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Measurement of Fronto-limbic Activity Using an Emotional Oddball Task in Children with Familial High Risk for Schizophrenia
Published on: December 2, 2015
Neurocognitive functioning in a group of offspring genetically at high-risk for schizophrenia in Eastern Turkey
Erol Ozan1, Erdem Deveci, Meltem Oral
1Ataturk University, School of Medicine, Department of Psychiatry, 25240 Erzurum, Turkey. erolozan@gmail.com
Insights
Children with a parent diagnosed with schizophrenia showed significant impairments in key cognitive functions, including working memory and executive functions. However, verbal and sustained attention remained unaffected, suggesting a complex cognitive endophenotype for schizophrenia.
Area of Science:
- Neuroscience
- Psychiatry
- Cognitive Psychology
Background:
- Schizophrenia has a significant genetic component.
- Identifying cognitive endophenotypes can aid in early detection and intervention.
- Children of parents with schizophrenia are at high risk for developing the disorder.
Purpose of the Study:
- To assess major cognitive domains in symptom-free children with a parent diagnosed with schizophrenia.
- To compare their neurocognitive performance against healthy children.
- To identify potential cognitive endophenotypes associated with schizophrenia risk.
Main Methods:
- Neurocognitive tests were administered to 30 children at high risk for schizophrenia and 37 matched healthy controls.
- Cognitive domains assessed included attention, memory, verbal-linguistic ability, and executive functions.
- Specific tests included the Stroop test, Wisconsin card sorting test, and Rey verbal learning test.
Main Results:
- High-risk children demonstrated significant deficits in working memory, focused attention, attention speed, divided attention, executive functions, verbal fluency, and declarative memory.
- No significant group differences were found in verbal attention or sustained attention.
- Performance was significantly poorer in the high-risk group across multiple cognitive domains.
Conclusions:
- Symptom-free children of parents with schizophrenia exhibit a broad range of cognitive impairments.
- These deficits may represent a cognitive endophenotype for schizophrenia.
- Further longitudinal studies with larger sample sizes and genetic analysis are recommended for a comprehensive understanding and to identify targets for early intervention.
Abstract:
We assessed major cognitive domains in symptom-free children of patients with schizophrenia compared to the healthy children of parents with no psychopathology using neurocognitive tests. We hypothesized that, offspring at high-risk for schizophrenia would have significant impairment in major domains: attention, memory, verbal-linguistic ability and executive functions. Thirty symptom-free children (17-males, 13-females; intelligence quotient=99.6+/-13.6; age=12.69+/-2.32 and education=5.8+/-2.3 years) having a parent diagnosed with schizophrenia and 37 healthy children matched for gender (19-males, 18-females), IQ (106.05+/-14.70), age (12.48+/-2.58) and years of education (6.0+/-2.5) were evaluated. The study group showed significant poor performance in cognitive domains, such as working memory (assessed with Auditory consonant trigram test), focused attention (Stroop test), attention speed (Trail making test), divided attention (Auditory consonant trigram test), executive functions (Wisconsin card sorting test), verbal fluency (Controlled word association test) and declarative memory (Rey verbal learning and Short-term memory test). However, no group differences were detected either on verbal attention (Digit span forward test) or sustained attention (TOVA, a continuous performance task); the latter as consistently reported to be a predictor of schizophrenia. In order to determine the cognitive endophenotype of schizophrenia, it seems more rational to conduct comprehensive evaluation of neurocognitive domains in well-matched groups via using sufficiently challenging tests to detect slight deficits. In addition, longitudinal studies with a larger sample size evaluating neurocognitive functions combined with genetic analysis may provide clues about explaining the genetic background of the disorder within the endophenocognitype concept and serve as new targets for early interventions.
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