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, September 23, 2023

Wearable Device May Detect Parkinson Disease 7 Years Before Symptom Onset

With your risk of Parkinsons you'd better hope you have a competent doctor that knows about this and has EXACT PROTOCOLS TO PREVENT PARKINSONS. 

Your risk of Parkinson's here:

Parkinson’s Disease May Have Link to Stroke March 2017 (Your doctor has had 6 years to put together Parkinson's prevention protocols.)

 

Wearable Device May Detect Parkinson Disease 7 Years Before Symptom Onset

Reduced daytime acceleration over 1 week was associated with a clinical diagnosis of Parkinson disease up to 7 years later.

A wearable device may be able to accurately identify individuals at an elevated risk of developing Parkinson disease (PD), according to study findings published in the journal Nature Medicine.

To date, treatment for PD consists of symptom management, with no current disease-modifying treatments available. Furthermore, at the onset of clinical manifestations, most patients will have undergone significant neuronal degeneration of dopaminergic tracts. There remains a need for reliable biomarkers that may detect the early pathologic changes that are associated with PD.

For the study, researchers aimed to investigate the effectiveness of digital accelerometer data as a prodromal marker for PD.

The researchers utilized a prospective, population-based cohort, termed the UK Biobank (UKBB). Accelerometry data was collected for 103,712 individuals aged 40-69, from 2013-2016. Comparison data was compiled, exploring whether accelerometers data can accurately serve as a prodromal marker for PD, by comparison of those diagnosed with PD to unaffected control individuals. Data was also compared with other current modalities, including genetic information, blood biochemistry, lifestyle, and prodromal symptoms.

Our results suggest that accelerometry collected with wearable devices in the general population could be used to identify those at elevated risk for PD on an unprecedented scale …

During the 2-year time of collection, 273 participants were diagnosed with PD; an additional 196 individuals were diagnosed ≥2 years after the data collection, forming a prodromal group for comparison. When comparing data between the prodromal and diagnosed PD cases to an age- and sex-matched unaffected control individuals (1:1), there was a significantly reduced daytime acceleration profile up to 7 years before diagnosis.

Linear regression models, when adjusted for age, sex and body mass index (BMI) for residual average acceleration, found a significant reduction of acceleration in diagnostic PD and prodromal PD when compared with unaffected control individuals. Additionally, no other investigated neurodegenerative disorders (Alzheimer disease, dystonia, all-cause dementia) were found to have a reduction in acceleration before a diagnosis, as was observed in PD. Depression, however, was the only other disorder that the researchers found to have a reduction in acceleration after diagnosis.

Prodromal and diagnosed PD could also be identified from the general population when using average acceleration with area under the precision recall curve (AUPRC) with values of 0.05±0.04 (prevalence =0.0034) and 0.06±0.05 (prevalence =0.0046), respectively. Comparing previous modalities used to identify prodromal PD (genetics, lifestyle, blood biochemistry), accelerometry data was also shown to have a better predictive value in identifying a future diagnosis of PD.

Of note, time dependent area under the receiver operator curve (AUROC) data identified accelerometry to be able to predict the probability of not receiving a diagnosis of PD better than any other single modality previously used; the findings highlight the ability to predict when a diagnosis of PD can be expected.

Study limitations include accelerometry data collection being restricted to a 7-day period, limiting analysis timeframe. Additional modalities with high predictive power, such as dopamine transporter imaging and motor examinations were also not included in the study.

The researchers concluded, “Our results suggest that accelerometry collected with wearable devices in the general population could be used to identify those at elevated risk for PD on an unprecedented scale and, importantly, individuals who will likely convert within the next few years can be included in studies for neuroprotective treatments.”

References:

Schalkamp AK, Peall KJ, Harrison NA, Sandor C. Wearable movement-tracking data identify Parkinson’s disease years before clinical diagnosis. Nat Med. Published online July 3, 2023. doi:10.1038/s41591-023-02440-2

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