Increase in apparent diffusion coefficient in normal appearing white matter following human traumatic brain injury correlates with injury severity

被引:49
作者
Goetz, P [1 ]
Blamire, A
Rajagopalan, B
Cadoux-Hudson, T
Young, D
Styles, P
机构
[1] John Radcliffe Hosp, MRC Biochem & Clin Magnet Resonance Unit, Oxford 0X3 9DU, England
[2] Radcliffe Infirm, Dept Neurosurg, NHS Trust, Oxford OX2 6HE, England
[3] John Radcliffe Hosp, Nuffield Dept Anaesthet, Oxford OX3 9DU, England
关键词
ADC; diffuse axonal injury; diffusion weighted imaging; T1; relaxation; T2; traumatic brain injury; white matter;
D O I
10.1089/0897715041269731
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Following diffuse traumatic brain injury, there may be persistent functional or psychological deficits despite the presence of normal conventional MR images. Previous experimental animal and human studies have shown diffusion abnormalities following focal brain injury. Our aim was to quantify changes in apparent diffusion coefficient (ADC) and absolute relaxation times of normal appearing white matter (NAWM) in humans following traumatic brain injury. Twenty-three patients admitted with a diagnosis of head injury (nine mild, eight moderate, and six severe) were scanned an average of 7.6 days after injury using a quantitative echo planar imaging acquisition to obtain co-registered T1, T2, and ADC parametric maps. Mean NAWM values were compared with a control group (n = 13). The patient group showed a small but significant increase in ADC in NAWM, with no significant change in T1 or T2 relaxation times. There was a correlation between injury severity and increasing ADC (p = 0.03) but no correlation with either T1 or T2, suggesting that ADC is a sensitive and independent marker of diffuse white matter tissue damage following traumatic insult. None of the patients had a reduced ADC, making ischaemia unlikely in this cohort. Pathophysiological mechanisms that may explain diffusely raised ADC include vasogenic edema, chronic ischemic phenomena, or changes in tissue cytoarchitecture or neurofilament alignment.
引用
收藏
页码:645 / 654
页数:10
相关论文
共 53 条
[1]   Axonal injury in falls [J].
AbouHamden, A ;
Blumbergs, PC ;
Scott, G ;
Manavis, J ;
Wainwright, H ;
Jones, N ;
McLean, J .
JOURNAL OF NEUROTRAUMA, 1997, 14 (10) :699-713
[2]  
Adams J H, 1983, Acta Neurochir Suppl (Wien), V32, P15
[3]   DIFFUSE AXONAL INJURY IN HEAD-INJURY - DEFINITION, DIAGNOSIS AND GRADING [J].
ADAMS, JH ;
DOYLE, D ;
FORD, I ;
GENNARELLI, TA ;
GRAHAM, DI ;
MCLELLAN, DR .
HISTOPATHOLOGY, 1989, 15 (01) :49-59
[4]   Diffusion and high resolution MRI of traumatic brain injury in rats: Time course and correlation with histology [J].
Albensi, BC ;
Knoblach, SM ;
Chew, BGM ;
O'Reilly, MP ;
Faden, AI ;
Pekar, JJ .
EXPERIMENTAL NEUROLOGY, 2000, 162 (01) :61-72
[5]   Detection of acute pathologic changes following experimental traumatic brain injury using diffusion-weighted magnetic resonance imaging [J].
Alsop, DC ;
Murai, H ;
Detre, JA ;
McIntosh, TK ;
Smith, DH .
JOURNAL OF NEUROTRAUMA, 1996, 13 (09) :515-521
[6]   Effects of osmotically driven cell volume changes on diffusion-weighted imaging of the rat optic nerve [J].
Anderson, AW ;
Zhong, JH ;
Petroff, OAC ;
Szafer, A ;
Ransom, BR ;
Prichard, JW ;
Gore, JC .
MAGNETIC RESONANCE IN MEDICINE, 1996, 35 (02) :162-167
[7]   Lesion volume, injury severity, and thalamic integrity following head injury [J].
Anderson, CV ;
Wood, DMG ;
Bigler, ED ;
Blatter, DD .
JOURNAL OF NEUROTRAUMA, 1996, 13 (02) :59-65
[8]  
Arfanakis K, 2002, AM J NEURORADIOL, V23, P794
[9]   Diffusion- and T-2-weighted MRI of closed-head injury in rats: A time course study and correlation with histology [J].
Assaf, Y ;
BeitYannai, E ;
Shohami, E ;
Berman, E ;
Cohen, Y .
MAGNETIC RESONANCE IMAGING, 1997, 15 (01) :77-85
[10]   Contribution of vasogenic and cellular edema to traumatic brain swelling measured by diffusion-weighted imaging [J].
Barzo, P ;
Marmarou, A ;
Fatouros, P ;
Hayasaki, K ;
Corwin, F .
JOURNAL OF NEUROSURGERY, 1997, 87 (06) :900-907