1H magnetic resonance spectroscopy in human hydrocephalus

被引:23
作者
Braun, KPJ
Gooskens, RHJM
Vandertop, WP
Tulleken, CAF
van der Grond, J
机构
[1] Univ Utrecht, Wilhelmina Childrens Hosp, Dept Child Neurol, Med Ctr, NL-3584 EA Utrecht, Netherlands
[2] Univ Utrecht, Dept Child Neurol, Med Ctr, Utrecht, Netherlands
[3] Univ Utrecht, Med Ctr, Dept Radiol, Utrecht, Netherlands
[4] Univ Utrecht, Med Ctr, Dept Neurosurg, Utrecht, Netherlands
[5] Vrije Univ Amsterdam, Univ Hosp, Dept Neurosurg, Amsterdam, Netherlands
关键词
hydrocephalus; magnetic resonance spectroscopy; lactate; ischemia; 3-hydroxybutyrate;
D O I
10.1002/jmri.10270
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: To evaluate cerebral metabolism in clinical hydrocephalus with H-1 magnetic resonance spectroscopy (MRS). Materials and Methods: In 24 children and adults with progressive, arrested, or normal pressure hydrocephalus, long-echo time H-1 MR spectra were acquired from periventricular white matter and intraventricular cerebrospinal fluid (CSF). Metabolite ratios, and the presence of lactate, were compared with 38 age-matched controls. Results: Metabolite ratios of patients were within the 95% confidence interval (CI) of controls. A small lactate resonance was detected in 20% of control and hydrocephalic subjects. Lactate was consistently visible in CSF spectra, though lactate concentrations were normal. The CSF lactate T-2 was long in comparison with the known intracellular metabolite T-2 relaxation times. In three neonates with hydrocephalus and spina bifida, 3-hydroxybutyrate was detected in CSF in vivo. Conclusion: Within the limits of the present methods, H-1 MRS could not detect cerebral metabolic abnormalities in human hydrocephalus and provided no additional diagnostic information. The long T-2 of lactate in CSF explains its high visibility. Hence, the detection of lactate in spectra acquired from voxels that contain CSF does not necessarily imply cerebral ischemia.
引用
收藏
页码:291 / 299
页数:9
相关论文
共 56 条
[1]   HIGH-RESOLUTION PROTON NUCLEAR-MAGNETIC-RESONANCE STUDIES OF HUMAN CEREBROSPINAL-FLUID [J].
BELL, JD ;
BROWN, JCC ;
SADLER, PJ ;
MACLEOD, AF ;
SONKSEN, PH ;
HUGHES, RD ;
WILLIAMS, R .
CLINICAL SCIENCE, 1987, 72 (05) :563-570
[2]   Differentiation between cortical atrophy and hydrocephalus using H-1 MRS [J].
Bluml, S ;
McComb, JG ;
Ross, BD .
MAGNETIC RESONANCE IN MEDICINE, 1997, 37 (03) :395-403
[3]   THE FASTING TEST IN PEDIATRICS - APPLICATION TO THE DIAGNOSIS OF PATHOLOGICAL HYPOKETOTIC AND HYPERKETOTIC STATES [J].
BONNEFONT, JP ;
SPECOLA, NB ;
VASSAULT, A ;
LOMBES, A ;
OGIER, H ;
DEKLERK, JBC ;
MUNNICH, A ;
COUDE, M ;
PATURNEAUJOUAS, M ;
SAUDUBRAY, JM .
EUROPEAN JOURNAL OF PEDIATRICS, 1990, 150 (02) :80-85
[4]   SPATIAL LOCALIZATION IN NMR-SPECTROSCOPY INVIVO [J].
BOTTOMLEY, PA .
ANNALS OF THE NEW YORK ACADEMY OF SCIENCES, 1987, 508 :333-348
[5]   KETONE-BODY TRANSPORT IN THE HUMAN NEONATE AND INFANT [J].
BOUGNERES, PF ;
LEMMEL, C ;
FERRE, P ;
BIER, DM .
JOURNAL OF CLINICAL INVESTIGATION, 1986, 77 (01) :42-48
[6]   In vivo 1H MR spectroscopic imaging and diffusion weighted MRI in experimental hydrocephalus [J].
Braun, KPJ ;
de Graaf, RA ;
Vandertop, WP ;
Gooskens, RHJM ;
Tulleken, KAF ;
Nicolay, K .
MAGNETIC RESONANCE IN MEDICINE, 1998, 40 (06) :832-839
[7]   Cerebral metabolism in experimental hydrocephalus:: an in vivo 1H and 31P magnetic resonance spectroscopy study [J].
Braun, KPJ ;
van Eijsden, P ;
Vandertop, WP ;
de Graaf, RA ;
Gooskens, RHJM ;
Tulleken, KAF ;
Nicolay, K .
JOURNAL OF NEUROSURGERY, 1999, 91 (04) :660-668
[8]  
Braun KPJ, 2000, NEUROL RES, V22, P51
[9]  
BRAUN KPJ, 1999, P 7 INT SOC MAGN RES, P626
[10]   DETECTION OF PROPAN-1,2-DIOL IN NEONATAL BRAIN BY IN-VIVO PROTON MAGNETIC-RESONANCE SPECTROSCOPY [J].
CADY, EB ;
LOREK, A ;
PENRICE, J ;
REYNOLDS, EOR ;
ILES, RA ;
BURNS, SP ;
COUTTS, GA ;
COWAN, FM .
MAGNETIC RESONANCE IN MEDICINE, 1994, 32 (06) :764-767