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Published on: January 9, 2015
Childhood-onset obsessive-compulsive disorder and tic disorders: case report and literature review
1Pediatrics and Developmental Neuropsychiatry Branch, National Institute of Mental Health, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892, USA. sniderl@intra.nimh.gov
Insights
Pediatric Autoimmune Neuropsychiatric Disorders Associated with Streptococcal Infections (PANDAS) involve autoimmune responses to GABHS infections. Immunomodulatory therapies like IVIG and plasma exchange show promise in treating PANDAS symptom severity.
Area of Science:
- Pediatric Neurology
- Immunology
- Infectious Disease
Background:
- A subset of childhood-onset obsessive-compulsive disorder (OCD) and tic disorders may stem from postinfectious autoimmune processes.
- Group A beta-hemolytic streptococci (GABHS) infections are implicated in the onset and exacerbation of symptoms in these children.
Observation:
- The PANDAS subgroup is defined by specific clinical criteria including prepubertal onset, sudden symptom exacerbations, neurological abnormalities during exacerbations, and a temporal link to GABHS infections.
- Clinical investigations have identified a subgroup of children with OCD and/or tic disorders experiencing symptom onset or worsening following GABHS infections.
Findings:
- A placebo-controlled trial demonstrated that both intravenous immunoglobulin (IVIG) and plasma exchange significantly reduced neuropsychiatric symptom severity in severely affected children within the PANDAS subgroup.
- IVIG and plasma exchange resulted in 40% and 55% symptom severity reductions, respectively.
Implications:
- The identified post-streptococcal inflammatory etiology offers potential avenues for targeted treatment and prevention strategies.
- Further research is needed to elucidate the mechanisms of treatment efficacy and explore the role of antibiotic prophylaxis in preventing symptom exacerbations.
Abstract:
A subgroup of childhood-onset obsessive-compulsive disorder (OCD) and tic disorders has been found to have a postinfectious autoimmune-mediated etiology. Clinical observations and systematic investigations have shown that a subgroup of children with OCD and/or tic disorders have the onset and subsequent exacerbations of their symptoms following infections with group A beta-hemolytic streptococci (GABHS). This subgroup has been designated by the acronym PANDAS: pediatric autoimmune neuropsychiatric disorders associated with streptococcal infections. Five clinical characteristics define the PANDAS subgroup: presence of OCD and/or tic disorder, prepubertal symptom onset, sudden onset or abrupt exacerbations, association with neurological abnormalities during exacerbations (adventitious movements or motoric hyperactivity), and the temporal association between symptom exacerbations and GABHS infections. The proposed poststreptococcal inflammatory etiology provides a unique opportunity for treatment and prevention, including immunomodulatory therapies such as plasma exchange and intravenous immunoglobulin. A placebo-controlled trial revealed that both intravenous immunoglobulin and plasma exchange were effective in reducing neuropsychiatric symptom severity (40 and 55% reductions, respectively) for a group of severely ill children in the PANDAS subgroup. Further research is required to determine why the treatments are helpful and to ascertain whether or not antibiotic prophylaxis can help prevent poststreptococcal symptom exacerbations.
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