Quantitative MRI assessment of Alzheimer’s disease

被引:0
作者
Joseph A. Helpern
Jens Jensen
Sang-Pil Lee
Maria F. Falangola
机构
[1] New York University School of Medicine,Department of Radiology, Center for Biomedical Imaging
[2] The Nathan Kline Institute,Center for Advanced Brain Imaging
来源
Journal of Molecular Neuroscience | 2004年 / 24卷
关键词
MRI; imaging; transgenic mice; Alzheimer’s disease; β-amyloid;
D O I
暂无
中图分类号
学科分类号
摘要
The development of a noninvasive method to detect early, subtle changes in the brains of patients with Alzheimer’s disease (AD) would have considerable clinical value as therapy. This therapy is most likely to be successful if intervention could occur before neurons were irreversibly damaged or lost. An ideal biological neuroimaging marker would be an early, sensitive, and valid indicator of brain changes, capable of discriminating the effects of normal aging. The introduction of high field-strength clinical magnetic resonance imaging (MRI) systems now offer a powerful new noninvasive tool that may be capable of detecting brain pathology resulting from AD. Here we present results from high field-strength MRI in transgenic mice along with a new MRI technique for imaging brain iron. The successful translation of this research to the clinic could prove important to both the early diagnosis and monitoring of the efficacy of potential therapies in humans.
引用
收藏
页码:45 / 48
页数:3
相关论文
共 78 条
[1]  
Bartzokis G.(2000)In vivo evaluation of brain iron in Alzheimer disease using magnetic resonance imaging Arch. Gen. Psychiatry 57 47-53
[2]  
Sultzer D.(2000)Endocytic pathway abnormalities precede beta-amyloid deposition in sporadic Alzheimer’s disease: differential effects of APOE genotype and presenilin mutations Am. J. Pathol. 157 277-286
[3]  
Cummings J.(1990)Cellular distribution of transferrin, ferritin, and iron in normal and aged human brains J. Neurosci. Res. 27 595-611
[4]  
Holt L. E.(1992)A histochemical study of iron, transferrin, and ferritin in Alzheimer’s diseased brains J. Neurosci. Res. 31 75-83
[5]  
Hance D. B.(2000)Graded reduction of cerebral blood flow in rat as detected by the nuclear magnetic resonance relaxation time T2: a theoretical and experimental approach J. Cereb. Blood Flow Metab. 20 316-326
[6]  
Henderson V. W.(1998)Regional distribution of neuritic plaques in the non-demented elderly and subjects with very mild Alzheimer disease [see Comments] Arch. Neurol. 55 1185-1191
[7]  
Mintz J.(1993)Histopathological correlations of nuclear magnetic resonance imaging parameters in experimental cerebral ischemia Mag. Reson. Imaging 11 241-246
[8]  
Cataldo A.(1998)Accelerated Alzheimer-type phenotype in transgenic mice carrying both mutant amyloid precursor protein and presenilin 1 transgenes Nat. Med. 4 97-100
[9]  
Peterhoff C.(2000)NMR relaxation in tissues with weak magnetic inhomogeneities Magn. Reson. Med. 44 144-156
[10]  
Troncoso J.(1994)Magnetic resonance imaging assessment of evolving focal cerebral ischemia: Comparson with histopathology in rats Stroke 25 1252-1262