Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder

Abstract Background Autism spectrum disorder (ASD) is a severe neurodevelopmental condition. Its incidence is on the rise worldwide, and in severe cases, it can lead to disability. While emerging evidence implicates cerebrovascular dysfunction in the pathophysiology of neurodevelopmental impairments...

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Main Authors: Xueyan Liu, Zhexuan Yang, Yu Lu, Shifang Tan, Kaiyu Wang, Changhao Wang, Ning Wang, Zhanqi Feng, Houjiang Wei, Meiying Cheng, Xin Zhao
Format: Article
Language:English
Published: BMC 2025-07-01
Series:European Journal of Medical Research
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Online Access:https://doi.org/10.1186/s40001-025-02815-w
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author Xueyan Liu
Zhexuan Yang
Yu Lu
Shifang Tan
Kaiyu Wang
Changhao Wang
Ning Wang
Zhanqi Feng
Houjiang Wei
Meiying Cheng
Xin Zhao
author_facet Xueyan Liu
Zhexuan Yang
Yu Lu
Shifang Tan
Kaiyu Wang
Changhao Wang
Ning Wang
Zhanqi Feng
Houjiang Wei
Meiying Cheng
Xin Zhao
author_sort Xueyan Liu
collection DOAJ
description Abstract Background Autism spectrum disorder (ASD) is a severe neurodevelopmental condition. Its incidence is on the rise worldwide, and in severe cases, it can lead to disability. While emerging evidence implicates cerebrovascular dysfunction in the pathophysiology of neurodevelopmental impairments associated with ASD, systematic characterization of cerebral hemodynamic variations across clinically stratified severity subgroups, particularly among mild–moderate and severe ASD presentations and typically developing (TD) children, remains a critical unmet research need. Methods This cross-sectional neuroimaging study enrolled 121 children aged 2 to 4 years: 16 with severe autism (Childhood Autism Rating Scale (CARS) score > 36), 60 with mild–moderate autism (CARS score between 30 and 36), and 45 TD children. CBF measurements were obtained from nine regions of interest (ROI) in both hemispheres: temporal lobe, parietal lobe, occipital lobe, putamen, thalamus, caudate nucleus, globus pallidus, hippocampus, and amygdala. Intergroup comparisons of CBF values were performed among the three groups. Particular emphasis was placed on analyzing the correlation between thalamic CBF values and serum zinc levels in autistic children. Results Children with severe autism exhibited significantly lower CBF in the temporal lobe, putamen, thalamus, and hippocampus compared to TD children (p < 0.05). Within the autism cohort, severe cases demonstrated further CBF reductions in the putamen and thalamus compared to mild–moderate cases (p < 0.05). Similarly, children with mild–moderate autism showed reduced CBF in the temporal lobe, putamen, thalamus, and hippocampus compared to TD children (p < 0.05). Notably, a significant difference in CBF was observed between the left and right thalamus in both mild–moderate and severe autism groups, with lower blood flow in the left thalamus (p < 0.05). A positive correlation was found between thalamic CBF values and serum zinc levels in the autism group. Conclusions Children with severe autism show significantly reduced CBF in critical brain regions. Thus, 3D-pCASL may enable the precise stratification of ASD severity in children and provide an imaging foundation for subsequent therapeutic evaluation.
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spelling doaj-art-df31feacb8a345e9b856be33146ac2be2025-08-20T04:01:25ZengBMCEuropean Journal of Medical Research2047-783X2025-07-013011910.1186/s40001-025-02815-wInvestigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorderXueyan Liu0Zhexuan Yang1Yu Lu2Shifang Tan3Kaiyu Wang4Changhao Wang5Ning Wang6Zhanqi Feng7Houjiang Wei8Meiying Cheng9Xin Zhao10Department of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityMR Research China, GE HealthcareDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Pediatrics, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityDepartment of Radiology, The Third Affiliated Hospital of Zhengzhou UniversityAbstract Background Autism spectrum disorder (ASD) is a severe neurodevelopmental condition. Its incidence is on the rise worldwide, and in severe cases, it can lead to disability. While emerging evidence implicates cerebrovascular dysfunction in the pathophysiology of neurodevelopmental impairments associated with ASD, systematic characterization of cerebral hemodynamic variations across clinically stratified severity subgroups, particularly among mild–moderate and severe ASD presentations and typically developing (TD) children, remains a critical unmet research need. Methods This cross-sectional neuroimaging study enrolled 121 children aged 2 to 4 years: 16 with severe autism (Childhood Autism Rating Scale (CARS) score > 36), 60 with mild–moderate autism (CARS score between 30 and 36), and 45 TD children. CBF measurements were obtained from nine regions of interest (ROI) in both hemispheres: temporal lobe, parietal lobe, occipital lobe, putamen, thalamus, caudate nucleus, globus pallidus, hippocampus, and amygdala. Intergroup comparisons of CBF values were performed among the three groups. Particular emphasis was placed on analyzing the correlation between thalamic CBF values and serum zinc levels in autistic children. Results Children with severe autism exhibited significantly lower CBF in the temporal lobe, putamen, thalamus, and hippocampus compared to TD children (p < 0.05). Within the autism cohort, severe cases demonstrated further CBF reductions in the putamen and thalamus compared to mild–moderate cases (p < 0.05). Similarly, children with mild–moderate autism showed reduced CBF in the temporal lobe, putamen, thalamus, and hippocampus compared to TD children (p < 0.05). Notably, a significant difference in CBF was observed between the left and right thalamus in both mild–moderate and severe autism groups, with lower blood flow in the left thalamus (p < 0.05). A positive correlation was found between thalamic CBF values and serum zinc levels in the autism group. Conclusions Children with severe autism show significantly reduced CBF in critical brain regions. Thus, 3D-pCASL may enable the precise stratification of ASD severity in children and provide an imaging foundation for subsequent therapeutic evaluation.https://doi.org/10.1186/s40001-025-02815-wCerebral blood flowASDZinc3D-pCASLNeurophysiology
spellingShingle Xueyan Liu
Zhexuan Yang
Yu Lu
Shifang Tan
Kaiyu Wang
Changhao Wang
Ning Wang
Zhanqi Feng
Houjiang Wei
Meiying Cheng
Xin Zhao
Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
European Journal of Medical Research
Cerebral blood flow
ASD
Zinc
3D-pCASL
Neurophysiology
title Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
title_full Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
title_fullStr Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
title_full_unstemmed Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
title_short Investigating cerebral blood flow dysregulation and serum zinc correlation in 2–4 year-old children with autism spectrum disorder
title_sort investigating cerebral blood flow dysregulation and serum zinc correlation in 2 4 year old children with autism spectrum disorder
topic Cerebral blood flow
ASD
Zinc
3D-pCASL
Neurophysiology
url https://doi.org/10.1186/s40001-025-02815-w
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