What causes PSP?
PSP occurs when brain cells in certain parts of the brain are damaged as a result of a build-up of a protein called tau.
Tau occurs naturally in the brain and is usually broken down before it reaches high levels.
In people with PSP, it isn't broken down properly and forms harmful clumps in brain cells.
The amount of abnormal tau in the brain can vary among people with PSP, as can the location of these clumps. This means the condition can have a wide range of symptoms.
The condition has been linked to changes in certain genes, but these genetic faults aren't inherited and the risk to other family members, including the children or siblings of someone with PSP, is very low.
The symptoms of PSP usually get gradually worse over time.
At first, they can be similar to some other conditions, which makes it difficult to diagnose early on.
Some of the main symptoms of PSP include:
- problems with balance and mobility, including frequent falls
- changes in behaviour, such as irritability or apathy (lack of interest)
- muscle stiffness
- an inability to control eye and eyelid movement, including focusing on specific objects or looking up or down at something
- slow, quiet or slurred speech
- difficulty swallowing (dysphagia)
- slowness of thought and some memory problems
The rate at which the symptoms progress can vary widely from person to person.
Read more about the symptoms of PSP.
There's no single test for PSP. Instead, the diagnosis is based on the pattern of your symptoms.
Your doctor will try to rule out other conditions that can cause similar symptoms, such as Parkinson's disease.
The large number of possible symptoms of PSP also makes it difficult to diagnose correctly and can mean it takes a while to get a definitive diagnosis.
You may need to have a brain scan to look for other possible causes of your symptoms, as well as tests of your memory, concentration and ability to understand language.
The diagnosis must be made or confirmed by a consultant with expertise in PSP. This will usually be a neurologist (a specialist in conditions affecting the brain and nerves).
Read more about how PSP is diagnosed.
Treatments for PSP
There's currently no cure for PSP, but research is continuing into new treatments that aim to relieve symptoms and prevent the condition getting worse.
Treatment currently focuses on relieving the symptoms while trying to make sure someone with PSP has the best possible quality of life.
As someone with PSP can be affected in many different ways, treatment and care is provided by a team of health and social care professionals working together.
Treatment will be tailored to meet the needs of each individual:
- medication to improve balance, stiffness and other symptoms
- physiotherapy to help with movement and balance difficulties
- speech and language therapy to help with speech or swallowing problems
- occupational therapy to help improve the skills needed for daily activities
- botox (botulinum toxin injections) or special glasses to help with eye problems
- feeding tubes to help manage dysphagia and avoid malnutrition or dehydration
Read more about how PSP is treated.
There's currently nothing that can be done to stop PSP gradually worsening, although research into new treatments gives hope that this may be possible in the future.
Good care and assistance can help someone with PSP to be more independent and enjoy a better quality of life, but the condition will eventually put them at risk of serious complications.
It's a good idea to talk to your doctor about what you'd like to happen when the condition reaches this stage.
Difficulty swallowing can cause choking or inhaling food or liquid into the airways. This can lead to pneumonia, which can be life threatening.
Help from a speech and language therapist at an early stage can lower this risk for as long as possible.
As a result of these complications, the average life expectancy for someone with PSP is around 6 or 7 years from when their symptoms start.
But it can be much longer, as the timespan varies from person to person.
Information about you
If you have PSP, your clinical team will pass information about you on to the National Congenital Anomaly and Rare Diseases Registration Service (NCARDRS).
This helps scientists look for better ways to prevent and treat this condition. You can opt out of the register at any time.