Brain scans reveal special case in frontotemporal dementia
People with early-onset dementia are often mistaken for having depression and now Australian research has discovered the cause: a profound loss of ability to experience pleasure related to degeneration of ‘hedonic hotspots’ in the brain where pleasure mechanisms are concentrated.
University of Sydney-led research has revealed marked degeneration, or atrophy, in frontal and striatal areas of the brain related to diminished reward-seeking, in patients with frontotemporal dementia (FTD).
The researchers believe it is the first study to demonstrate profound anhedonia, the clinical definition for a loss of ability to experience pleasure, in people with FTD.
Anhedonia is also common in people with depression, bipolar disorder and obsessive-compulsive disorder and can be particularly disabling for the individual.
In the study, patients with FTD, which generally affects people aged 40-65, displayed a dramatic decline from pre-disease onset, in contrast to patients with Alzheimer’s disease, who were not found to show clinically significant anhedonia.
The results point to the importance of considering anhedonia as a primary presenting feature of FTD, where researchers found neural drivers in areas that are distinct from apathy or depression.
The findings were published in the leading neuroscience journal, Brain.
The paper’s senior author, Professor Muireann Irish from the School of Psychology, notes that despite increasing evidence of motivational disturbances, no study had previously explored the capacity to experience pleasure in people with FTD.
“Much of human experience is motivated by the drive to experience pleasure but we often take this capacity for granted," said Professor Irish, who is also a member of the University of Sydney’s Brain and Mind Centre and recently published a paper in Brain about moral reasoning in FTD.
“But consider what it might be like to lose the capacity to enjoy the simple pleasures of life – this has stark implications for the wellbeing of people affected by these neurodegenerative disorders.
“Our findings also reflect the workings of a complex network of regions in the brain, signalling potential treatments.
“Future studies will be essential to address the impact of anhedonia on everyday activities, and to inform the development of targeted interventions to improve quality of life in patients and their families.”
This is the first study, to the researchers’ knowledge, to demonstrate profound anhedonia in FTD, reflecting loss of grey matter density in the frontal and striatal regions of the brain.
Interestingly, anhedonia was not present in a group of participants with Alzheimer’s disease, suggesting this symptom is specific to FTD.
A total of 172 participants were recruited, including 87 FTD, 34 Alzheimer’s disease participants.
Using brain imaging, researchers found that the loss of pleasure related to degeneration in a discrete set of regions in the so-called pleasure system of the brain.
The study led by the University of Sydney includes researchers with affiliations with the ARC Centre of Excellence in Cognition and its Disorders, the Royal Prince Alfred Hospital and the Black Dog Institute.
Declaration: The authors have no competing interests to declare.