1 in 3 People Could Develop This Alzheimer’s-Like Disease by Age 85

A new disease mimics Alzheimer's symptoms in people aged 85 and older—but it's entirely different. Get the facts on LATE.

brain scansAtthapon Raksthaput/Shutterstock

Each year, 500,000 people learn that they have Alzheimer’s, a progressive brain disease marked by problems with memory and thinking that interfere with daily life. Now new research suggests some of these people—especially those aged 85 and older—may actually have a newly coined form of dementia known as LATE: limbic-predominant age-related TDP-43 encephalopathy. The acronym is apt since the condition tends to strike people later in life than Alzheimer’s.

“Approximately one in three of all persons over age 85 diagnosed with Alzheimer’s may actually have LATE,” says study author Peter Nelson, MD, PhD, a professor at the University of Kentucky in Lexington.

The new report, which appears in the journal Brain, is based on a National Institute on Aging (NIA) project on LATE, and it included researchers from more than 20 institutions in six countries.

Alzheimer’s versus LATE

While Alzheimer’s disease is the most common type of dementia, it is far from the only type. There are several lesser-known types that are equally devastating. LATE seems to be the most similar to AD in terms of symptoms, namely memory loss and confusion, but there are some important distinctions. Here’s how to know if your memory loss might be Alzheimer’s.

For starters, LATE tends to hit people aged 85 and older, while Alzheimer’s often starts around age 65 and up. What’s more, LATE tends to progress at a slower pace than Alzheimer’s—unless the two diseases travel together, in which case there is a more rapid decline.

Alzheimer’s can have a genetic link, but LATE is not hereditary, says Howard Fillit, MD, founding Executive Director and Chief Science Officer of the Alzheimer’s Drug Discovery Foundation.

Like Alzheimer’s, LATE can only be definitively diagnosed after death during an autopsy of the brain, but the brains of people with LATE look a whole lot different than those of people with Alzheimer’s. “With LATE, the brain can look quite devastated in the region that serves to consolidate short-term memory called the hippocampus,” Dr. Nelson says. There is also an abundance of a toxic protein called TDP-43 in the brains of people with LATE, which suggests a different cause than Alzheimer’s.

The tell-tale signs of Alzheimer’s in the brain include tangles of a protein called tau along with plaques of amyloid-beta, explains Julie A. Schneider, MD, MS, The Deborah R. And Edgar D. Jannotta Presidential Professor of Pathology and Neurological Sciences Associate Director, Rush Alzheimer’s Disease Center, Rush University Medical Center. Alzheimer’s damage starts in the hippocampus but eventually attacks other areas of the brain.

LATE: What’s in a name?

“Recent research and clinical trials in Alzheimer’s disease have taught us two things: First, not all of the people we thought had Alzheimer’s have it; second, it is very important to understand the other contributors to dementia,” says Nina Silverberg, PhD, director of the Alzheimer’s Disease Centers Program at the NIA, in a news release.

Dr. Nelson agrees: “A growing awareness of non-Alzheimer’s diseases that underlie the clinical syndrome of dementia will assist in both clinical trials for Alzheimer’s, and also for the non-Alzheimer’s dementias such as LATE,” he says. “I hope that we can now get on to better tailoring the right therapeutic strategies to the right groups of individuals.”

Time is of the essence, Dr. Fillit adds. “The old-old or individuals aged 85 and older are the fastest growing segment of our population.”

Can LATE be treated?

Like Alzheimer’s the disease is incurable. Doctors can and do use some of the same drugs to ease symptoms of LATE as they do for Alzheimer’s, but in the future, there may be targeted drugs that work better for each type of dementia.

When doctors treat cancer today, they analyze a tumor’s genetic makeup and pair it with therapies that are more likely to be effective. Such “precision medicine” may one day play a role in treating dementia. “We hope to identify subtypes of dementia with cheap and non-invasive blood tests and then have tailored treatments,” Dr. Fillit says. Because of the new report, “we can now say, it’s probably LATE, and we know about TDP-43, which ultimately gives us a drug target.” Learn more about the differences between dementia and Alzheimer’s disease.

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Denise Mann, MS
Denise Mann is a freelance health writer whose articles regularly appear in Reader’s Digest. She has received numerous awards, including the Arthritis Foundation's Northeast Region Prize for Online Journalism; the Excellence in Women's Health Research Journalism Award; the Journalistic Achievement Award from the American Society for Aesthetic Plastic Surgery; National Newsmaker of the Year by the Community Anti-Drug Coalitions of America; the Gold Award for Best Service Journalism from the Magazine Association of the Southeast; a Bronze Award from The American Society of Healthcare Publication Editors; and an honorable mention in the International Osteoporosis Foundation Journalism Awards. Mann received a graduate degree from the Medill School of Journalism at Northwestern University in Evanston, Ill., and her undergraduate degree from Lehigh University in Bethlehem, Pa. She lives in New York with her husband David; sons Teddy and Evan; and their miniature schnauzer, Perri Winkle Blu, and rescue chihuahua-pitbull, Thomas.