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Published on: July 24, 2016
Long-term psychiatric outcomes in youth with enterovirus A71 central nervous system involvement
Hsiang-Yuan Lin1,2,3, Yi-Lung Chen4, Pei-Hsuan Chou5
1Azrieli Adult Neurodevelopmental Centre, Campbell Family Mental Health Research Institute, Centre for Addiction and Mental Health, Toronto, Ontario, Canada.
Insights
Enterovirus A71 central nervous system (CNS) infection in youth significantly increases the risk of developing Attention-Deficit/Hyperactivity Disorder (ADHD) later in life. Early identification and intervention are crucial for managing these long-term psychiatric and developmental outcomes.
Area of Science:
- Neurology
- Neurodevelopmental Disorders
- Psychiatry
Background:
- Enterovirus A71 (EV-A71) central nervous system (CNS) infection can lead to long-term neurological and neurodevelopmental issues.
- The impact of early-life EV-A71 CNS infection on the subsequent development of psychiatric disorders remains under-investigated.
- No prior longitudinal studies have systematically examined these long-term psychiatric consequences.
Purpose of the Study:
- To investigate the long-term psychiatric sequelae of childhood EV-A71 CNS infection.
- To compare the prevalence of psychiatric disorders in EV-A71 CNS-infected youth with national and community-based cohorts.
- To assess emotional, behavioral, and cognitive outcomes in a cohort of youth with a history of EV-A71 CNS infection.
Main Methods:
- A naturalistic longitudinal follow-up study of 43 youth with a history of EV-A71 CNS involvement (6-18 years prior).
- Psychiatric assessment via diagnostic interviews, parent/self-rated questionnaires, and neuropsychological testing.
- Comparison of psychiatric disorder prevalence to a national cohort and comparison of emotional/behavioral/cognitive function to matched ADHD and healthy control groups.
Main Results:
- Youth with a history of EV-A71 CNS involvement had a threefold increased odds of receiving an Attention-Deficit/Hyperactivity Disorder (ADHD) diagnosis compared to the national sample (34.9% vs. 10.1%).
- No other psychiatric diagnoses were found to be more common in the EV-A71 CNS-infected group.
- EV-A71 CNS-infected youth with psychiatric disorders exhibited comparable ADHD symptoms, oppositional behaviors, autistic features, and attention deficits to community-based ADHD youth, all more severe than healthy controls.
- Autistic features were similarly present in EV-A71 CNS-infected youth (with or without psychiatric disorders) and ADHD youth.
Conclusions:
- Childhood EV-A71 CNS infection is associated with a significantly higher risk of developing ADHD in later life.
- Long-term psychiatric outcomes may include ADHD, alongside social, communication, and emotional difficulties, and autistic features.
- Earlier identification and intervention for these developmental and psychiatric problems in children with a history of EV-A71 CNS infection are recommended.
Abstract:
Long-term neurological and neurodevelopmental sequelae are a concerning issue for people with Enterovirus A71 (EV-A71) central nervous system (CNS) infection. Unfortunately, no longitudinal prospective clinical study has systematically investigated the consequences of EV-A71 CNS infection during early life on the later development of other psychiatric disorders. In this naturalistic longitudinal follow-up design, we followed forty-three youth, who got EV-A71 CNS involvement 6-18 years ago and were enrolled in other EV-A71 clinical studies then. Their psychiatric presentation, emotional/behavioral problems, and cognitive issues were examined using a psychiatrist-conducted diagnostic interview, parent- and self-rated questionnaires, and neuropsychological tests, respectively. We compared the prevalence of psychiatric disorders in youth with EV-A71 CNS involvement to a nationally representative cohort. Emotion/behavior and cognition in EV-A71-CNS-infected youth were compared to those in a matched community-based sample of healthy controls and youth with attention-deficit/hyperactivity disorder (ADHD). Compared to a national sample (absolute ADHD prevalence 10.1%), youth with EV-A71 CNS involvement had three times the odds of receiving an ADHD diagnosis (standardized prevalence ratio, 95% CI = 1.8, 4.2; absolute ADHD prevalence 34.9%). No other psychiatric diagnoses were more common in EV-A71-CNS-infected youth. Compared to community-based ADHD youth, EV-A71-CNS-infected youth with psychiatric disorders showed comparable core ADHD symptoms, opposition/defiance, autistic features, and suboptimal sustained attention performance (based on the Conners' Continuous Performance Test), all of which were more severe than healthy controls. EV-A71-CNS-infected youth without psychiatric disorders showed comparable autistic features to EV-A71-CNS-infected youth with psychiatric disorders and ADHD youth. EV-A71 CNS involvement may cause long-term, adverse psychiatric outcomes that develop into an ADHD diagnosis alongside social/communication/emotion problems and autistic features. We recommend earlier identification and intervention of these problems among these children.
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