Information provided by the Alzheimers Society
Frontotemporal dementia (FTD) is one of the less common types of dementia. The term covers a wide range of different conditions. It is sometimes called Pick’s disease or frontal lobe dementia. This factsheet explains what FTD is, its symptoms, and who gets it. It also describes how it is diagnosed and the treatment and support that is available.
The word ‘frontotemporal’ refers to the lobes of the brain that are damaged in this type of dementia. The frontal lobes of the brain, found behind the forehead, deal with behaviour, problem-solving, planning and the control of emotions. An area of usually the left frontal lobe also controls speech.
The temporal lobes – on either side of the brain – have several roles. The left temporal lobe usually deals with the meaning of words and the names of objects. The right temporal lobe is usually involved in recognising faces and familiar objects. For more see factsheet 456, Dementia and the brain.
Frontotemporal dementia occurs when nerve cells in the frontal and/or temporal lobes of the brain die, and the pathways that connect the lobes change. Some of the chemical messengers that transmit signals between nerve cells are also lost. Over time, as more and more nerve cells die, the brain tissue in the frontal and temporal lobes shrinks.
When the frontal and/or temporal lobes are damaged in this way, this causes the symptoms of FTD. These include changes in personality and behaviour, and difficulties with language. These symptoms are different from the memory loss often associated with more common types of dementia, such as Alzheimer’s disease.
As FTD is a less common form of dementia, many people (including some health professionals) may not have heard of it.
Frontotemporal dementia is much less common than other forms of dementia, such as Alzheimer’s disease or vascular dementia. However, it is a significant cause of dementia in younger people – that is, those under the age of 65. Frontotemporal dementia is probably the third most common cause of dementia in this age group and some studies even place it second most common. It affects men and women roughly equally.
Frontotemporal dementia is most often diagnosed between the ages of 45 and 65. However, it can also affect people younger or older than this, and it is probably under-recognised in older people. Even so, this ‘peak age’ for FTD (the age at which it is most often diagnosed) is much younger than the age at which people are most often diagnosed with the more common types of dementia, such as Alzheimer’s disease.
Being diagnosed at a younger age is likely to present someone with a different set of challenges. They may still be working, have financial commitments or dependent children, and want different services and support. For more information about these issues see factsheet 440, What is young-onset dementia?
The symptoms of FTD dementia vary depending on which areas of the frontal and temporal lobes are damaged. A person may have one of three main types of FTD:
As with most forms of dementia, the symptoms can be very subtle at first, but they slowly get worse as the disease progresses.
This is the most common type of FTD. Two thirds of people with FTD are diagnosed with this type. During the early stages, changes are seen in the person’s personality and behaviour.
A person with behavioural variant FTD may:
It is common for a person with behavioural variant FTD to struggle with planning, organising and making decisions. These difficulties may first appear at work or with managing finances.
In contrast to those with Alzheimer’s disease, people in the early stages of behavioural variant FTD tend not to have problems with day-to-day memory or with visuospatial skills (judging relationships and distances between objects). Someone with FTD may go walking without obvious purpose but, unlike a person with Alzheimer’s, will often find their way home without getting lost.
Recent research shows that FTD can also affect the sensitivity of people with dementia to physical or environmental stimulation such as temperature, sounds and even pain.
It is unusual for a person with behavioural variant FTD to be aware of the extent of their problems. Even early on, people generally lack control over their behaviour or insight into what is happening to them. Their symptoms are more often noticed by the people close to them.
In the other two types of FTD, the early symptoms are difficulties with language that progressively get worse. These difficulties become apparent slowly, often over two or more years.
In progressive non-fluent aphasia, these problems are with speech – ‘aphasia’ means loss of language. Common early symptoms may include:
slow, hesitant speech which may seem difficult to produce – a person may stutter before they can get the right word out, or may mispronounce it when they do
In semantic dementia, speech is fluent but people begin to lose their vocabulary and understanding of what objects are. Common early symptoms may include:
In the early stages of both language forms of FTD, other mental abilities (such as memory, visuospatial skills, planning and organising) tend to be unaffected.
The rate at which FTD progresses varies greatly, with life expectancy ranging from less than two years to 10 years or more. Research shows that on average, people live for about six to eight years after the start of symptoms but this varies widely.
As FTD progresses, the differences between the three types become much less obvious. People with the behavioural variant tend to develop language problems as their condition progresses. They may eventually lose all speech, like a person with one of the language variants.
Similarly, over several years a person with a language variant of FTD (especially semantic dementia) will tend to develop the behavioural problems typical of behavioural variant FTD.
In the later stages of all types of FTD, more of the brain becomes damaged. As a result, the symptoms are often similar to those of the later stages of Alzheimer’s disease. The person may become less interested in people and things and have limited communication. They may become restless or agitated, or behave aggressively. At this late stage, they may no longer recognise friends and family, and are likely to need full-time care to meet their needs.
About 10–20 per cent of people with FTD also develop a motor disorder, either before or after the start of dementia. A motor disorder is one that causes difficulties with movement. These motor disorders, which are generally uncommon but more likely in people with this form of dementia, are:
The symptoms of these three conditions are similar and can include twitching, stiffness, slow movements and loss of balance or co-ordination. In the later stages, they can often cause difficulties with swallowing. Progressive supranuclear palsy and corticobasal degeneration share some symptoms with Parkinson’s disease and are sometimes called ‘atypical parkinsonism’. For more information see factsheet 442, Rarer causes of dementia.
These motor disorders are all degenerative diseases of the nervous system, meaning that they will get worse over time. If a person has both FTD and motor neurone disease, they can deteriorate more quickly than someone with FTD alone. On average, a person with both conditions will live for two or three years after diagnosis.
We don’t know exactly what causes FTD. Experts think that the disease is due to a mixture of genetic, medical and lifestyle factors. Even allowing for its under-recognition in older people, FTD does not show the very strong link with ageing seen for more common dementias such as Alzheimer’s disease or vascular dementia.
Autopsy studies show that the death of nerve cells in the frontal and temporal lobes is linked to clumps of abnormal proteins inside the cells, including proteins called tau and TDP-43. The tau protein may take the form of Pick bodies, which gave FTD its original name of Pick’s disease – after Dr Arnold Pick who first studied the dementia.
Frontotemporal dementia is much more likely to run in families than the more common forms of dementia are. About one third of people with the condition have some family history of dementia.
About 10–15 per cent of people with FTD have a very strong family history of the condition, with several close relatives in different generations affected. This pattern is most common in the behavioural type of FTD and least common in semantic dementia. Typically in these cases, FTD is inherited from a parent as a defect (mutation) in one of three genes: MAPT, GRN or C9ORF72.
Each of the children or siblings of someone with a mutation that is known to cause FTD has a 50 per cent chance of carrying the same mutation. Families with a known mutation should be offered a referral to a specialist genetics service for counselling. For more about genetic testing see factsheet 405, Genetics of dementia.