Nordberg Agneta
Karolinska Institutet, Department of Neurobiology, Care Sciences and Society, Division of Alzheimer Neurobiology, Karolinska University Hospital Huddinge, Novum 5th floor, Stockholm, Sweden.
Eur J Nucl Med Mol Imaging. 2008 Mar;35 Suppl 1:S46-50. doi: 10.1007/s00259-007-0700-2.
Alzheimer's disease (AD) is a very complex neurodegenerative disorder, the exact cause of which is still not known. The major histopathological features, amyloid plaques and neurofibrillary tangles, already described by Alois Alzheimer, have been the focus in research for decades. Despite a probable whole cascade of events in the brain leading to impairment of cognition, amyloid is still the target for diagnosis and treatment.
The rapid development of molecular imaging techniques now allows imaging of amyloid plaques in vivo in Alzheimer patients by PET amyloid ligands such as Pittsburgh compound B (PIB). Studies so far have revealed high (11)C-PIB retention in brain at prodromal stages of AD and a possibility to discriminate AD from other dementia disorders by (11)C-PIB. Ongoing studies are focussing to understand the relationship between brain and CSF amyloid processes and cognitive processes.
In vivo imaging of amyloid will be important for early diagnosis and evaluation of new anti-amyloid therapies in AD.
阿尔茨海默病(AD)是一种非常复杂的神经退行性疾病,其确切病因尚不清楚。阿洛伊斯·阿尔茨海默早已描述过的主要组织病理学特征——淀粉样斑块和神经原纤维缠结,数十年来一直是研究的焦点。尽管大脑中可能存在一系列导致认知障碍的事件,但淀粉样蛋白仍是诊断和治疗的靶点。
分子成像技术的快速发展现在使得通过正电子发射断层显像(PET)淀粉样配体,如匹兹堡化合物B(PIB),在体内对阿尔茨海默病患者的淀粉样斑块进行成像成为可能。迄今为止的研究表明,在AD的前驱期大脑中(11)C-PIB保留率很高,并且有可能通过(11)C-PIB将AD与其他痴呆症区分开来。正在进行的研究集中于了解大脑与脑脊液淀粉样蛋白过程和认知过程之间的关系。
淀粉样蛋白的体内成像对于AD的早期诊断和新的抗淀粉样蛋白疗法的评估将具有重要意义。