Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study

AIM: To measure the local cerebral metabolic rate for glucose (LCMRGlc) in neonatal brains during maturation using positron emission tomography (PET) and 2-[18F]fluoro-2-deoxy-D-glucose (FDG). METHODS: Twenty infants were studied using PET during the neonatal period. The postconceptional age ranged...

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Veröffentlicht in:Archives of disease in childhood. Fetal and neonatal edition 1996-05, Vol.74 (3), p.F153-F157
Hauptverfasser: Kinnala, A., Suhonen-Polvi, H., Aärimaa, T., Kero, P., Korvenranta, H., Ruotsalainen, U., Bergman, J., Haaparanta, M., Solin, O., Nuutila, P., Wegelius, U.
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container_end_page F157
container_issue 3
container_start_page F153
container_title Archives of disease in childhood. Fetal and neonatal edition
container_volume 74
creator Kinnala, A.
Suhonen-Polvi, H.
Aärimaa, T.
Kero, P.
Korvenranta, H.
Ruotsalainen, U.
Bergman, J.
Haaparanta, M.
Solin, O.
Nuutila, P.
Wegelius, U.
description AIM: To measure the local cerebral metabolic rate for glucose (LCMRGlc) in neonatal brains during maturation using positron emission tomography (PET) and 2-[18F]fluoro-2-deoxy-D-glucose (FDG). METHODS: Twenty infants were studied using PET during the neonatal period. The postconceptional age ranged from 32.7 to 60.3 weeks. All infants had normal neurodevelopment and were normoglycaemic. The development of the infants was carefully evaluated (follow up 12-36 months) clinically, and by using a method based on Gesell Amatruda's developmental diagnosis. LCMRGlc was quantitated using PET derived from FDG kinetics and calculated in the whole brain and for regional brain structures. RESULTS: LCMRGlc for various cortical brain regions and the basal ganglia was low at birth (from 4 to 16 mumol/100 g/minute). In infants 2 months of age and younger LCMRGlc was highest in the sensorimotor cortex, thalamus, and brain stem. By 5 months, LCMRGlc had increased in the frontal, parietal, temporal, occipital and cerebellar cortical regions. In general, the whole brain LCMRGlc correlated with postconceptional age (r = 0.90; P < 0.001). The change in the glucose metabolic pattern observed in the neonatal brain reflects the functional maturation of these brain regions. CONCLUSION: These findings show that LCMRGlc in infants increases with maturation. Accordingly, when LCMRGlc is measured during infancy, the postconceptional age has to be taken into account when interpretating the results.
doi_str_mv 10.1136/fn.74.3.F153
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METHODS: Twenty infants were studied using PET during the neonatal period. The postconceptional age ranged from 32.7 to 60.3 weeks. All infants had normal neurodevelopment and were normoglycaemic. The development of the infants was carefully evaluated (follow up 12-36 months) clinically, and by using a method based on Gesell Amatruda's developmental diagnosis. LCMRGlc was quantitated using PET derived from FDG kinetics and calculated in the whole brain and for regional brain structures. RESULTS: LCMRGlc for various cortical brain regions and the basal ganglia was low at birth (from 4 to 16 mumol/100 g/minute). In infants 2 months of age and younger LCMRGlc was highest in the sensorimotor cortex, thalamus, and brain stem. By 5 months, LCMRGlc had increased in the frontal, parietal, temporal, occipital and cerebellar cortical regions. In general, the whole brain LCMRGlc correlated with postconceptional age (r = 0.90; P &lt; 0.001). The change in the glucose metabolic pattern observed in the neonatal brain reflects the functional maturation of these brain regions. CONCLUSION: These findings show that LCMRGlc in infants increases with maturation. Accordingly, when LCMRGlc is measured during infancy, the postconceptional age has to be taken into account when interpretating the results.</description><identifier>ISSN: 1359-2998</identifier><identifier>EISSN: 1468-2052</identifier><identifier>DOI: 10.1136/fn.74.3.F153</identifier><identifier>PMID: 8777676</identifier><language>eng</language><publisher>England: BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</publisher><subject>Age Factors ; Brain - diagnostic imaging ; Brain - metabolism ; Brain Stem - metabolism ; Cerebellar Cortex - metabolism ; Cerebellum - metabolism ; Cerebral Cortex - metabolism ; Child, Preschool ; Deoxyglucose - analogs &amp; derivatives ; Emission measurements ; Female ; Fluorine Radioisotopes ; Fluorodeoxyglucose F18 ; Follow-Up Studies ; Glucose - metabolism ; Humans ; Infant ; Infant, Newborn ; Infant, Premature ; Infants ; Male ; Retrospective Studies ; Thalamus - metabolism ; Tomography, Emission-Computed</subject><ispartof>Archives of disease in childhood. 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Fetal and neonatal edition</title><addtitle>Arch Dis Child Fetal Neonatal Ed</addtitle><description>AIM: To measure the local cerebral metabolic rate for glucose (LCMRGlc) in neonatal brains during maturation using positron emission tomography (PET) and 2-[18F]fluoro-2-deoxy-D-glucose (FDG). METHODS: Twenty infants were studied using PET during the neonatal period. The postconceptional age ranged from 32.7 to 60.3 weeks. All infants had normal neurodevelopment and were normoglycaemic. The development of the infants was carefully evaluated (follow up 12-36 months) clinically, and by using a method based on Gesell Amatruda's developmental diagnosis. LCMRGlc was quantitated using PET derived from FDG kinetics and calculated in the whole brain and for regional brain structures. RESULTS: LCMRGlc for various cortical brain regions and the basal ganglia was low at birth (from 4 to 16 mumol/100 g/minute). In infants 2 months of age and younger LCMRGlc was highest in the sensorimotor cortex, thalamus, and brain stem. By 5 months, LCMRGlc had increased in the frontal, parietal, temporal, occipital and cerebellar cortical regions. In general, the whole brain LCMRGlc correlated with postconceptional age (r = 0.90; P &lt; 0.001). The change in the glucose metabolic pattern observed in the neonatal brain reflects the functional maturation of these brain regions. CONCLUSION: These findings show that LCMRGlc in infants increases with maturation. 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Suhonen-Polvi, H. ; Aärimaa, T. ; Kero, P. ; Korvenranta, H. ; Ruotsalainen, U. ; Bergman, J. ; Haaparanta, M. ; Solin, O. ; Nuutila, P. ; Wegelius, U.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-b543t-6779fb9da7c2a3c922b1559af1bf7d8439e6a6ac5a4b15c1a555c8eb8acb5783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1996</creationdate><topic>Age Factors</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - metabolism</topic><topic>Brain Stem - metabolism</topic><topic>Cerebellar Cortex - metabolism</topic><topic>Cerebellum - metabolism</topic><topic>Cerebral Cortex - metabolism</topic><topic>Child, Preschool</topic><topic>Deoxyglucose - analogs &amp; derivatives</topic><topic>Emission measurements</topic><topic>Female</topic><topic>Fluorine Radioisotopes</topic><topic>Fluorodeoxyglucose F18</topic><topic>Follow-Up Studies</topic><topic>Glucose - metabolism</topic><topic>Humans</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>Infant, Premature</topic><topic>Infants</topic><topic>Male</topic><topic>Retrospective Studies</topic><topic>Thalamus - metabolism</topic><topic>Tomography, Emission-Computed</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kinnala, A.</creatorcontrib><creatorcontrib>Suhonen-Polvi, H.</creatorcontrib><creatorcontrib>Aärimaa, T.</creatorcontrib><creatorcontrib>Kero, P.</creatorcontrib><creatorcontrib>Korvenranta, H.</creatorcontrib><creatorcontrib>Ruotsalainen, U.</creatorcontrib><creatorcontrib>Bergman, J.</creatorcontrib><creatorcontrib>Haaparanta, M.</creatorcontrib><creatorcontrib>Solin, O.</creatorcontrib><creatorcontrib>Nuutila, P.</creatorcontrib><creatorcontrib>Wegelius, U.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Health &amp; 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Fetal and neonatal edition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kinnala, A.</au><au>Suhonen-Polvi, H.</au><au>Aärimaa, T.</au><au>Kero, P.</au><au>Korvenranta, H.</au><au>Ruotsalainen, U.</au><au>Bergman, J.</au><au>Haaparanta, M.</au><au>Solin, O.</au><au>Nuutila, P.</au><au>Wegelius, U.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study</atitle><jtitle>Archives of disease in childhood. Fetal and neonatal edition</jtitle><addtitle>Arch Dis Child Fetal Neonatal Ed</addtitle><date>1996-05-01</date><risdate>1996</risdate><volume>74</volume><issue>3</issue><spage>F153</spage><epage>F157</epage><pages>F153-F157</pages><issn>1359-2998</issn><eissn>1468-2052</eissn><abstract>AIM: To measure the local cerebral metabolic rate for glucose (LCMRGlc) in neonatal brains during maturation using positron emission tomography (PET) and 2-[18F]fluoro-2-deoxy-D-glucose (FDG). METHODS: Twenty infants were studied using PET during the neonatal period. The postconceptional age ranged from 32.7 to 60.3 weeks. All infants had normal neurodevelopment and were normoglycaemic. The development of the infants was carefully evaluated (follow up 12-36 months) clinically, and by using a method based on Gesell Amatruda's developmental diagnosis. LCMRGlc was quantitated using PET derived from FDG kinetics and calculated in the whole brain and for regional brain structures. RESULTS: LCMRGlc for various cortical brain regions and the basal ganglia was low at birth (from 4 to 16 mumol/100 g/minute). In infants 2 months of age and younger LCMRGlc was highest in the sensorimotor cortex, thalamus, and brain stem. By 5 months, LCMRGlc had increased in the frontal, parietal, temporal, occipital and cerebellar cortical regions. In general, the whole brain LCMRGlc correlated with postconceptional age (r = 0.90; P &lt; 0.001). The change in the glucose metabolic pattern observed in the neonatal brain reflects the functional maturation of these brain regions. CONCLUSION: These findings show that LCMRGlc in infants increases with maturation. Accordingly, when LCMRGlc is measured during infancy, the postconceptional age has to be taken into account when interpretating the results.</abstract><cop>England</cop><pub>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</pub><pmid>8777676</pmid><doi>10.1136/fn.74.3.F153</doi><oa>free_for_read</oa></addata></record>
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subjects Age Factors
Brain - diagnostic imaging
Brain - metabolism
Brain Stem - metabolism
Cerebellar Cortex - metabolism
Cerebellum - metabolism
Cerebral Cortex - metabolism
Child, Preschool
Deoxyglucose - analogs & derivatives
Emission measurements
Female
Fluorine Radioisotopes
Fluorodeoxyglucose F18
Follow-Up Studies
Glucose - metabolism
Humans
Infant
Infant, Newborn
Infant, Premature
Infants
Male
Retrospective Studies
Thalamus - metabolism
Tomography, Emission-Computed
title Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study
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