“Historically, diagnostic studies for cognitive impairment and dementia have been limited to structural brain imaging, but increasingly there’s a recognition that we can use the bloodstream as an available but imperfect tool to understand who maximally benefits from those structural and functional imaging tools,” said UCLA Associate Professor and Vice Chair of Research in Neurology Jason Hinman, MD, PhD, the study’s lead author. “It may also tell us who might be the best candidates for some of the really new emerging drugs that are available on the market to treat cognitive impairment and dementia.”
The study represents some of the first validation results reported by a NIH-funded consortium of academic medical centers working to identify biomarkers associated with vascular drivers behind cognitive impairment to help inform diagnosis and treatment. The consortium, known as MarkVCID, was formed in 2016 after researchers recognized they needed a better handle on precisely how vascular brain injury was contributing to dementia.
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Researchers identified signaling involved in angiogenesis as potential biomarkers, theorizing that the body may respond to damaged small blood vessels in the brain with intensified efforts to grow more. For this study, researchers focused on just one of those signals, PlGF, which has previously been associated with cerebral blood flow regulation. Data also gathered by the consortium had suggested this may be a useful biomarker for identifying patients with cognitive impairment and dementia due to vascular brain injury.
At UCLA and four other research sites, 335 patients underwent brain imaging, cognitive testing and blood collection. Researchers found those in the top quartile for PlGF measurement were three times as likely to have cognitive impairment or dementia compared to those in the bottom quartile. Every unit increase in total PlGF in the bloodstream was also associated with a 22% increase in the likelihood of having cognitive impairment and a 16% increase in the likelihood of having imaging evidence of cerebral small vessel disease.
“The addition of a blood-based biomarker that is associated with the traditional measures of vascular injury could allow a provider to be able to distinguish the patient that has Alzheimer’s-predominant dementia versus a significant vascular contribution,” Dr. Hinman said. “Right now it’s kind of the clinician’s best guess. This work can directly inform this diagnostic decision.”
Source: Eurekalert
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