ForeFront

RESEARCH CENTRE

About us

ForeFront provides a unique combination of clinical and laboratory-based research which together aim to unravel the mechanisms behind frontotemporal dementia (FTD) and motor neurone disease (MND) and help to develop effective treatments.

ForeFront comprises two government funded research groups across four themes:

FTD and MND NHMRC Program grant

Neuropathology
Animal modelling and cellular/molecular biology
Neurological research clinics

Memory node of the ARC Centre of Excellence in Cognition and its Disorders

Cognition and neuroimaging

Who’s involved?

Neuropathology

What regions and cell types are vulnerable? What proteins are affected?

Prof Glenda Halliday and Professor Jillian Kril

Animal modelling and cellular/molecular biology

What proteins are toxic and how do they cause pathogenesis? What cells are vulnerability and how can we prevent this?
Professor Jürgen Götz and Assoc. Professor Lars Ittner

Clinical

How does the disease spread through the brain? How can we develop identification tools and test symptomatic treatments?

Prof John Hodges and Prof Matthew Kiernan

Cognition and neuroimaging

What brain functions are impaired? What brain areas are impaired and which functions do they subserve?

Assoc Professor Olivier Piguet and Dr Michael Hornberger

For more information on the clinical aspects of these disease click here

For more information on the laboratory-based research on these diseases click here

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Neuroimaging biomarkers of bipolar disorder risk

Bipolar Disorder is a highly heritable mood disorder characterised by oscillating periods of depression and mania. Previous research has established that this illness is accompanied by widespread changes in brain structure and function. However, the causes of these changes remain unknown. Are these changes a result of the illness process? Are they a product of the medications used to manage Bipolar symptoms? Do they represent the underlying cause of the clinical symptoms observed in this disorder? The Bipolar "Kids and Sibs" Study attempts to answer these questions by studying the young first-degree relatives of Bipolar Disorder patients, who are at increased risk of developing Bipolar Disorder or another related mental illness in the future themselves. As these young “at-risk” individuals have not received a Bipolar diagnosis and are free from medication, they provide a unique opportunity to examine brain differences that relate to both risk for and resilience to Bipolar Disorder. The aim of this study is to identify neuroimaging biomarkers that may differentiate individuals who will ultimately go on to develop Bipolar Disorder or another mental illness, from individuals who are resilient and will remain well. This may assist in identifying those who are most at risk before they become unwell, and allow for interventions that prevent progression to illness or minimise the impact of this condition.

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