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| Name | Class |
|---|---|
| Barnham Benevolent Foundation | UNKNOWN |
| Jason and Daphne Mermikides Charitable Trust | UNKNOWN |
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Higher than average blood sugar (glucose) levels are linked to an increased risk of developing type 2 diabetes. As such, there is interest in identifying dietary factors that could lower blood glucose to help reduce the number of people with this disease. Findings from some human studies indicate that dairy products, especially a milk protein (whey), may help the control of blood glucose levels. However, there is a need for further studies to confirm these findings in individuals without diabetes but with higher than average blood glucose levels.
In the UK, more than 700 people are diagnosed with type 2 diabetes each day. Higher than average (raised) fasting blood sugar (glucose) is a characteristic of those at risk of developing this disease and as a result there is significant interest in dietary factors that could reduce levels of blood glucose, lowering the frequency of type 2 diabetes in the population. Existing scientific evidence suggests an important role of dairy products and especially of whey protein in the control of blood glucose levels. However, there is a need for further studies to confirm these findings in individuals without diabetes but with higher than average blood glucose levels.
Milk contains high quality proteins, of which 80% are caseins and 20% are whey proteins. Whey proteins are a rich source of branched-chain amino acids (such as leucine) which are thought to play an important role in regulating blood glucose control and other aspects of cardiovascular disease development in both healthy and type 2 diabetic subjects. However, very few studies in non-diabetic subjects with moderately raised HbA1c, characteristic of long-term poor glucose control, have been performed to investigate how whey protein affects blood glucose levels in the body especially when consumed over the longer term in the daily diet. Furthermore, data are limited on whether the leucine content of protein plays an important role in controlling blood glucose levels.
Study aims The main aims of this study is to investigate in adults without diabetes but with moderately raised HbA1c (a long- term marker of blood glucose control) whether a protein obtained from milk and dairy products (whey) has a beneficial effect on fasting and day-long blood glucose and insulin levels compared with a plant based protein (such as wheat). The researchers will also determine if leucine, a particular amino acid (building blocks of protein) found in higher levels in whey protein plays an important role in controlling blood glucose levels.
A secondary aim will determine whether the protein interventions influence risk markers for developing heart disease and diabetes including the level of blood lipids, hormones regulating blood sugar levels and blood vessel health.
This study will test the hypothesis that the incorporation of whey protein (total protein dose 50 g/d) in the habitual diet for 8 weeks will result in an improvement in fasting and day-long blood glucose and insulin levels, and other risk markers of heart disease and diabetes compared with wheat protein (total protein dose 50 g/d), and that the addition of leucine to wheat (to match the content found in whey protein) will improve blood glucose control.
Study design This study will be a long term, double-blind, randomised, controlled, three-way, cross-over study, in which the participants will receive the protein supplements (in random order) for 8 weeks each, with a 4 week wash-out period between the different protein treatments. At the beginning and end of each protein intervention, a fasting blood sample will be collected to determine the longer term effects of the assigned protein supplement on fasting glycaemic control, insulin sensitivity, endothelial function and other cardio-metabolic risk markers, as well as non-invasive measures of blood vessel health. At the beginning of each intervention period, a subset of participants will also undergo a day-long test meal investigation to determine the short-term (postprandial) effects of the protein interventions on the study outcome measures in response to standard sequential test meals containing the assigned protein interventions.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Whey Protein Isolate | Experimental | Subjects are asked to supplement their habitual diet with 56 g of whey protein isolate a day for 8 weeks |
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| Wheat Protein | Experimental | Subjects are asked to supplement their habitual diet with 56 g of wheat protein a day for 8 weeks |
|
| Wheat protein with leucine | Experimental | Subjects are asked to supplement their habitual diet with 56 g of wheat protein with leucine a day for 8 weeks |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Whey Protein Isolate | Dietary Supplement | Whey protein product isolated from whole milk. 79% Protein with minimal carbohydrate and fat. 50 grams of total supplemental protein/amino acids from whey protein powder consumed in two 25g (total protein/amino acids) nutrition shakes twice per day for 8 weeks in the form of a nutritional shake. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in fasting and day long glucose levels | Blood glucose levels will be measured using a clinical chemistry analyser | Before and after each 8 week intervention. |
| Change in fasting and day long insulin levels | Blood insulin levels will be measured using ELISA | Before and after each 8 week intervention. |
| Measure | Description | Time Frame |
|---|---|---|
| Change in vascular reactivity measured by Laser Doppler Imaging with iontophoresis | Fasting and day long measurement of vascular reactivity in the microcirculation. | Before and after each 8 week intervention. |
| Change in the total and HDL-cholesterol |
| Measure | Description | Time Frame |
|---|---|---|
| Metabonomics | Urinary biomarkers will be measured using NMR | Before and after each 8 week intervention |
Inclusion Criteria:
Exclusion Criteria:
• Females who are breast-feeding, may be pregnant, or if of child-bearing potential and are not using effective contraceptive precautions
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Julie Lovegrove, Professor | Contact | 0044(0)1183786418 | 6418 | j.a.lovegrove@reading.ac.uk |
| Drew Price, Masters | Contact | 00447905106167 | a.j.price@pgr.reading.ac.uk |
| Name | Affiliation | Role |
|---|---|---|
| Julie Lovegrove, Professor | University of Reading | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Hugh Sinclair Unit of Human Nutrition, Department of Food and Nutritional Sciences, University of Reading | Reading | Berkshire | RG6 6AP | United Kingdom |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 20377924 | Background | Pal S, Ellis V, Dhaliwal S. Effects of whey protein isolate on body composition, lipids, insulin and glucose in overweight and obese individuals. Br J Nutr. 2010 Sep;104(5):716-23. doi: 10.1017/S0007114510000991. Epub 2010 Apr 9. | |
| 15531672 | Background | Nilsson M, Stenberg M, Frid AH, Holst JJ, Bjorck IM. Glycemia and insulinemia in healthy subjects after lactose-equivalent meals of milk and other food proteins: the role of plasma amino acids and incretins. Am J Clin Nutr. 2004 Nov;80(5):1246-53. doi: 10.1093/ajcn/80.5.1246. |
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| ID | Term |
|---|---|
| D018149 | Glucose Intolerance |
| ID | Term |
|---|---|
| D006943 | Hyperglycemia |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| D007930 | Leucine |
| ID | Term |
|---|---|
| D000597 | Amino Acids, Branched-Chain |
| D000596 | Amino Acids |
| D000602 | Amino Acids, Peptides, and Proteins |
| D000601 | Amino Acids, Essential |
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Double-blind, randomised, controlled, 3-way, cross-over study
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Coded protein products will be used.
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| Wheat Protein | Dietary Supplement | Enzymatically hydrolysed wheat protein containing wheat peptides. 75% Protein with minimal carbohydrate and fat. 50 grams of total supplemental protein/amino acids from whet protein peptide powder consumed in two 25g (total protein/amino acids) nutrition shakes twice per day for 8 weeks in the form of a nutritional shake. |
|
| Wheat Protein with Leucine | Dietary Supplement | Enzymatically hydrolysed wheat protein containing wheat peptides with and additional 1.4g of L-leucine. 75% Protein with minimal carbohydrate and fat and a L-leucine concentration equal to whey protein isolate. 50 grams of total supplemental protein/amino acids from wheat protein peptide powder, with added leucine to equal the total content of the whey protein condition, consumed in two 25g (total protein/amino acids) nutrition shakes twice per day for 8 weeks. |
|
Fasting total cholesterol and HDL-C will be measured using a clinical chemistry analyser. LDL-C will be calculated using the Friedewald formula
| Before and after each 8 week intervention |
| Change in fructosamine | Fructosamine will be measured using a clinical chemistry analyser | Before and after each 8 week intervention |
| Change in C-reactive protein | C-reactive protein | Before and after each 8 week intervention |
| Change in pulse wave analysis | Pulse wave analysis will be measured using the Mobil-O-Graph device | Before and after each 8 week intervention |
| Change in blood pressure | Systolic blood pressure, diastolic blood pressure and pulse pressure | Before and after each 8 week intervention |
| Change in cellular adhesion molecule | VCAM and ICAM will be measured by Luminex, ICAM, P-selectin and E-selectin | Before and after each 8 week intervention |
| Change in selectins | P-selectin and E-selectin will be measured using Luminex | Before the start of the intervention |
| Change in beta-hydroxy butyrate | Beta-hydroxy butyrate will be measured using a clinical chemistry analyser as a marker of ketone bodies | Before and after each 8 week intervention |
| Change in insulin sensitivity | Glucose and insulin levels will be used to estimate insulin sensitivity using the Homeostatic model assessment calculation | Before and after each 8 week intervention |
| Change in non-esterified fatty acids | Non-esterified fatty acids will be measured using a clinical chemistry analyser | Before and after each 8 week intervention |
| Measurement of height | Height will be measured using a stadiometer | Before the start of the intervention |
| Change in body weight | Body weight will be measured using the Tanita scale | Before and after each 8 week intervention |
| Change in body mass index | Body mass index will be calculated from body weight and height measurement | Before and after each 8 week intervention |
| Change in body composition | Body composition will be measured using bioelectrical impedance. | Before and after each 8 week intervention |