IMAGE: Brain scans
These images of brain scans released by the University of Rochester, N.Y., show a healthy brain, left, and the brain of a patient with neuroAIDS. The white areas indicate brain cell loss.
updated 10/2/2006 10:04:45 PM ET 2006-10-03T02:04:45

It’s an Achilles’ heel of HIV therapy: The AIDS virus can sneak into the brain to cause dementia, despite today’s best medicines.

Now scientists are beginning to test drugs that may protect against the memory loss and other symptoms of so-called neuroAIDS, which afflicts at least one in five people with HIV and is becoming more common as patients live longer.

With almost 1 million Americans, and almost 40 million people worldwide, living with HIV, that’s a large and underrecognized toll.

“That means HIV is the commonest cause of cognitive dysfunction in young people worldwide,” says Dr. Justin McArthur, vice chairman of neurology at Baltimore’s Johns Hopkins University, who treats neuroAIDS. “There’s no question it’s a major public health issue.”

While today’s most powerful anti-HIV drugs do help by suppressing levels of the virus in blood — so that there’s less to continually bathe the brain — they can’t cure neuroAIDS. Why? HIV seeps into the brain very soon after someone is infected, and few anti-HIV drugs can penetrate the brain to chase it down.

Protecting the brain
“Despite the best efforts of (anti-HIV) therapy, brain is failing,” says Dr. Harris Gelbard, a neurologist at the University of Rochester Medical Center. He is part of a major new effort funded by the National Institutes of Health to find the first brain-protecting treatments.

What’s now called neuroAIDS is much different from the AIDS dementia of the epidemic’s early years, when patients often had horrific brain symptoms similar to end-stage Alzheimer’s, unable to move or talk. They’d die within six months.

Today, anti-HIV medication has resulted in a more subtle dementia that strikes four years or more before death: At first, patients forget phone numbers and their movements slow. They become less able to juggle multiple tasks.

Some worsen until they can’t hold a job or perform other activities, but not everyone worsens — and doctors can’t predict who will. In a vicious cycle, the memory loss makes many forget their anti-HIV pills, so the virus rebounds.

Gelbard estimates that neuroAIDS reduces patients’ mental function by 25 percent.

If HIV patients live long enough, many specialists worry, nearly all of them may suffer at least some brain symptoms.

“They’re living longer with HIV in the brain,” explains Kathy Kopnisky of the NIH’s National Institute of Mental Health, which is spending about $60 million investigating neuroAIDS. “And they’re aging, so they’re going through the normal brain aging-related processes” that can make people vulnerable to Alzheimer’s and other brain diseases.

Unique type of dementia
Biologically, this is a different type of dementia from any caused by Alzheimer’s or Parkinson’s, and drugs for those brain-degenerating diseases so far are proving disappointing against neuroAIDS.

So the government-funded attack has two fronts:

  • First, figure out which of the powerful anti-HIV cocktails are the best bet for HIV patients with memory problems.

A few of today’s HIV-suppressing drugs, such as nevirapine, abacavir, AZT and indinavir, can penetrate the blood-brain barrier, says Dr. Ron Ellis of the University of California, San Diego.

But no one knows if using those drugs instead of others will slow the brain damage once neuroAIDS symptoms begin. Early next year, Ellis will begin a study of 120 such patients — at UCSD, Hopkins and Washington University in St. Louis — to try to tell, by randomly assigning them to either a brain-penetrating cocktail or different drugs.

  • Second, find drugs that protect nerve cells from the inflammation-triggered toxic chain reaction that seems to be how HIV wreaks its damage.

The brainTopping the candidates are the epilepsy drug valproic acid and lithium, a drug long used in manic-depression. Both inhibit an enzyme, called GSK-3b. The body normally makes the enzyme, but too much is poisonous. In the brain, HIV knocks that careful balancing act out of whack, leading to death of connections key to memory and other neuronal functions.

In a recent pilot study, Gelbard found tantalizing signs that valproic acid might increase brain connections in a few neuroAIDS patients, and improve their symptoms. He’s about to begin a second-stage study to try to tell if the effect is real; a similar pilot trial with lithium is under way.

Seeking a one-two punch, Gelbard also hopes to soon begin a human study of an experimental drug that targets a second inflammatory protein that HIV uses, this one to trigger brain cells to kill themselves.

© 2012 The Associated Press. All rights reserved. This material may not be published, broadcast, rewritten or redistributed.


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