West Australian researchers will use fresh funding to investigate how a single gene change causes insulin resistance and type 2 diabetes.

The research by University of WA Professor Aleksandra Filipovska, supported by a newly-announced $60,000 grant from Diabetes Research WA, will also look at how diet and exercise may be able to target a gene change to reveal ways to prevent and manage the onset of type 2 diabetes.

Also the head of the Mitochondrial Medicine and Biology laboratory at the Harry Perkins Institute of Medical Research, Professor Filipovska said the gene change was known to be a significant contributor to metabolic disease.

“This common variation of a gene inside mitochondria, which are microscopic energy producing machines within our cells, can change energy production and breakdown of fats and sugars to cause insulin resistance and type 2 diabetes, and is commonly found in the population,” she explained.

“Using a new model we’ve created using the latest genome editing technology, we hope this project will build on findings from our pilot study to show how this gene is linked to the predisposition to and cause of insulin resistance and its contribution to the development of type 2 diabetes,” said Professor Filipovska.

“We will also test how this single gene change may be impacted by different diets and exercise to understand how we can prevent the onset of type 2 diabetes by altering our nutrition and energy usage.

“Pinpointing the molecular mechanisms linked to this gene change will also help uncover important drug targets for new medicines, test available drugs and antioxidants that may be able to delay insulin resistance, and provide new avenues for tests to diagnose the conditions.”

Diabetes Research WA executive director Sherl Westlund said the charity was pleased to be supporting such vital research.

“Insulin resistance is one of the main features of type 2 diabetes, which is the seventh leading cause of death nationally, so the potential positive impact of this project on the health of Australians is immense,” she said.

“Being able to identify how energy levels fail as type 2 diabetes develops is an important piece of the puzzle in tackling the condition.”

More than 100,000 Australians have developed diabetes in the past year and the total cost impact of diabetes in Australia is estimated at ~$14 billion.

Professor Oliver Rackham from Curtin University, Dr Stefan Siira and Judith Ermer, both from The University of WA are also part of the research team.

Diabetes Research WA, based at Royal Perth Hospital, was established in 1976 to stimulate research into diabetes in Western Australia.

$60,000 has been awarded for a project investigating a new way to tackle disease-inducing chronic inflammation linked to type 2 diabetes.

Professor Pfleger and Dr Elizabeth Johnstone (pictured above) and the Molecular Endocrinology and Pharmacology Laboratory team at the Harry Perkins Institute of Medical Research, in collaboration with colleagues at Monash University, hope to reduce health complications of type 2 diabetes by blocking a newly-discovered pathway.

Inflammation is increased in type 2 diabetes and we’ve found this pathway effectively stokes the fires of inflammation in the body, making it burn more fiercely, increasing the risk of it getting out of control and causing collateral health damage.

The group has found that key proteins on the surface of cells involved in chronic inflammation – known as Immunoglobulin-like Cell Adhesion Molecules – are turned on by a process called transactivation when other G protein-coupled receptor molecules on the cell surface are themselves turned on. They aim is to develop smart inhibitors of this pathway in order to keep inflammation under control and, in doing so, treat and prevent type 2 diabetes complications, such as atherosclerosis – which is the formation of fatty deposits in arteries – and kidney disease.

This new funding will support research into the underlying molecular mechanisms driving this transactivation process and test peptides that modulate the pathway, to expand the number of potential type 2 diabetes drug targets.

Additionally, the work will involve use of BRET – bioluminescence resonance energy transfer – technology, which Professor Pfleger’s laboratory is a world-leader in using to study protein-protein interactions.

Dr Mary Abraham from the Telethon Kids Institute and Perth Children’s Hospital has secured $60,000 from our 2022 Diabetes Research Grants program to launch a pilot study into the use of oral insulin in type 1 diabetes – a medication intervention that could be a game-changer for those with the chronic condition.

Oral insulin had so far predominantly been tested in those with type 2 diabetes while insulin injections or insulin pump therapy are the cornerstone of type 1 diabetes treatment but still, most people remain unable to achieve optimal blood glucose levels, so there’s a very real need to improve on treatment.

Oral insulin has enormous benefits of being a non-invasive form of insulin and offers the hope of reducing the risk of blood sugar levels falling dangerously low in people with diabetes, and it may also help to minimise weight gain that can be an issue with subcutaneous insulin because it causes high insulin levels in the body. It is also believed oral insulin may reduce the long-term risk of diabetes-related vascular complications, as well as possibly restore beta cell function.

This 12-week study aimed to see if oral insulin could be used alongside injected insulin. The success of oral insulin has so far been limited due to absorption issues. This trial of an improved oral drug delivery system has been designed to overcome this challenge. If it can be used to reduce the amount of insulin that needs to be injected by people with type 1 diabetes or mean they require less total insulin, this would be a very welcome breakthrough.

2022 Diabetes Research Grants Announced.

On Monday 15 November 2021, coinciding with the Annual World Diabetes Day, the DRWA 2022 Research Grants were awarded to two very deserving recipients.

Clinical/Translational Research

Dr Mary Abraham from the Telethon Kids Institute and Perth Children’s Hospital has secured $60,000 from our 2022 Diabetes Research Grants program to launch a pilot study into the use of oral insulin in type 1 diabetes – a medication intervention that could be a game-changer for those with the chronic condition.

Oral insulin had so far predominantly been tested in those with type 2 diabetes while insulin injections or insulin pump therapy are the cornerstone of type 1 diabetes treatment but still, most people remain unable to achieve optimal blood glucose levels, so there’s a very real need to improve on treatment.

Oral insulin has enormous benefits of being a non-invasive form of insulin and offers the hope of reducing the risk of blood sugar levels falling dangerously low in people with diabetes, and it may also help to minimise weight gain that can be an issue with subcutaneous insulin because it causes high insulin levels in the body. It is also believed oral insulin may reduce the long-term risk of diabetes-related vascular complications, as well as possibly restore beta cell function.

This 12-week study aimed to see if oral insulin could be used alongside injected insulin. The success of oral insulin has so far been limited due to absorption issues. This trial of an improved oral drug delivery system has been designed to overcome this challenge. If it can be used to reduce the amount of insulin that needs to be injected by people with type 1 diabetes or mean they require less total insulin, this would be a very welcome breakthrough.

Fundamental/Basic Science

$60,000 has been awarded for a project investigating a new way to tackle disease-inducing chronic inflammation linked to type 2 diabetes.

Professor Pfleger and Dr Elizabeth Johnstone (pictured above) and the Molecular Endocrinology and Pharmacology Laboratory team at the Harry Perkins Institute of Medical Research, in collaboration with colleagues at Monash University, hope to reduce health complications of type 2 diabetes by blocking a newly-discovered pathway.

Inflammation is increased in type 2 diabetes and we’ve found this pathway effectively stokes the fires of inflammation in the body, making it burn more fiercely, increasing the risk of it getting out of control and causing collateral health damage.

The group has found that key proteins on the surface of cells involved in chronic inflammation – known as Immunoglobulin-like Cell Adhesion Molecules – are turned on by a process called transactivation when other G protein-coupled receptor molecules on the cell surface are themselves turned on. They aim is to develop smart inhibitors of this pathway in order to keep inflammation under control and, in doing so, treat and prevent type 2 diabetes complications, such as atherosclerosis – which is the formation of fatty deposits in arteries – and kidney disease.

This new funding will support research into the underlying molecular mechanisms driving this transactivation process and test peptides that modulate the pathway, to expand the number of potential type 2 diabetes drug targets.

Additionally, the work will involve use of BRET – bioluminescence resonance energy transfer – technology, which Professor Pfleger’s laboratory is a world-leader in using to study protein-protein interactions.

A $60,000 grant has been awarded to research fellow Dr Aveni Haynes

A $60,000 grant has been awarded to research fellow Dr Aveni Haynes from the Children’s Diabetes Centre at Telethon Kids Institute, and her team, to investigate continuous glucose monitoring (CGM) for measuring blood sugar levels in children at high-risk of developing type 1 diabetes but who are not yet showing clinical signs of the condition.

Dr Haynes said the project will involve children enrolled in the Australia-wide Environmental Determinants of Islet Autoimmunity (ENDIA) study who have either a parent or sibling with type 1 diabetes and who have developed type 1 diabetes-specific autoantibodies that indicate they are on the path towards developing the autoimmune condition.

“There’s evidence that blood sugar levels in these high-risk children could be abnormal some months to years before they develop type 1 diabetes symptoms. Previously these children have been monitored using blood tests which only reflect a snapshot in time,” explained Dr Haynes.

“Our work is looking to find early changes in the pattern of blood glucose levels in very young children in more detail and the CGM will show us what’s happening to those levels 24 hours a day.”

Dr Haynes said given these children had a much higher risk of being diagnosed with clinical type 1 diabetes, their parents may experience anxiety related to this. This project could help alleviate some of that anxiety by giving parents more information about whether or not there were any signs of changes in their child’s day-to-day blood glucose levels.

“The information could also be used in future research aimed to reverse, delay or slow the progression of these children developing symptomatic or clinical type 1 diabetes; perhaps by helping to preserve insulin-producing cells that are lost in type 1 diabetes, or using other possible treatments earlier than is standard practice now,” she said.

“And we want to reduce the chances these at-risk children will first present to hospital with diabetic ketoacidosis which can be life-threatening and is caused by blood sugar levels being too high for too long.”

This project holds enormous potential to impact future treatment and prevention of type 1 diabetes.