Brain-specific proteins in the cerebrospinal fluid of severely asphyxiated newborn infants

被引:86
作者
Blennow, M
Sävman, K
Ilves, P
Thoresen, M
Rosengren, L
机构
[1] Univ Gothenburg, Dept Cell Biol & Histol, Gothenburg, Sweden
[2] Ullevaal Univ Hosp, Oslo, Norway
[3] Univ Bristol, St Michaels Hosp, Dept Child Hlth, Bristol, Avon, England
[4] Tartu Univ Hosp, Dept Paediat, Tartu, Estonia
[5] Sahlgrens Univ Hosp, Dept Paediat, S-41345 Gothenburg, Sweden
[6] Karolinska Inst, Astrid Lindgrens Childrens Hosp, Neonatal Programme, Stockholm, Sweden
[7] Huddinge Univ Hosp, Dept Paediat, Stockholm, Sweden
关键词
birth asphyxia; brain proteins; cerebrospinal fluid; glial fibrillary protein; neurofilament protein; neuron-specific enolase; protein S-100;
D O I
10.1080/080352501317061594
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Upcoming trials of neuroprotective strategies in severely asphyxiated newborn infants emphasize the need for early and objective markers of both good and bad long-term prognosis. Traditional markers such as neurological depression and seizures are not specific. Aim: To study whether measurement in the cerebrospinal fluid of some proteins known to be specific to the central nervous system was in covariance with the clinical course and long-term prognosis. Methods: Twenty-two asphyxiated infants were included in the study and compared with a control group of 8 infants without signs of perinatal asphyxia. Cerebrospinal fluid (CSF) was collected during the first 4 d of life and analysed for neurofilament protein (NFp), glial fibrillary acidic protein (GFAp), protein S-100 and neuron-specific enolase (NSE). Results: The concentrations of all four proteins were significantly increased in the CSF of asphyxiated infants. The concentrations correlated significantly with other indicators of long-term prognosis and to neurological impairment at 1 y of age, or death before that time. Specifically, concentrations were excessively high in the five infants who died. Conclusions: High concentrations of brain-specific proteins are released into the CSF of asphyxiated infants. It might therefore be useful to measure these concentrations when excluding patients with the gravest prognosis from neuroprotective trials.
引用
收藏
页码:1171 / 1175
页数:5
相关论文
共 17 条
[1]   EARLY PATTERN-RECOGNITION IN SEVERE PERINATAL ASPHYXIA - A PROSPECTIVE MRI STUDY [J].
BAENZIGER, O ;
MARTIN, E ;
STEINLIN, M ;
GOOD, M ;
LARGO, R ;
BURGER, R ;
FANCONI, S ;
DUC, G ;
BUCHLI, R ;
RUMPEL, H ;
BOLTSHAUSER, E .
NEURORADIOLOGY, 1993, 35 (06) :437-442
[2]   BRAIN-TYPICAL CREATINE-KINASE IN SERUM OF NEWBORN-INFANTS WITH PERINATAL BRAIN-DAMAGE [J].
BECKER, M ;
MENZEL, K .
ACTA PAEDIATRICA SCANDINAVICA, 1978, 67 (02) :177-180
[3]   GLIAL FIBRILLARY ACIDIC PROTEIN IN THE CEREBROSPINAL-FLUID - A POSSIBLE INDICATOR OF PROGNOSIS IN FULL-TERM ASPHYXIATED NEWBORN-INFANTS [J].
BLENNOW, M ;
HAGBERG, H ;
ROSENGREN, L .
PEDIATRIC RESEARCH, 1995, 37 (03) :260-264
[4]   THE DEFINITION OF ACUTE PERINATAL ASPHYXIA [J].
CARTER, BS ;
HAVERKAMP, AD ;
MERENSTEIN, GB .
CLINICS IN PERINATOLOGY, 1993, 20 (02) :287-304
[5]   Neonatal encephalopathies - Time to reconsider the cause of encephalopathies [J].
Edwards, AD ;
Nelson, KB .
BMJ-BRITISH MEDICAL JOURNAL, 1998, 317 (7172) :1537-1538
[6]  
GARCIAALIX A, 1994, PEDIATRICS, V93, P234
[7]   PREDICTIVE VALUE OF EARLY CONTINUOUS AMPLITUDE INTEGRATED EEG RECORDINGS ON OUTCOME AFTER SEVERE BIRTH ASPHYXIA IN FULL-TERM INFANTS [J].
HELLSTROMWESTAS, L ;
ROSEN, I ;
SVENNINGSEN, NW .
ARCHIVES OF DISEASE IN CHILDHOOD-FETAL AND NEONATAL EDITION, 1995, 72 (01) :F34-F38
[8]   COMPARISON OF 2 METHODS OF PREDICTING OUTCOME IN PERINATAL ASPHYXIA [J].
LEVENE, MI ;
GRINDULIS, H ;
SANDS, C ;
MOORE, JR .
LANCET, 1986, 1 (8472) :67-69
[9]   Early biochemical indicators of hypoxic-ischemic encephalopathy after birth asphyxia [J].
Nagdyman, N ;
Kömen, W ;
Ko, HK ;
Müller, C ;
Obladen, M .
PEDIATRIC RESEARCH, 2001, 49 (04) :502-506
[10]   POSTISCHEMIC NEURONAL DAMAGE CAUSES ASTROGLIAL ACTIVATION AND INCREASE IN LOCAL CEREBRAL GLUCOSE-UTILIZATION OF RAT HIPPOCAMPUS [J].
RISCHKE, R ;
KRIEGLSTEIN, J .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 1991, 11 (01) :106-113