Normal cerebral FDG uptake during childhood

被引:23
作者
London, Kevin [1 ,2 ]
Howman-Giles, Robert [1 ,2 ,3 ]
机构
[1] Childrens Hosp Westmead, Dept Nucl Med, Sydney, NSW 2145, Australia
[2] Univ Sydney, Sydney Med Sch, Discipline Paediat & Child Hlth, Sydney, NSW 2006, Australia
[3] Univ Sydney, Sydney Med Sch, Discipline Imaging, Sydney, NSW 2006, Australia
基金
英国医学研究理事会;
关键词
FDG PET/CT; Cerebral metabolism; Paediatrics; Neurology; POSITRON-EMISSION-TOMOGRAPHY; BRAIN-DEVELOPMENT; GLUCOSE-METABOLISM; BLOOD-FLOW; CHILDREN; ADOLESCENTS; MATURATION; INFANTS; HEALTHY; AGE;
D O I
10.1007/s00259-013-2639-9
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Purpose Current understanding of cerebral FDG uptake during childhood originates from a small number of studies in patients with neurological abnormalities. Our aim was to describe cerebral FDG uptake in a dataset of FDG PET scans in children more likely to represent a normal population. Methods We reviewed cerebral FDG PET scans in children up to 16 years of age with suspected/proven extracranial malignancies and the following exclusions: central nervous system metastases, previous malignancies, previous chemotherapy or radiotherapy, development of cerebral metastases during therapy, neurological conditions, taking antiepileptic medication or medications likely to interfere with cerebral metabolism, and general anaesthesia within 24 h. White matter, basal ganglia, thalamus and the cerebellar cortex were analysed using regional SUVmax, and the cerebral cortex, basal ganglia, thalamus and cerebellum were analysed using a regional relative uptake analysis in comparison to maximal cortical uptake. Results Scans from 30 patients (age range 11 months to 16 years, mean age 10 years 5 months) were included. All regions showed increasing SUVmax with age. The parietal, occipital, lateral temporal and medial temporal lobes showed lower rates of increasing FDG uptake causing changing patterns of regional FDG uptake during childhood. The cortical regions showing the most intense uptake in early childhood were the parietal and occipital lobes. At approximately 7 years of age these regions had relatively less uptake than the frontal lobes and at approximately 10 years of age these regions had relatively less uptake than the thalamus. Conclusion Relative FDG uptake in the brain has not reached an adult pattern by 1 year of age, but continues to change up to 16 years of age. The changing pattern is due to different regional rates of increasing cortical FDG uptake, which is less rapid in the parietal, occipital and temporal lobes than in the frontal lobes.
引用
收藏
页码:723 / 735
页数:13
相关论文
共 26 条
[1]  
CHIRON C, 1992, J NUCL MED, V33, P696
[2]   POSITRON EMISSION TOMOGRAPHY STUDY OF HUMAN-BRAIN FUNCTIONAL-DEVELOPMENT [J].
CHUGANI, HT ;
PHELPS, ME ;
MAZZIOTTA, JC .
ANNALS OF NEUROLOGY, 1987, 22 (04) :487-497
[3]   MATURATIONAL CHANGES IN CEREBRAL FUNCTION IN INFANTS DETERMINED BY F-18 DG POSITRON EMISSION TOMOGRAPHY [J].
CHUGANI, HT ;
PHELPS, ME .
SCIENCE, 1986, 231 (4740) :840-843
[4]   A critical period of brain development: Studies of cerebral glucose utilization with PET [J].
Chugani, HT .
PREVENTIVE MEDICINE, 1998, 27 (02) :184-188
[5]   Working memory performance in typically developing children and adolescents: Behavioral evidence of protracted frontal lobe development [J].
Conklin, Heather M. ;
Luciana, Monica ;
Hooper, Catalina J. ;
Yarger, Rebecca S. .
DEVELOPMENTAL NEUROPSYCHOLOGY, 2007, 31 (01) :103-128
[6]   Effect of valproate on cerebral metabolism and blood flow: An F-18-2-deoxyglusose and O-15 water positron emission tomography study [J].
Gaillard, WD ;
Zeffiro, T ;
Fazilat, S ;
DeCarli, C ;
Theodore, WH .
EPILEPSIA, 1996, 37 (06) :515-521
[7]   Brain development during childhood and adolescence: a longitudinal MRI study [J].
Giedd, JN ;
Blumenthal, J ;
Jeffries, NO ;
Castellanos, FX ;
Liu, H ;
Zijdenbos, A ;
Paus, T ;
Evans, AC ;
Rapoport, JL .
NATURE NEUROSCIENCE, 1999, 2 (10) :861-863
[8]   Brain development in healthy, hyperactive, and psychotic children [J].
Gogtay, N ;
Giedd, J ;
Rapoport, JL .
ARCHIVES OF NEUROLOGY, 2002, 59 (08) :1244-1248
[9]  
HUTTENLOCHER PR, 1987, HUM NEUROBIOL, V6, P1
[10]  
KEYES JW, 1995, J NUCL MED, V36, P1836