Neuron-specific enolase levels and neuroimaging in asphyxiated term newborns

被引:21
作者
Ezgü, FS
Atalay, Y
Gücüyener, K
Tunç, S
Koç, E
Ergenekon, E
Tiras, U
机构
[1] Gazi Univ, Fac Med, Dept Pediat, Ankara, Turkey
[2] Sevgi Hosp, Dept Biochem, Ankara, Turkey
[3] Ankara Hosp, Dept Pediat, Ankara, Turkey
关键词
D O I
10.1177/08830738020170111301
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The study was designed to investigate the cerebrospinal fluid and serum levels of neuron-specific enolase, along with cranial ultrasonography, magnetic resonance imaging (MRI), and electroencephalography (EEG), for predicting the clinical state and neurologic outcome of 26 asphyxiated term newborns. The babies were graded according to the Sarnat and Sarnat classification. Cerebrospinal fluid neuron-specific enolase levels of the 18 babies in the whole hypoxic-ischemic encephalopathy group were higher than the 8 babies in the "no encephalopathy" group. Cerebrospinal fluid neuron-specific enolase levels of 13 cases in the hypoxic-ischemic encephalopathy grade 2 and 3 groups (high-risk group) were higher than both the no encephalopathy and hypoxic-ischemic encephalopathy grade 1 groups when pooled. Cerebrospinal fluid neuron-specific enolase levels of the 7 newborns in the hypoxic-ischemic encephalopathy grade 3 group were also significantly higher than the 5 in the hypoxic-ischemic encephalopathy grade 1 group. The findings of cranial MRI, EEG, and cerebrospinal fluid neuron-specific enolase levels were correlated with each other and the clinical grade of the patients and also were predictive of the neurologic outcome at 1 year of age. Cerebrospinal fluid neuron-specific enolase levels, cranial MRI, and EEG are predictive of outcome of hypoxic-ischemic brain damage in asphyxiated newborns, and this predictivity would increase with the combination of these diagnostic parameters.
引用
收藏
页码:824 / 829
页数:6
相关论文
共 23 条
[1]   NEONATAL HYPOXIA AND EPILEPTIC RISK - A CLINICAL PROSPECTIVE-STUDY [J].
BERGAMASCO, B ;
BENNA, P ;
FERRERO, P ;
GAVINELLI, R .
EPILEPSIA, 1984, 25 (02) :131-136
[2]   Combined use of electroencephalogram and magnetic resonance imaging in full-term neonates with acute encephalopathy [J].
Biagioni, E ;
Mercuri, E ;
Rutherford, M ;
Cowan, F ;
Azzopardi, D ;
Frisone, MF ;
Cioni, G ;
Dubowitz, L .
PEDIATRICS, 2001, 107 (03) :461-468
[3]   Brain-specific proteins in the cerebrospinal fluid of severely asphyxiated newborn infants [J].
Blennow, M ;
Sävman, K ;
Ilves, P ;
Thoresen, M ;
Rosengren, L .
ACTA PAEDIATRICA, 2001, 90 (10) :1171-1175
[4]   THE DEFINITION OF ACUTE PERINATAL ASPHYXIA [J].
CARTER, BS ;
HAVERKAMP, AD ;
MERENSTEIN, GB .
CLINICS IN PERINATOLOGY, 1993, 20 (02) :287-304
[5]  
DAWSONSAUNDERS B, 1998, BASIC CLIN BIOSTATIS, P117
[6]  
GARCIAALIX A, 1994, PEDIATRICS, V93, P234
[7]   S-100 PROTEIN AND NEURON-SPECIFIC ENOLASE IN CSF AFTER EXPERIMENTAL TRAUMATIC OR FOCAL ISCHEMIC BRAIN-DAMAGE [J].
HARDEMARK, HG ;
ERICSSON, N ;
KOTWICA, Z ;
RUNDSTROM, G ;
MENDELHARTVIG, I ;
OLSSON, Y ;
PAHLMAN, S ;
PERSSON, L .
JOURNAL OF NEUROSURGERY, 1989, 71 (05) :727-731
[8]   CLINICAL RELEVANCE OF INCREASED NEURON-SPECIFIC ENOLASE CONCENTRATION IN CEREBROSPINAL-FLUID [J].
JACOBI, C ;
REIBER, H .
CLINICA CHIMICA ACTA, 1988, 177 (01) :49-54
[9]   HIGHLY SENSITIVE IMMUNOASSAYS FOR 3 FORMS OF RAT-BRAIN ENOLASE [J].
KATO, K ;
SUZUKI, F ;
UMEDA, Y .
JOURNAL OF NEUROCHEMISTRY, 1981, 36 (03) :793-797
[10]  
LAMERS KJB, 1995, ACTA NEUROL SCAND, V92, P247