University of Otago researchers are closer to preventing immature death and improving the overall health of people with diabetes.
More than 60 per cent of people worldwide with type 2 diabetes die from some sort of heart disease.
Associate Professor Rajesh Katare, of the Department of Physiology, leads a team of Otago researchers who have been working to develop a treatment for people with type 2 diabetes who develop heart disease.
Previously, the group identified molecular regulators (microRNA) which play a major role in the development of heart disease and modified them before they changed, to prevent the disease in diabetics.
“However, in reality and in clinic, we do not see patients before they develop any form of disease,” Associate Professor Katare says.
“In fact, people don't go to a GP or hospital unless there is a problem.”
Using mouse models, which react in a similar way to humans with type 2 diabetes, the group set out to treat heart disease.
“We identified that our treatment was able to restore the heart function by reducing the death of heart cells,” Associate Professor Katare says.
“This is an exciting result, as we are able to initiate the treatment after the development of the disease but still improve the heart function. This result has given us the confidence that microRNA therapy can be used in clinic.”
Associate Professor Katare says the impact will be huge, particularly among the Māori community due to the simple nature of the treatment and the use of cell-free products, making it culturally safe to use.
It will improve the health of people with type 2 diabetes and reduce immature death, he says.
“This in turn will have a massive impact on the whole whānau.”
The next stage of the project is to test if there will be similar improvements in larger animal models.
“If funded, this will take our research findings one more step closer towards translating into the clinic.”
Therapeutic knockdown of miR-320 improves deteriorated cardiac function in a pre-clinical model of non-ischemic diabetic heart disease.
Nilanjan Ghosh, Sonya Fenton, Isabelle van Hout, Gregory T. Jones, Sean Coffey, Michael J. A. Williams, Ramanen Sugunesegran, Dominic Parry, Philip Davis, Daryl O. Schwenke, Aniruddha Chatterjee, and Rajesh Katare.
Molecular Therapy Nucleic Acids
For more information, please contact:
Associate Professor Rajesh Katare
Department of Physiology
University of Otago
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