This means the disease may be curable and a vaccine possible. Bacteria in periodontitis seems to be the culprit. Reported amyloid and tau buildups may be a response, not a cause. Compelling research offers a genuine reason for optimism. Dementia is now the fifth leading cause of death around the world, and 70% of that is due to Alzheimer's disease. Until now, experts have been baffled by what causes it, and powerless at slowing or reversing the cruel progress of this condition. Alzheimer's pulls its victims away from reality as their families watch, hearts breaking, until death delivers the final blow. That may be about to change, though, thanks to new research that finds what causes Alzheimer's is actually bacteria, P gingivalis, in gum disease. Has the role of protein deposits in patients’ brains been misunderstood? Brain exhibiting plaque build-up, in blue It's been known for a while that the brains of Alzheimer's victims have unusually high amounts of amyloid and tau proteins.This has lead, naturally, to a suspicion that these proteins cause the disease. However, it turns out that some older people with exceptionally good memories have significant amounts of amyloid and tau proteins in their brains. This has called into question their causal role in the disease, and has led scientists to investigations of the possibility that the proteins may be appearing as a response to the actual culprit. Gum disease in mice P. gingivalis Research from 2009 had identified a gum-disease bacteria, P gingivalis IgG, as a frequent malady of Alzheimers suffers and frequently present in their brains. It was unclear, however, whether the patients' periodontitis had something to do with the disease or was simply a condition sufferers acquired after its onset. A number of research teams conducted P gingivalis experiments and found that its presence worsens Alzheimer's symptoms — including amyloid buildup — in mice bred to have the disease, and actually causes Alzheimer's in healthy mice. An early clue A few years back, Massachusetts General Hospital's Robert Moir started looking into the behaviors of a particular sequence of amino acids in beta amyloids. It exists in 70% of vertebrates, as well as some other animals, intriguing Moir, who told New Scientist, "This is a very old peptide doing something that's important." He found that the protein was a bacterial microbe killer. This suggested that the familiar buildups could be defending the brain against invading bacteria. The smoking gun The new study reveals that toxic enzymes, gingipains, that allow P gingivalisto feed on human flesh were found in 96% of the tissue they examined from 54 Alzheimers' victims. Also, when they examined the DNA of three Alzheimer brains they, found the P gingivalis in them all. Researcher Sim Singhrao of University of Central Lancashire, not involved in the study, tells New Scientist, ""This is the first report showing P. gingivalis DNA in human brains, and the associated gingipains, co-lococalising with plaques." As further confirmation, there was more of both the bacteria and its gingipains — and amyloid and tau buildup — in patients experiencing more advanced dementia. The study also found that the gingipains mangle tau proteins so that they begin killing neurons. The result? Dementia. What this means Altogether, this may finally be the Alzheimer's breakthrough scientists have been waiting for. First off, the researchers discovered P gingivalis in the spinal fluid of living patients, suggesting a means of early diagnosis since Alzheimer's may take from 10 to 20 years to develop before becoming symptomatic. Second, the bacteria may be vulnerable to treatment. Pharmaceutical firm Cortexyme is testing gingipain blockers that has resulted in improvement for Alzheimer's patients. Larger trials are imminent. Third, another team in Melbourne Australia is working on a vaccine against gum disease and thus Alzheimer's. The beginning of the end of Alzheimer’s? We've gotten our hopes up before, but the new research provides genuine reason for optimism. The cause of this tragic condition may finally have been identified. As Cortexyme's Casey Lynch says, "We believe this is a universal hypothesis of pathogenesis." Source
