Our annual funding round is designed to support bright young researchers, as well as established institutions, as they strive to make the kind of life-changing breakthrough our diabetes community is hoping for. 

Our first research award was made in 1999 for a small equipment grant and since that time, we have committed more than £12 million to diabetes research in the UK and as part of the International Diabetes Wellness Network, around the world.

To read more about our research strategy, click here

Our Funded Research 

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2014

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DECS, Diabetic Eye disease in Children Study: incidence, detection/presentation, clinical characteristics and putcomes of diabetic eye disease in childhood in the UK

Recipient: Professor Jugnoo Rahi
Institution: UCL Institute of Child Health
City: London
Amount: £19,978

Description - click here to read
Despite the recent and on-going increase in the frequency of childhood diabetes, little is known about childhood diabetic eye disease, particularly how common it is in the UK, how it develops, and its consequences for future vision. We propose to address this paucity of information in order to help plan the services and treatments children need to prevent visual loss and improve overall disease management. This study will provide currently unavailable data which cannot be accessed from existing routine sources. We plan a national incidence study of childhood diabetic eye disease (retinopathy / cataract) and diabetes-related visual disability, investigating variations (eg by age, gender, ethnicity), clinical characteristics, patterns of detection and short term outcomes. The cohort established by the proposed study will also enable future longer term studies of outcomes. ‘Cases’ will be ascertained through active surveillance by ophthalmologists reporting to the long-established British Ophthalmic Surveillance Unit, which has facilitated all the key recent national studies of childhood eye disorders, including studies carried out by our team (referenced below). As with our prior studies, we will establish at the outset a clinical research network comprising ophthalmologists who manage children with diabetes, as the forum for implementing the study and for translating findings into practice to directly impact on care.

2014

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Does low vitamin D cause adipose tissue inflammation and insulin resistance?

Recipient: Professor John Wilding
Institution: University of Liverpool
City: Liverpool
Amount: £20,000

Description - click here to read

Vitamin D is an important hormone which performs a number of vital functions in the body, and lack of it for a period can cause a variety of health problems, many of which relate to bone damage. However, it is common for obese individuals to have a low level of vitamin D in their blood. Research work suggests that low blood levels of vitamin D might make individuals more likely to develop type 2 diabetes, a condition in which the body’s cells become less responsive to insulin, the hormone which tells these cells to take sugar out of the blood for storage. This is why people with untreated diabetes can have dangerously high levels of sugar in their blood. Obese individuals tend to have bigger fat cells. These bigger fat cells are less responsive to insulin than normal sized cells, and also release ‘messengers’ that cause inflammation. This inflammation also makes it more difficult for insulin to work properly. We have done some research in this area already and our work has shown that vitamin D may reduce this inflammation in fat, which could ultimately make the body more sensitive to insulin, thus reducing the risk of type 2 diabetes. We also want to know if obese people have high levels in their bodies of a substance which might block vitamin D from reducing this inflammation. In this study, we shall take samples of fat from the abdomens of people who are having planned abdominal surgery, and use these fat biopsies to measure how much inflammation there is. We would also measure vitamin D levels in their blood and perform a number of non-invasive tests to determine the total body fat mass and where that fat is being stored. We would then analyse these results and be in a better position to say whether people with low vitamin D levels have more inflammation in their fat and therefore don’t respond to insulin as they should.

2014

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Influence of n-3FA intake on high-fat diet induced changes in anabolic signalling in healthy adults

Recipient: Dr Oliver Witard
Institution: University of Stirling
City: Stirling
Amount: £5,160

Description - click here to read
High calorie-high fat ‘westernized’ diets that lead to obesity may lead to impairments in the ability of our muscles to grow in response to nutrients. In this research project, first we plan to investigate the potential adverse effect that a high calorie-high fat diet may have on preserving normal quantities of muscle mass. We hypothesize that a high calorie-high fat diet will impair the capability of signalling proteins within skeletal muscle that control muscle growth to respond to nutrient provision. Therefore, we anticipate the capacity to maintain normal quantities of muscle mass will be reduced by a high calorie-high fat diet. Part 2 of this research project investigates the effectiveness of fish oil as an intervention to maintain muscle mass during high calorie-high fat dieting. By feeding fish oil, thereby increasing intake of omega-3 fatty acids, we aimed to investigate the capacity for fish oil to maintain muscle mass during high calorie-high fat dieting. We hypothesize that feeding fish oils during high calorie-high fat dieting will help maintain the capability of signalling proteins within skeletal muscle that control muscle growth to respond to nutrient provision.

2014

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Investigating inflammatory changes in human diabetic bladder dysfunction

Recipient: Dr Andy Grant
Institution: King’s College London
City: London
Amount: £17,360

Description - click here to read

Many people with diabetes are affected by some form of bladder dysfunction, where the bladder muscle becomes overactive and can cause urinary urgency (a sudden and intense urge to use the toilet), nocturia (waking from sleep to urinate multiple times in a night) and urinary incontinence (leakage of urine). Together, these symptoms can dramatically reduce quality of life. Recent studies in patients with overactive bladder muscles (which can also occur without the presence of diabetes) and animal models of diabetic bladder dysfunction have identified altered levels of cytokines in urine and bladder tissue samples. These are a group of chemicals with important roles in regulating the immune system, which can also affect the behaviour of other organs, so they may cause the changes in bladder muscle activity. In this study we plan to collect samples of bladder tissue from patients with normal bladders and from patients with diabetes, in both cases with or without overactive bladders. By quantifying the amounts of cytokines in these tissue samples and comparing them to measurements of bladder function, we hope to further our understanding of the changes that occur in the bladder to cause the debilitating symptoms of diabetic bladder dysfunction.

2014

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Reducing fear of hypoglycaemia in families and Improving metabolic control in Children and young people with diabetes (RICHes): A feasibility pilot study

Recipient: Dr Deborah Christie
Institution: University College London
City: London
Amount: £20,000

Description - click here to read

Fears about hypoglycaemia and associated seizures can result in blood glucose (BG) concentration being run higher than recommended. This fear is underpinned by a) anxiety about frequent monitoring; b) the relentless nature of daily management and c) lack of confidence that others are able or willing to provide appropriate care. The resulting higher HbA1c significantly increases the risk of long-term complications. This study will evaluate an intervention to reduce anxiety and increase confidence in self-management that will result in improved diabetes control for children and young people, and improved quality of life for the whole family.

2014

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The prevalence and risk factors for non-alcoholic fatty liver disease in patients with type 2 diabetes mellitus

Recipient: Dr William Alazawi
Institution: Queen Mary University of London and Barts Health NHS Trust
City: London
Amount: £11,000

Description - click here to read

Deaths from liver disease are rising more rapidly than any other cause of death in the UK. The most common cause of chronic liver injury in the developed world is non-alcoholic fatty liver disease (NAFLD), which is found in up to 75% of patients with diabetes. NAFLD is a spectrum of disease that includes simple fat deposition to the more aggressive form involving inflammation and scarring in the liver (non-alcoholic steatohepatitis (NASH) that can progress to cirrhosis, liver failure and liver cancer. The factors that determine whether an individual patient will develop the more aggressive NASH are not fully understood although a combination of genetic, environmental and lifestyle factors are likely to play a role. There has been recent interest in the effect of ethnicity in the progression of NAFLD and our group has recently reported that NAFLD is three times more common among patients of Bangladeshi origin compared to other ethnic groups – including other South Asian groups. Our aim is to study the degree to which NAFLD and NASH affect patients with diabetes from different ethnicities and to develop guidelines to help doctors manage patients with NAFLD in an ethnically diverse population, such as ours.

2014

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The Professor David Matthews Non-Clinical Fellowship

To use Mendelian randomisation to understanding the causal relationship between circulating biomarkers and Type 2 Diabetes in the UK Biobank.

Recipient: Dr Jessica Tyrrell
Institution: University of Exeter Medical School
City: Exeter
Amount: £172,389

Description - click here to read

Type 2 diabetes represents a huge health burden worldwide (in the UK, it costs the NHS £296 per second), and research is underway to determine how this burden can be reduced. It is a complex disease, with many factors contributing to disease development. Epidemiological studies have demonstrated that type 2 diabetes is associated with a myriad of biomarkers, often as a consequence, rather than cause of the disease process. Understanding which biomarkers play a causal role in type 2 diabetes is of critical importance for understanding disease aetiology, improving diagnosis, and successfully developing treatments. This study will use one of the largest UK population-based studies, the UK Biobank and apply genetic and statistical techniques to investigate the causal relationship between more than 40 biomarkers and type 2 diabetes. The size of UK Biobank will provide a powerful resource for these studies and enable us to draw robust conclusions about which biomarkers are causally linked to diabetes. This project will investigate causality using a Mendelian randomisation approach; a technique that has already helped further our understanding of type 2 diabetes aetiology. This project will be organised in three sequential stages. In Stage 1, we will investigate the association between biomarkers and incident (~3,500 January 2014) and prevalent type 2 diabetes cases (n=14,486) using regression models. In stage 2, we will identify genetic variants associated with our selected biomarkers using regression models. Finally in stage 3, we will utilise instrumental variable analysis to assess the causal relationship between circulating biomarkers and type 2 diabetes. This project will be of critical importance. Identifying the likely small number of biomarkers that truly influence disease aetiology will be incredibly important – it will highlight the pathways and systems that researchers and pharmaceutical companies should focus on if they want to prevent disease or improve treatments.

2014

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Young people with type 1 diabetes (16 – 25 years old) with good and poor glycaemic control: adopting a resilience approach to enhance understanding of differences in this transitional group with generally poor clinical performance.

Recipient: Professor Jorg Huber
Institution: University of Northampton
City: Northampton
Amount: £19,821

Description - click here to read

Young people with type 1 diabetes find it difficult to adjust to and deal effectively with their illness as evidenced by poor blood sugar control, serious complications and high mortality. The problem is particularly pronounced in England in the 16 – 25 age group. Our understanding of this national failure is very limited, particularly as scant recent research is available for the UK. Instead of focusing on the negative aspects of diabetes, we want to find out how young people successfully adjust to and integrate the condition into their day-to-day life. They are living through an important transitional period where crucial developments are taking place, which impact on partner, career and other life-style choices. We adopt a novel approach focusing on resilience, which others and ourselves have successfully researched in groups without diabetes. Resilience is the ability to deal effectively with adversity and bounce back from poor wellbeing/mental health and this will be explored in our study. We will use questionnaire data to assess resilience and associated factors such as attachment, social support, self-esteem and recent life events. We will use in-depth interviews and personal diaries exploring issues of self-care, the challenges of the condition and the way individuals deal with these challenges with the aim to develop a deeper understanding of the role of resilience in dealing with a complex and demanding illness. A key element will be the comparison of individuals with good glycaemic control with those with poor control; in line with the resilience approach a key aim will be to provide an initial resilience profile of the young adult with type 1 diabetes with good blood glucose control. This initial study will provide the basis for further applications carrying out a longitudinal study, possibly incorporating neurobiological assessments, and contributing to the development of targeted interventions.

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