Did rapid brain evolution make humans susceptible to Alzheimers?

To Bruce Yankner, professor of pathology and neurology at Harvard Medical School (HMS), it’s pretty clear that evolution is to blame.

“Something has occurred in evolution that makes our brain susceptible to age-related change,” Yankner said in a talk last night sponsored by the Harvard Museum of Natural History as part of its “Evolution Matters” lecture series.

Yankner, whose HMS lab studies brain aging and how getting old gives rise to the pathology of Alzheimer’s and Parkinson’s diseases, said Alzheimer’s is one of the most rapidly emerging diseases of this century. As medical science lengthens human lifespan, the proportion of the population that is elderly is growing. Considering that as many as half of those over age 85 develop Alzheimer’s, there is a growing urgency to understand the disease more fully and to develop more effective interventions.

“It is clear that cognitive impairment and decline is one of the emerging health threats of the 21st century,” Yankner said.

Yankner said that scientific evidence shows that some cognitive decline — beginning in middle age and accelerating after age 70 — is normal as we grow older. This decline is also seen in other animals, including mice and monkeys. It is marked by wide variation among individuals, with some individuals maintaining cognitive abilities similar to those much younger.

The puzzling question, Yankner said, is why humans develop the severe disabilities of Alzheimer’s disease. Studies of other creatures show no sign of similar conditions even in our closest animal relatives. That means susceptibility to Alzheimer’s evolved recently, likely during a period marked by a rapid increase in our brain size. Size alone probably isn’t the determining factor, though, Yankner said, since other animals are known to have even larger brains, including whales, elephants, and even our extinct relative the Neanderthal.

Instead, he said, it is likely that brain complexity and the new large number of cells in the human brain have something to do with it.

Recent research, in Yankner’s lab and elsewhere, has used genetic tools to probe the differences between young and old brains in humans, monkeys, and mice. The work shows that gene function in the aging brain slows — dramatically in ones with Alzheimer’s — and that the genes that shut off the most are those that protect the brain against genetic damage from environmental and other factors.

Yankner said he believes that cognitive decline is due to a slow accumulation of genetic damage in the aging brain, with Alzheimer’s showing the most severe form of this damage, called double strand breaks. Though the source of the damage is not yet clear, one culprit, he said, may be the accumulation of metals in the brain over time, particularly iron.

Neurons use more energy than most other cells, Yankner said. With the brain’s increase in complexity over time, its energy demands also rose. Iron plays a key role in a cell’s energy-producing mitochondria, and so iron accumulation leading to genetic damage could be a byproduct of our neuron-rich, energy-gobbling brains.

“Aging is a balance between wear and tear and repair. Where you wind up in that balance determines how you do,” Yankner said.

Provided by Harvard University (news : web)