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. Did your doctor somehow miss the recovery protocol that Pedro Bach-y-Rita used to recover fully back in 1958 with only a partial brain?

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.

Tuesday, October 27, 2026

A clinical and biomarker model for predicting post-stroke cognitive impairment: a prospective cohort study

 

 Describing a problem with NO solution is a fireable offense in any business!

Let's check how long you have NOT BEEN SOLVING THE PROBLEM!

A clinical and biomarker model for predicting post-stroke cognitive impairment: a prospective cohort study


  • X

    Xinyu Zhang 1†

  • X

    Xiangwen Hao 2†

  • Y

    Yanyang Li 2

  • J

    Jingqi Chen 2

  • X

    Xiaoyan Zheng 2

  • A

    Anren Zhang 3*

  • Qiuhong Man

    Qiuhong Man 2*

  • 1. School of Health Preservation and Rehabilitation, Chengdu University of Traditional Chinese Medicine, Chengdu, China

  • 2. Department of Clinical Laboratory, Shanghai Fourth People's Hospital, School of Medicine, Tongji University, Shanghai, China

Abstract


Background and objectives: 


Post-stroke cognitive impairment (PSCI) is highly prevalent and substantially compromises functional recovery and quality of life; however, early identification remains challenging. This study aimed to develop and validate an early prediction model for PSCI by integrating routinely available blood biomarkers with clinical characteristics.


Methods: 


Patients with acute ischemic stroke were prospectively enrolled at Shanghai Fourth People's Hospital between March and November 2024. Cognitive function was assessed 3 months after stroke using the Telephone Montreal Cognitive Assessment (T-MoCA), a telephone-based cognitive screening instrument, with PSCI defined as a corrected T-MoCA score <19. Univariable logistic regression, Spearman correlation analysis, and variance inflation factor analysis were performed to characterize associations and predictor redundancy. Bootstrap least absolute shrinkage and selection operator (LASSO) logistic regression with 1,000 resampling iterations was used to assess variable-selection stability, followed by multivariable logistic regression and nomogram construction. Model performance was evaluated using receiver operating characteristic (ROC) analysis, calibration analysis, decision curve analysis (DCA), and clinical impact curves (CIC), with 1,000 bootstrap iterations used for internal validation.


Results: 


A total of 198 patients were included, of whom 138 developed PSCI and 60 were classified as post-stroke cognitively normal (PSCN, non-PSCI group). The final prediction model incorporated age, prior stroke history, diabetes mellitus, small dense low-density lipoprotein (sdLDL), apolipoprotein A-I (ApoA-I), homocysteine, cystatin C, and D-dimer. The model achieved an apparent AUC of 0.798. Following 1,000 bootstrap resampling iterations, the mean AUC was 0.777 (95% CI, 0.733–0.802), and the optimism-corrected AUC was 0.762. Calibration analysis suggested reasonable agreement between predicted and observed risks, while DCA and CIC analyses indicated potential utility for PSCI risk stratification.


Conclusions: 


This study developed and internally validated a multivariable model combining clinical characteristics and circulating biomarkers to estimate PSCI risk after acute ischemic stroke. The model showed acceptable predictive performance and may support early risk stratification.

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