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New Blood Test Offers Insights into Alzheimer's Detection

A new blood test may improve detection of Alzheimer's and other brain diseases.

Ramiro Eduardo Rea Reyes, Rachael E. Wilson, Rebecca E. Langhough, Rachel L. Studer, Erin M. Jonaitis, Julie E. Oomens, Elizabeth M. Planalp, Barbara B. Bendlin, Nathaniel A. Chin, Sanjay Asthana, Henrik Zetterberg, Sterling C Johnson

― 6 min read


Revolutionary Blood Test Revolutionary Blood Test for Alzheimer’s brain disorders through blood analysis. New test detects Alzheimer’s and other
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Alzheimer's disease (AD) is a serious illness that affects the brain, leading to problems with memory and thinking. It's like a pesky thief that steals not just your keys but also your ability to remember where you left them! One of the main traits of Alzheimer’s is the buildup of two types of proteins in the brain: amyloid-beta plaques and neurofibrillary tau tangles. These two troublemakers help doctors figure out if someone has Alzheimer’s and how serious it is.

The Tools to Detect Alzheimer’s

To catch the sneaky amyloid and tau proteins, doctors use a few different methods. They can take a sample of your brain fluid (called cerebrospinal fluid, or CSF). They can also use a fancy scanning machine (like a super cool camera) called positron emission tomography (PET). Recently, testing Blood Samples has become a helpful and quicker way to look for these proteins.

But Alzheimer’s isn’t the only condition that causes problems with thinking. Many people can have other brain issues along with Alzheimer's, and detecting these can be really important. For example, protein related to another condition, known as alpha-synuclein, often pops up with Alzheimer’s problems. So, it’s good to find a way to check for both Alzheimer’s and other brain diseases at the same time.

A New Way to Check for Brain Issues

Researchers are now using a method called the Nucleic Acid-Linked Immuno-Sandwich Assay CNS panel, or NULISAseq for short (try saying that five times fast!). This high-tech approach lets us measure many proteins in a small amount of blood. This is pretty exciting because it means we can learn a lot about what's happening in the brain in just one test.

In one study, scientists picked 252 blood samples from participants in two large programs that focus on Alzheimer’s. They wanted to see how well the NULISAseq method could identify the bad guys (amyloid and tau proteins) in the blood. They also wanted to find out if they could spot other troublesome proteins related to different brain diseases.

Who Were the Study Participants?

The study participants were mainly adults in their late middle age. Most of them were doing well mentally, meaning they could remember to buy bread and milk at the store! However, some showed early signs of memory issues.

The researchers went through a lot of effort to carefully select whose blood they would test. They made sure to have blood samples from participants who had undergone PET scans to check for amyloid and tau. This way, they could compare their findings with the new testing method they were using.

Testing the Samples

After gathering the blood samples, they prepared them for testing. The blood was spun around in a machine (like a mini rollercoaster ride for the blood!) to separate out what they needed for the analysis. Then, using the NULISAseq kit, they looked for specific proteins that might indicate problems in the brain.

The results were collected and compared with another well-established test called the Simoa assay to see if these new methods were just as good at detecting amyloid and tau proteins.

Assessing Memory and Brain Skills

All study participants underwent extensive brain function tests. This means they had to do things like remember lists of words, solve puzzles, and figure out tricky patterns. These tests helped determine the participants' cognitive status. Some were doing great, while others had mild cognitive impairment (MCI) or even dementia.

Researchers also looked at brain images to see how well each participant’s brain was working. They checked for any signs of shrinkage or other problems that might indicate declining brain health.

What Did They Find?

The study threw up some interesting results. When comparing the performance of the NULISAseq method to Simoa, it appeared to work just as well for spotting amyloid proteins in the blood. Finding these markers correctly is important because if they are present, it signals that a person may have Alzheimer’s.

As for tau proteins, while both methods worked well, Simoa was slightly better at detecting them. This makes sense since tau proteins behave differently compared to amyloid, which can be a bit sneaky on its own.

Identifying Other Brain Issues

The researchers didn’t stop there. They also wanted to check how well they could identify other brain conditions from the blood samples. They found several different proteins linked to other issues.

For example, people with MCI had higher levels of certain proteins, including some connected to different neurodegenerative diseases. This suggests that even if someone shows early signs of memory trouble, there might be other things going on in their brain.

Notably, one protein in particular, pTDP43-409, was found at higher levels in those with cognitive issues. This was exciting because it could mean a connection to another condition called limbic associated TDP-43 encephalopathy (LATE). So, this could point to the possibility that other brain diseases are contributing to memory loss, not just Alzheimer’s.

The Importance of These Findings

Understanding all these factors is crucial. Many patients present symptoms that don’t fit neatly into just one category. By using a panel to evaluate multiple proteins at once, it could help doctors create a clearer picture of what’s happening in a patient’s brain.

This is particularly useful since treatments for Alzheimer’s and other conditions can vary. If a person doesn’t have Alzheimer’s but has a different issue causing their Cognitive Decline, it’s important to know for their treatment plan.

What’s Next?

The researchers pointed out that while their study yielded promising results, it's still early days. They want to dig deeper and conduct more studies with larger groups. This way, they can understand better how these various proteins work and how they relate to different forms of dementia.

Moreover, researchers hope to understand how these proteins change over time in patients. This can help predict who might be at risk of developing serious cognitive issues down the line.

Final Thoughts

In conclusion, this research provides a glimpse into the future of brain health evaluations. By using advanced testing techniques, we can potentially catch problems faster and in more detail than ever before. This approach could lead to better treatments and brighter futures for everyone affected by Alzheimer’s and other brain diseases.

Just remember, if you ever misplace your keys and can't remember where they are, you might just be having a normal day or maybe a sneak peek of what it's like to be part of a study on Alzheimer’s – and thankfully, there are smart people working hard to keep those pesky proteins in check!

Original Source

Title: Targeted Proteomic Biomarker Profiling Using NULISA in a cohort enriched with risk for Alzheimer's Disease and Related Dementias

Abstract: Structured AbstractO_ST_ABSINTRODUCTIONC_ST_ABSTargeted proteomic assays may be useful for diagnosing and staging Alzheimers disease and related dementias (ADRD). We evaluated the performance of a 120-marker central nervous system (CNS) NUcleic acid-Linked Immuno-Sandwich Assay (NULISA) panel in samples spanning the AD spectrum. METHODSCross-sectional plasma samples (n=252) were analyzed using Alamars NULISAseq CNS panel. ROC analyses demonstrated NULISAseq-pTau217 accuracy in detecting amyloid (A) and tau (T) PET positivity. Differentially expressed proteins were identified using volcano plots. RESULTSNULISAseq-pTau217 accurately classified A/T PET status with ROC AUCs of 0.92/0.86. pTau217 was upregulated in A+, T+, and impaired groups with log2-fold changes of 1.21, 0.57 and 4.63, respectively, compared to A-. Interestingly, pTDP43-409 was also upregulated in the impaired group and correlated with declining hippocampal volume and cognitive trajectories. DISCUSSIONThis study shows the potential of a targeted proteomics panel for characterizing brain changes pertinent to ADRD. The promising pTDP43-409 findings require further replication.

Authors: Ramiro Eduardo Rea Reyes, Rachael E. Wilson, Rebecca E. Langhough, Rachel L. Studer, Erin M. Jonaitis, Julie E. Oomens, Elizabeth M. Planalp, Barbara B. Bendlin, Nathaniel A. Chin, Sanjay Asthana, Henrik Zetterberg, Sterling C Johnson

Last Update: 2024-11-29 00:00:00

Language: English

Source URL: https://www.medrxiv.org/content/10.1101/2024.11.28.24318162

Source PDF: https://www.medrxiv.org/content/10.1101/2024.11.28.24318162.full.pdf

Licence: https://creativecommons.org/licenses/by/4.0/

Changes: This summary was created with assistance from AI and may have inaccuracies. For accurate information, please refer to the original source documents linked here.

Thank you to medrxiv for use of its open access interoperability.

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