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Ankylosing spondylitis (AS) is a long-term (chronic) condition in which the spine and other areas of the body become inflamed.
AS tends to first develop in teenagers and young adults. It's also around three times more common in men than in women.
The symptoms of AS can vary, but usually involve:
These symptoms tend to develop gradually, usually over several months or years, and may come and go over time.
In some people the condition gets better with time, but for others it can get slowly worse.
Read about symptoms of ankylosing spondylitis.
You should see your GP if you have persistent symptoms of AS.
If your GP thinks you may have the condition, they should refer you to a specialist in conditions affecting muscles and joints (rheumatologist) for further tests and any necessary treatment.
Further tests may include blood tests and imaging tests.
Read about diagnosing ankylosing spondylitis.
It's not known what causes the condition, but there's thought to be a link with a particular gene known as HLA-B27.
Read about the causes of ankylosing spondylitis.
There's no cure for AS and it's not possible to reverse the damage caused by the condition. However, treatment is available to relieve the symptoms and help prevent or delay its progression.
In most cases treatment involves a combination of:
Surgery is sometimes needed to repair significantly damaged joints or correct severe bends in the spine, but this is uncommon.
Read about treating ankylosing spondylitis.
The outlook for AS is highly variable. For some people the condition improves after an initial period of inflammation, whereas for others it can get progressively worse over time.
Around 70-90% of people with AS remain fully independent or minimally disabled in the long term.
However, some people eventually become severely disabled as a result of the bones in their spine fusing in a fixed position and damage to other joints, such as the hips or knees.
With modern treatments, AS doesn't normally affect life expectancy significantly, although the condition is associated with an increased risk of other potentially life-threatening problems.
For example, AS can lead to:
Read about the complications of ankylosing spondylitis.
If you have AS, 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.
Find out more about the AS register.
The symptoms of ankylosing spondylitis (AS) usually develop slowly over several months or years. The symptoms may come and go, and improve or get worse, over many years.
AS usually first starts to develop during the later teenage years or early adulthood.
The main symptoms of AS are described below, although you may not develop all of these if you have the condition.
Back pain and stiffness are usually the main symptoms of AS. You may find:
As well as causing symptoms in your back and spine, AS can also cause inflammation of the joints (arthritis) in other parts of your body, such as your hips and knees.
The main symptoms associated with arthritis are:
Enthesitis is painful inflammation where a bone is joined to a tendon (a tough cord of tissue that connects muscles to bones) or a ligament (a band of tissue that connects bones to bones).
Common sites for enthesitis are:
If your ribs are affected, you may experience chest pain and find it difficult to expand your chest when breathing deeply.
Fatigue is a common symptom of untreated AS. It can make you feel tired and lacking in energy.
In ankylosing spondylitis (AS) several parts of the lower spine become inflamed, including the bones in the spine (vertebrae) and spinal joints.
Over time this can damage the spine and lead to the growth of new bone. In some cases this can cause parts of the spine to join up (fuse) and lose flexibility (ankylosis).
It's not known exactly what causes AS, but in many cases there seems to be a link with a particular gene known as HLA-B27.
Research has shown more than 9 out of 10 people with AS carry a particular gene known as human leukocyte antigen B27 (HLA-B27).
Having this gene doesn't necessarily mean you'll develop AS. It's estimated 8 in every 100 people in the general population have the HLA-B27 gene, but most don't have AS.
It's thought having this gene may make you more vulnerable to developing AS. The condition may be triggered by one or more environmental factors, although it's not known what these are.
Testing for this gene may be carried out if AS is suspected. However, this test isn't a very reliable method of diagnosing the condition because some people can have the HLA-B27 gene but not have ankylosing spondylitis.
Read about how ankylosing spondylitis is diagnosed.
AS can run in families, and the HLA-B27 gene can be inherited from another family member.
If you have AS and tests have shown you carry the HLA-B27 gene, the chance of any children you have developing the condition is less than 20%.
If you have AS but don't carry the HLA-B27 gene, the chance of any children you have developing the condition is less than 10%.
If you have a close relative who has AS, such as a parent or a brother or sister, you're three times more likely to develop the condition compared with someone who doesn't have a relative with the condition.
Ankylosing spondylitis (AS) can be difficult to diagnose because the condition develops slowly and there's no definitive test.
The first thing you should do if you think you have AS is to see your GP. They'll ask about your symptoms, including:
Back pain associated with AS can be quite distinctive. For example, it usually doesn't improve with rest and may wake you up during the night.
If your GP suspects AS, they may arrange blood tests to check for signs of inflammation in your body. Inflammation in your spine and joints is one of the main symptoms of the condition.
If your results suggest you do have inflammation, you'll be referred to a rheumatologist for further tests. A rheumatologist is a specialist in conditions that affect muscles and joints.
Your rheumatologist will carry out imaging tests to examine the appearance of your spine and pelvis, as well as further blood tests.
These may include:
A genetic blood test may sometimes be carried out to see if you carry the HLA-B27 gene, which is found in most people with AS.
This can contribute towards a diagnosis of AS, but it's not entirely reliable as not everyone with the condition has this gene and some people have the gene without ever developing AS.
Although scans can sometimes show spinal inflammation and fusing of the spine (ankylosis), damage to the spine can't always be picked up in the early stages of AS.
This is why diagnosis is often difficult. In many cases confirming a diagnosis is a long process that can take years.
A diagnosis of AS can usually be confirmed if an X-ray shows inflammation of the sacroiliac joints (sacroiliitis) and you have at least one of the following:
If you have all three of these features but don't have sacroiliitis – or if you only have sacroiliitis – you'll be diagnosed with probable ankylosing spondylitis.
There's no cure for ankylosing spondylitis (AS), but treatment is available to help relieve the symptoms.
Treatment can also help delay or prevent the process of the spine joining up (fusing) and stiffening.
In most cases treatment involves a combination of:
You can also read a summary of the pros and cons of the available treatments to compare your options.
Keeping active can improve your posture and range of spinal movement, along with preventing your spine becoming stiff and painful.
As well as keeping active, physiotherapy is a key part of treating AS. A physiotherapist can advise about the most effective exercises and draw up an exercise programme that suits you.
Types of physiotherapy recommended for AS include:
Some people prefer to swim or play sport to keep flexible. This is usually fine, although some daily stretching and exercise is also important.
If you're ever in doubt, speak to your physiotherapist or rheumatologist before taking up a new form of sport or exercise.
The National Ankylosing Spondylitis Society (NASS) provides detailed information about different types of exercise to help you manage your condition.
You may need painkillers to manage your condition while you're being referred to a rheumatologist. The rheumatologist may continue prescribing painkillers, although not everyone needs them all the time.
The first type of painkiller usually prescribed is a non-steroidal anti-inflammatory drug (NSAID). As well as helping ease pain, NSAIDs can help relieve swelling (inflammation) in your joints.
Examples of NSAIDs include:
When prescribing NSAIDs, your GP or rheumatologist will try to find the one that suits you and the lowest possible dose that relieves your symptoms. Your dose will be monitored and reviewed as necessary.
If NSAIDs are unsuitable for you, an alternative painkiller, such as paracetamol, may be recommended.
Paracetamol rarely causes side effects and can be used in women who are pregnant or breastfeeding. However, paracetamol may not be suitable for people with liver problems or those dependent on alcohol.
If necessary, you may also be prescribed a stronger type of painkiller called codeine as well as paracetamol.
Codeine can cause side effects, including:
If your symptoms can't be controlled using painkillers or exercising and stretching, anti-tumour necrosis factor (TNF) medication may be recommended. TNF is a chemical produced by cells when tissue is inflamed.
Anti-TNF medications are given by injection and work by preventing the effects of TNF, as well as reducing the inflammation in your joints caused by ankylosing spondylitis.
Examples of anti-TNF medication include:
These are relatively new treatments for AS and their long-term effects are unknown. However, they have been used for longer in people with rheumatoid arthritis and this is providing clearer information about their long-term safety.
If your rheumatologist recommends using anti-TNF medication, the decision about whether they're right for you must be discussed carefully, and your progress will be closely monitored.
In rare cases anti-TNF medication can interfere with the immune system, increasing your risk of developing potentially serious infections.
The National Institute for Health and Care Excellence (NICE) has produced guidance about the use of anti-TNF medication for AS.
NICE states adalimumab, etanercept and golimumab may only be used if:
After 12 weeks of treatment with anti-TNF medication, your pain score and BASDAI will be tested again to see whether they've improved enough to make continuing treatment worthwhile.
If they have, treatment will continue and you'll be tested every 12 weeks. If there's not enough improvement after 12 weeks, you'll be tested again at a later date or the treatment will be stopped.
Corticosteroids have a powerful anti-inflammatory effect and can be taken as tablets or injections by people with AS.
If a particular joint is inflamed, corticosteroids can be injected directly into the joint. You'll need to rest the joint for up to 48 hours after the injection.
It's usually considered wise to have a corticosteroid injection up to three times in one year, with at least three months between injections in the same joint.
This is because corticosteroids injections can cause a number of side effects, such as:
Corticosteroids may also calm down painful swollen joints when taken as tablets.
Disease-modifying anti-rheumatic drugs (DMARDs) are an alternative type of medication often used to treat other types of arthritis.
DMARDs may be prescribed for AS, although they're only beneficial in treating pain and inflammation in joints in areas of the body other than the spine.
Sulfasalazine is the main DMARD sometimes used to treat inflammation of joints other than the spine.
Most people with AS won't need surgery. However, joint replacement surgery may be recommended to improve pain and movement in the affected joint if the joint has become severely damaged.
For example, if the hip joints are affected, a hip replacement may be carried out.
In rare cases corrective surgery may be needed if the spine becomes badly bent.
As the symptoms of AS develop slowly and tend to come and go, you'll need to see your rheumatologist or GP for regular check-ups.
They'll make sure your treatment is working properly and may carry out physical assessments to assess how your condition is progressing. This may involve further sets of the same blood tests or X-rays you had at the time of your diagnosis.
Any complications of ankylosing spondylitis that arise will be treated as they develop.
Ankylosing spondylitis (AS) is a complex condition that can affect many parts of your body. It can cause complications in your day-to-day life and lead to additional health conditions.
Some complications associated with AS are outlined below.
Although most people with AS remain fully independent or minimally disabled in the long term, some people with the condition eventually have severely restricted movement in their spine.
This usually only affects the lower back and is the result of the bones in the spine joining up (fusing).
Fusing of the spine can make it difficult to move your back and can mean your posture becomes fixed in one position, although it doesn't lead to severe disability in most cases.
In rare cases surgery may be recommended to correct severe bends in the spine.
AS can cause joints such as the hips and knees to become inflamed. This can damage the affected joints over time, making them painful and difficult to move.
If a joint becomes particularly damaged, you may need surgery to replace it with an artificial one.
Iritis, also known as anterior uveitis, is a condition sometimes associated with AS where the front part of the eye becomes red and swollen. It usually only affects one eye, rather than both.
If you have iritis, your eye may become red, painful and sensitive to light (photophobia). Your vision may also become blurred or cloudy.
You should visit your GP as soon as possible if you have AS and think you may have developed iritis, as the condition can cause the loss of some or all of your vision if not treated promptly.
If your GP thinks you have iritis, they'll refer you urgently to an ophthalmologist, a medical doctor who specialises in eye problems, for treatment.
Iritis can usually be treated with corticosteroid eye drops.
Osteoporosis is where the bones become weak and brittle. In AS osteoporosis can develop in the spine and increase your risk of fracturing the bones in your backbone. The longer you have the condition, the more this risk increases.
If you do develop osteoporosis, you'll usually need to take medication to help strengthen your bones.
There are a number of medications that can be used to treat osteoporosis, which can be taken by mouth (orally) as tablets or given by injection.
Read about treating osteoporosis.
If you have AS, you may also have an increased risk of developing cardiovascular disease (CVD). CVD is a general term that describes a disease of the heart or blood vessels, such as heart disease and stroke.
Because of this increased risk, it's important to take steps to minimise your chances of developing CVD.
Your rheumatologist, a specialist in treating muscle and joint conditions, can advise about lifestyle changes you should make to minimise your risk of developing a CVD.
These changes may include:
You may also be prescribed medication to reduce your blood pressure or blood cholesterol level.
Cauda equina syndrome is a very rare complication of AS that occurs when nerves at the bottom of your spine become compressed (compacted).
Cauda equina syndrome causes:
See your GP as soon as possible if you have AS and you develop any of these symptoms.
In very rare cases it's possible to develop a condition called amyloidosis as a complication of AS.
Amyloid is a protein produced by cells in your bone marrow, the spongy material found in the centres of some hollow bones.
Amyloidosis is a condition where amyloid builds up in organs such as your heart, kidneys and liver.
It can cause a wide range of symptoms, including:
Over time AS can increasingly affect your ability to work. Some people with the condition may be unable to work at all, and others may need to make changes to their working life, such as working part-time, working from home, or avoiding physically demanding work.
When at work, it's important to maintain a good posture when sitting or standing for long periods of time. You should get up, stretch and move around regularly. This could mean adjusting your work station or ensuring you take regular breaks.
Read about how to sit correctly.
The National Ankylosing Spondylitis Society (NASS) has more information on living with Ankylosing Spondylitis, including advice about the condition and employment.