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, June 6, 2019

Use of Antihypertensives Associated With Decreased Risk of Dementia

I want to know if coffee is better for dementia prevention or my Nifedipine use (a calcium channel blocker). WHOM will know that answer? It is a fuckingly simple question. I don't care that the answer will be hard to figure out. Living with a stroke is hard.

Coffee May Lower Your Risk of Dementia Feb. 2013

 

Use of Antihypertensives Associated With Decreased Risk of Dementia

Antihypertensive drug use is negatively associated with dementia in elderly persons followed in general practices in Germany, according to a study published in the Journal of Alzheimer’s Disease.

“After another setback for the anti-amyloid strategy, dementia prevention is increasingly becoming an area of interest,” said Jens Bohlken, MD, Institute of Social Medicine, Occupational Health and Public Health (ISAP), University of Leipzig, Leipzig, Germany. “In view of this, our most important task is to find existing therapies that are associated with a reduction in dementia risk or at least an extension of the time to dementia onset.”

This study was based on data from the Disease Analyzer database (IQVIA), which compiles drug prescriptions, diagnoses, and basic medical and demographic data obtained directly and in anonymous format from computer systems used in the practices of general practitioners and specialists.

Researchers included 12,405 patients with documented blood pressure values and an initial diagnosis of all-cause dementia in 739 general practices in Germany between January 2013 and December 2017 (index date). Inclusion criteria were as follows: age 60 years at the index date, observation time of at least 12 months prior to the index date, and hypertension diagnosis prior to the index date.

After applying similar inclusion criteria, dementia cases were matched to 12,405 controls without dementia using propensity scores based on age, sex, index year, and co-diagnoses (ie, diabetes, hyperlipidaemia, stroke, heart disease, depression, intracranial injury, Parkinson’s disease, osteoporosis, and epilepsy). For the controls, the index date was that of a randomly selected visit between January 2013 and December 2017.

The primary outcome was the incidence of dementia as a function of the use of antihypertensive drugs.

The use of angiotensin II receptor blockers (odds ratios [ORs], 0.74-0.79), angiotensin-converting enzyme (ACE) inhibitors (ORs, 0.85-0.88), calcium channel blockers (ORs, 0.82-0.89), and beta blockers (OR = .88) were all associated with a decrease in dementia incidence.

In patients treated with calcium channel blockers, increasing the duration of treatment decreased the incidence of dementia.

“Antihypertensive therapy alone cannot guarantee that dementia will never occur,” noted Karel Kostev, PhD, IQVIA, Germany, Mannheim, Germany. “However, these findings highlight the importance of the prescription of antihypertensive drugs in the context of preventing hypertension-associated cognitive decline.”

The authors of the study also noted that further studies are needed to gain a better understanding of the medications associated with a decreased risk of dementia.

“We plan to investigate the role of lipid-lowering drugs, antidepressants, and further medications in the future,” they said.

The study is subject to some limitations, as the patients in the study were all aged 60 years or older, and this inclusion criterion was necessary for identifying dementia. However, previous research has shown that it is important for a life course-related prevention strategy to initiate hypertension treatment at a younger age. Moreover, data on patients’ lifestyle factors, including smoking and physical activity, education, and job, were also lacking. The strengths of this study are the number of patients available for analysis, which allowed the use of a case-control design, and the use of real-world data, with different diagnoses and medications available for analysis.

Reference: http://dx.doi.org/10.3233/JAD-190362

SOURCE: IOS Press

The Inflammatory Potential of the Diet is Directly Associated with Incident Depressive Symptoms Among French Adults

Useless, no explanation of what this diet is as compared to the French paradox. 

The French paradox: lessons for other countries - NCBI

The French Diet Is Le Bullshit - The Daily Beast

The Inflammatory Potential of the Diet is Directly Associated with Incident Depressive Symptoms Among French Adults

The Journal of Nutrition, nxz045, https://doi.org/10.1093/jn/nxz045
Published:
01 June 2019
Article history

ABSTRACT


Background
Low-grade chronic inflammation has been suggested to play a substantial role in the etiology of depression; however, studies on the prospective association between the inflammatory potential of the diet and depression are limited.
Objective
The aim of this study was to investigate the association between the inflammatory potential of the diet (measured using the Alternate Dietary Inflammatory Index, ADII) and incident depressive symptoms. We also tested the potential modulating effect of sex, age, BMI, and lifestyle indicators.
Methods
The study sample consisted of 26,730 participants (aged 18–86 y) from the NutriNet-Santé study. Baseline ADII was computed using repeated 24-h dietary records collected during the first 2 y of the follow-up. Incident cases of depressive symptoms were defined by a Center for Epidemiologic Studies Depression scale ≥17 for men and ≥23 for women at least once during follow-up. HR and 95% CI were estimated using multivariable Cox proportional hazards models.
Results
A total of 2221 incident cases of depressive symptoms were identified over a mean follow-up of 5.4 y. After accounting for a wide range of potential confounders, the highest quartile of the ADII was associated with a 15% (95% CI: 2, 31) increase in the risk of depressive symptoms compared with the lowest quartile. In the stratified analyses, associations were statistically significant only among women (HRquartile4 vs. quartile1: 1.19; 95% CI: 1.02, 1.37), middle-age adults (HRquartile4 vs. quartile1: 1.16; 95% CI: 1.00, 1.35), and participants with a BMI ≥25 (HRquartile4 vs. quartile1: 1.29; 95% CI: 1.04, 1.60).
Conclusions
Overall, a proinflammatory diet was associated with a higher risk of depressive symptoms, especially among women, middle-age adults, and participants with overweight or obesity. These findings contribute to the increasing scientific evidence showing a detrimental role of the proinflammatory diet. The NutriNet-Santé study is registered at clinicaltrials.gov as NCT03335644.

This article is published and distributed under the terms of the Oxford University Press, Standard Journals Publication Model (https://academic.oup.com/journals/pages/open_access/funder_policies/chorus/standard_publication_model)
You do not currently have access to this article.

Study: Cholesterol in eggs tied to cardiac disease, death

Once again it is your doctors responsibility to determine the correct answer specifically for you. I never could figure out why dietary cholesterol would translate into blood cholesterol. Don't listen to me, I'm not medically trained, is your doctor? An easy question for your doctor; 'How does dietary cholesterol cause higher cardiac disease?'  Don't let them get away with not answering.

Are you in this group? Does your doctor know about this group?

Why Dietary Cholesterol Does Not Matter (for most people)

The latest here:

 

Study: Cholesterol in eggs tied to cardiac disease, death

MedicalXpress Breaking News-and-Events | June 05, 2019
The risk of heart disease and death increases with the number of eggs an individual consumes, according to a UMass Lowell nutrition expert who has studied the issue.

Research that tracked the diets, health, and lifestyle habits of nearly 30,000 adults across the country for as long as 31 years has found that cholesterol in eggs, when consumed in large quantities, is associated with ill health effects, according to Katherine Tucker, a biomedical and nutritional sciences professor in UMass Lowell's Zuckerberg College of Health Sciences, who co-authored the analysis. The study was published in the Journal of the American Medical Association.
The study results come as egg consumption in the country continues to rise. In 2017, people ate an average of 279 eggs per year, compared with 254 eggs in 2012, according to the US Department of Agriculture.
Current US Dietary Guidelines for Americans do not offer advice on the number of eggs individuals should eat each day. The guidelines, which are updated every 5 years, do not include this because nutrition experts had begun to believe saturated fats were the driving factor behind high cholesterol levels, rather than eggs, according to Tucker. However, prior to 2015, the guidelines did recommend individuals consume no more than 300 milligrams of cholesterol a day, she said.
One large egg contains nearly 200 milligrams of cholesterol, roughly the same amount as an 8-ounce steak, according to the USDA. Other foods that contain high levels of cholesterol include processed meats, cheese, and high-fat dairy products.
While the new research does not offer specific recommendations on egg or cholesterol consumption, it found that each additional 300 milligrams of cholesterol consumed beyond a baseline of 300 milligrams per day was associated with a 17% higher risk of cardiovascular disease and an 18% higher risk of death.
Eating several eggs a week "is reasonable," said Tucker, who noted they include nutrients beneficial to eye and bone health. "But I recommend people avoid eating three-egg omelets every day. Nutrition is all about moderation and balance."
Research results also determined that study participants' exercise regimen and overall diet quality, including the amount and type of fat they consumed, did not change the link between cholesterol in one's diet and risk of cardiovascular disease and death.
"This is a strong study because the modeling adjusted for factors such as the quality of the diet
," Tucker said. "Even for people on healthy diets, the harmful effect of higher intake of eggs and cholesterol was consistent."
To read more, click here.


Wednesday, June 5, 2019

White Meat Increases Cholesterol Levels Similar to Red Meat

 You'll have to ask your doctor to explain EXACTLY how dietary red and white meat translate into cholesterol in the blood.  You do expect them to know that easy question?

White Meat Increases Cholesterol Levels Similar to Red Meat

A new study found that red meat isn’t the only type of meat that raises blood cholesterol levels.

By Alexa Lardieri, Staff Writer June 4, 2019, at 10:21 a.m.
More Study: Chicken Increases Cholesterol Researchers concluded that restricting white meat in addition to red meat is recommended for lowering cholesterol. Consuming white meat, such as poultry, has an equal effect on blood cholesterol levels as consuming red meat.
A study published Tuesday in the American Journal of Clinical Nutrition debunked previous assumptions that only red meat had an impact on cholesterol. Researchers were surprised to discover that eating white meat also increases blood cholesterol levels more than consuming a comparable amount of plant proteins.

Researchers observed this change in study participants regardless of whether their diet contained high levels of saturated fat. Dr. Ronald Krauss, study author and director of atherosclerosis research at the Children's Hospital Oakland Research Institute, said in a press release that grass-fed beef, fish and processed products like bacon and sausages were not studied.
"When we planned this study, we expected red meat to have a more adverse effect on blood cholesterol levels than white meat, but we were surprised that this was not the case – their effects on cholesterol are identical when saturated fat levels are equivalent," Krauss said.
Researchers concluded that restricting white meat in addition to red meat is recommended for lowering cholesterol. According to the study, plant proteins, such as vegetables, beans and legumes, are the healthiest for blood cholesterol levels.
The study also found that red and white meat, and diets high in saturated fat, increased amounts of large cholesterol-enriched low-density lipoprotein particles. LDL is known as the "bad" cholesterol and it is connected to cardiovascular disease.
While government dietary guidelines have recommended decreasing consumption of red meat and increasing consumption of poultry, the study's results suggest more research is needed and a change to guidelines may be necessary.
Alexa Lardieri, Staff Writer
Alexa Lardieri is a reporter and digital producer at U.S. News & World Report. You can follow ...  Read more

Door-in-Door-Out Time at Primary Stroke Centers May Predict Outcome for Emergent Large Vessel Occlusion Patients

I'm sure your definition of favorable is not anywhere close to 100% recovery. Even with your bad definition you had a 65% failure rate.  You have a fucking lot of work to accomplish 100% recovery for all.  WHEN THE HELL ARE YOU GOING TO GET THERE? After you are the 1 in 4 that per WHO will have a stroke? Too late at that point in time. Is that goal even on your radar?

Door-in-Door-Out Time at Primary Stroke Centers May Predict Outcome for Emergent Large Vessel Occlusion Patients

Originally publishedhttps://doi.org/10.1161/STROKEAHA.118.021936Stroke. 2018;49:2969–2974

Abstract

Background and Purpose—

Interfacility transfers for thrombectomy in stroke patients with emergent large vessel occlusion (ELVO) are associated with longer treatment times and worse outcomes. In this series, we examined the association between Primary Stroke Center (PSC) door-in to door-out (DIDO) times and outcomes for confirmed ELVO stroke transfers and factors that may modify the interaction.

Methods—

We retrospectively identified 160 patients transferred to a single Comprehensive Stroke Center (CSC) with anterior circulation ELVO between July 1, 2015 and May 30, 2017. We included patients with acute occlusions of the internal carotid artery or proximal middle cerebral artery (M1 or M2 segments), with a National Institutes of Health Stroke Scale score of ≥6. Workflow metrics included time from onset to recanalization, PSC DIDO, interfacility transfer time, CSC arrival to arterial puncture, and arterial puncture to recanalization. Primary outcome measure was National Institutes of Health Stroke Scale at discharge and modified Rankin Scale (mRS) score at 90 days.

Results—

The median (Q1–Q3) age and National Institutes of Health Stroke Scale of the 130 ELVO transfers analyzed was 75 (64–84) and 17 (11–22). Intravenous alteplase was administered to 64% of patients. Regarding specific workflow metrics, median (Q1–Q3) times (in minutes) were 241 (199–332) for onset to recanalization, 85 (68–111) for PSC DIDO, 26 (17–32) for interfacility transport, 21 (16–39) for CSC door to arterial puncture, and 24 (15–35) for puncture to recanalization. Median discharge National Institutes of Health Stroke Scale score was 5 (2–16), and 46 (35%) patients had a favorable outcome at 90 days. Complete reperfusion (modified Thrombolysis in Cerebral Ischemia 2c/3) modified the deleterious association of DIDO on outcome.

Conclusions—

For patients diagnosed with ELVO at a PSC who are being transferred to a CSC for thrombectomy, longer DIDO times may have a deleterious effect on outcomes and may represent the single biggest modifiable factor in onset to recanalization time. PSCs should make efforts to decrease DIDO and routine use of DIDO as a performance measure is encouraged.

Drug companies decided not to pursue Enbrel for Alzheimer's


Enbrel(etanercept) is the drug that Dr. Tobinick(19 posts) seems to have never even entertained trying to get his uses of etanercept  for stroke tested in a clinical trial.
Here is an analysis of Dr. Tobinick's use of Enbrel for whatever.

Enbrel for Stroke and Alzheimer’s

 
CHICAGO, June 5, 2019 — “Any science that has promise for Alzheimer’s disease and other dementias and is not genuinely pursued, or shared with the research community, does a disservice to the millions of individuals facing the disease today and in the future. Alzheimer's is a personally devastating and fatal disease, the sixth leading cause of death in the United States, with the number of people impacted by the disease increasing daily. No stone should be left unturned. The expectation of the Alzheimer’s Association and our millions of constituents is that every possible path is pursued thoroughly and aggressively with people living with the disease as a priority.”

— Maria C. Carrillo, Ph.D., chief science officer, Alzheimer’s Association

Tuesday, June 4, 2019

Allopregnanolone as a Therapeutic to Regenerate the Degenerated Brain

We'll never know if this would be useful post stroke since there is NO STROKE LEADER to go to to update the stroke strategy and start research on these questions. You're screwed as long as we don't have stroke survivors running stroke associations. 

Allopregnanolone as a Therapeutic to Regenerate the Degenerated Brain


  • Gerson D. Hernandez
  • Roberta Diaz BrintonEmail author
  • Gerson D. Hernandez
    • 1
  • Roberta Diaz Brinton
    • 1
    Email author
  1. 1.Center for Innovation in Brain Science, College of MedicineUniversity of ArizonaTucsonUSA
Chapter

Part of the ISGE Series book series (ISGE)


Abstract

Neurosteroids regulate both regeneration and repair systems in the brain. Among this class of molecules, allopregnanolone (Allo) is the first regenerative therapeutic that has been extensively investigated in animal models and more recently in humans for its capacity to promote regeneration in the central and peripheral nervous system. In preclinical analyses, Allo induced generation and survival of new neurons in the hippocampus of aged mice and in transgenic mouse models of Alzheimer’s disease (AD), which was associated with restoration of learning and memory function. Allo is a proliferative factor for both neural stem cells and pre-progenitor oligodendrocytes, increasing both the number of newly generated cells and their survival. Safety characteristics of Allo regulation of neurogenesis indicate that the regenerative system it affects is tightly regulated with closely guarded thresholds for both activation and magnitude of proliferation. In the brain of mice with AD, Allo increased liver X receptor and pregnane X receptor expression, reduced ß-amyloid and microglial activation, and increased markers of white matter generation. Results of preclinical studies indicate that an optimal treatment regimen of Allo to promote endogenous regeneration is one that is administered once per week over the course of several months. Allo dose and frequency of exposure are determining factors regulating its therapeutic efficacy. Previous and current human safety exposure data supported by extensive preclinical efficacy data are strong foundations for the clinical development of Allo as a therapeutic to regenerate the degenerated brain.

Keywords

Neurosteroid Allopregnanolone Neurodegeneration Regeneration Aging brain 


Specific nutrient patterns are associated with higher structural brain integrity in dementia-free older adults

Damn it all, we need specifics, not this 'higher amounts' crapola. 

Specific nutrient patterns are associated with higher structural brain integrity in dementia-free older adults

LauraFratiglioniacGrégoriaKalpouzosaMassimoMusiccobFulvioAdornibIngegerdJohanssondAnnaMarsegliaaWeiliXuae

Highlights

Exploring the association between nutrient patterns and structural brain integrity.
Five nutrient dietary patterns were derived using principal component analysis.
Specific nutrient's intake combinations were associated with brain integrity.
Future studies including repeated measures of exposures and MRI measures are necessary.

Abstract

Optimal nutrition may play a beneficial role in maintaining a healthy brain. However, the relationship between nutrient intake and brain integrity is largely unknown. We investigated the association of specific nutrient dietary patterns with structural characteristics of the brain. Within the population-based Swedish National study on Aging and Care-Kungsholmen (SNAC-K), a cross-sectional study of 417 dementia-free participants aged ≥60 years who underwent structural magnetic resonance imaging (MRI) scans during 2001–2003, was carried-out. Data on dietary intake were collected using a food frequency questionnaire, from which intake of 21 nutrients was estimated. By principal component analysis, five nutrient patterns were extracted: (1) NP1 was characterized by fiber, vitamin C, E, β-carotene, and folate [Fiber&Antioxidants], (2) NP2 by eicosapentaenoic (EPA, 20:5 ω-3) and docosahexaenoic (DHA, 22:6 ω-3) polyunsaturated fatty acids (PUFAs), proteins, cholesterol, vitamin B3, B12, and D [long chain (LC) ω-3PUFAs&Proteins], (3) NP3 by α-linoleic (18:2 ω-6) and α-linolenic (18:3 ω-3) PUFAs, monounsaturated fatty acids (MUFAs), and vitamin E [MUFAs&ω-3,6PUFAs], (4) NP4 by saturated fatty acids (SFAs), trans fats, MUFAs, and cholesterol [SFAs&Trans fats], (5) NP5 by B-vitamins, retinol, and proteins [B-Vitamins&Retinol]. Nutrient patterns scores were tertiled with the lowest tertile as reference, and were related to total brain volume (TBV) and white matter hyperintensities volume (WMHV) using linear regression models adjusting for potential confounders. In the multi-adjusted model, compared to the lowest intake for each pattern, the highest intake of NP1 (β = 11.11, P = 0.009), NP2 (β = 7.47, P = 0.052), and NP3 (β = 10.54, P = 0.005) was associated with larger TBV whereas NP5 was related to smaller TBV (β = −12.82, P = 0.001). The highest intake of NP1 was associated with lower WMHV (β = −0.32, P = 0.049), whereas NP4 was associated with greater WMHV (β = 0.31, P = 0.036). In sum, our results suggest that the identified brain-health specific nutrient combinations characterized by higher intake of fruit, vegetables, legumes, olive and seed oils, fish, lean red meat, poultry and low in milk and dairy products, cream, butter, processed meat and offal, were strongly associated with greater brain integrity among older adults.

Keywords

Nutrient patterns
Total brain volume
White matter hyper intensity volume
Brain integrity
Cross-sectional study

Research data for this article

Data not available / Data will be made available on request
About research data

Quality of life and disability after severe stroke and early neurological rehabilitation

Pretty much useless, there was no objective analysis of the starting point and the therapy delivered to the results achieved.  ISN'T THAT THE WHOLE FUCKING POINT OF STROKE THERAPY? WHAT WORKS AND WHAT DOESN'T? The mentors and senior researchers involved in this need to be fired.

Quality of life and disability after severe stroke and early neurological rehabilitation

Abstract

BACKGROUND: Data on the long-term effects on quality of life of patients after severe stroke and discharge from early institutional rehabilitation are important for guiding the early rehabilitation phase and the further outpatient care.
OBJECTIVE: Analysis of the outcome of patients following severe stroke 3 and 12 months after discharge from early neurological rehabilitation.(What the fuck stupid objective is this? It should be; What interventions provide the best outcomes.)
METHODS: Analysis of the Asklepios Hamburg multicenter early stroke rehabilitation registry (ICD 10: I61, I60, I63 and OPS 8‑552). Structured interviews with documentation of disabilities using the early rehabilitation Barthel index (ERBI), modified Rankin scale (mRS) and quality of life (12-item short form health survey, SF-12). Assessment of further treatment and complications 3 and 12 months after discharge from the early rehabilitation departments by telephone interviews. RESULTS: Out of 1045 treated stroke patients 270 were enrolled between October 2015 and November 2017 and 200 and 151 patients could be followed up after 3 and 12 months, respectively. There was a significant improvement (p < 0.001) in the median ERBI (151 patients at 12 months). Factors influencing a poorer functional outcome (higher mRS) at 12 months were a higher mRS at discharge (OR 5.43 [1.18, 25.09], p = 0.03) and age (per decade OR 1.5 [1.09, 2.02]; p = 0.01). Female sex reduced the risk for a poorer outcome after 12 months (OR 0.49 [0.25, 0.96]; p = 0.04). Quality of life (SF-12) was not different over time. The mental quality of life showed no differences (p = 0.32) compared to a historical, significantly less (p<0.001) handicapped stroke collective.
CONCLUSION: The surviving severe stroke patients recovered significantly up to 12 months after discharge. The mental quality of life did not differ from that of a historical less handicapped collective.(Then you didn't ask the right questions, with the caregiver not present. You browbeat them into accepting your tyranny of low expectations.)

Real-time foot clearance biofeedback to assist gait rehabilitation following stroke: a randomized controlled trial protocol

Interesting, I was just immediately given an AFO, then a hinged AFO.  I seriously believe that an AFO actually hinders recovery, you do no training of your dorsiflexion while wearing an AFO.  I went cold turkey on using one on a 21 day canoe trip in Canada and Alaska, 3 years after stroke. It forced me to immediately strengthen my ankle to keep it from rolling and get toe clearance. Didn't fall on that trip. 

Real-time foot clearance biofeedback to assist gait rehabilitation following stroke: a randomized controlled trial protocol

Trials201920:317
  • Received: 20 December 2018
  • Accepted: 6 May 2019
  • Published:
Open Peer Review reports

Abstract

Background

The risk of falling is significantly higher in people with chronic stroke and it is, therefore, important to design interventions to improve mobility and decrease falls risk. Minimum toe clearance (MTC) is the key gait cycle event for predicting tripping-falls because it occurs mid-swing during the walking cycle where forward velocity of the foot is maximum.
High forward velocity coupled with low MTC increases the probability of unanticipated foot-ground contacts. Training procedures to increase toe-ground clearance (MTC) have potential, therefore, as a falls-prevention intervention. The aim of this project is to determine whether augmented sensory information via real-time visual biofeedback during gait training can increase MTC.

Methods

Participants will be aged > 18 years, have sustained a single stroke (ischemic or hemorrhagic) at least six months previously, able to walk 50 m independently, and capable of informed consent. Using a secure web-based application (REDCap), 150 participants will be randomly assigned to either no-feedback (Control) or feedback (Experimental) groups; all will receive 10 sessions of treadmill training for up to 10 min at a self-selected speed over 5–6 weeks. The intervention group will receive real-time, visual biofeedback of MTC during training and will be asked to modify their gait pattern to match a required “target” criterion. Biofeedback is continuous for the first six sessions then progressively reduced (faded) across the remaining four sessions. Control participants will walk on the treadmill without biofeedback. Gait assessments are conducted at baseline, immediately following the final training session and then during follow-up, at one, three, and six months. The primary outcome measure is MTC. Monthly falls calendars will also be collected for 12 months from enrolment.

Discussion

The project will contribute to understanding how stroke-related changes to sensory and motor processes influence gait biomechanics and associated tripping risk. The research findings will guide our work in gait rehabilitation following stroke and may reduce falls rates. Treadmill training procedures incorporating continuous real-time feedback may need to be modified to accommodate stroke patients who have greater difficulties with treadmill walking.

Trial registration

Australia New Zealand Clinical Trials Registry, ACTRN12617000250336. Registered on 17 February 2017.

Keywords

  • Gait
  • Stroke
  • Biofeedback
  • Falls
  • Tripping
  • Minimum toe clearance (MTC)

Background

Stroke affects > 60,000 Australians every year, with 50% unable to walk one week following the event [1]. Impaired walking impacts independence by reducing the ability to perform everyday activities and limiting community participation [2, 3]. Falls risk is significantly higher in people with chronic stroke [4] and approximately 50% of people living at home after a stroke will fall within 12 months [9], with up to half sustaining multiple falls. Furthermore, in community-dwelling people with stroke, up to 77% of falls occurred during walking. While there has been considerable research investigating falls risk management for older people generally, high-risk groups, such as those who have had a stroke, have not been extensively studied with respect to targeted falls prevention. Traditional exercise-based falls-prevention programs are useful for the general older adult community but are not effective in people with stroke. For example, Batchelor et al. found that a multifactorial intervention including a home-based balance and strength program did not reduce falls in people with stroke [10]. Another study confirmed that a group- and home-based exercise program incorporating balance and strength training did not reduce falls [11]. This suggests that alternative, targeted treatments to reduce falls risk in people with stroke are urgently needed.
Stroke adversely affects sensorimotor function and muscle strength, inhibiting the capacity to activate appropriate muscles and increasing the risk of contact between the foot and either the supporting surface or objects on it. Said et al. [15] found, for example, that stroke participants who had difficulty in stepping over small obstacles (4 cm high) had greater falls rates. The key gait variable for predicting tripping-falls is minimum toe clearance (MTC), an event mid-swing in the walking cycle [5, 6, 7, 8]. Low MTC increases the probability of unanticipated foot-ground contacts [7]. Given that tripping directly results from unsuccessful toe clearance, previous research with both young and older populations has focused on toe trajectory control during walking [6, 7, 8, 12, 13, 14]. Training individuals to increase MTC, therefore, has potential as a falls-prevention intervention.
The aim of this project is to determine whether real-time biofeedback of toe clearance during gait training can significantly minimize tripping risk in people with stroke. We will test the efficacy of real-time biofeedback as an intervention to increase MTC using a randomized controlled trial (RCT) design incorporating both a training or “acquisition” phase with biofeedback. Retention tests will be conducted to confirm learning, as demonstrated by the longer-term or “relative permanence” of the targeted behavior.
The primary objective is to determine whether real-time biofeedback of MTC during gait training will significantly increase MTC in people with stroke. We will also determine whether changes in MTC achieved on a treadmill transfer to overground walking. It is hypothesized that, compared to no-biofeedback training, visual biofeedback of foot clearance parameters during gait training will significantly increase toe-ground clearance (MTC) and MTC during biofeedback training will be retained in the longer term. It is also hypothesized that increases in MTC demonstrated in treadmill training will transfer to overground walking, such that tripping-risk in people with stroke is significantly reduced.

Parasitic Worms for the Treatment of Neurodegeneration

I'm not sure you are going to want to try this for your likely descent into dementia.  But then they renamed rat poison to warfarin and made it a ubiquitous treatment for blood thinning. Your doctors thoughts?

1. A documented 33% dementia chance post-stroke from an Australian study?   May 2012.

2. Then this study came out and seems to have a range from 17-66%. December 2013.

3. A 20% chance in this research.   July 2013.

4. Dementia Risk Doubled in Patients Following Stroke September 2018

 

Parasitic Worms for the Treatment of Neurodegeneration

The article discusses the current status and prospects of clinical use of immunomodulatory parasitic worms in the treatment of autoimmune and inflammatory diseases, including MS and AD. Here, we present our current understanding of the diversity of CD8 (+) iTregs effector cells and possible contribution of nematode factors to this process.

14 more pages.  

Nurture the Miracle of Neuroplasticity

You can read this yourself, but I quit immediately because of the promotion of Dr. Jill Bolte Taylor’s “My Stroke of Insight.” TED talk.  Because of her promotion of the bogus left brain/right brain stuff.

Nurture the Miracle of Neuroplasticity

 

P75-T Adaptation of the motor system is associated with neuroplasticity

I got absolutely nothing out of this. Did your doctor? 

P75-T Adaptation of the motor system is associated with neuroplasticity

Background

Repetition suppression (RS), i.e., adaption of neural excitability in response to a repeated stimulus, manifests as a decrement in the amplitude of the motor evoked potentials (MEPs) following repeated transcranial magnetic stimulation (TMS) of the motor cortex. RS is associated with abnormal adaptation to external stimuli and may be indicative of neuroplastic capacity.

Objective

To investigate the association between RS and experimentally induced plasticity.

Methods

Fourteen healthy subjects (7 males, aged 22–42 years) were studied with a RS paradigm, which was applied prior and following (0 min, 10 min, and 20 min) paired associative stimulation (PAS). The RS paradigm, consisting of twenty trains of four TMS pulses with an inter-stimulus interval (ISI) of 1 s and an inter-train interval (ITI) of 17 s, was applied to abductor pollicis brevis muscle ‘hotspot’. During PAS, median nerve stimulation was delivered 25 ms prior to TMS pulses given at 0.2 Hz for 15 min.

Results

A two-way repeated ANOVA identified 6 subjects with an interaction effect of RS and PAS (p < 0.05). Furthermore, the linear mixed model revealed a significant effect of PAS on RS by time in the responders ((F10min = 4.965, p10min = 0.033) and (F20min = 7.519, p20min = 0.010)). An independent samples t-test revealed that the resting motor threshold was significantly lower in responders than in non-responders (p = 0.05).

Conclusion

Our results demonstrate that RS is facilitated in subjects showing the interaction effect. This interaction might be mediated by the GABAergic inhibitory system during activation of the negative thalamo-cortical feedback loop due to the homeostatic plasticity.

Nerve Stimulation Therapy May Help Some People Recover After a Stroke

Is your hospital following this and figuring out how to implement in their hospital? Or are they doing FUCKING NOTHING? Do you prefer their incompetence to be NOT KNOWING? OR NOT DOING?

Nerve Stimulation Therapy May Help Some People Recover After a Stroke

Electrical stimulation may help people recover after having a common type of stroke.




Each year, more than 795,000 people in the United States have a stroke.
Of them, nearly 40 percent go on to experience moderate to severe physical and mental complications, estimates the National Stroke Association. Another 25 percent have minor issues in the aftermath of a stroke.
Now stroke patients may have access to a new type of treatment that may help minimize the degree of complications.
The therapy, known as active nerve cell cluster stimulation, uses a small device implanted through the roof of the mouth that sends electrical stimulation to the nerves behind the nose.
When administered within 24 hours after a stroke, the nerve stimulation treatment was found to reduce the degree of disability in stroke patients three months after having the most common type of stroke, according to a new study published in The LancetTrusted Source last month.
The new treatment could be a safe, effective option for many stroke patients who are not eligible to receive traditional clot-busting medications, the researchers said.
“This study opens the avenues to develop treatment options for patients with acute ischemic stroke who are not eligible for standard of care acute stroke therapy to improve functional outcomes and to reduce long-term disabilities,” Dr. Anand Patel, a vascular neurologist at North Shore University Hospital in Manhasset, New York, told Healthline.

To measure just how effective the therapy is, researchers from multiple institutions, including UCLA and Northwestern University, studied 1,000 participants who had an acute cortical ischemic stroke. In this type of stroke, blood flow to the brain is obstructed.
The participants were randomly assigned into two groups: one that received the stimulation therapy and another that underwent a placebo therapy.
Throughout the study, the first group received stimulation to the nerve-cell cluster behind the nose four hours per day for five consecutive days.
In a subgroup of 520 participants who’d experienced major deficits and injury to the brain, nearly half of the participants who received the new, experimental nerve therapy experienced favorable outcomes, versus 40 percent of the participants who didn’t receive the stimulation.
Although these findings aren’t statistically significant, the researchers note, when the results are combined with previous research from earlier trials, there’s enough evidence to suggest that the therapy is a safe, effective stroke treatment when given anywhere from 8 to 24 hours after a stroke.


During a stroke, there’s an interruption of blood supply to the brain.
The key to treating a stroke and minimizing long-term damage is to quickly and effectively restore blood flow to the brain.
Typically, doctors treat stroke by opening blocked arteries or removing a clot. They do this with either clot-dissolving medications or surgically reopening clotted blood vessels.
However, the medication’s effectiveness drops significantly if it’s given more than three hours after a stroke. The medicine also doesn’t work for all patients, and some aren’t able to take it due to other health issues.
Furthermore, not every medical center has the proper expertise needed to treat patients with clot-retrieval devices.
Stimulating the nerve cells behind the nose may improve stroke outcomes in one of three ways, according to health experts.
“First, stimulation of this nerve bundle actually improved blood flow to the brain starved of oxygen during a stroke. Second, stimulation seems to fortify the blood-brain barrier, thereby [decreasing] the leakiness that causes swelling after a stroke,” said Dr. Jason Tarpley, a stroke neurologist and director of the Stroke and Aneurysm Center at Providence St. Joseph Health Pacific Neuroscience Institute.
“Finally, stimulation enhances plasticity of the brain, in which noninjured parts of the brain can pick up the job of the injured brain areas,” Tarpley added.
In other words, this therapy can quickly feed oxygen to the brain and protect tons of brain cells.