Frontotemporal dementia is a rare type of dementia that tends to run in families.
The term 'dementia' describes a loss of mental ability that is more than would be expected with ageing. It is sufficient to affect day-to-day activities and gets progressively worse.
Frontotemporal dementia is similar to Alzheimer's disease in that it is caused by a build-up of abnormal proteins in the brain, leading to a progressive loss of brain cells. The affected areas of the brain gradually function less well and shrink.
It tends to affect the frontal and temporal lobes of the brain (the front and sides) in particular, and often starts at a younger age than usually seen in Alzheimer's disease.
The frontal lobes are at the front of the brain, behind the forehead – they regulate our ability to plan and organise ourselves and are important in regulating our behaviour. The temporal lobes are on either side of the brain above and behind the ears, and they organise memory and language.
Several different conditions can affect these lobes and 'frontotemporal dementia' is the broad term to describe them all (read about the types of frontotemporal dementia). Symptoms vary depending on the exact areas of the brain affected.
Generally, frontotemporal dementia causes slowly progressive problems with language, thinking, emotions and behaviour. It can profoundly alter a person's character and social conduct – for example, they may either become impulsive and much more outgoing, or uninterested and lacking in energy, depending on the type of disease they have.
Other typical symptoms include inappropriate behaviour in social situations and difficulty with speech.
Frontotemporal dementia typically starts between the ages of 45 and 65, although it can sometimes affect younger people as well as the elderly.
Learn more about the symptoms of frontotemporal dementia.
The disease worsens over a period of time – typically three to 10 years – although it varies widely between patients (some cases can be more rapid; in others it can be much slower).
Over time, new symptoms may develop that can be quite different to those already present. Past problems might disappear and new ones emerge.
People with frontotemporal dementia can become isolated and socially withdrawn as the illness progresses. They may not want to spend time in the company of others, or when in company, may lack empathy and concern for others. They may behave in rude or insulting ways.
Some lack the motivation to care for themselves well and may need supervision and prompting. Home-based help is often needed, and some people will eventually need residential care in a nursing home.
Frontotemporal dementia is caused by a build-up of abnormal proteins in the brain.
The abnormal proteins clump together and become toxic to the brain cells, causing them to die. The frontal and temporal lobes of the brain are typically most affected and as cells are lost, the brain areas shrink over time.
It's not fully understood why these abnormal proteins build up, but there is often a genetic cause. About a third to a half of cases of frontotemporal dementia are inherited and run in families.
Learn more about the causes of frontotemporal dementia.
If your doctor thinks you may have dementia, you may be referred to a memory clinic or another specialist clinic, where you will be asked about your symptoms and have a physical check-up, memory test and cognitive test. You may also have blood tests and brain scans.
Learn more about the diagnosis of frontotemporal dementia.
There is currently no cure for frontotemporal dementia, nor any drugs that will slow the progress of the disease.
Behaviour modification may help control challenging or dangerous behaviours, and antidepressants can be effective in improving some of the symptoms. Learn more about the management of frontotemporal dementia.
Rehabilitative support such as physiotherapy, occupational therapy and speech therapy aim to help with adapting to lost functions, and dementia activities such as 'memory cafes' and some psychological therapies can help with managing the symptoms.
If you have dementia, your future health and social care needs will need to be assessed and a care plan will be drawn up.
For more information, read about the management of frontotemporal dementia.
People with frontotemporal dementia tend to have problems with emotions, communication and behaviour. They will not usually be aware of these changes.
The early symptoms depend on which area of the brain is affected.
Generally, symptoms gradually worsen over a period of three to 10 years.
Behavioural and emotional changes vary widely from person to person – for example, some may be uninterested and seem to have no drive, while others may be impulsive and more outgoing, with no inhibitions.
Typical signs are:
As the disease progresses, people with frontotemporal dementia may become socially isolated and withdrawn.
People with frontotemporal dementia tend to gradually lose the ability to speak, eventually becoming mute.
Many people with frontotemporal dementia lose the ability to think for themselves. Signs are:
In the later stages, many people with frontotemporal dementia may develop problems with movement. They may no longer initiate movements and may become rigid.
Frontotemporal dementia is caused by a build-up of abnormal proteins affecting the frontal and temporal areas of the brain (behind the forehead and above and behind the ears).
The abnormal proteins clump together and become toxic to the brain cells, causing them to die. The frontal and temporal lobes are most affected and shrink over time.
It's not yet fully understood why these abnormal proteins build up, but there is often a strong genetic cause. About a third to a half of cases of frontotemporal dementia are inherited and run in families.
Mutations (alterations) in three genes account for the majority of these inherited cases:
Tau protein is involved in some cases of frontotemporal dementia. This protein is present in all nerve cells and has an important role in transporting other essential proteins between nerve cells in the brain.
A mutation in the gene that codes for tau protein causes abnormal tau to build up. This particular mutation is found on chromosome 17 (see the box, top right, for an explanation of genes and chromosomes).
Without a usable form of tau protein, and with an abnormal form of the protein building up, the brain cells cannot function properly and so they die.
Other types of frontotemporal dementia will be associated with different genes, proteins and chromosomes. In other words, there is no single common cause of frontotemporal dementia.
Confirming a diagnosis of dementia can be difficult, particularly when the condition is in its early stages. This is because many of the symptoms of dementia can be caused by other conditions.
When you visit your doctor it can be helpful if you and a close relative or friend are seen together, because they can help you remember what is happening.
For frontotemporal dementia to be diagnosed correctly, you will have a number of tests and assessments, including:
Some of these tests can be carried out by your doctor. Some will be carried out by specialists, such as a neurologist (an expert in treating conditions that affect the brain and nervous system), an elderly care physician, or a psychiatrist with experience in treating dementia.
Questionnaires are sometimes used to help test your mental abilities and how severe your symptoms are. One widely used questionnaire is the Mini Mental State Examination (MMSE).
The MMSE can be used to assess a number of different mental abilities, including:
The MMSE is a series of questions, each carrying a score with a maximum of 30 points. Example questions include:
The MMSE is not a test to diagnose dementia. However, it is useful for assessing the level of mental impairment that a person with dementia may have.
Scores on these and other tests only help to assess the problem and must be taken into context. For example, someone who cannot read or write very well may score less than someone else, but they may not have dementia. Similarly, someone with a higher level of education may achieve a higher score but still have dementia.
More detailed psychological tests (including tests of frontal lobe function, language, memory and thinking) may also be used by a specialist psychologist.
Once you've been diagnosed with frontotemporal dementia, your future health and social care needs will need to be assessed and a care plan drawn up.
A care plan is a way of ensuring you receive the right treatment for your needs – you can read more about it in the box on this page.
There is currently no cure for frontotemporal dementia, but certain medication and psychological therapy can help in managing the symptoms. These are detailed below.
Unfortunately, acetylcholinesterase inhibitors such as donepezil, which are normally prescribed for Alzheimer's disease and vascular dementia, are not effective in frontotemporal dementia.
There is some evidence that selective serotonin reuptake inhibitors (SSRIs), a type of antidepressant, may help control the loss of inhibitions, overeating and compulsive behaviour seen in some people with frontotemporal dementia.
Learn more about SSRIs, including how they work and the side effects.
Antipsychotics such as haloperidol are only really used for treating severely challenging behaviour that is putting you or others at risk of harm.
This is because the drugs can cause a range of serious side effects, including rigidity and immobility.
If antipsychotics are needed, they will be prescribed at the lowest possible dose and for the shortest possible time, and your health will be carefully monitored.
The medication may cause drowsiness and/or shaking. You can [look up your antipsychotic medication] to find out more about it, including the side effects.
Psychological treatments do not slow down the progression of dementia, but they can help you to cope with the symptoms.
Some psychological treatments are outlined below.
Cognitive stimulation involves taking part in activities and exercises designed to improve your memory, problem-solving skills and language ability.
Reality orientation therapy is a type of therapy that reduces feelings of mental disorientation, memory loss and confusion, while improving feelings of self-esteem.
The therapy may involve group work in a classroom, in which a board prominently displays information such as:
The group members repeat a series of tasks designed to give mental stimulation. The tasks also reinforce information regarding the time, the place and the people involved in the group. You will be involved in discussions about a variety of topics, as well as taking part in word and memory games.
Reality orientation may be beneficial in some cases, but the benefits can be small and are often only apparent with continued effort. The technique is also often considered unsuitable for use in care home settings.
Behavioural therapy uses a problem-solving approach where possible motivations and reasons for troublesome behaviour are identified. Different strategies are adopted to try to change that behaviour.
For example, a person with dementia may have a history of wandering out of their home or care centre because they feel restless. Therefore, encouraging them to take part in regular physical exercise may help to decrease their restlessness.
Behavioural therapy can be used to treat many of the behavioural problems associated with dementia, such as depression, aggression, and delusional thinking. It is usually given by a carer, such as a trained friend or relative, or by an employed carer. It is supervised by a healthcare professional.
Important: Our website provides useful information but is not a substitute for medical advice. You should always seek the advice of your doctor when making decisions about your health.