People with dementia whose parents also had dementia develop symptoms an average of six years earlier than their parents did, according to new research.
Family history, variations in certain genes, and medical conditions such as cardiovascular disease and diabetes influence a person’s chance of developing dementia. But less clear are the factors that affect when the first symptoms of forgetfulness and confusion will arise.
Factors such as education, blood pressure, and carrying the genetic variant APOE4, which increases the risk of dementia, accounted for less than a third of the variation in the age at onset—meaning that more than two-thirds remains to be explained.
“It’s important to know who is going to get dementia, but it’s also important to know when symptoms will develop,” says first author Gregory Day, an assistant professor of neurology and an investigator at the Charles F. and Joanne Knight Alzheimer’s Disease Research Center at Washington University School of Medicine in St. Louis.
“…people with two parents with dementia developed the disease much younger than people with one parent.”
“If we can better understand the factors that delay or accelerate the age at onset, we eventually could get to the point where we collect this information at a doctor’s visit, put it through our calculator, and determine an expected age at onset for any adult child of a person with dementia.”
Alzheimer’s disease is the most common cause of dementia, affecting an estimated 5.8 million people in the United States. Between 10% and 15% of the children of Alzheimer’s patients go on to develop symptoms of the disease themselves.
The researchers studied people with dementia who were participating in research studies at the Knight ADRC. They identified 164 people with dementia who had at least one parent who had been diagnosed with dementia.
Using medical records and interviews with participants and knowledgeable friends or family members, the researchers determined the age at onset of dementia for each participant and his or her parent or parents. People with one parent with dementia developed symptoms an average of 6.1 years earlier than the parent had. If both parents had dementia, the age at onset was 13 years earlier than the average of the parents’ ages at diagnosis.
It’s not just the diagnosis
Changes over the past few decades in diagnostic criteria and social attitudes toward cognitive decline in later life partially explain why the study participants received diagnoses at younger ages than their parents, the researchers say. But other factors were likely at play as well.
“Nowadays there’s less of a tendency to brush off confusion and forgetfulness as signs of getting older,” Day says. “People who watched their parents decline with Alzheimer’s disease are especially unlikely to dismiss such concerns.
“What’s most interesting, I think, is that people with two parents with dementia developed the disease much younger than people with one parent. That suggests that it’s more than just changes in diagnostic criteria or social attitudes. People with two parents with dementia may have a double dose of genetic or other risk factors that pushes them toward a younger age at onset.”
Mysterious risk factors
As part of this study, the researchers analyzed a large set of known risk factors for Alzheimer’s disease. They studied heritable factors such as ethnicity, race, genetic variants, and which parent had the disease. They also looked at education, body mass index, diabetes, cardiovascular disease, blood pressure, blood cholesterol level, depression, tobacco use, excessive alcohol use, and histories of traumatic brain injury.
All of the factors together only accounted for 29% of the variability, meaning that researchers have not identified most of what influences the age of dementia onset. Intriguingly, the researchers found that people who received an Alzheimer’s disease diagnosis at unexpectedly younger or older ages than their parents were more likely than people diagnosed at the expected age to have certain mutations in Alzheimer’s genes—although it wasn’t clear what effect these mutations have.
“These people are really interesting. We don’t know why their symptoms began earlier or later than expected,” Day says.
“There were no other risk factors we could identify. We started this project looking for factors that we could target to give people more time before they start experiencing dementia. Although we’re not yet at the point where we can modify people’s genes, we can begin to explore how these genes may accelerate or slow down the onset of dementia in these individuals. By learning more about the effect of these genes on Alzheimer’s disease, we may be able to develop novel treatments.”
The study is available online in JAMA Network Open.
Support for this study came from the National Institute on Aging, and the National Institutes of Health.
