Arthritis is commonly perceived as a condition that only affects older adults. However, children are not immune to this disease either. Juvenile Idiopathic Arthritis (JIA) is the most common type of arthritis in children, and unlike age-related osteoarthritis, it is an autoimmune condition. This means the body’s immune system mistakenly attacks its own joint tissues, leading to pain, stiffness, and swelling. Recognizing early signs, understanding the disease, and ensuring timely intervention can prevent long-term joint damage and improve a child’s quality of life.
- Juvenile Arthritis Is an Autoimmune Disease – JIA develops when a child’s immune system attacks healthy tissues in the joints, causing inflammation. It is not caused by overuse or injury. While the exact cause remains unknown, genetics and environmental triggers may play a role. JIA includes several subtypes, each with unique features, but all involve persistent joint inflammation lasting six weeks or more in children under 16.
- Early Symptoms May Be Subtle and Easily Missed – Parents may notice symptoms like morning stiffness, joint swelling, or a child limping without an obvious injury. Children may also become more fatigued, irritable, or lose interest in physical activities. Some may even develop low-grade fever or a rash, especially during flare-ups. If these symptoms persist, it’s important to seek medical evaluation.
- Severity Can Range from Mild to Debilitating – JIA can vary in severity. Mild cases may cause intermittent stiffness and discomfort in a single joint, particularly in the mornings. Moderate cases might include visibly swollen, warm, or red joints, with reduced mobility. In severe cases, multiple joints may be involved, and deformities can develop, significantly impacting the child’s ability to walk, write, or play.
- Physical and Emotional Impact Is Significant – Children may struggle to express or understand their pain, leading to frustration or emotional distress. The unpredictability of symptoms—better on some days and worse on others—can interfere with school, play, and social life. Prolonged pain and reduced mobility may also lead to poor sleep and affect a child’s confidence and mood.
- Early Diagnosis Makes a Big Difference – If symptoms continue for more than six weeks, consult a Pediatric Rheumatologist. Diagnosis involves a thorough history, physical examination, blood tests (checking for inflammation and specific antibodies), and imaging such as X-rays or MRIs. Identifying the condition early is crucial to prevent permanent joint damage and preserve function.
- Eye Screening Is Essential – Children with JIA are at risk for uveitis, a silent inflammation of the eye that can lead to vision loss or blindness if left untreated. Regular eye exams by an ophthalmologist are necessary, even if the child has no visual complaints.
- Treatment Requires a Multidisciplinary Approach – JIA treatment typically includes anti-inflammatory medications, immunosuppressants, and in some cases, biologic drugs that target specific immune pathways. A Pediatric Rheumatologist coordinates care with other specialists like ophthalmologists, physiotherapists, and pediatricians to manage the child’s overall health and development.
- Physical Therapy Is Vital to Preserve Mobility – Regular physiotherapy helps maintain joint flexibility, reduce stiffness, and improve strength. Activities should be supervised by a trained pediatric physiotherapist and tailored to your child’s needs. Physical therapy works best when combined with medication and regular monitoring.
Juvenile arthritis can affect every aspect of a child’s life, from movement to mood. But with early recognition, proper treatment, and consistent follow-up, most children with JIA can lead active, fulfilling lives. The key lies in timely diagnosis, a multidisciplinary care approach, and ongoing support for both the child and the family.
Dr Jyothi Raghuram, Senior Consultant – Pediatrics & Pediatric Rheumatology, Aster Whitefield Hospital, Bengaluru