Rapid new blood diagnostic test for ALS
Neurally-derived extracellular vesicles extracted from a standard blood sample contain microRNA sequences used to diagnose ALS. Credit: Paul Cox.

A highly accurate diagnostic blood test has been developed for amyotrophic lateral sclerosis (ALS), a progressive neurodegenerative disease that affects neurons in the brain and spinal cord.

ALS leads to gradual paralysis, ultimately resulting in the inability to walk, speak, or, in later stages, move. Currently, diagnosis is based on a thorough clinical examination, but it can take up to 12 months to provide a definitive diagnosis, by which time many patients have significantly deteriorated. Misdiagnosis rates vary widely, occurring in as many as 68% of cases, further complicating timely and accurate treatment.

Researchers from the not-for-profit Brain Chemistry Labs in Jackson Hole, Wyoming, published the paper, “A microRNA diagnostic biomarker for amyotrophic lateral sclerosis” in Brain Communications.

The diagnostic test requires only a simple blood draw and is based on small sequences of nucleic acids, known as microRNA, extracted from tiny vesicles released by the brain and nervous system.

Analysis of microRNA sequences from hundreds of patient samples allowed researchers to develop a unique “ALS fingerprint” comprising eight distinct microRNA sequences. These sequences can sensitively and specifically distinguish blood samples of ALS patients from healthy controls and from patients with conditions that mimic ALS in its early stages, with an overall accuracy of up to 98%.

Rapid new blood diagnostic test for ALS
Dr. Sandra Banack pipettes blood samples from ALS patients at the Brain Chemistry Labs in Jackson Hole. Credit: Paul Cox.

Scientists hope the test will become a tool to help neurologists make more rapid diagnoses.

“Rapid diagnosis will allow treatment to begin earlier, leading to better outcomes for ALS patients,” said Brain Chemistry Labs scientist Dr. Sandra Banack, senior author on the paper.

This new test follows on the heels of three prior validation studies using different patient cohorts for a total sample size of 471, with many of the samples provided by the U.S. National ALS Biorepository.

Dr. Paul Alan Cox, Executive Director of the Brain Chemistry Labs, hopes to make this test widely available within 18 to 24 months to neurologists by securing a diagnostic company partnership.

More information:
Sandra Banack et al, A microRNA diagnostic biomarker for amyotrophic lateral sclerosis, Brain Communications (2024). DOI: academic.oup.com/braincomms/ar … 3/braincomms/fcae268

Provided by
Brain Chemistry Labs

Citation:
Rapid blood diagnostic test developed for amyotrophic lateral sclerosis (2024, September 12)
retrieved 13 September 2024
from https://medicalxpress.com/news/2024-09-rapid-blood-diagnostic-amyotrophic-lateral.html

This document is subject to copyright. Apart from any fair dealing for the purpose of private study or research, no
part may be reproduced without the written permission. The content is provided for information purposes only.





Source link

Leave a Reply

Your email address will not be published. Required fields are marked *

Before you post, please prove you are sentient.

What is 5 times 5?

Explore More

Glaucoma drug shows promise against neurodegenerative diseases, animal studies suggest

A drug commonly used to treat glaucoma has been shown in zebrafish and mice to protect against the build-up in the brain of the protein tau, which causes various forms

New research identifies potential therapeutic target for amyotrophic lateral sclerosis

Credit: Cell Reports (2024). DOI: 10.1016/j.celrep.2024.114719 Amyotrophic lateral sclerosis (ALS), also known as Lou Gehrig’s disease, is the most common degenerative motor neuron disease in adults. It is characterized by

Some shunts used after epilepsy surgery may risk brain shifting and chronic headaches

Surgeons who observe persistent fluid buildup after disconnecting epileptic and healthy brain areas should think twice before installing low-pressure nonprogrammable drainage shunts, according to a study co-authored by Rutgers pediatric