days consumption of a cocoa drink high in flavanols, in subjects with diabetes, with and without peripheral neuropathy.
Cocoa flavanols form part of the family of polyphenols (also found in red wine and tea) which have aroused interest due to epidemiological studies suggesting that diets high in these substances might reduce risks of heart disease. However, it is difficult to account for all sources of polyphenols in these epidemiological studies, and the level of cocoa product consumption was generally not well documented. Furthermore, in readily available cocoa products, processing may remove most of the flavanols, leading to such products varying considerably in flavanol content. Recently, laboratory studies of the effects of cocoa flavanols have suggested an effect on the relaxation of smooth muscle in blood vessel walls, specifically the element mediated by the endothelium (blood vessel wall). Studies using ultrasound methods in healthy volunteers have shown an increase in blood flow in the arm following temporary arterial occlusion.
As endothelial dysfunction is now thought to play a central role in the complications of diabetes, novel ways to mitigate this are constantly being sought. It is well recognised that diabetic peripheral nerve damage leads to abnormal foot blood flow, including impaired superficial skin blood flow, and that this is one of the factors delaying wound healing in diabetic foot ulcers (the single largest cost in secondary care diabetes).
Several techniques are currently used to monitor blood flow to the limbs, including venous occlusion plethysmography (VOP), laser Doppler methods and nuclear medicine techniques. These techniques have low spatial resolution, low specificity, are labour intensive, or require the use of injected radioactive contrast agents (which pose a particular risk to diabetic patients). Radiation dose also limits repeat studies.
The arterial spin labelling magnetic resonance (ASL MR) technique is non-invasive, but yields a quantifiable measure of blood flow with high resolution, and allows measurements to be repeated several times, as the technique uses no external contrast agents.
The present study aims to use non-invasive magnetic resonance imaging (MRI) to measure peripheral (foot) and brain blood flow at baseline and in response to a cocoa drink high in flavanols, in subjects with type 2 diabetes, with and without peripheral neuropathy.
Subjects will attend an initial screening visit. Measures of HbA1c, kidney function and blood pressure will be checked, along with ankle-brachial pressure index (to check for poor circulation), foot pulses, and examination for peripheral nerve damage and cardiac neuropathy.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| High Flavanol Cocoa | Experimental | Cocoa drink containing ~450mg cocoa flavanols and 10g carbohydrate per serving. Subject consumes 2 servings per day, for 7 days. |
|
| Low Flavanol Cocoa | Placebo Comparator | Cocoa drink containing ~25mg cocoa flavanols and 10g carbohydrate per serving. Subject consumes 2 servings per day, for 7 days. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| High Flavanol Cocoa | Dietary Supplement | Total daily flavanol intake provided by the high flavanol drink is ~900mg |
|
| Measure | Description | Time Frame |
|---|---|---|
| Change in Fasting Brain Blood Flow | Measured by ASL-MR at Day 0 and after 7d consumption of a cocoa drink to detect a change following intervention | Day 0 and after 7d consumption of a cocoa drink |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Brain blood flow after acute consumption of cocoa | Measured at day 0, (before intervention commences)and after 7days consumption of a cocoa drink | 1,3,5 and 8hrs after cocoa consumption |
| Change in Fasting foot blood flow |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Affiliation | Role |
|---|---|---|
| Simon Paige, MD | University Hospitals NHS Trust | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Nottingham | Nottingham | Notts | NG72UH | United Kingdom |
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| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D010523 | Peripheral Nervous System Diseases |
| ID | Term |
|---|---|
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
| D004700 | Endocrine System Diseases |
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| Low Flavanol Cocoa | Dietary Supplement |
|
Measured using ASL-MR
| Day 0 and after 7d consumption of a cocoa drink |
| Change in Foot blood flow after acute consumption of cocoa | Measured at day 0, (before intervention commences)and after 7days consumption of a cocoa drink | 1,3,5 and 8hrs after cocoa consumption |
| Change in Blood Flavanol concentration | Measured at day 0, (before intervention commences)and after 7days consumption of a cocoa drink | Day 0 and after 7d consumption of a cocoa drink |
| Change in Fasting oxidative stress status | Oxidative stress assessed by measuring concentration of homocysteine, CRP, 8-isoprostaglandin, arginine and nitric oxide metabolites in the blood. | Day 0 and after 7 days of consuming a cocoa drink |
| Change in diabetes control | Assessment made from HbA1c, glucose and insulin concentration in the blood | Day 0 and after 7days of consuming a cocoa drink daily |
| D009468 | Neuromuscular Diseases |
| D009422 | Nervous System Diseases |