Obsessive-Compulsive Disorder Clinical Trial
Official title:
The Characterization of Childhood Onset Obsessive Compulsive Disorder and the PANDAS Subgroup
The purpose of this study is to learn more about Obsessive-compulsive Disorder (OCD) in
children. OCD usually has a slow onset, and symptoms that may remain at a stable level over
time. A subset of children with OCD has a sudden onset and symptoms that fluctuate in
severity over time. This study will also compare healthy children to those with OCD. This is
an observational study; children who participate will not receive any new or experimental
therapies.
OCD affects nearly 1% of the pediatric population. The symptoms of this illness can interrupt
development, causing significant psychological distress and producing life-long impairments
in social, academic, and occupational functioning. A subgroup of pediatric OCD has been
designated by the acronym PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated
with Streptococcal Infections). This type of OCD is characterized by sudden symptom onset and
a relapsing-remitting course of illness; exacerbation of symptoms occurs with scarlet fever
or strep. throat infections. This study will identify factors that distinguish children with
PANDAS OCD from children with non-PANDAS OCD, and will compare both groups to healthy
children.
Children with OCD and their parents are screened with interviews and a review of the child's
medical records. Participants have an initial evaluation that includes a psychiatric,
physical and neuromotor exam, neuropsychological testing, psychological interviews, and a
blood test. Structural magnetic resonance imaging (MRS) scans of the brain are also obtained.
The MRS scan does not use radiation.
After the initial evaluation, children with OCD have follow-up visits every 6 weeks for 12 to
24 months. They are seen yearly for 8 years after the study. If they have a significant
improvement or worsening of their symptoms, they are asked to make a maximum of two extra
visits. Parents of OCD patients are called four times a year to discuss any changes in the
child's condition between yearly visits. All participants have a 1-year follow-up visit upon
study completion.
Obsessive-compulsive disorder (OCD) affects nearly 1% of the pediatric population. The
intrusive symptoms of this illness can interrupt normative development, causing significant
psychological distress and producing life-long impairments in social, academic, and
occupational functioning. Current research supports a neurobiologic model for OCD. Converging
lines of evidence suggest that a post-infectious autoimmune-mediated process may be
associated with the pathogenesis of some pediatric cases. This subgroup has been designated
by the acronym, PANDAS (Pediatric Autoimmune Neuropsychiatric Disorders Associated with
Streptococcal infections). The abrupt symptom onset and relapsing-remitting course of illness
characteristic of the PANDAS subgroup appears to define a distinct cohort of patients, in
whom symptom exacerbations occur synchronously with Group A beta-hemolytic streptococcal
(GABHS) infections.
We propose to perform prospective, longitudinal evaluations of a group of 72 children with
recent onset OCD and 72 age-/sex-matched healthy volunteers. All children will undergo a
comprehensive baseline assessment, including physical, neurological and psychiatric
evaluations, neuropsychological testing, structural MRI and MRS scans, and laboratory assays.
The children with OCD will be evaluated in the NIMH outpatient clinic at six-week intervals
for a 28-month period to obtain prospective ratings of neuropsychiatric symptom severity,
physical and neurological assessments, and anti-streptococcal antibody titers. At the end of
the observation period, each OCD patient will be placed into a cohort based on the course of
his or her symptoms: those displaying an acute onset and episodic course of OCD will be
assigned to the "episodic" group, while those children with a gradual onset and stable course
will comprise the "persistent" group. We hypothesize that the episodic group will have GABHS
infections concurrent with their neuropsychiatric symptoms exacerbations and will meet
criteria for the PANDAS subgroup. In contrast, children in the persistent group are not
expected to have distinct periods of relapse nor a temporal association between GABHS
infections and worsening of their symptoms. We expect that children in the PANDAS subgroup
will demonstrate cross-reactive antibodies (antistreptococcal/antineuronal) during symptom
exacerbations. At the conclusion of the study, we will perform group comparisons between the
episodic OCD and persistent OCD cohorts, as well as between the patients and controls. The
purpose of these comparisons is to identify baseline markers of membership in the PANDAS
subgroup. The possibilities include distinctive HLA subtypes, quantitative differences in
cytokines distribution, unique MRS chemical profiles, or a specific pattern of deficits on
neuropsychological tests of basal ganglia function.
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