from Section IV - Cognitive Disorders
Published online by Cambridge University Press: 10 January 2011
Abstract
Neurochemical imaging offers an opportunity to study at a molecular level in-vivo the neuronal substrates that underpin Alzheimer's disease (AD) and related disorders, such as mild cognitive impairment (MCI). In particular, proton magnetic resonance spectroscopic imaging (1H MRSI) is unique among diagnostic imaging modalities because the method can measure several different brain metabolites simultaneously, including N-acetylaspartate (NAA), a neuronal integrity marker, and myo-inositol (MI), a potential glial marker. The goal of this chapter is to review key findings of 1H MRSI in AD, MCI and aging, and to discuss the potential value of this technology for diagnosis and prognosis of AD as well as for the assessment of therapeutic intervention. Other neurochemical imaging technologies such as direct mapping of neurotransmitter systems using emission tomography (PET) tracers and new trends, such as amyloid PET imaging are also briefly discussed.
Introduction
Alzheimer's disease (AD) is the most common cause of dementia and a growing health problem globally, affecting 20% of the population over 80 years of age (Ferri et al., 2005). Currently, the definite diagnosis of AD can only be made through autopsy to find the pathological hallmarks of the disease: microscopic amyloid plaques and neurofibrillary tangles. Macroscopically, AD is characterized by progressive loss of brain tissue that leads to a rapid decline in cognitive function.
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