The diagnosis of juvenile spondyloarthritis (JSpA) can be difficult because the symptoms are sometimes episodic and unpredictable. However, it is important to get a correct diagnosis as soon as possible in order to begin treatment. This is the role of a pediatric rheumatologist –– a physician with special training in diagnosing and treating arthritis in children. It is important to note that even in the care of the most experienced rheumatologist, a diagnosis can involve extensive testing and time.
In order to make the diagnosis, the physician will commonly do a physical exam and evaluate your child's history of symptoms as well as perform laboratory tests. Note that X-rays are not always useful in the diagnosis of JSpA in that the changes due to spondylitis normally seen in adults are rarely present in children. Moreover, the X-rays can be difficult to interpret in teenagers since the bones are growing along the joints.
SAA receives no government funding and relies on the
generous donations from individuals to create and maintain the programs and
services aimed at improving the futures of the 2.7 million Americans affected
by spondylitis and its family of related diseases.
A complete physical exam is commonly performed including evaluating for arthritis; asking careful questions about, and examining for, inflammation/pain –– specifically enthesitis –– inflammation of the area where a ligament or tendon attaches to the bone. The physician may also test spinal mobility and tenderness in the sacroiliac (SI) joints (the joints at the base of the spine, where the spine meets the pelvis), as well as check movement with breathing.
A clinical history of symptoms is also important. This can include checking the family history of AS and related diseases since heredity does play a factor.
It is important to note that there is no specific laboratory test for JSpA. Blood tests show that children with JSpA do not have rheumatoid factor or antinuclear antibodies common in other types of chronic childhood arthritis. A positive test for the HLA-B27 genetic marker often correlates with the presence of JSpA in a child with arthritis. The presence of the HLA-B27 genetic marker in spondyloarthritis varies by race, so while the HLA-B27 test is important, it is not diagnostic for juvenile spondyloarthritis. Also note that HLA-B27 is a normal gene found in 8 percent of the Caucasian population. Generally speaking, no more than 2 percent of people born with this gene will eventually develop a form of spondyloarthritis.
Sometimes, children with JSpA may encounter other problems such as Crohn's disease or ulcerative colitis (inflammation of the intestine), uveitis or iritis (inflammation of the eye), or psoriasis (a scaly rash that occurs most frequently on the elbows, knees, and scalp, but can cover much of the body).
Posted June 2015
Visit our S.W.I.F.T. website
Posted December 2012
Spondylitis Association of America (SAA): Can you describe the following blood tests and what they look for? Also, how...
PO Box 5872
Sherman Oaks, CA 91413
(800) 777-8189 U.S. only
or (818) 892-1616