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 |
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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 < 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 & 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. Fetal and neonatal edition, 1996-05, Vol.74 (3), p.F153-F157</ispartof><rights>Copyright BMJ Publishing Group LTD May 1996</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-b543t-6779fb9da7c2a3c922b1559af1bf7d8439e6a6ac5a4b15c1a555c8eb8acb5783</citedby><cites>FETCH-LOGICAL-b543t-6779fb9da7c2a3c922b1559af1bf7d8439e6a6ac5a4b15c1a555c8eb8acb5783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528340/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC2528340/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/8777676$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study</title><title>Archives of disease in childhood. 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 < 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><subject>Age Factors</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - metabolism</subject><subject>Brain Stem - metabolism</subject><subject>Cerebellar Cortex - metabolism</subject><subject>Cerebellum - metabolism</subject><subject>Cerebral Cortex - metabolism</subject><subject>Child, Preschool</subject><subject>Deoxyglucose - analogs & derivatives</subject><subject>Emission measurements</subject><subject>Female</subject><subject>Fluorine Radioisotopes</subject><subject>Fluorodeoxyglucose F18</subject><subject>Follow-Up Studies</subject><subject>Glucose - metabolism</subject><subject>Humans</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>Infant, Premature</subject><subject>Infants</subject><subject>Male</subject><subject>Retrospective Studies</subject><subject>Thalamus - metabolism</subject><subject>Tomography, Emission-Computed</subject><issn>1359-2998</issn><issn>1468-2052</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1996</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kcGLEzEUxoMo67p68yoEBL04NZlMJhkPgoy2FZZVcPEakkzSps4kNcnI9r83S0tRD57eI9-PL-97D4DnGC0wJu1b6xesWZDFElPyAFzipuVVjWj9sPSEdlXddfwxeJLSDiGEGWMX4IKX0rL2EsTeRKOiHOFkslRhdBpGmQ20IcLNOOuQDBzm6PwG5m15djFlmNwdnILP2wSDhaOz5h2UHi4_ruA-JJdj8NBMLiVXmhymsIlyvz3AlOfh8BQ8snJM5tmpXoHb5afbfl1df1l97j9cV4o2JFctY51V3SCZriXRXV0rTGknLVaWDbwhnWllKzWVTRE0lpRSzY3iUivKOLkC74-2-1lNZtDG5xJT7KObZDyIIJ34W_FuKzbhl6hpzUmDisGrk0EMP2eTsiiJtBlH6U2Yk2C8rJc3XQFf_gPuwhx9ySbKuhEiGDNaqDdHSseQUjT2PApG4v6QwnrBGkHE_SEL_uLP8c_w6XJFr466S9ncnWUZf4iWEUbFzfderPnN8lv_dS1WhX995NW0-__PvwFp-rd8</recordid><startdate>19960501</startdate><enddate>19960501</enddate><creator>Kinnala, A.</creator><creator>Suhonen-Polvi, H.</creator><creator>Aärimaa, T.</creator><creator>Kero, P.</creator><creator>Korvenranta, H.</creator><creator>Ruotsalainen, U.</creator><creator>Bergman, J.</creator><creator>Haaparanta, M.</creator><creator>Solin, O.</creator><creator>Nuutila, P.</creator><creator>Wegelius, U.</creator><general>BMJ Publishing Group Ltd and Royal College of Paediatrics and Child Health</general><general>BMJ Publishing Group LTD</general><general>BMJ Group</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>K9.</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>19960501</creationdate><title>Cerebral metabolic rate for glucose during the first six months of life: an FDG positron emission tomography study</title><author>Kinnala, A. ; 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 & 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 & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Archives of disease in childhood. 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 < 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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