New model designed to better understand the causes of Alzheimer’s disease
Scientists from Cardiff University have brought together all known risk factors for Alzheimer’s disease for the first time to produce a new model of the disease which it is hoped will help speed up the discovery of new treatments.
The Multiplex Model is a new way of looking at Alzheimer’s disease developed by Professor Julie Williams, Dr Rebecca Sims and Dr Matt Hill at Cardiff University’s UK Dementia Research Institute (UKDRI)
The findings have been published in Nature Neuroscience.
Cardiff University says the model was produced by looking at all known genetic risk factors to further understanding of what triggers Alzheimer’s and how it develops.
More than fifty risk genes have already been identified and this new theory uses these, and the impact of thousands of other genes, to create the most detailed look at the basis of the disease yet.
There are eight hundred and fifty thousand people with dementia in the UK and Alzheimer’s is the most common form. There is no cure for the condition, which causes problems with memory and thinking.
Julie Williams, director of the UKDRI at Cardiff, said “The genetic breakthroughs we and other scientists have made over the past 20 years have shown us that Alzheimer’s is a multi-component disease.
“The Multiplex Model assumes that changes to one or all of these components work together to form a disease cascade. In other words, we now know that Alzheimer’s can be triggered by a number of different defects in the genetic make-up.
“By using this multi-faceted approach, we can pinpoint our research and work even faster towards developing new therapies.”
Researchers are already able to predict those likely to get Alzheimer’s with about 80% accuracy through looking at the combined effect of all contributing genes. For those with highest genetic risk they can currently predict the likelihood in most cases.
The model of Alzheimer’s used for the past twenty years, the amyloid hypothesis, has been limited to looking at the plaques of amyloid protein formed in the brain triggering dementia, but this approach has yet to yield new treatments that work.
This new model looks at the combined effects of many genes, along with a breakdown in cellular processes linked to Alzheimer’s, such as abnormalities in the brain’s immune response or differences in the way the brain processes cholesterol. It also considers environmental factors, such as ageing and vascular issues.
Julie Williams said “Alzheimer’s disease begins some 20 years before symptoms emerge, and at the moment we just don’t know what triggers it.
“This new approach allows us to look at all of the different factors and components involved – once we know more about exactly what is happening in the earliest stages of disease at a cellular and genetic level we can identify new targets for treatment and preventative therapies.
“It’s likely that there won’t be a single cure for Alzheimer’s – there’ll be lots of different treatments that target various processes, similar to heart disease. Our research is attacking this complex disease from many different angles.”
Bart De Strooper, director of the UKDRI, said “We are proud of this great overview of the genetic basis of Alzheimer’s disease from one of our world-leading teams in the UK Dementia Research Institute. The huge progress in understanding the complex genetics underlying this condition will greatly help us in deciphering the early disease phases, when treatment intervention is most likely to be effective.
“This further emphasises the need for a multi-angle, holistic approach to studying neurodegenerative disease. In order to make breakthroughs, we will have to harness wide-ranging expertise from across the research field, ensuring new knowledge gained is brought together to provide a complete picture of the causes and drivers of dementia.”
Cardiff University’s £20m dementia research centre is one of seven UK centres looking at finding new ways to understand diagnose, treat, prevent and care for people with dementia.