Objective PET study of glucose metabolism asymmetries in children with epilepsy: Implications for normal brain development
Clinical interpretation of cerebral positron emission tomography with 2‐deoxy‐2[F‐18]fluoro‐d‐glucose (FDG‐PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age‐related variations in regional cortical glucose metabolism asymmetries in the developing...
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Published in | Human brain mapping Vol. 40; no. 1; pp. 53 - 64 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Hoboken, USA
John Wiley & Sons, Inc
01.01.2019
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Subjects | |
Online Access | Get full text |
ISSN | 1065-9471 1097-0193 1097-0193 |
DOI | 10.1002/hbm.24354 |
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Abstract | Clinical interpretation of cerebral positron emission tomography with 2‐deoxy‐2[F‐18]fluoro‐d‐glucose (FDG‐PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age‐related variations in regional cortical glucose metabolism asymmetries in the developing human brain. FDG‐PET scans of 58 children (age: 1–18 years) were selected from a large single‐center pediatric PET database. All children had a history of epilepsy, normal MRI, and normal pattern of glucose metabolism on visual evaluation. PET images were analyzed objectively by statistical parametric mapping with the use of age‐specific FDG‐PET templates. Regional FDG uptake was measured in 35 cortical regions in both hemispheres using an automated anatomical labeling atlas, and left/right ratios were correlated with age, gender, and epilepsy variables. Cortical glucose metabolism was mostly symmetric in young children and became increasingly asymmetric in older subjects. Specifically, several frontal cortical regions showed an age‐related increase of left > right asymmetries (mean: up to 10%), while right > left asymmetries emerged in posterior cortex (including portions of the occipital, parietal, and temporal lobe) in older children (up to 9%). Similar trends were seen in a subgroup of 39 children with known right‐handedness. Age‐related correlations of regional metabolic asymmetries showed no robust gender differences and were not affected by epilepsy variables. These data demonstrate a region‐specific emergence of cortical metabolic asymmetries between age 1–18 years, with left > right asymmetry in frontal and right > left asymmetry in posterior regions. The findings can facilitate correct interpretation of cortical regional asymmetries on pediatric FDG‐PET images across a wide age range. |
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AbstractList | Clinical interpretation of cerebral positron emission tomography with 2‐deoxy‐2[F‐18]fluoro‐
d
‐glucose (FDG‐PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age‐related variations in regional cortical glucose metabolism asymmetries in the developing human brain. FDG‐PET scans of 58 children (age: 1–18 years) were selected from a large single‐center pediatric PET database. All children had a history of epilepsy, normal MRI, and normal pattern of glucose metabolism on visual evaluation. PET images were analyzed objectively by statistical parametric mapping with the use of age‐specific FDG‐PET templates. Regional FDG uptake was measured in 35 cortical regions in both hemispheres using an automated anatomical labeling atlas, and left/right ratios were correlated with age, gender, and epilepsy variables. Cortical glucose metabolism was mostly symmetric in young children and became increasingly asymmetric in older subjects. Specifically, several frontal cortical regions showed an age‐related increase of left > right asymmetries (mean: up to 10%), while right > left asymmetries emerged in posterior cortex (including portions of the occipital, parietal, and temporal lobe) in older children (up to 9%). Similar trends were seen in a subgroup of 39 children with known right‐handedness. Age‐related correlations of regional metabolic asymmetries showed no robust gender differences and were not affected by epilepsy variables. These data demonstrate a region‐specific emergence of cortical metabolic asymmetries between age 1–18 years, with left > right asymmetry in frontal and right > left asymmetry in posterior regions. The findings can facilitate correct interpretation of cortical regional asymmetries on pediatric FDG‐PET images across a wide age range. Clinical interpretation of cerebral positron emission tomography with 2‐deoxy‐2[F‐18]fluoro‐d‐glucose (FDG‐PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age‐related variations in regional cortical glucose metabolism asymmetries in the developing human brain. FDG‐PET scans of 58 children (age: 1–18 years) were selected from a large single‐center pediatric PET database. All children had a history of epilepsy, normal MRI, and normal pattern of glucose metabolism on visual evaluation. PET images were analyzed objectively by statistical parametric mapping with the use of age‐specific FDG‐PET templates. Regional FDG uptake was measured in 35 cortical regions in both hemispheres using an automated anatomical labeling atlas, and left/right ratios were correlated with age, gender, and epilepsy variables. Cortical glucose metabolism was mostly symmetric in young children and became increasingly asymmetric in older subjects. Specifically, several frontal cortical regions showed an age‐related increase of left > right asymmetries (mean: up to 10%), while right > left asymmetries emerged in posterior cortex (including portions of the occipital, parietal, and temporal lobe) in older children (up to 9%). Similar trends were seen in a subgroup of 39 children with known right‐handedness. Age‐related correlations of regional metabolic asymmetries showed no robust gender differences and were not affected by epilepsy variables. These data demonstrate a region‐specific emergence of cortical metabolic asymmetries between age 1–18 years, with left > right asymmetry in frontal and right > left asymmetry in posterior regions. The findings can facilitate correct interpretation of cortical regional asymmetries on pediatric FDG‐PET images across a wide age range. Clinical interpretation of cerebral positron emission tomography with 2-deoxy-2[F-18]fluoro-d-glucose (FDG-PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age-related variations in regional cortical glucose metabolism asymmetries in the developing human brain. FDG-PET scans of 58 children (age: 1-18 years) were selected from a large single-center pediatric PET database. All children had a history of epilepsy, normal MRI, and normal pattern of glucose metabolism on visual evaluation. PET images were analyzed objectively by statistical parametric mapping with the use of age-specific FDG-PET templates. Regional FDG uptake was measured in 35 cortical regions in both hemispheres using an automated anatomical labeling atlas, and left/right ratios were correlated with age, gender, and epilepsy variables. Cortical glucose metabolism was mostly symmetric in young children and became increasingly asymmetric in older subjects. Specifically, several frontal cortical regions showed an age-related increase of left > right asymmetries (mean: up to 10%), while right > left asymmetries emerged in posterior cortex (including portions of the occipital, parietal, and temporal lobe) in older children (up to 9%). Similar trends were seen in a subgroup of 39 children with known right-handedness. Age-related correlations of regional metabolic asymmetries showed no robust gender differences and were not affected by epilepsy variables. These data demonstrate a region-specific emergence of cortical metabolic asymmetries between age 1-18 years, with left > right asymmetry in frontal and right > left asymmetry in posterior regions. The findings can facilitate correct interpretation of cortical regional asymmetries on pediatric FDG-PET images across a wide age range.Clinical interpretation of cerebral positron emission tomography with 2-deoxy-2[F-18]fluoro-d-glucose (FDG-PET) images often relies on evaluation of regional asymmetries. This study was designed to establish age-related variations in regional cortical glucose metabolism asymmetries in the developing human brain. FDG-PET scans of 58 children (age: 1-18 years) were selected from a large single-center pediatric PET database. All children had a history of epilepsy, normal MRI, and normal pattern of glucose metabolism on visual evaluation. PET images were analyzed objectively by statistical parametric mapping with the use of age-specific FDG-PET templates. Regional FDG uptake was measured in 35 cortical regions in both hemispheres using an automated anatomical labeling atlas, and left/right ratios were correlated with age, gender, and epilepsy variables. Cortical glucose metabolism was mostly symmetric in young children and became increasingly asymmetric in older subjects. Specifically, several frontal cortical regions showed an age-related increase of left > right asymmetries (mean: up to 10%), while right > left asymmetries emerged in posterior cortex (including portions of the occipital, parietal, and temporal lobe) in older children (up to 9%). Similar trends were seen in a subgroup of 39 children with known right-handedness. Age-related correlations of regional metabolic asymmetries showed no robust gender differences and were not affected by epilepsy variables. These data demonstrate a region-specific emergence of cortical metabolic asymmetries between age 1-18 years, with left > right asymmetry in frontal and right > left asymmetry in posterior regions. The findings can facilitate correct interpretation of cortical regional asymmetries on pediatric FDG-PET images across a wide age range. |
Author | Pilli, Vinod K. Jeong, Jeong‐Won Chugani, Harry T. Juhász, Csaba Kumar, Ajay Konka, Praneetha |
AuthorAffiliation | 1 The Carman and Ann Adams Department of Pediatrics Wayne State University Detroit Michigan 3 PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan Detroit Michigan 2 Department of Neurology Wayne State University Detroit Michigan |
AuthorAffiliation_xml | – name: 2 Department of Neurology Wayne State University Detroit Michigan – name: 1 The Carman and Ann Adams Department of Pediatrics Wayne State University Detroit Michigan – name: 3 PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan Detroit Michigan |
Author_xml | – sequence: 1 givenname: Vinod K. surname: Pilli fullname: Pilli, Vinod K. organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan – sequence: 2 givenname: Jeong‐Won orcidid: 0000-0003-4498-0939 surname: Jeong fullname: Jeong, Jeong‐Won organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan – sequence: 3 givenname: Praneetha surname: Konka fullname: Konka, Praneetha organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan – sequence: 4 givenname: Ajay surname: Kumar fullname: Kumar, Ajay organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan – sequence: 5 givenname: Harry T. surname: Chugani fullname: Chugani, Harry T. organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan – sequence: 6 givenname: Csaba orcidid: 0000-0002-5067-5554 surname: Juhász fullname: Juhász, Csaba email: csaba.juhasz@wayne.edu organization: PET Center and Translational Imaging Laboratory, Children's Hospital of Michigan |
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CitedBy_id | crossref_primary_10_22141_2224_0713_20_3_2024_1065 crossref_primary_10_1007_s00406_019_01052_7 crossref_primary_10_3389_fneur_2022_1083775 crossref_primary_10_3389_fneur_2022_844911 crossref_primary_10_1016_j_seizure_2019_05_008 crossref_primary_10_1007_s00247_023_05794_4 crossref_primary_10_1364_BOE_449341 crossref_primary_10_1155_2021_2714222 crossref_primary_10_3390_sym13010105 crossref_primary_10_1002_hbm_26063 crossref_primary_10_1523_JNEUROSCI_1043_23_2023 |
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Keywords | brain development cortex asymmetry positron emission tomography children glucose metabolism |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 Present address Harry T. Chugani, Division of Neurology, Nemours/Alfred I. DuPont Hospital for Children, Wilmington, DE, USA, and Department of Neurology, Thomas Jefferson University School of Medicine, Philadelphia, PA, USA Funding information National Institute of Neurological Disorders and Stroke, Grant/Award Numbers: NS041922, NS089659 |
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SubjectTerms | Adolescent Age Asymmetry Brain brain development Cerebral Cortex - growth & development Cerebral Cortex - metabolism Cerebral Cortex - physiopathology Child Child, Preschool Children cortex Epilepsy Epilepsy - diagnostic imaging Epilepsy - metabolism Evaluation Female Fluorodeoxyglucose F18 Functional Laterality - physiology Gender aspects Glucose Glucose - metabolism Handedness Hemispheres Hemispheric laterality Humans Infant Magnetic resonance imaging Male Mapping Medical imaging Metabolism Pediatrics Positron emission Positron emission tomography Radiopharmaceuticals Regional analysis Regional development Sex differences Subgroups Temporal cortex Temporal lobe Tomography Visual cortex |
Title | Objective PET study of glucose metabolism asymmetries in children with epilepsy: Implications for normal brain development |
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