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 can vary. This type of dementia resembles Alzheimer's disease in that it also involves a progressive degeneration of brain cells that is irreversible.
With this form of dementia, a person may have symptoms such as sudden onset of memory loss, behaviour changes, or difficulties with speech and movement.
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 shrink or die. In other cases, the brain cells in these areas get larger, containing round, silver "Pick's bodies". Pick's disease refers to a subtype of frontotemporal dementia that has these specific abnormalities. In frontotemporal dementia, the changes in the brain affect the person's ability to function. Researchers estimate that approximately two to five per cent of all dementia cases are frontotemporal dementia.
Other names often used for frontotemporal dementia, in addition to Pick's disease, include:
- Semantic dementia
- Frontal lobe dementia
- Primary progressive aphasia
- Corticobasal degeneration
- Pick's complex
Symptoms of frontotemporal dementia
Since the frontal and temporal areas of the brain can be affected, early symptoms often affect either behaviour and/or speech (language).
- Changes in behaviour may include becoming either withdrawn or disinhibited (e.g., losing the ability to restrain one's behaviour and actions).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 the disease.
Other possible changes in behaviour include
- Inappropriate social behaviour, e.g. they may say inappropriate things or come across as rude or tactless
- Loss of insight into the behaviours of oneself and others (making it seem as if they don’t care)
- Changes in food preferences
- Blunted emotions
- Decreased energy and motivation
- Changes in personality, e.g. more outgoing people may become quieter and quiet people may become more extroverted
- Problems with speech (language) can range from speaking less to total loss of speech, i.e. becoming mute. They may have difficulty finding the right words and may use circumlocution, i.e., talking around the words or describing what they mean. 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 memory is not a problem 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 occur.
Diagnosis of frontotemporal dementia
Assessment is important to rule out other problems, for example, primary psychiatric disorder, for which it may be mistaken. 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. Cognitive (thinking) tests may be done to assess which brain functions are affected. A history will be taken from the person, family and caregivers, to get a detailed picture of what has been happening. Brain imaging (such as with an MRI) can also be helpful in making a diagnosis of frontotemporal dementia.
Risk factors for frontotemporal dementia
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 one extremely rare type of frontotemporal dementia which can be passed from generation to generation.
Treatment for frontotemporal dementia
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.
Much can be done, however, to help manage the symptoms. It is important to learn as much as possible about the disease, to help understand and respond to the person’s new behaviours. People around the individual will need to seek support to learn coping strategies to work around the individual’s behaviour, rather than trying to get the person to change. Speech pathologists may be helpful in teaching strategies to work around the communication problems.
For more information, check out the full brochure on Frontotemporal Dementia.
More information and resources
- Frontotemporal Dementia: Facing the Challenges for Patients, Family Members, and Clinicians
The first half of this presentation will briefly describe some of the challenges associated with diagnosing of FTD, with a focus on the contributions of neuropsychological assessment and interprofessional team collaboration. The second half of the presentation will describe a unique telehealth-delivered support group for spouses of individuals diagnosed with FTD and other atypical dementia, and the lessons learned from our caregiver participants about family member needs and the essential ingredients of therapeutic group interventions. Hosted by brainXchange in partnership with the Alzheimer Society of Canada and the Canadian Dementia Resource and Knowledge Exchange (CDRAKE).
- Behavioural variant frontotemporal dementia
This webinar discusses behavioural variant frontotemporal dementia (bvFTD), a type of frontotemporal dementia. In this presentation, you’ll learn about the criteria physicians use to diagnose bvFTD, the basics of its pathology, genetics and treatment options. Presented by Dr. Carmela Tartaglia, Assistant Professor at the University of Toronto. Hosted by brainXchange in partnership with the Alzheimer Society of Canada and the Canadian Consortium of Neurodegeneration in Aging (CCNA).
Fact sheets and booklets
- Understanding the Genetics of FTD: A guide for patients and their families, The Association for Frontotemporal Degeneration
- What about the kids? Frontotemporal degeneration: Information for parents with young children and teens, The Association for Frontotemporal Degeneration
- The doctor thinks its FTD. Now what? A guide for managing a new diagnosis (FTD), The Association for Frontotemporal Degeneration
- Frontotemporal dementia support, Rare Dementia Support
- Frontotemporal dementia, The Mayo Clinic
- Improving the care of persons with dementia in rural and remote areas, Rural Dementia Action Research
- Contact your local Alzheimer Society to find out about more resources