Magnetic Resonance Imaging to Detect Structural Brain Changes in Huntington's Disease: A Review of Data from Mouse Models

被引:1
作者
Hanrahan, Jenna [1 ]
Locke, Drew P. [1 ]
Cahill, Lindsay S. [1 ,2 ]
机构
[1] Mem Univ Newfoundland, Dept Chem, Arctic Ave, St John, NF A1C 5S7, Canada
[2] Mem Univ Newfoundland, Discipline Radiol, St John, NF, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Brain structure; Huntington's disease; magnetic resonance imaging; mouse models; neuroanatomy; VOXEL-BASED MORPHOMETRY; CAG REPEAT-LENGTH; NATURAL-HISTORY; MOTOR DEFICITS; ANIMAL-MODELS; MRI; ATROPHY; MICE; HD; PHENOTYPE;
D O I
10.3233/JHD-240045
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Structural magnetic resonance imaging (MRI) is a powerful tool to visualize 3D neuroanatomy and assess pathology and disease progression in neurodegenerative disorders such as Huntington's disease (HD). The development of mouse models of HD that reproduce many of the psychiatric, motor and cognitive impairments observed in human HD has improved our understanding of the disease and provided opportunities for testing novel therapies. Similar to the clinical scenario, MRI of mouse models of HD demonstrates onset and progression of brain pathology. Here, we provided an overview of the articles that used structural MRI in mouse models of HD to date, highlighting the differences between studies and models and describing gaps in the current state of knowledge and recommendations for future studies.
引用
收藏
页码:279 / 299
页数:21
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