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, April 21, 2022

Telomere Length and Stroke Recurrence after Ischemic Stroke and TIA

 So no real association found but even so nothing on how to increase telomere length.

This is why you want long telomeres:

Frontiers | Telomere Length as a Marker of Biological Age

And how to do it.

Physical Activity and Nutrition: Two Promising Strategies for Telomere Maintenance?

The latest here:

Telomere Length and Stroke Recurrence after Ischemic Stroke and TIA

First Published April 14, 2022 Research Article 

Background and Objective

Shortening telomere length (TL), as an indicator of aging, has been associated with increased risk of cardiovascular disease and incident stroke. However, there is limited data relating to the association between TL and recurrent stroke.

Methods

Patients from the Third China National Stroke Registry who had whole genome sequencing (WGS) were selected. TL was estimated by using TelSeq based on binary sequence alignment/map files derived from WGS data. Cox proportional hazards regression models were performed to assess the association of TL with recurrent stroke.

Results

8041 patients with ischemic stroke or transient ischemic attack were included. Mean TL was 2.14±0.82 kb. Patients in the lowest tertile of TL had higher incidence of stroke recurrence compared to those in the middle and highest tertile (6.4% vs 5.9% vs 5.2%), but the difference was not longer significant after adjusting for age, sex, cardiovascular risk factors and stroke severity. Similarly, when analysing TL as a continuous variable, the HR per 1000bp increase in TL was significant 0.88 (0.79-0.98), but after adjusting for co-variates, was no longer significant (0.91; 95% CI, 0.81-1.02). In patients aged >65 years, but not in younger patients, after adjusting for co-variates, TL was significantly associated with stroke recurrence. Compared to the lowest tertile, HRs (95%CI) after adjustment for all co-variates for the middle and highest tertiles were 0.78 (0.55-1.10) and 0.67 (0.46-0.98) respectively, with p for trend of 0.03. In analyses using TL as a continuous variable, adjusted HR (95%CI) per 1000bp increase in TL was 0.80 (0.66-0.96). However, there was no significant interaction between TL and age on risk of stroke recurrence (p for interaction=0.09).

Conclusions

In Chinese ischemic stroke or transient ischemic attack patients, no independent association was found between TL and risk of stroke recurrence after adjusting for co-variates. We found a possible association in older patients but this needs replicating.

 

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