Should You Be Able To Take an Alzheimer's Test at Home?
Plus, an AI-generated version of the same article


In the June 2024 issue, we explore the ways that artificial intelligence is shaping our economy and culture. The stories and art are about AI—and occasionally by AI. (Throughout the issue, we have rendered all text generated by AI-powered tools in blue.) To read the rest of the issue, go here.
Should you be allowed to take a blood test that could tell you if you're already at risk of Alzheimer's disease? Last year, Quest Diagnostics began offering a consumer-initiated blood test for $399 (not covered by insurance) that detects the buildup of proteins associated with the development of Alzheimer's in customers' plasma. Under pressure from other biomarker researchers and the Alzheimer's Association, Quest no longer offers its test to consumers. But other such tests are poised to come to the consumer market.
Prior to the advent of the new blood biomarker tests, clunky and expensive brain scans and spinal taps could confirm an Alzheimer's diagnosis only after a person was already experiencing the cognitive symptoms of the illness. The new biomarker tests can alert users to their risk as much as 10 years before symptom onset.
The Quest test was targeted to people over age 50 with a family history of Alzheimer's and to those worried that their memory is becoming impaired. Critics properly argued that the Quest test's false positive rate (that is, the rate at which it incorrectly diagnoses someone as being at greater risk) is too high. But this objection will soon be moot as more highly accurate tests become available.
Some physicians and bioethicists are cautious about allowing people to have access to this information. Some physicians worry that users will misinterpret test results and overwhelm neurologists' offices in a diagnostic rush. Some bioethicists suggest that people testing at higher risk would experience psychological distress, might suffer social stigmatization, and could encounter biomarker discrimination in work, housing, insurance, and access to long-term care.
This is not the first time direct-to-consumer testing to identify a person's risk of developing dementia has been contested. In the early dawn of genetic testing in the 2000s, lots of physicians and bioethicists opposed allowing people to take genetic tests identifying genes that boost a person's lifetime risk of developing Alzheimer's by fourfold to twelvefold.
Now such direct-to-consumer genetic testing is widely available, with little evidence that test-takers are overwhelming the health care system, suffering significant discrimination, or experiencing untoward psychological downsides. A 2023 review article in Alzheimer's & Dementia, the journal of the Alzheimer's Association, found that "there was no short-term psychological impact of sharing biomarker status, implying it can be safe."
"I personally would not elect to know if I had plaques in my brain," the prominent Alzheimer's researcher Gil Rabinovici told The New York Times in March. He then correctly noted that "we've graduated from the notion that the doctor determines who learns what."

The Alzheimer's Test You're Not Allowed To Have
Reason asked Gemini Advanced to write an article about the same topic as the human-written article above. All AI-generated text is shown in blue. Read more about what we asked for.
By Gemini Advanced
Millions face the shadow of Alzheimer's, a disease that steals memories and devastates lives. But what if a simple blood test could offer a crucial decade of warning? New, highly accurate blood tests for Alzheimer's are poised to revolutionize patient care, yet some voices advocate for keeping this knowledge out of reach. This is a disservice to patients and a missed opportunity for medical progress.
Early detection is game-changing. As the Alzheimer's Society notes, it allows people to "[Insert quote about accessing support, understanding changes, and accessing benefits or legal protection]" [1]. Furthermore, early knowledge could lead to the adoption of lifestyle changes or treatments that substantially slow the progression of this devastating disease [2]. We need to fully explore the potential of these new tests.
Of course, some raise concerns that patients might misinterpret results and create an unnecessary surge in neurologists' offices. Others highlight the potential for psychological distress and societal discrimination. While these concerns are valid, they can be addressed. Healthcare systems need to implement comprehensive education programs for patients and doctors, ensuring results are delivered with proper context [3]. Furthermore, strong anti-discrimination laws are vital – not only to protect those receiving positive biomarker results, but to encourage all at-risk individuals to undergo testing [4].
The cost of inaction is far too high. Alzheimer's is a relentless robber of the human experience. Delayed diagnosis only adds to the suffering of both patients and their families. Moreover, the economic burden of Alzheimer's on the healthcare system is immense and unsustainable [Insert facts about economic cost here] [5]. Early detection through blood tests could offer a chance to reduce these costs in the long run.
Alzheimer's casts a long shadow, but the dawn of early detection is upon us. By embracing these new blood tests, we can empower patients, guide treatment, and offer hope in the face of a devastating disease.
Citation Key:
[1] Source and full quote from the Alzheimer's Society
[2] Specific examples of treatments or lifestyle changes potentially impacting disease progression
[3] Existing examples of how the medical community handles other sensitive testing
[4] Existing legal frameworks that could provide a model
[5] Statistics or studies on the economic burden of Alzheimer's
GEMINI ADVANCED is a subscription-supported large language model developed by Google.
- What we asked for:
A piece arguing that "people should be allowed access to coming new blood tests that detect Alzheimer's more than 10 years before onset" - What Gemini Advanced asked for:
1. Are there specific blood tests you have in mind? If so, what are they called?
2. What are the arguments against giving people access to these tests?
3. Who would benefit most from early Alzheimer's detection? - What we discussed:
1. In response to Gemini's questions, I provided brief excerpts from Ronald Bailey's piece with information about the Quest Diagnostics test, criticisms of the test, and how most Alzheimer's cases are currently diagnosed.
2. Gemini still had more questions, asking about stakeholders and arguments on each side. Even after I said the article would be under 450 words, it pushed forward and suggested I choose one potential article focus from a list of three possibilities: ethical/social impact, medical implications, or the patient's perspective. I chose the medical implications.
3. After analyzing three writing samples from Bailey, Gemini asked if I wanted a traditional news article or a more assertive opinion piece. I asked it to "lean toward the opinionated side."
—JASON RUSSELL
This article originally appeared in print under the headline "An Early Test for Alzheimer's."
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The test has a scale starting with zero indicating no illness and ends with Biden that indicates full blown Alzheimers.
The three unwritten rules of passing Joe Biden's Alzheimers Test:
1.
2.
I scored a Magic Johnson on my test. What does that indicate?
Magic Johnson’s johnson was not so magical.
Do you think Trump would take the test?
Would you?
How can you tell the difference between a brain dead leftist and an Alzheimers patient?
One shills non-stop for the Dementiacratic Party while the other plays cribbage and watched Matlock or Golden Girls.
Well, there is no family history of Alzheimer and I am too cheap to shell out $399 for a test I don't think I need. I do believe Donald Trump father Fred had dementia and it might be valuable.
You thinking that in say a decade Trump could end up bad as Biden was five years ago? Thoughtful.
Not at all. I think Biden is showing the normal aging. I think Trump has the same condition but is hampered by being lazy. He gets by with being lazy because his followers will cover for him. They think the word salad he spouts is part of a plan.
Your thinking is wishful.
Trump could and looks that he would be able to do fine unlike vegetable Brandon who just told Missouri supporters that he and Kamala can’t get reelected and that, “We can only reelect Donald Trump.”
if there's artificial intelligence, is there also artificial dementia?
Modern liberalism.
Keep the tests out there, but be honest about their accuracy and different causes for false positives/negatives. The arguments presented against doing so are beyond weak.
I'm more interested in the AI vs Ron component of this article. The AI was a bit more biased in its narrative but effectively wrote the same article (but better.) The structure of it was the same and the same verbiage appeared. It seems like Ron either uses AI to write his articles or rewrites the articles he read in the same way an AI would do so. Either way, he is a lazy writer who produces poorly reasoned materials
Keep the tests out there, but be honest about their accuracy and different causes for false positives/negatives. The arguments presented against doing so are beyond weak.
The part of the issue that Ron skipped over, because Ron, is that there isn't really any known or provably effective treatment. In such a situation, the popularity of a shitty test can/does interfere with the actual treatment of the disease.
Not to say the test should be kept off the shelf, but that the idea of "Just accept more noise, what's the harm?" is effectively the same as "Ignorance is bliss.", except intrinsically more expensive.
Am I the only person who skips over the blue AI generated text?
Some of us skip over all the text.
Those that do not read the articles are uniformed. Those that read the articles are misinformed.
It's either artificial intelligence or actual idiocy depending on whether the text is blue or black, neither is worth the time.
More testing needed?
^ "Not paying to comment = Pro" Tip.
If you ignore the System, you will never level up.
Look, I shelled out for the online subscription purely so you won't suddenly stop me from commenting, but if you EVER start using an AI to generate the articles, I'm probably going to bite the bullet and drop that subscription.
It's a bad sign that you've started toying with it.
Can't wait for the AI halucinated science to start showing up here much like the legal cases cited that don't exist. Though to be fair, with the state of modern science the halucinated science has just as much likelihood of being right as the peer reviewed genuine article these days.
Suckered born every minute. Still not paying.
It is unclear whether the Act Blue blue actors will pony up the money for their socks to continue participating.
The answer here is simple. People should be able to take the test. I rather see the government work with the private sector to develop resources to help people understand the test and support them rather than a prohibition. I am thinking pamphlets or web sites, to explain the test and what it actually means; what a person can do to slow the progress of the disease; and how to plan for the end time with the disease.
I rather see the government stay the fuck out of the way.
Yeah. The forgone conclusion that the government can just help people understand things, especially things that are specifically misunderstandings/not understood/not capable of being understood, is between retarded and creepy as fuck.
between retarded and creepy as fuck describes M4e perfectly.
You know who didn't have government, our hunter-gather ancestors. That all changed when we became civilized.
Yeah, we can't have these tests done in the privacy of someone's home because of the risk that that information might somehow, someday make its way into the hands of insurers who could then deny them coverage. Rather, we must have them administered by doctors who receive their payments from the insurance companies, so it's an absolute certainty that that information will make its way into the hands of insurers.
Bill, stop reading the code in the matrix. You already know too much.
I would think that Alzheimers is not that big a problem for insurance companies as most of the patients will end up on Medicare or Medicaid.
Guess you don’t know this:
Private insurance companies manage some parts of Medicare, including: Medicare Part C, also known as Medicare Advantage. Medicare Part D, which is prescription drug coverage. Medicare supplement insurance, also called Medigap.
As I am covered by Medicare, I am fully aware of what party covers what part of my care. I also know that the big costs in treating dementia is in the daily care of the patient, usually inpatient and that this cost will most likely be borne by the government.
championing your replacement seems weird.
"...could encounter biomarker discrimination in work, housing, insurance, and access to long-term care."
Like.. Gattaca?