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.

Wednesday, April 19, 2023

Test Predicts Transition From Normal to Impaired Cognition

With your good chance of MCI/demntia post stroke it is your doctor's responsibility to use this test on you and provide EXACT PROTOCOLS that will prevent transition to dementia.  I can't find any example of this test, your doctor is responsible for that. 

Approximately 30% of stroke patients develop dementia within 1 year of stroke onset.

Test Predicts Transition From Normal to Impaired Cognition

Sensitive, simple test detects subtle deficit at its earliest stage

A photo of a senior man performing a memory test while sitting across a desk from a male physician.

The Stages of Objective Memory Impairment (SOMI) system predicted transitions from normal cognition to incident symptomatic cognitive impairment, longitudinal data showed.

Over a mean follow-up of about 6 years, cognitively normal older adults with memory tests scores reflecting moderate retrieval impairment (SOMI-2) were twice as likely to progress to incident cognitive impairment as those whose memory was intact (SOMI-0), according to Ellen Grober, PhD, of Albert Einstein College of Medicine in the New York City and co-authors.

Participants with memory storage deficits (SOMI-3 or SOMI-4) were three times as likely to progress, the researchers reported in Neurologyopens in a new tab or window. After adjusting for all biomarkers, SOMI stage remained an independent predictor of incident cognitive impairment.

"There is increasing evidence that some people with no thinking and memory problems may actually have very subtle signs of early cognitive impairment," Grober said in a statement.

"In our study, a sensitive and simple memory test predicted the risk of developing cognitive impairment in people who were otherwise considered to have normal cognition," she added. "Our results support the use of the SOMI system to identify people most likely to develop cognitive impairment."

Earlier studies have linked SOMI outcomes with the presence of Alzheimer's disease pathologyopens in a new tab or window in cognitively unimpaired people in the Anti-Amyloid Treatment in Asymptomatic Alzheimer's (A4) clinical trial.

SOMI is based on the Free and Cued Selective Reminding Test (FCSRT). The test begins with a study phase in which people are shown four cards, each with drawings of four items, and are asked to identify an item belonging to a particular category (for example, an apple would belong to the fruit category). Participants are then asked to recall the items; if they're stuck, they're given category cues to prompt them.

"The FCSRT provides measures of memory retrieval (free recall) and memory storage (total recall)," Grober and co-authors wrote. "Free recall scores predict incident mild cognitive impairment and incident dementia, particularly dementia due to Alzheimer's disease, and often outperform other cognitive tests."

The SOMI system maps free recall and total recall scores into stages. At SOMI-0, free recall and total recall are normal. SOMI-1 and SOMI-2 reflect increasing retrieval difficulty with declining free recall in the context of intact total recall, beginning 7-8 years before clinical dementia. In SOMI-3 and SOMI-4, cuing fails to recover all the items missed in free recall, indicating a memory storage deficit occurring about 1 to 3 years before clinical dementia.

Grober and colleagues followed 969 cognitively normal people from the Knight Alzheimer Disease Research Centeropens in a new tab or window in St. Louis who had a Clinical Dementia Rating (CDRopens in a new tab or window) of 0 at baseline. Mean age was about 69, mean follow-up was 6.36 years, and 59.6% were female.

About a third (33.8%) of participants were APOE4 positive. A total of 555 people had cerebrospinal fluid and structural MRI measures (the biomarker subgroup) and 144 were amyloid-positive. Findings were adjusted for age, sex, education, and APOE4 status.

Participants in SOMI-1 through SOMI-4 had elevated hazard ratios for transitioning from normal cognition to symptomatic cognitive impairment, which was defined as CDR≥0.5.

SOMI-2 (HR 2.07, 95% CI 1.32-3.01) and SOMI-3/4 (HR 3.11, 95% CI 1.94-4.97) were significantly associated with incident cognitive impairment compared with SOMI-0 (P<0.001 for both). In subgroups with biomarkers and amyloid-positive status, SOMI-1 participants also showed increased cognitive impairment risk.

In models including measures of amyloid and tau pathology and hippocampal volume, SOMI remained a significant predictor of time to CDR≥0.5.

Only 4.9% of participants (47 people) were classified as SOMI-3 or SOMI-4, limiting interpretation of data from this group, Grober and co-authors said. Most participants were white and highly educated, and results may not apply to others.

  • Judy George covers neurology and neuroscience news for MedPage Today, writing about brain aging, Alzheimer’s, dementia, MS, rare diseases, epilepsy, autism, headache, stroke, Parkinson’s, ALS, concussion, CTE, sleep, pain, and more. Follow

Disclosures

The study was funded by the NIH, the Alzheimer's Association, Cure Alzheimer Fund, and the Leonard and Sylvia Marx Foundation.

Grober receives a small royalty for commercial use of the Free and Cued Selective Reminding Test with Immediate Recall; the test is available at no cost to researchers and clinicians. One co-author disclosed relationships with AbbVie, American Academy of Neurology, American Headache Society, Amgen, Biohaven, Eli Lilly, GlaxoSmithKline, Grifols, Lundbeck, Merck, Pfizer, Teva, Vector, and Vedanta. No other relationships relevant to the manuscript were reported.

Primary Source

Neurology

Source Reference: opens in a new tab or windowGrober E, et al "Association of stages of objective memory impairment with incident symptomatic cognitive impairment in cognitively normal individuals" Neurology 2023; DOI:10.1212/WNL.0000000000207276.

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