Single-dose effects on the P3no-go ERP component predict clinical response to stimulants in pediatric ADHD
Geir Ogrim1, Ida Emilia Aasen2, Jan Ferenc Brunner3
1Neuropsychiatric Unit, Østfold Hospital Trust, Aasebraatveien 27, 1605 Fredrikstad, Norway; Institute of Psychology, Norwegian University of Science and Technology, 7491 Trondheim, Norway.
Insights
Predicting attention-deficit/hyperactivity disorder (ADHD) stimulant response is possible. Changes in the P3no-go event-related potential (ERP) component after a single stimulant dose can identify responders and non-responders in children and adolescents.
Area of Science:
- Neuroscience
- Child and Adolescent Psychiatry
- Pharmacology
Background:
- Approximately 30% of children and adolescents with ADHD are non-responders to stimulant medication.
- Predicting stimulant response in ADHD is challenging due to a lack of reliable biomarkers.
- Event-Related Potentials (ERPs) offer a potential objective measure for predicting treatment outcomes.
Purpose of the Study:
- To investigate whether changes in ERPs after a single stimulant dose can predict clinical response in ADHD patients.
- To identify specific ERP components that differentiate between responders and non-responders to stimulant treatment.
Main Methods:
- 87 children and adolescents with ADHD (aged 8-18) underwent ERP recordings during a go/no-go task before and after a single stimulant dose.
- Participants were categorized as responders (REs) or non-responders (non-REs) after a 4-week systematic medication trial.
- Changes in ERP components (e.g., P3no-go, cue-P3, CNV) and behavioral measures were compared between REs and non-REs.
Main Results:
- Significant differences were observed between REs and non-REs in medication-induced changes in P3no-go amplitude, cue-P3, CNV, omission errors, reaction time, and reaction-time variability.
- The P3no-go amplitude showed the largest effect size (d=1.76, p<.001).
- Changes in P3no-go and omission errors achieved 90% accuracy in classifying REs and 76% in classifying non-REs, after controlling for age.
Conclusions:
- Single-dose stimulant-induced changes in the P3no-go ERP component amplitude can predict clinical response in ADHD.
- The P3no-go component may serve as a valuable clinical biomarker for predicting stimulant treatment efficacy in pediatric ADHD patients.
Objective:
Approximately 30% of children and adolescents diagnosed with attention-deficit/hyperactivity disorder (ADHD) and treated with stimulants are considered non-responders (non-REs). Reliable predictors of response are missing. We examined changes in Event-Related Potentials (ERPs) induced by a single dose of stimulant medication in order to predict later clinical response.
Methods:
ERPs were registered twice during performance of a visual cued go/no-go task in 87 ADHD patients (27 girls) aged 8-18years; the second recording on a single dose of stimulant medication, followed by a systematic medication trial lasting 4weeks. Based on the four-week trial, participants were categorized as responders (REs, N=62) or non-REs (N=25). Changes among REs and non-REs in ERP components (cueP3, CNV, P3go, N2no-go, P3no-go) and behavioral-test variables were then compared.
Results:
REs and non-REs differed significantly in medication-induced changes in P3no-go, cue-P3, CNV, omission errors, reaction time, and reaction-time variability. The largest effect size was found for P3no-go amplitude (p<.001; d=1.76). Changes in P3no-go and omission errors correctly classified 90% of the REs and 76% of the non-REs, when controlling for the age of the participants.
Conclusion:
Clinical response to stimulants can be predicted by assessing single-dose changes in the P3no-go ERP component amplitude.
Significance:
Changes in P3no-go may be a clinically useful marker of response to stimulants.
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