Related Experiment Video
Updated: Feb 4, 2026

Exploring Cognitive Functions in Babies, Children & Adults with Near Infrared Spectroscopy
Published on: July 28, 2009
Cognitive characteristics of mitochondrial diseases in children
Hillary Shurtleff1, Dwight Barry2, Sirisak Chanprasert3
1Department of Neurology, University of Washington, Seattle, WA, USA; Seattle Children's Hospital, Seattle, WA, USA.
Insights
Children with mitochondrial disorders and seizures have significantly lower intelligence scores compared to those without seizures. Early onset and intractable seizures indicate a worse cognitive profile in pediatric mitochondrial disease.
Area of Science:
- Neurology
- Genetics
- Pediatrics
Background:
- Mitochondrial disorders are a group of inherited metabolic diseases.
- Intelligence profiles in children with mitochondrial disorders are not well-defined, especially concerning seizures and age of onset.
Purpose of the Study:
- To define intelligence profiles in pediatric patients with mitochondrial disorders.
- To investigate the impact of seizures and age of symptom onset on cognitive function.
Main Methods:
- Retrospective descriptive study of 49 pediatric patients with mitochondrial diseases.
- Intelligence assessed using Wechsler Intellectual Quotient (IQ) testing or Vineland Adaptive Behavior Scales.
- Exploratory data analysis to compare cognitive outcomes between groups with and without seizures.
Main Results:
- Patients with seizures had a lower median Full Scale IQ (FSIQ) of 67 compared to 100 in those without seizures.
- Performance IQ (PIQ) was significantly lower in the seizure group (median 63) versus the non-seizure group (median 100).
- Patients with intractable epilepsy showed the lowest adaptive functioning scores.
Conclusions:
- Mitochondrial disease patients with seizures and early onset exhibit a worse cognitive phenotype.
- Absence of seizures may be associated with average intelligence in pediatric mitochondrial disease.
- Seizure activity is a significant factor influencing cognitive outcomes in mitochondrial disorders.
Introduction:
This retrospective descriptive study was undertaken to further define the intelligence profiles of children with mitochondrial disorders, in the context of seizures and age of symptom onset.
Methods:
We retrospectively identified forty-nine pediatric patients with definitive mitochondrial disease diagnoses and complete intelligence or adaptive functioning testing data. Patients were 0-216 months at onset of symptoms and 61-250 months of age at testing. Twenty-four of 49 patients had seizures. Twenty-one of the 24 patients with seizures had medically intractable seizures. All patients had Wechsler Intellectual Quotient (IQ) testing, except nine patients with seizures who were unable to engage in IQ testing and were assessed with a structured parent interview measure, the Vineland Adaptive Behavior Scales. We used descriptive and exploratory data analysis methods to characterize test results.
Results:
Distribution of ages for patients with the Vineland assessment was younger than those given the Wechsler. The median overall score (combining Wechsler and Vineland summary scores) for all patients was 85 (interquartile range [IQR]: 50, 102), with the group without seizures obtaining a higher median Full Scale IQ (FSIQ) of 100 (IQR: 86, 109), compared to the group with seizures with a median FSIQ of 67 (IQR: 49.5, 89), a difference that is both statistically and clinically different (Δ = 33; 95% CI: 9, 52). The adaptive function measure was composed of patients only with intractable epilepsy and yielded the lowest overall median summary score of 43 (IQR: 37, 50). This general trend in differences between the FSIQ scores of the groups with and without seizures was also seen across all subscale measures analyzed-IQ index scores and two subtest scores, Digit Span and Coding-though differences were not always statistically different. Vargha-Delaney's A effect sizes ranged between 0.68 and 0.90, trends that mirrored those of distributional and median differences. Groups without versus with seizures differed most distinctly in Performance IQ (PIQ), with the group without seizures' median PIQ being 100 (IQR 94, 112) versus the group with seizures' median PIQ being 63 (IQR 54, 84), a difference of 37 points (95% CI).
Discussion:
Results suggest that patients with mitochondrial diseases with seizures and early onset disease represent a worse cognitive phenotype, as compared with those with no seizures, who can have average intelligence. Results are discussed in the context of current literature.
Related Concept Videos
Animal Mitochondrial Genetics
Cognitive Dissonance
Characteristics of Life
Comparing Mitochondrial, Chloroplast, and Prokaryotic Genomes
Export of Mitochondrial and Chloroplast Genes
Characteristics of Fluids

