Cognitive functioning and mental health in children with a primary mitochondrial disease
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Published on: July 9, 2016
Kim F E van de Loo1,2, José A E Custers3, Lonneke de Boer4
1Radboud Center for Mitochondrial Medicine, Department of Medical Psychology, Radboud Institute for Health Sciences, Amalia Children's Hospital, Radboud University Medical Center, Geert Grooteplein Zuid 10, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.
Insights
Children with mitochondrial disease (MD) often experience cognitive and mental health issues, impacting their quality of life. Early assessment is crucial, even in mild cases, to improve patient care and research.
Area of Science:
- Pediatric Neurology
- Neurodevelopmental Disorders
- Mitochondrial Diseases
Background:
- Cognitive and mental health functioning in children with mitochondrial disease (MD) are understudied.
- These aspects significantly impact quality of life (QoL) and require further investigation.
- Understanding these issues is vital for improving patient care and guiding future research.
Purpose of the Study:
- To map cognitive functioning in children with MD.
- To assess mental health in children with MD.
- To analyze the relationship between cognitive/mental health and disease-specific factors.
Main Methods:
- Included pediatric patients (<18 years) with genetically confirmed MD.
- Assessed demographic and disease-specific factors using the International Paediatric Mitochondrial Disease Scale (IPMDS).
- Evaluated cognitive functions (intelligence, attention, working memory) and mental health (psychological functioning, QoL).
Main Results:
- 33 children with MD included; intellectual functioning varied widely.
- High rates of cognitive impairments (e.g., attention, working memory) and mental health issues (behavioral problems, anxiety, depression) were observed.
- Children with lower intellectual functioning had more disease-related impairments compared to those with average or above-average intellectual functioning.
Conclusions:
- Significant cognitive and mental health impairments are prevalent in children with MD, irrespective of intellectual functioning level.
- Even children with average or above-average intellectual functioning exhibit specific cognitive deficits.
- Structural assessment of cognitive and mental health is essential for all children with MD, including those with mild symptoms.
Background:
Studies regarding cognitive and mental health functioning in children with mitochondrial disease (MD) are scarce, while both are important issues given their impact on QoL. Knowledge on these aspects of functioning and its relationship with disease parameters is essential to gather more insight in working mechanisms and provide recommendations for future research and patientcare. The aim of this study was to map the cognitive functioning and mental health in children with MD in relation to disease specific factors.
Methods:
Pediatric patients (< 18 year) with a genetically confirmed MD were included. Demographic and disease specific factors (International Paediatric Mitochondrial Disease Scale) were assessed, as well as cognitive functioning (intelligence, attention, working memory (WM)), and mental health (psychological functioning and quality of life). Individual patient data was described.
Results:
Thirty-three children with MD were included. Intellectual functioning ranged from a clinically low IQ (36% of the patients, N = 12/33) to an average or above average IQ (39%, N = 13/33). A higher verbal versus performance IQ was observed (36% N = 5/14), a lower processing speed (43%, N = 6/14), attentional problems (50%, N = 7/14), and verbal WM problems (11%, N = 2/18). Regarding mental health, general behavioral problems were reported (45%, N = 10/22), and on subscale level, attention problems (45%, N = 10), withdrawn/depressed (36%, N = 8/22) and anxious/depressed behavior (14%, N = 3/22). Furthermore, QoL impairments were reported (42%, N = 5/12). The specific intelligence profiles, cognitive impairments, behavioral problems and QoL impairments occurred in every intelligence subgroup. Children with an average or above general intellectual functioning had a generally lower and less variability in IPMDS scores, less frequently epilepsy, vision and hearing problems, and a relatively later age of onset, as compared to patients with a clinically low intellectual functioning.
Conclusions:
Despite considerable heterogeneity, overall results showed a high rate of impairments in both cognitive and mental health functioning. Also in children with an average or above level of intellectual functioning, specific cognitive impairments were observed. Children with a clinically low intellectual functioning more often had disease related impairments compared to children with a higher intellectual functioning. The importance of structural assessment of cognitive functioning and mental health is warranted, also in children with mild disease related symptoms.
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