(Content reproduced with permission from the Alzheimer Society of Canada)
What is Frontotemporal Dementia?
Unlike Alzheimer's disease, which generally affects most areas of the brain,
Frontotemporal Dementia is an umbrella term for a group of rare disorders that
primarily affect the frontal and temporal lobes of the brain – the areas
generally associated with personality and behaviour. In some cases, brain cells
in these areas can shrink or die. In other cases, the brain cells in these areas
get larger, containing round, silver "Pick's bodies." The term "Pick's
Disease" is used to describe this subtype of Frontotemporal Dementia that
has these specific abnormalities. In both situations, the changes in the brain
affect the person's ability to function. Researchers estimate that approximately
2% of all dementia cases are Frontotemporal Dementia.
Other names for Frontotemporal Dementia include:
• Pick's Disease
• Semantic Dementia
• Frontal Lobe Dementia
• Primary Progressive Aphasia
• Corticobasal Degeneration
• Pick's Complex
How does Frontotemporal Dementia affect the person?
Since the frontal and temporal areas of the brain can be affected in different
ways, early symptoms often affect either behaviour and/or speech
• Changes in behaviour may include becoming either withdrawn or disinhibited (e.g., losing the ability to restrain one's behaviour and actions).
The person may lose interest in personal hygiene, become easily distracted or
repeat the same action over and over again. Overeating or compulsively putting
objects in the mouth may occur. Sometimes incontinence is an early symptom of
• Problems with speech (language) can range from reduction
of speech to total loss, i.e. becoming mute. Echoing what has been said by others
and stuttering are common symptoms. The person may have difficulty sustaining
a train of thought or maintaining a conversation for any length of time.Writing
and reading are also affected.
In the early stage of Frontotemporal Dementia, behaviour changes or problems
with speech (language) can appear separately. As the disease progresses, these
two areas will overlap. Unlike Alzheimer's disease, a person with Frontotemporal
Dementia often remains oriented to time and has preserved memory in the early
stages. In the later stages of the disease, general symptoms of dementia arise,
i.e. confusion and forgetfulness. Motor skills are lost and swallowing difficulties
How is Frontotemporal Dementia assessed?
No single test can diagnose Frontotemporal Dementia. Doctors diagnose the disease
through a process of identifying characteristic features of the disease and
ruling out other possible causes. Brain imaging (such as with an MRI) can also
be helpful in making a diagnosis of Frontotemporal Dementia.
What are the risk factors for Frontotemporal Dementia?
Frontotemporal Dementia tends to occur at a younger age than Alzheimer's disease
and can affect both men and women. The average length of the disease is 2-10
years. Little is known about the cause of Frontotemporal Dementia and risk factors
have yet to be identified. While most cases are not inherited, there is an autosomal
dominant gene (chromosome 17) which can be passed from generation to generation.
This type of Frontotemporal Dementia is extremely rare.
Is there a treatment?
At present, there is no known cure and no effective way to slow its progression.
Cholinesterase inhibitors, used as treatment for Alzheimer's disease, usually
do not work for the treatment of Frontotemporal Dementia, as different areas
of the brain are affected. Treatment currently focuses on managing symptoms.
For more information:
• Call your
local Alzheimer Society.
• Visit the Pick's Disease Support
(The contents of this document are provided for information purposes only,
and do not represent advice, an endorsement or a recommendation, with respect
to any product, service or enterprise, and/or the claims and properties thereof,
by the Alzheimer Society of Canada. The Information Sheet is not intended to
replace clinical diagnosis by a health professional.)