Changing stroke rehab and research worldwide now.Time is Brain! trillions and trillions of neurons that DIE each day because there are NO effective hyperacute therapies besides tPA(only 12% effective). I have 523 posts on hyperacute therapy, enough for researchers to spend decades proving them out. These are my personal ideas and blog on stroke rehabilitation and stroke research. Do not attempt any of these without checking with your medical provider. Unless you join me in agitating, when you need these therapies they won't be there.

What this blog is for:

My blog is not to help survivors recover, it is to have the 10 million yearly stroke survivors light fires underneath their doctors, stroke hospitals and stroke researchers to get stroke solved. 100% recovery. The stroke medical world is completely failing at that goal, they don't even have it as a goal. Shortly after getting out of the hospital and getting NO information on the process or protocols of stroke rehabilitation and recovery I started searching on the internet and found that no other survivor received useful information. This is an attempt to cover all stroke rehabilitation information that should be readily available to survivors so they can talk with informed knowledge to their medical staff. It lays out what needs to be done to get stroke survivors closer to 100% recovery. It's quite disgusting that this information is not available from every stroke association and doctors group.

Saturday, January 18, 2025

Novel blood-based biomarker may reliably detect Alzheimer’s-related brain abnormalities

 

With your extra risk of dementia post stroke; has this been rolled out in your hospital so EXACT DEMENTIA PREVENTION PROTOCOLS CAN BE INITIATED?

1. A documented 33% dementia chance post-stroke from an Australian study?   May 2012.

2. Then this study came out and seems to have a range from 17-66%. December 2013.`    

3. A 20% chance in this research.   July 2013.

4. Dementia Risk Doubled in Patients Following Stroke September 2018 

Novel blood-based biomarker may reliably detect Alzheimer’s-related brain abnormalities

Key takeaways:

  • Higher placental growth factor was associated with a higher Clinical Dementia Rating score.
  • The biomarker may be valuable for screening younger adults as an early Alzheimer’s intervention.

Placental growth factor, a blood-based protein, may be a reliable method to detect abnormalities in the brain that presage cognitive impairment indicative of Alzheimer’s disease, data show.

“Blood-based biomarkers are sorely needed to help diagnose and monitor patients at risk for vascular cognitive impairment, as, currently, brain MRI is the predominant method used for assessing a patient's burden of cerebrovascular disease,” Kyle C. Kern, MD, lead author of the study published in Alzheimer’s & Dementia and vascular neurologist at UCLA Health, told Healio in an email. “Placental growth factor is a promising blood-based biomarker that would be more cost-effective and accessible.”

Source: Adobe Stock.
A novel blood-based biomarker, placental growth factor, may be feasible in detecting brain abnormalities associated with Alzheimer’s disease. Image: Adobe Stock

A blood-based protein, placental growth factor (PlGF), may regulate cerebrovascular permeability and has the potential to be utilized as a biomarker to detect Alzheimer’s disease, Kern and colleagues wrote. They hypothesized that white-matter interstitial fluid accumulation, estimated by MRI imaging free water (FW), would clarify associations between elevated PlGF, white matter hyperintensities (WMH) in the brain and cognitive impairment indicative of disease presence.

Their cross-sectional study analyzed data of 370 older adults (mean age 72 years; 61% women; 83% white) from six sites across the Mark VCID consortium. The consortium was established to validate candidate biomarkers for cerebral small vessel disease by recruiting a diverse swath of candidates who possess a range of vascular risk factors and varied degrees of cognitive impairment. Records of all patients included testing for plasma PlGF as well as brain MRI.

Kyle C. Kern

All participants underwent a cognitive battery with the primary assessments being the Clinical Dementia Rating (CDR) and the Uniform Data Set version 3 composite of executive function (UDS3-EF).

Imaging across all study sites was performed with a trio of 3T MRI models, with researchers subsequently conducting a cross-sectional analysis of FW to determine if it mediated associations between PlGF and WMH, or PlGF and cognition, as measured by scores from CDR and UDS3-EF.

According to results, higher PlGF was associated with higher FW, higher WMH and higher CDR, but not UDS3-EF. Conversely, higher FW was associated with higher WMH and CDR, but lower UDS3-EF.

Kern and colleagues also reported that FW accounted for 26% of the association between PlGF and CDR, and 73% of that between PlGF and WMH.

Based on these data, the researchers suggested this biomarker may be valuable for screening younger adults as an early intervention to forestall potential vascular injury and cognitive decline.

“By demonstrating how elevated [placental growth factor] relates to MRI markers of cerebrovascular disease and worse cognitive status, this study bolsters our understanding of how [it] might be used clinically to diagnose or monitor vascular cognitive impairment,” Kern told Healio.

Reference:

Study supports new blood-based biomarker to detect early brain changes leading to cognitive impairment and dementia. https://www.uclahealth.org/news/release/study-supports-new-blood-based-biomarker-detect-early-brain. Published Dec. 18, 2024. Accessed Jan. 3, 2025.

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