One region especially affected was the parietal cortex, which is involved in functions including spatial orientation and navigation.
Professor Scott Small, director of the Alzheimer's Disease Research Center at Columbia University in New York, said: "It has been known for years that Alzheimer's starts in a brain region known as the entorhinal cortex. But this study is the first to show in living patients that it begins specifically in the lateral entorhinal cortex, or LEC.
"The LEC is considered to be a gateway to the hippocampus, which plays a key role in the consolidation of long-term memory, among other functions. If the LEC is affected, other aspects of the hippocampus will also be affected."
The scientists suspect that Alzheimer's spreads by a domino effect: neurons are compromised in the LEC, which in turn reduces the integrity of their neighbours.
Two of the hallmarks of Alzheimer's disease are sticky protein deposits in the brain called beta amyloid plaques, and "tangles" of tau protein.
A first step to accumulating beta amyloid is the production of amyloid precursor protein (APP).
Professor Karen Duff, also of Columbia University and co-author of the report, said: "The LEC is especially vulnerable to Alzheimer's because it normally accumulates tau, which sensitises the LEC to the accumulation of APP.
"Together, these two proteins damage neurons in the LEC, setting the stage for Alzheimer's."
Prof Small said: "Now that we've pinpointed where Alzheimer's starts, and shown that those changes are observable ... we may be able to detect Alzheimer's at its earliest preclinical stage, when the disease might be more treatable and before it spreads to other brain regions."
- PAA
