In vivo viscoelastic properties of the brain in normal pressure hydrocephalus

被引:143
作者
Streitberger, Kaspar-Josche [2 ]
Wiener, Edzard [3 ]
Hoffmann, Jan [4 ,5 ]
Freimann, Florian Baptist [6 ]
Klatt, Dieter [2 ]
Braun, Juergen [7 ]
Lin, Kui [1 ,8 ]
McLaughlin, Joyce [1 ,8 ]
Sprung, Christian [6 ]
Klingebiel, Randolf [1 ,3 ]
Sack, Ingolf [2 ]
机构
[1] Klin Pk, Neuroradiol & Radiol Inst, CH-8027 Zurich, Switzerland
[2] Charite, Dept Radiol, D-10117 Berlin, Germany
[3] Charite, Dept Neuroradiol, D-10117 Berlin, Germany
[4] Charite, Dept Neurol, D-10117 Berlin, Germany
[5] Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94143 USA
[6] Charite, Dept Neurosurg, Berlin, Germany
[7] Charite, Inst Med Informat, D-10117 Berlin, Germany
[8] Rensselaer Polytech Inst, Dept Math, Troy, NY USA
关键词
MR elastography; brain; viscoelasticity; springpot; normal pressure hydrocephalus; MAGNETIC-RESONANCE ELASTOGRAPHY; MR ELASTOGRAPHY; ISCHEMIA; BEHAVIOR; DIAGNOSIS; DISEASE; LIVER; MODEL;
D O I
10.1002/nbm.1602
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Nearly half a century after the first report of normal pressure hydrocephalus (NPH), the pathophysiological cause of the disease still remains unclear. Several theories about the cause and development of NPH emphasize disease-related alterations of the mechanical properties of the brain. MR elastography (MRE) uniquely allows the measurement of viscoelastic constants of the living brain without intervention. In this study, 20 patients (mean age, 69.1 years; nine men, 11 women) with idiopathic (n = 15) and secondary (n = 5) NPH were examined by cerebral multifrequency MRE and compared with 25 healthy volunteers (mean age, 62.1 years; 10 men, 15 women). Viscoelastic constants related to the stiffness (mu) and micromechanical connectivity (alpha) of brain tissue were derived from the dynamics of storage and loss moduli within the experimentally achieved frequency range of 25-62.5 Hz. In patients with NPH, both storage and loss rnoduli decreased, corresponding to a softening of brain tissue of about 20% compared with healthy volunteers (p < 0.001). This loss of rigidity was accompanied by alpha decreasing a parameter (9%, p < 0.001), indicating an alteration in the microstructural connectivity of brain tissue during NPH. This disease-related decrease in viscoelastic constants was even more pronounced in the periventricular region of the brain. The results demonstrate distinct tissue degradation associated with NPH. Further studies are required to investigate the source of mechanical tissue damage as a potential cause of NPH-related ventricular expansions and clinical symptoms. Copyright (C) 2010 John Wiley & Sons, Ltd.
引用
收藏
页码:385 / 392
页数:8
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