Early detection of Alzheimer’s disease (AD) is
important to reveal preclinical pathological alterations, to monitor
disease progression, and to evaluate response to therapy. The study of
cerebral glucose metabolism through 18F-fluoro-deoxy-glucose
positron emission tomography (FDG-PET) plays a leading role in early
detection of AD because the decrease of cerebral glucose metabolism
largely precedes the onset of AD symptoms. This technique demonstrated
high sensitivity in early diagnosis of AD, allowing a qualitative and
quantitative estimate of cerebral glucose metabolism. Furthermore
FDG-PET imaging may help to discriminate the subjects of a high-risk
population (like patients with mild cognitive impairment) who more
probably will develop AD: an early stage of AD generally shows
hypometabolism of medial temporal lobes and parietotemporal posterior
cortices; other cerebral cortices are later involved. The combination of
FDG-PET with other biomarkers, such as genotype, cerebrospinal fluid
markers, and amyloid plaque imaging, may increase the preclinical
diagnostic accuracy and offer promising approaches to assess individual
prognosis in AD patients.
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