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PMID: 3501693 Published · ppublish English Journal Article Research Support, U.S. Gov't, Non-P.H.S. Research Support, U.S. Gov't, P.H.S.

Positron emission tomography study of human brain functional development.

Annals of neurology ·Vol. 22 ·No. 4 ·1987-10-00 ·Pages 487-97

Chugani HT, Phelps ME, Mazziotta JC

Abstract

From over 100 children studied with 2-deoxy-2[18F]fluoro-D-glucose and positron emission tomography we selected 29 children (aged 5 days to 15.1 years) who had suffered transient neurological events not significantly affecting normal neurodevelopment. These 29 children were reasonably representative of normal children and provided an otherwise unobtainable population in which to study developmental changes in local cerebral metabolic rates for glucose (lCMRGlc). In infants less than 5 weeks old lCMRGlc was highest in sensorimotor cortex, thalamus, brainstem, and cerebellar vermis. By 3 months, lCMRGlc had increased in parietal, temporal, and occipital cortices; basal ganglia; and cerebellar cortex. Frontal and dorsolateral occipital cortical regions displayed a maturational rise in lCMRGlc by approximately 6 to 8 months. Absolute values of lCMRGlc for various grey matter regions were low at birth (13 to 25 mumol/min/100 gm), and rapidly rose to reach adult values (19 to 33 mumol/min/100 gm) by 2 years. lCMRGlc continued to rise until, by 3 to 4 years, it reached values of 49 to 65 mumol/min/100 gm in most regions. These high rates were maintained until approximately 9 years, when they began to decline, and reached adult rates again by the latter part of the second decade. The highest increases of lCMRGlc over adult values occurred in cerebral cortical structures; lesser increases were seen in subcortical structures and in the cerebellum. This time course of lCMRGlc changes matches that describing the process of initial overproduction and subsequent elimination of excessive neurons, synapses, and dendritic spines known to occur in the developing brain. The determination of changing metabolic patterns accompanying normal brain development is a necessary prelude to the study of abnormal brain development with positron emission tomography.

MeSH Terms
Adolescent Aging/metabolism Brain/diagnostic imaging,growth & development,metabolism Child Child, Preschool Deoxyglucose/analogs & derivatives Female Fluorodeoxyglucose F18 Glucose/metabolism Humans Infant Infant, Newborn Male Tomography, Emission-Computed
Chemicals
Fluorodeoxyglucose F18 Deoxyglucose Glucose
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Chugani H T
Department of Neurology, UCLA School of Medicine 90024.
Phelps M E
Mazziotta J C
Article Info
Journal
Annals of neurology
Abbr.
Ann Neurol
ISSN
0364-5134
Published
1987-10-00
Pages
487-97
Language
English
Region
United States
NLM ID
7707449
Subset
IM
Grants
NINDS NIH HHS · 1-K07-NS00886-03 · United States
NINDS NIH HHS · 2P01-NS15654-06 · United States
NIMH NIH HHS · 5R01-MH37916-04 · United States
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