What is axial spondyloarthritis?
Axial spondyloarthritis [pronounced: AK-see-ul SPON-dee-low-ar-THRY-tis] is a form of inflammatory arthritis that can affect the spine and pelvic region, including the hips and sacroiliac [SAY-kroh-IL-ee-ak] joints.
Axial refers to the central skeleton (spine and pelvis). Spondylo- refers to vertebra (bones that make up joints of the spine), and arthritis means joint inflammation. Axial spondyloarthritis (axSpA) as a whole term means inflammation affecting joints of the spine and pelvic region.
AxSpA is an autoimmune disease, meaning the body’s own immune system attacks its healthy tissues by mistake. This can lead to back and hip pain and changes to the joints of the spine, caused by inflammation. AxSpA can be very painful, and in some cases limit mobility.
Learning more about axSpA can help you manage symptoms and understand when to seek help from a doctor or healthcare team.
Forms of axial spondyloarthritis
Learn more about the different forms of axSpA
Axial spondyloarthritis is a term used for multiple forms of arthritis that affect the spine and pelvic region. In the past, doctors may have given a diagnosis of axial psoriatic arthritis, reactive arthritis, or enteropathic arthritis. Now, these types of arthritis are considered different forms of axial spondyloarthritis because they share similar signs and symptoms, genetic markers, test results, and treatments.
Radiographic axial spondyloarthritis (ankylosing spondylitis)
Radiographic axial spondyloarthritis (r-axSpA) is the most common form of axSpA. When joints become inflamed over an extended period, this can lead to changes that show up on medical imaging. To receive a diagnosis of r-axSpA, changes must be visible on x-ray of the sacroiliac joints.Until recently, the term ankylosing spondylitis (AS) was used to refer to a diagnosis of r-axSpA. This term is still commonly used to describe symptoms or when making a diagnosis. Ankylosing means fusing and spondylitis means inflammation of the spine. Since not everyone with r-axSpA will experience spinal or bone fusing, it was decided that the term radiographic axial spondyloarthritis is a more accurate name to describe the disease.
Early diagnosis of r-axSpA and intervention is important to long-term health. If left untreated, r-axSpA can lead to bone fusion, chronic pain, and limited mobility. Typically, people with r-axSpA develop symptoms at a younger age, more commonly between late teens and 30, though it can be diagnosed at any age.
Non-radiographic axial spondyloarthritis
Non-radiographic axial spondyloarthritis (nr-axSpA) is not visible on x-ray imaging. People with symptoms and test results strongly suggestive of axSpA, but who have no visible changes to their sacroiliac joints on x-ray may receive a diagnosis of nr-axSpA. Although not visible on x-ray, small changes are sometimes visible using magnetic resonance imaging (MRI).
Juvenile spondyloarthritis
Children can develop axSpA, though symptoms in children typically begin as a form of peripheral arthritis affecting larger joints, or enthesitis, which is inflammation of the entheses (where ligaments attach to bone). Children might experience pain in the hips, knees, ankles, back or spine. They may also have other symptoms that affect their eyes (uveitis), skin (psoriasis), or may experience unusual or painful bowel symptoms (inflammatory bowel disease). Some children might have symptoms that come and go, which can be difficult to diagnose. Children under the age of 16 who experience symptoms of joint pain may receive a diagnosis of juvenile idiopathic arthritis (JIA), and may later develop symptoms of axSpA. For those who experience persistent or recurrent joint pain or inflammation, it is best to see a doctor such as a rheumatologist as early as possible to determine what might be the cause.
Other forms of arthritis included under axSpA include:
Peripheral spondyloarthritis
Peripheral spondyloarthritis does not always affect the spine or sacroiliac joints. Peripheral refers to activity happening outside the core of the body, commonly in the extremities (arms, legs, hands, and feet). In cases of peripheral axSpA, symptoms may be present in joints such as the elbows, hips, knees and ankles, and commonly in the fingers or toes (dactylitis). Some patients may have both axial and peripheral involvement.
Axial psoriatic arthritis
Axial psoriatic arthritis (axPsA) is a form of psoriatic arthritis (PsA) that involves inflammation or pain in the spine or sacroiliac joints. While people with psoriatic arthritis can have symptoms of axSpA in the early stages of their disease, it is more commonly diagnosed among those who have been living with PsA for several years.The likelihood of developing axPsA varies. There are some risk factors, such as having peripheral arthritis in addition to PsA, or testing positive for a gene called HLA-B27, which is linked to inflammation in the spine. More research is needed to better understand how often people with PsA develop axSpA.Since axPsA is typically discovered through x-ray or other medical imaging, it is important to tell your healthcare team if you are experiencing new pain or inflammation around your spine or peripheral joints (elbows, wrists, knees, ankles) so they can help monitor any disease progression.
To learn more, visit our page about Psoriatic Arthritis.
Reactive arthritis
Reactive arthritis is a form of arthritis that develops after an illness, such as an infection – for example, food poisoning or other infection of the intestine. Even though reactive arthritis symptoms start after having an illness, reactive arthritis itself is not contagious. It can happen when your immune system responds to fight the infection and triggers an autoimmune response in your joints.Signs include stiffness, pain and swelling typically of a large joint (knee, elbow, ankle, wrist) that occurs roughly 2-4 weeks after an infection. Classic infections known to trigger reactive arthritis include E. Coli, Yersinia, Shigella, Camphylobacter, and Chlamydia. The spine may also be involved, with signs and symptoms similar to r-axSpA. Many people will get better spontaneously, although a some will develop chronic inflammation in the joints.
To learn more, visit our page about Reactive Arthritis.
Enteropathic arthritis
Enteropathic arthritis (EnA) is a form of arthritis that occurs in people who have inflammatory bowel disease (IBD). EnA most commonly affects the joints of the lower limbs, and sometimes the spine. It causes swelling, inflammation, and joint pain. People living with EnA experience inflammation in both the joints and the digestive tract. Some medications used to treat IBD will also help alleviate symptoms of EnA.
Risk Factors
Below are some of the risk factors that may contribute to developing axSpA.
- Genetics/Family History
- While there are some genetic components that can help determine if someone has an increased likelihood of developing axSpA, not everyone who receives a diagnosis of axSpA will have these genetic markers.
- HLA-B27 Gene
- Human leukocyte antigens, or HLAs, are proteins found on the surface of white blood cells. These proteins help your immune system tell the difference between your own body and infections or other threats to your body.
- HLA-B27 is a gene variant that indicates a person may have an increased likelihood of developing an autoimmune condition, where the body has difficulty telling the difference between your own cells and infections or other foreign substances. HLA-B27 is also connected to some inflammatory conditions. While we’re not exactly sure why this is the case, HLA-B27 has been linked to:
- Axial spondyloarthritis
- Axial psoriatic arthritis
- Reactive arthritis
- Uveitis
- Enteropathic arthritis
- Your doctor may order a blood test to check if you have the HLA-B27 gene to help diagnose your symptoms. If the test is positive, you may have a higher-than-average risk of having or developing an autoimmune condition, including axSpA.
- It is important to note that while this blood test can help provide more information to your doctors about your symptoms, having a positive result for HLA-B27 does not always mean that you have or will develop axSpA. Conversely, you could have a negative test result for HLA-B27 and still have symptoms and receive a diagnosis of axSpA.
- Sex and gender
- Axial spondyloarthritis affects males and females in similar numbers, though males typically develop the disease at an earlier age and are at higher risk of spinal fusion.
- It is not known how often axSpA occurs in people who are intersex or who are trans identified.
- Women may experience additional delays in receiving a diagnosis due to misconceptions about the disease being more common in men.
- Hormones
- More research is needed to better understand the role of hormones in people with axSpA. Hormone fluctuations during menstrual cycles, pregnancy, menopause, or through hormone replacement therapy (HRT) may impact symptoms of axSpA. If you have concerns about how hormones may be affecting your symptoms, speak with your healthcare team.
- Age
- Symptoms of axSpA can appear at any time but typically begin between the ages of 20-30, with almost all people experiencing symptoms before the age of 45.
- Environment
- Symptoms of axSpA can appear for the first time after an infection. While axSpA is not contagious, some infections are known to trigger the immune system in a way that may contribute to its development. Other environmental factors such as stress or smoking could also lead to the onset of symptoms.
- Smoking
- Cigarette smoking can increase disease activity, inflammation and contribute to worse physical functioning and overall quality of life for people with axSpA.
Symptoms and Diagnosis
Symptoms
Symptoms of axial spondyloarthritis (axSpA) can appear in many forms, which can make diagnosis difficult. It can sometimes take doctors and medical teams a long time to rule out other conditions that might share similar symptoms, or to wait to see how symptoms develop over time. In Canada, it can take almost a decade to receive a diagnosis – a barrier that researchers and clinicians are working hard to change.
Receiving a diagnosis and starting treatment early are important. People who experience symptoms for a shorter period of time typically have a better response to treatment.
Being able to recognize symptoms early is key to seeking support from a doctor, and getting set on the path to diagnosis.
The most common symptom of axSpA is chronic low back pain that seems to come and go, or ‘flare’ for no apparent reason. Pain and stiffness are generally worse in the morning or after prolonged periods of rest, and they improve with stretching and exercise as the day progresses. People with axSpA tend to feel better after exercise and worse after rest. AxSpA back pain generally persists for weeks or months, rather than hours or days.
Most people will experience back pain at some point in their lives. Studies show about 25% (1 in 4) of people will develop chronic back pain, and roughly 5% (1 in 20) of those cases are caused by spondyloarthritis.
It is important to pay attention to your symptoms if you have back pain that lasts longer than two weeks. If you have not done any activities that could have caused back pain, it is best to talk to a doctor to find out what may be causing your pain.
Back Pain
Acute back pain
Acute back pain lasts less than six weeks and typically occurs after or alongside an injury or sudden change in a chronic illness. If pain lasts longer than 12 weeks, it may have another source.
Mechanical back pain
Mechanical back pain (MBP) typically improves with rest and may feel worse with movement. It can be caused by a physical injury or could result from another condition affecting the vertebrae (bones that make up sections of the spine), disc herniation (when the rubbery tissue between vertebrae is bulged or pushed out of place), muscle strain, or related to posture or occupational stressors. Mechanical back pain typically has a physical source and should be investigated further by your doctor or healthcare team if it lasts longer than three months.
Inflammatory back pain
Inflammatory back pain (IBP) often causes stiffness in the morning, or after a period of rest, but typically this pain improves after movement or exercise. Inflammation may be part of a flare or could be longer lasting. Inflammatory back pain often develops before the age of 40 and can improve with the help of anti-inflammatory medications.
An estimated 300,000 people living in Canada have axSpA, while about 6.5 million people living in Canada experience chronic mechanical back pain. Separating the two is important since treatments for each type of back pain are very different.
Dactylitis
In some people, painful swelling of the entire toe or finger can occur. This is called dactylitis or ‘sausage’ digit(s).
Enthesitis
The place where a tendon or ligament attaches to bone is called an enthesis (plural: entheses). There are over 100 entheses in your body with many ligaments and tendons attaching to bones. When these areas become swollen or inflamed, it is called enthesitis. People with axSpA may also experience pain in the tendons or ligaments due to inflammation caused by enthesitis. This can be experienced in addition to painful joints.
Some of the more common spots for enthesitis are underneath or on the back of the heels (Achilles tendon, plantar fascia), on the sides of the elbows (tennis/golfer’s elbow), and on the outside of the hips (greater trochanters).
Eye Health
Uveitis
Uveitis [u-vee-i-tis] is an inflammatory condition that affects the uvea (middle layer of the eye). It can cause pain, redness, and inflammation in one or both eyes. It can also cause blurred or distorted vision and may cause permanent damage or vision loss if not treated. Typically, people with axSpA experience a form called anterior uveitis (also called iritis).
Uveitis affects about 40% of people with axSpA. It is important to monitor your symptoms and let your doctor or healthcare team know if you experience pain in or behind your eyes, have blurry vision, become light sensitive, or have other vision changes with no other known cause. Catching symptoms early is important to minimizing changes to your vision.
Fatigue
Fatigue is common among people with inflammatory arthritis. This could be related to inflammation or from years of disrupted sleep caused by pain. It can be difficult to tell what is causing fatigue, and while some people notice an improvement in their level of fatigue from treatment, others do not, even though they may have symptom relief from pain and stiffness. In these cases, fatigue may be caused by more than just disease activity.
Joint Fusion
When symptoms of axSpA go untreated, some people may develop fusion of the ligaments and rubbery discs between the vertebrae. When this happens, it may be difficult for them to bend their spine or rotate their necks. While not all people with axSpA develop fusion, people who are male are at an increased risk. Other risk factors include, elevated inflammation markers, inflammation on imaging, positive HLA-B27 gene testing, and smoking.
Skin Rashes
Psoriasis
Psoriasis is a skin condition recognized by clearly defined, raised patches of skin (called plaques) that are often red and covered with flaky skin (called scale). These patches can be very itchy but are rarely painful. In people with darker skin, plaques may be thicker, darker, and have a purplish, grey or brown colour. For people with lighter skin, the plaques may appear red or have a silvery white scale made of built-up dead skin cells.
Diagnosis
Early, accurate diagnosis of axial spondyloarthritis (axSpA) is important because the damage it causes is difficult if not impossible to reverse; however, early detection and treatment can prevent lasting damage to the spine.
AxSpA can be difficult to diagnose since it has such a wide range of symptoms, and some people may not realize their symptoms are a sign of something more serious until they have already started to progress. In Canada, it takes an average of 9 years to receive a diagnosis.
Since some people only experience episodes, or flares of mild back pain, symptoms may go unnoticed for years. If you are concerned your symptoms are too vague or you are not sure if it is serious enough, it is always best to get checked out anyway.
If you have symptoms of axSpA, it is important to talk to a doctor so they can help determine what might be causing your symptoms. Your doctor will also want to know what kind of back or joint pain you have been experiencing, how long you have had it, and if you have found relief from movement, or other activities.
If you have chronic back pain and history of uveitis, psoriasis, or inflammatory bowel disease (ulcerative colitis or Crohn’s disease), you should be assessed by a rheumatologist.
Using a symptom tracker can help you communicate symptoms to your doctor.
Imaging
To help make a diagnosis, your doctor will order imaging, such as x-ray or MRI. The images will help your doctor see if there are any unusual growths on your bones, or changes to your joints that may be causing your symptoms.
Blood Test
HLA-B27
To help make a diagnosis, your doctor will likely order a blood test to check if you have a gene called HLA-B27.
If you are positive for the HLA-B27 gene, it can be an indication that you are at higher-than-average risk for developing an autoimmune condition. If you have symptoms of axSpA, and a positive blood test for HLA-B27, it can help in making a diagnosis. Roughly 2% of individuals with this gene will develop axSpA although this increases to 30% if an individual also has chronic back pain. It is also possible to have a negative test result and still receive a diagnosis for axSpA. This test is just one tool doctors use to help make a diagnosis.
Treatment

Early intervention and treatment of axSpA is important to help prevent or slow disease progression. While diet and exercise can be helpful in managing some symptoms, some people with axSpA will need to take medication to help keep symptoms under control and prevent or reduce further damage to joints and ligaments.
Once a diagnosis of axSpA has been confirmed, your doctor will work with you to develop a treatment plan. Sometimes this may mean trying different medications until you find something that works for you.
Medications
The goal of treatment for axSpA is to relieve pain and stiffness so you can continue with daily activities.
There are many different types of medications that can help relieve symptoms, but they do not all work in the same way. These medications can be very complex, so you are encouraged to ask for in-depth explanations from your healthcare team – including pharmacists, who are an excellent source of information.
To learn more information about specific medications, visit Arthritis Society Canada’s Medication Reference Guide.
EXPLORE: Watch the video Biologics, Biosimilars and JAK Inhibitors.
NSAIDs
Nonsteroidal anti-inflammatory drugs (NSAIDs) are usually the first type of medication prescribed for pain and inflammation. NSAIDs do not treat the underlying cause of axSpA, but they may be helpful in relieving acute symptoms of pain and inflammation.
NSAIDs work by reducing the amount of a hormone called prostaglandin, which your body creates to respond to pain and inflammation. The most effective way to use NSAIDs for predictable forms of pain is to take your recommended dose as soon as you begin feeling pain or inflammation. This will help limit the amount of prostaglandin your body creates and maximize the medication’s ability to reduce pain and inflammation. Many people with axSpA take NSAIDs daily. The risks and benefits of long term NSAID use should be discussed with your rheumatologist.
Using NSAIDs long-term can irritate the stomach, so it is recommended to take these medications with food, and you may be given an additional medication to help protect your stomach. NSAID use can also worsen conditions such as high blood pressure and kidney disease. Your healthcare team will monitor you for these kinds of complications.
It is important to always follow the directions given to you by your doctor on how to take medications, as they will have information that is specific to you and your health needs. If NSAIDs are ineffective or cannot be used, your doctor or nurse practitioner may recommend another form of medication.
Disease Modifying Anti-Rheumatic Drugs
Disease Modifying Anti-Rheumatic Drugs (DMARDs) are a class of arthritis medications that are designed to suppress and modify the immune system’s inflammation response. These medications are often taken long-term and can take weeks before their effects are felt. Since each person can have a different response to each type of DMARD, sometimes a combination of medications, known as combination therapy, is needed to be most effective at relieving symptoms and controlling the disease.
Biologics and Biosimilars
Inflammation is the body’s natural response to fighting infections or healing trauma. Diseases such as axSpA cause abnormal amounts of inflammation in joints, tendons, and bone which causes pain, swelling, and stiffness. Chronic inflammation can result in irreversible destruction of cartilage in joints, which may lead to joint deformity and loss of function.
Biologics and biosimilars are a form of DMARD created from living cells. Biologic or biosimilar drugs work by blocking specific inflammation signals, improving pain and preventing damage to joints.
A common target for biologics is a small protein in the body called tumor necrosis factor alpha (TNF-α), which is responsible for much of the inflammation, pain, and bone deformities that can occur. Medications that target TNF-α include:
Alternative treatments to TNF-α inhibitors include interleukin-17a (IL-17a) blockers such as:
Less commonly, an oral medication called sulfasalazine may be used in people who cannot take NSAIDs. It is also helpful for some people with peripheral joint involvement.
Janus Kinase (JAK) inhibitors
Janus Kinase or JAK inhibitors are another type of DMARD, belonging to a family of drugs called tsDMARDs (targeted synthetic disease-modifying anti-rheumatic drugs). These drugs block specific enzymes in the body (e.g., JAK1, JAK2, JAK3, TYK2) to reduce the body’s overactive immune response by interrupting how signals are sent throughout the cells.
Commonly used JAK inhibitors include:
Corticosteroids
Corticosteroids such as prednisone are in a class of medication that help alleviate inflammation. They are often fast-acting and very potent. Corticosteroids are sometimes prescribed during the early stages of symptom development or during a flare to help get pain and inflammation under better control before deciding on a longer-term treatment plan. Long-term use of prednisone is not recommended except in rare circumstances.
Long-term use is associated with many side effects including weight gain, diabetes, high blood pressure, cardiovascular disease, fractures, infections, cataracts, glaucoma, and adrenal insufficiency. It is important to follow directions on how to take this type of medication, and how and when to stop.
Surgery
Those with severe, advanced r-axSpA may require surgery for badly damaged joints. Surgery usually involves replacing a joint with an artificial joint. This is called a total joint replacement, most often used for end-stage damage to the hip or knee joints. Benefits include less pain, better movement, and restored function. Spinal surgery is complex and is only used in those with severe deformity.
For more information on hip, knee or ankle replacements, please visit our comprehensive section on surgery.
Self-Management
Explore forms of self-management for inflammatory arthritis, including joint protection, exercises, relaxation techniques, and eating well.
Contributors
This information was last updated May 2025, with expert advice from:
Dr. Jonathan Chan
MD, FRCPC – Rheumatology
Clinical Fellowship in Spondyloarthritis
Clinical Associate Professor, University of British Columbia
Clinical Investigator, Arthritis Research Canada
For more information and resources about axial spondyloarthritis, visit, Canadian Spondyloarthritis Association.
References:
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8811359/
- https://pubmed.ncbi.nlm.nih.gov/36033135/
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645460/
- https://pubmed.ncbi.nlm.nih.gov/34260699/
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9312440
- https://pubmed.ncbi.nlm.nih.gov/18973732
- https://pubmed.ncbi.nlm.nih.gov/37663655/
- https://pubmed.ncbi.nlm.nih.gov/32935330/
- https://www.ncbi.nlm.nih.gov/books/NBK538173/
- https://link.springer.com/article/10.1007/s11916-008-0069-3
- https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10645460
- https://pmc.ncbi.nlm.nih.gov/articles/PMC5470065
- https://pmc.ncbi.nlm.nih.gov/articles/PMC6812897
