Abstract
To investigate the metabolic consequences of germinal matrix hemorrhage(GMH) we used volume-selective 1H magnetic resonance spectroscopy in the striatal region in 12 preterm infants with predominantly small GMH. Both sides of the brain were investigated twice. Metabolite indices were calculated as the metabolite signal, recorded with TR = 1.6 s and TE = 272 ms, divided by the fully relaxed water signal corrected for transverse relaxation time constant (T2) decay. At the first investigation, when the infants were 32.5 ± 2.0 (mean ± SD) wk postmenstrual age, the hemorrhage was unilateral or markedly asymmetrical in size in 10 of 12 infants. The lactate index was higher (p < 0.01) and the phosphocreatine + creatine(Cr) (p < 0.05) and N-acetyl-L-aspartate (NAA)(p < 0.05) indices lower in the side with the larger hemorrhage. At the second investigation, 54.1 ± 2.7 wk postmenstrual age, no sign of a previous GMH could be seen on magnetic resonance imaging in three of 10 infants. Lactate could be detected in two of 10 infants only, and the Cr and NAA indices did not differ between sides. However, the choline index was significantly higher in the side with the larger hemorrhage (p < 0.01). We conclude that GMH is initially followed by lactate accumulation and possibly a delay in maturation as indicated by the transiently low Cr and NAA indices. Moreover, an increased choline index at the corrected age of 3 mo indicates a more persistent metabolic change after small GMH.
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Abbreviations
- Cho:
-
choline-containing compounds
- GMH:
-
germinal matrix hemorrhage
- 1H MRS:
-
proton magnetic resonance spectroscopy
- MRI:
-
magnetic resonance imaging
- NAA:
-
N-acetyl-L-aspartate
- Cr:
-
phosphocreatine + creatine
- T1:
-
longitudinal relaxation time constant
- T2:
-
transverse relaxation time constant
References
Volpe JJ 1995 Intracranial hemorrhage: germinal matrix-intraventricular hemorrhage of the premature infant. In: Neurology of the Newborn. WB Saunders. Philadelphia, pp 403–463
Pape KE, Wigglesworth JS 1979 The clinico-pathological relationships and aethiological aspects of intraventricular haemorrhage. In: Haemorrhage, Ischaemia and the Perinatal Brain. William Heineman Medical Books, London, pp 133–148
Funato M, Tamai H, Kodaka R, Taki H, Yoshioka Y, Shimada S 1988 The moment of intraventricular hemorrhage. Brain Dev 10: 325–327
Lou HC, Lassen NA, Friis Hansen B 1979 Impaired autoregulation of cerebral blood flow in the distressed newborn infant. J Pediatr 94: 118–121
Pryds O 1991 Control of cerebral circulation in the high-risk neonate. Ann Neurol 30: 321–329
Volpe JJ, Herscovitch P, Perlman JM, Raichle ME 1983 Positron emission tomography in the newborn: extensive impairment of regional cerebral blood flow with intraventricular hemorrhage and hemorrhagic intracerebral involvement. Pediatrics 72: 589–601
Younkin D, Medoff Cooper B, Guillet R, Sinwell T, Chance B, Delivoria Papadopoulos M 1988 In vivo31P nuclear magnetic resonance measurement of chronic changes in cerebral metabolites following neonatal intraventricular hemorrhage. Pediatrics 82: 331–336
Papile L, Burstein J, Burstein R, Koffler H 1978 Incidence and evolution of subependymal and intraventricular hemorrhage: a study of infants with birth weights less than 1,500 gm. J Pediatr 92: 529–534
Volpe JJ 1989 Intraventricular hemorrhage in the premature infant-current concepts. Part I. Ann Neurol 25: 3–11
Pape KE, Wigglesworth JS 1979 Pathological anatomy of intraventricular haemorrhage. In: Haemorrhage, Ischaemia and the Perinatal Brain. Spastics International Medical Publications. JB Lippincott, Philadelphia, pp 118–132
Gould SJ, Howard S, Hope PL, Reynolds EO 1987 Periventricular intraparenchymal cerebral haemorrhage in preterm infants: the role of venous infarction. J Pathol 151: 197–202
Larsen T, Petersen S, Greisen G, Larsen JF 1990 Normal fetal growth evaluated by longitudinal ultrasound examinations. Early Hum Dev 24: 37–45
Peden CJ, Cowan FM, Bryant DJ, Sargentoni J, Cox IJ, Menon DK, Gadian DG, Bell JD, Dubowitz LM 1990 Proton MR spectroscopy of the brain in infants. J Comput Assist Tomogr 14: 886–894
van der Knaap MS, van der Grond J, van Rijen PC, Faber JA, Valk J, Willemse K 1990 Age-dependent changes in localized proton and phosphorus MR spectroscopy of the brain. Radiology 176: 509–515
Huppi PS, Posse S, Lazeyras F, Burri R, Bossi E, Herschkowitz N 1991 Magnetic resonance in preterm and term newborns;1 H-spectroscopy in developing human brain. Pediatr Res 6: 574–578
Kreis R, Ernst T, Ross BD 1993 Development of the human brain: in vivo quantification of metabolite and water content with proton magnetic resonance spectroscopy. Magn Reson Med 30: 424–437
Toft PB, Leth H, Lou HC, Pryds O, Henriksen O 1994 Brain metabolite concentrations in the developing brain estimated by proton magnetic resonance spectroscopy. J Magn Reson Imaging 4: 674–680
Leth H, Toft PB, Pryds O, Peitersen B, Lou HC, Henriksen O 1995 Brain Lactate in preterm and growth-retarded neonates. Acta Paediatr Scand 84: 495–499
Hubbard AM, Markowitz RI, Kimmel B, Kroger M, Bartko MB 1992 Sedation for pediatric patients undergoing CT and MRI. J Comput Assist Tomogr 16: 3–6
Frahm J, Michaelis T, Merboldt KD, Bruhn H, Gyngell ML, Hanicke W 1990 Improvements in localized proton NMR spectroscopy of human brain. Water suppression, short echo times, and 1 mL resolution. J Magn Reson 90: 464–473
Ordidge RJ, Cresshull ID 1986 The correction of transient B0 field shifts following the application of pulsed gradients by phase correction in the time domain. J Magn Reson 69: 151–155
Frahm J, Bruhn H, Gyngell ML, Merboldt KD, Hanicke W, Sauter R 1989 Localized high-resolution proton NMR spectroscopy using stimulated echoes: initial applications to human brain in vivo. Magn Reson Med 9: 79–93
Christiansen P, Henriksen O, Stubgaard M, Gideon P, Larsson HBW 1993 In Vivo quantification of brain metabolites by1 H-MRS using water as an internal standard. J Magn Reson Imaging 11: 107–118
Dobbing J, Sands J 1973 Quantitative growth and development of human brain. Arch Dis Child 48: 757–767
Toft PB, Leth H, Pryds O, Peitersen B, Lou HC, Henriksen O 1994 Periventricular lactate accumulation in prematurity: accentuation in intrauterine growth retardation. In: Lou HC, Greisen G, Falck Larsen J (eds) Brain Lesion in the Newborn (Alfred Benzon Symposium 37). Munksgaard, Copenhagen, pp 302–313
Zuerrer M, Martin E, Boltshauser E 1991 MR imaging of intracranial hemorrhage in neonates and infants at 2.35 Tesla. Neuroradiology 33: 223–229
Edvinsson L, Lou HC, Tvede K 1986 On the pathogenesis of regional cerebral ischemia in intracranial hemorrhage: a causal influence of potassium?. Pediatr Res 20: 478–480
Pranzatelli MR, Stumpf DA 1985 The metabolic consequences of experimental intraventricular hemorrhage. Neurology 35: 1299–1303
Penrice J, Cady EB, Amess PN, Wylezinska M, Wyatt JS, Reynolds EOR 1995 Regional variation in 1H-metabolite concentrations in the brains of newborn infants. Pediatr Res 38: 449( abstr)
Birken DL, Oldendorf WH 1989 N-acetyl-L-Aspartic acid: a literature review of a compound prominent in 1H-NMR spectroscopic studies of brain. Neurosci Biobehav Rev 13: 23–31
Cady EB, Lorek A, Penrice J, Wylezinska M, Cooper CE, Brown GC, Owen-Reece H, Kirkbride V, Wyatt JS, Reynolds EOR 1994 Brain-metabolite transverse relaxation times in magnetic resonance spectroscopy increase as adenosine triphosphate depletes during secondary energy failure following acute hypoxia-ischaemia in the newborn piglet. Neurosci Lett 182: 201–204
Miller BL 1991 A review of chemical issues in 1H NMR spectroscopy: N-acetyl-L-aspartate, creatine and choline. NMR Biomed 4: 47–52
Lowe J, Papile L 1990 Neurodevelopmental performance of very-low-birth-weight infants with mild periventricular, intraventricular hemorrhage. Outcome at 5 to 6 years of age. Am J Dis Child 144: 1242–1245
Blackman JA, McGuinness GA, Bale JF Jr, Smith WL 1991 Large postnatally acquired porencephalic cysts: unexpected developmental outcomes. J Child Neurol 6: 58–64
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Supported by the Danish Medical Research Council No. 12-96356, by the Dannin foundation, and by the Ludvig and Sara Elsass foundation.
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Toft, P., Leth, H., Peitersen, B. et al. Metabolic Changes in the Striatum after Germinal Matrix Hemorrhage in the Preterm Infant. Pediatr Res 41, 309–316 (1997). https://doi.org/10.1203/00006450-199703000-00001
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DOI: https://doi.org/10.1203/00006450-199703000-00001
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