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.

Thursday, September 10, 2026

Plasma Cluster of Differentiation 147 and Cognitive Impairment After Acute Ischemic Stroke

 Describing this problem DOES NOTHING TO PREVENT COGNITIVE IMPAIRMENT! I'd have everyone involved fired for incompetence in not knowing that the only goal of survivors IS RECOVERY!

Check how long incompetence has prevailed in NOT SOLVING THE PROBLEM!

Plasma Cluster of Differentiation 147 and Cognitive Impairment After Acute Ischemic Stroke


Abstract

Background

Cluster of differentiation 147 (CD147) is a multifunctional transmembrane glycoprotein, but its effect on poststroke cognitive impairment (PSCI) is unclear.

Methods

The current study included 612 patients with ischemic stroke with plasma CD147 levels from a preplanned ancillary study of CATIS (China Antihypertensive Trial in Acute Ischemic Stroke). Mini‐Mental State Examination and Montreal Cognitive Assessment were used to evaluate cognitive function at the 3‐month follow‐up visit. PSCI was defined as a score of <27 for Mini‐Mental State Examination or <25 for Montreal Cognitive Assessment. Logistic regression models and restricted cubic spline analyses were used to assess the associations between CD147 and PSCI.

Results

As defined by Mini‐Mental State Examination, 317 participants developed PSCI. After multivariate adjustment, elevated plasma CD147 levels were significantly associated with higher odds of PSCI (odds ratio, 1.75 [95% CI, 1.21–2.51]). Multiple‐adjusted spline regression model showed a linear association between plasma CD147 level and PSCI (P for linearity=0.038). Furthermore, adding plasma CD147 to conventional risk factors improved the discriminatory power (C statistics, 0.695 versus 0.711; P=0.047). Similar findings were observed when PSCI was defined by the Montreal Cognitive Assessment.

Conclusions

Elevated plasma CD147 levels at admission were associated with higher odds of cognitive impairment at 3 months after stroke among patients with acute ischemic stroke, suggesting its potential role in the pathophysiological processes of PSCI.

Registration

URL: https://clinicaltrials.gov/study/NCT01840072; Unique Identifier: NCT01840072.




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