Regional specificity of magnetic resonance imaging and histopathology following cerebral ischemia in preterm fetal sheep

被引:16
作者
Fraser, Mhoyra [1 ]
Bennet, Laura [2 ]
Helliwell, Rachel [3 ]
Wells, Scott [4 ]
Williams, Christopher [1 ]
Gluckman, Peter [1 ]
Gunn, Alistair J. [2 ]
Inder, Terrie [5 ]
机构
[1] Univ Auckland, Fac Med & Hlth Sci, Liggins Inst, Auckland 1, New Zealand
[2] Univ Auckland, Fac Med & Hlth Sci, Dept Physiol, Auckland 1, New Zealand
[3] Univ Auckland, Fac Med & Hlth Sci, Dept Anat Radiol, Auckland 1, New Zealand
[4] Canterbury Hlth, Dept Radiol, Christchurch, New Zealand
[5] Washington Univ, Dept Pediat, St Louis, MO 63130 USA
关键词
magnetic resonance imaging; white matter injury; fetal sheep; cerebral ischemia;
D O I
10.1177/1933719107299612
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Early and accurate evaluation of the nature and extent of cerebral injury in the preterm infant brain is important for prognostication and decision making in the neonatal intensive care unit. The capability of magnetic resonance imaging (MRI) to define acute ischemic changes in white and gray matter in comparison to contemporaneous histopathology has not been adequately ascertained. The aim of this study is to assess whether postmortem MRI predicts the nature and extent of brain injury in a preterm fetal sheep model of cerebral hypoperfusion. MRI examinations were performed on fetal sheep brains (d99-100 gestation), perfusion fixed 72 hours after an ischemic insult (n = 7) with left-hemispheric placement Of a microdialysis probe and compared with sham-occlusion (n = 3) and unoperated-control fetuses (n = 4). Cerebral ischemia was associated with MRI changes including global cerebral injury and diffuse white matter signal abnormality, which corresponded closely with histological damage. However, histological changes in deep structures, including the corona radiata, thalamus, and globus pallidus were not reliably detected on MRI. These findings confirm that in preterm fetal sheep, MRI can accurately assess cortical gray matter and subcortical and periventricular white matter abnormalities 3 days after hypoxic-ischemic injury but appears to have limited sensitivity to detect injury to deep structures.
引用
收藏
页码:182 / 191
页数:10
相关论文
共 54 条
  • [1] Reduced development of cerebral cortex in extremely preterm infants
    Ajayi-Obe, M
    Saeed, N
    Cowan, FM
    Rutherford, MA
    Edwards, AD
    [J]. LANCET, 2000, 356 (9236) : 1162 - 1163
  • [2] MRI measurements of the pons and cerebellum in children born preterm; associations with the severity of periventricular leukomalacia and perinatal risk factors
    Argyropoulou, MI
    Xydis, V
    Drougia, A
    Argyropoulou, PI
    Tzoufi, M
    Bassounas, A
    Andronikou, S
    Efremidis, SC
    [J]. NEURORADIOLOGY, 2003, 45 (10) : 730 - 734
  • [3] Selective vulnerability of preterm white matter to oxidative damage defined by F2-isoprostanes
    Back, SA
    Luo, NL
    Mallinson, RA
    O'Malley, JP
    Wallen, LD
    Frei, B
    Morrow, JD
    Petito, CK
    Roberts, CT
    Murdoch, GH
    Montine, TJ
    [J]. ANNALS OF NEUROLOGY, 2005, 58 (01) : 108 - 120
  • [4] Back SA, 2001, J NEUROSCI, V21, P1302
  • [5] Selective vulnerability of late oligodendrocyte progenitors to hypoxia-ischemia
    Back, SA
    Han, BH
    Luo, NL
    Chricton, CA
    Xanthoudakis, S
    Tam, J
    Arvin, KL
    Holtzman, DM
    [J]. JOURNAL OF NEUROSCIENCE, 2002, 22 (02) : 455 - 463
  • [6] BARKOVICH AJ, 1990, AM J NEURORADIOL, V11, P1087
  • [7] BARKOVICH AJ, 1995, AM J NEURORADIOL, V16, P1837
  • [8] FOETAL SHEEP - MORPHOGENESIS OF NERVOUS SYSTEM AND HISTOCHEMICAL ASPECTS OF MYELINATION
    BARLOW, RM
    [J]. JOURNAL OF COMPARATIVE NEUROLOGY, 1969, 135 (03) : 249 - &
  • [9] Brain damage and axonal injury in a Scottish cohort of neonatal deaths
    Bell, JE
    Becher, JC
    Wyatt, B
    Keeling, JW
    McIntosh, N
    [J]. BRAIN, 2005, 128 : 1070 - 1081
  • [10] MR microscopy and high resolution'small animal MRI: applications in neuroscience research
    Benveniste, H
    Blackband, S
    [J]. PROGRESS IN NEUROBIOLOGY, 2002, 67 (05) : 393 - 420