PET Reveals First Image of Amyloid Deposits with Alzheimer's Disease

A Swedish medical university study provides clues into the pathologic course of Alzheimer's disease (AD). The brain of the first Alzheimer's patient to display amyloids demonstrable with a positron emission tomography (PET) scanner has been studied, both during progression of the disease and after death.

One pathologic characteristic of AD is the accumulation in the brain of beta-amyloid proteins to form amyloid plaques. However, it is not known how early the plaques form in the brain, whether they are the primary cause of the disease, or what pathogenic role is played by other changes in the brain.


The very first PET scan in the world of amyloid plaque in a living patient with the amyloid-binding compound ¹¹C-PIB (Pittsburgh compound B) was performed in 2002 by Prof. Agneta Nordberg, from the Karolinska Institutet (Stockholm, Sweden) , and provides insights into the pathologic course of AD on the brain of the first on a 56-year old Alzheimer's patient. The researchers then monitored the patient as the disease progressed with routine PET scans and memory tests. After the patient died, the investigators performed pathologic and neurochemical analyses of the brain tissue.

The combined result analyses, which was published online December 14, 2010, in the journal Brain, give a detailed picture of how Alzheimer's disease develops. For example, the results reveal that high concentrations of amyloid plaques were discovered at an early stage of the disease when the patient suffered slight memory loss. The levels remained unchanged during the course of the disease, in contrast to the increasingly declining energy metabolism in the brain, which was also measured using PET as the patient's memory gradually worsened.

One formerly unknown connection that was discovered in the study is that the greater accumulation of plaque is accompanied by a decrease in the number of neuronal nicotinic receptors in the brain. These receptors are vital to memory function, and this new evidence demonstrates that the receptors are affected early on in the disease development. Furthermore, inflammatory changes were measured in brain regions with low levels of plaques, which suggest that the neuroinflammation related to AD might have a different cause and evolve at different stage of the disease compared to that of amyloid accumulation. Studies on this are currently being carried out on living patients using PET imaging technology.

Today, over 1,000 patients around the world have undergone PET scans for measuring amyloid concentrations in the brain. PIB-PET was recently recommended as the earliest clinical diagnostic biomarker for discovering AD, following the diagnostic guidelines provided by the American Alzheimer's Association (Chicago, IL, USA). However, if clinicians are to gain additional insight into the importance of these PET examinations, a follow up of the results obtained from conducted PET studies should be performed in the brain tissue of deceased patients.

"If we combine different examinations, we will be able to affirm that complex changes take place at the same time in the brain during the development of Alzheimer's disease,” said Prof. Nordberg. "Our study shows that new, modern imaging technology known as molecular imaging makes it possible to discover the disease at an early stage. This opens up new opportunities for early diagnosis and for understanding the causes of the disease and identifying patients who can be expected to respond well to future Alzheimer's therapy.”

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