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Alzheimer's mutations found in brain cells

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Alzheimer's mutations found in brain cells

2004-07-06 11:35:11

 

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WASHINGTON (Reuters) - The genetic mutations that lie behind most

cases of Alzheimer's disease may be found inside cell powerhouses

known as mitochondria, U.S. researchers said on Monday.

 

They said they found mutations in mitochondrial DNA in 65 percent of

patients in a study who died of Alzheimer's, and none of the

patients who died of something else.

 

Their finding, published this week in the Proceedings of the

National Academy of Sciences, could help shed light on the most

common form of Alzheimer's, which affects more than 4 million people

in the United States alone.

 

Most DNA is carried on the chromosomes. But an important form is

found in the mitochondria of cells, which are structures that help

provide energy.

 

Douglas Wallace of the Center for Molecular and Mitochondrial

Medicine and Genetics at the University of California at Irvine and

colleagues looked at the brains of 23 people who died of Alzheimer's

and 40 people who died free of dementia.

 

They looked especially for mutations in mitochondrial DNA. They

found variations of a particular mutation in 65 percent of the

brains of Alzheimer's patients and none of the others.

 

Several mutations have been linked to early-onset Alzheimer's, but

it has been difficult to pin down a cause of the most common form,

known as late-onset, sporadic Alzheimer's.

 

The mutations are associated with reductions in the total amount of

mitochondrial DNA, Wallace's team said. It could be that they impair

energy production in the cells, increase the generation of free

radicals that can damage cells, and destroy the connections between

brain cells, they said.

 

Or the mutations could be a symptom rather than a cause.

 

" The question remains: is the increase in (the mitochondrial DNA)

mutations seen in AD brains simply a reflection of accelerated

aging, or is it a distinct pathological phenomenon? " they wrote.

 

 

 

 

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Copyright 2003 Reuters.

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