
Exploring Blood-Based Biomarkers and Treatment Eligibility in Alzheimer Disease: Gil Rabinovici, MD
The professor of neurology and radiology at University of California, San Francisco, discussed the potential of blood-based biomarkers in Alzheimer treatment eligibility, highlighting current limitations and the importance of safety monitoring. [WATCH TIME: 7 minutes]
WATCH TIME: 7 minutes
"The consensus of the committee ultimately was that the blood-based biomarkers are very close, and maybe in the near future, a positive blood-based biomarker would be sufficient to establish eligibility for treatment. But we're not quite there yet."
Alzheimer disease (AD), a progressive neurodegenerative disorder, affects millions globally and remains a leading cause of dementia. Characterized by cognitive decline and memory loss, AD poses significant challenges to patients, families, and healthcare systems. Advancements in diagnostic tools and treatments could be crucial to managing this complex condition effectively. In recent research, studies have focused on the potential of blood-based biomarkers to streamline AD diagnostics and treatment eligibility.
These biomarkers could offer a less invasive alternative to positron emission tomography (PET) scans and spinal taps, which are currently used to detect amyloid plaques and other indicators. However, variability in performance and the lack of FDA approval limit their immediate application. As new treatments emerge, such as those targeting amyloid-related imaging abnormalities (ARIA), rigorous patient monitoring, including frequent MRIs, may be essential to mitigate risks and ensure efficacy.
At the
Newsletter
Keep your finger on the pulse of neurology—subscribe to NeurologyLive for expert interviews, new data, and breakthrough treatment updates.