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.

Showing posts with label Leukoaraiosis. Show all posts
Showing posts with label Leukoaraiosis. Show all posts

Monday, August 26, 2024

Correlation of silent brain infarcts and leukoaraiosis in middle-aged ischemic stroke patients: a retrospective study

So your competent? doctor is required to have EXACT PROTOCOLS that restore myelin. Is your doctor competent in this regard? Or don't you have a functioning stroke doctor? Does your doctor even know this problem needs to be fixed?

 Leukoaraiosis is the rarefaction of the brain white matter caused by loss of axons and myelin due to ischemic injury and appears to be of central importance in the neurocognitive defects associated with HD.

The latest here:

Correlation of silent brain infarcts and leukoaraiosis in middle-aged ischemic stroke patients: a retrospective study

Mohammad Fathi AbdulsalamMohammad Fathi Abdulsalam1Nour Shaheen
&#x;Nour Shaheen2*Ahmed ShaheenAhmed Shaheen2Yasmeen Jamal AlabdallatYasmeen Jamal Alabdallat3Abdelraouf RamadanAbdelraouf Ramadan4Mostafa MeshrefMostafa Meshref1Fathy Mahmoud MansourFathy Mahmoud Mansour1Elsayed AbedElsayed Abed1Abdel-Ghaffar I. FayedAbdel-Ghaffar I. Fayed1Mohamed Ahmed ZakiMohamed Ahmed Zaki1Ahmad F. El-AdawyAhmad F. El-Adawy1Oliver FloutyOliver Flouty5Mohamed HamedMohamed Hamed1
  • 1Department of Neurology, Faculty of Medicine, Al-Azhar University, Cairo, Egypt
  • 2Alexandria Faculty of Medicine, Alexandria University, Alexandria, Egypt
  • 3Faculty of Medicine, Hashemite University, Zarqa, Jordan
  • 4Kasr Alainy Faculty of Medicine, Cairo University, Cairo, Egypt
  • 5Department of Neurosurgery and Brain Repair, University of South Florida, Tampa, FL, United States

Background: Cerebrovascular diseases of the brain are usually defined by transient ischemic attacks and strokes. However, they can also cause brain injuries without neurological events. Silent brain infarcts (SBI) and leukoaraiosis are symptoms of both vascular and neurological abnormalities. This study aims to investigate the association between SBI, leukoaraiosis, and middle-aged patients with ischemic stroke.

Methods: A single-center retrospective study of 50 middle-aged, ischemic stroke patients were studied from November 2022 and May 2023. The patients were divided into two groups based on the presence or absence of leukoaraiosis. History taking, physical examination, brain CT scan, and MRI were all part of the diagnostic process. Metabolic syndrome (MetS) was also assessed through various factors. The statistical analysis included descriptive statistics, logistic regression analysis, and chi-square test.

Results: Out of the cohort comprising 50 patients, characterized by a mean age of 52.26 years (SD 5.29), 32 were male, constituting 64% of the sample. Among these patients, 26 individuals exhibited leukoaraiosis, with 17 of them (65.4%) also presenting with SBI. Moreover, within this cohort, 22 patients were diagnosed with MetS, representing 84.6% of those affected. The Multivariate logistic regression analysis showed a strong and independent association between leukoaraiosis and SBI. Individuals with leukoaraiosis were nearly five times more likely to have SBI compared to those without leukoaraiosis.

Conclusion: The study highlights leukoaraiosis as a significant risk factor for SBI, alongside MetS. Advanced imaging techniques have facilitated their detection, revealing a higher prevalence among stroke patients, particularly associated with age and hypertension. Further research is needed to fully understand their complex relationship and develop better management strategies for cerebrovascular diseases, ultimately improving patient outcomes.

Introduction

Historically, cerebrovascular disease of the brain has been defined by the symptoms and signs of transient ischemic attack or stroke. However, neuropathological studies in highly selected populations have revealed that vascular disease can cause brain injury in the absence of these acute neurological events. The advent of advanced brain-imaging techniques, such as computerized tomography (CT) and Magnetic resonance imaging (MRI), has allowed similar observations to be made in patient groups and healthy individuals, necessitating a reconsideration of the definition of cerebrovascular disease (1, 2). Signs of cerebral small vessel disease on conventional MRI include leukoaraiosis, recent subcortical lacunar infarcts (clinically symptomatic), lacunes (clinically silent), cerebral microbleeds, prominent perivascular spaces, and cerebral atrophy (3). These brain infarcts, while often asymptomatic, demand increased attention to mitigate the deleterious effects of vascular disease in the brain. Silent brain infarctions (SBIs) comprise two subtypes: lacunar and non-lacunar, resulting from small perforating artery occlusion and embolism or athero-sclerotic stenosis, respectively. The advancement of MRI technology enables the distinction between these subtypes (46). Therefore, exploring the distinct risk factors between the two subtypes, especially in the case of SBI, could lead to the development of specific prevention strategies, particularly for middle-aged individuals. Hypertension (HTN), apart from age, is the most widely accepted risk factor associated with SBI. Furthermore, the consistent correlation between hypertension and these infarcts suggests a critical role for hypertensive small-vessel disease in their pathogenesis (7). However, further research is necessary to better define the association between hypertension and brain infarcts, particularly in terms of preventing SBI through effective hypertension control. SBI and leukoaraiosis (LA) are intricate cerebral manifestations that have garnered considerable attention due to their association with diverse vascular and metabolic abnormalities. Hence, comprehending the intricate relationship between these cerebral alterations and MetS is of paramount importance for elucidating their underlying mechanisms and devising effective prevention and management strategies. Leukoaraiosis was observed through MRI and manifests as increased signal intensity in the white matter, often attributed to small vessel disease and pathological processes such as demyelination, gliosis, and vessel lipo hyalinosis (8). Conversely, SBIs denote brain tissue damage resulting from inadequate blood supply without acute neurological symptoms. Though often asymptomatic, SBIs pose a substantial risk for future stroke and cognitive decline (9). MetS plays a pivotal role in the development of LA and SBIs, operating through mechanisms such as vascular dysfunction, inflammation, insulin resistance, and dyslipidemia (10). The diagnosis of LA and SBIs primarily relies on MRI techniques, with fluid-attenuated inversion recovery (FLAIR) imaging sequences commonly employed to detect and assess the extent of white matter changes (11). Epidemiological data indicate a higher prevalence of LA and SBIs with advancing age, affecting a significant proportion of individuals over 65 years. This research aims to investigate the association between LA, SBIs, and middle-aged patients with ischemic stroke. The study focuses on middle-aged stroke patients to address the critical period in stroke epidemiology, capture a substantial portion of stroke cases in a relatively younger age group, identify early risk factors and pathophysiological mechanisms, and provide clinically relevant insights for healthcare providers in terms of risk stratification, diagnostics, and treatment strategies.

More at link.

Saturday, March 19, 2022

Leukoaraiosis Mediates the Association of Total White Blood Cell Count With Post-Stroke Cognitive Impairment

So you described a problem, offered NO SOLUTION. Useless. Prevent that cognitive impairment instead of this useless shit you did. 

Oops, I'm not playing by the polite rules of Dale Carnegie,  'How to Win Friends and Influence People'. 

Telling stroke medical persons they know nothing about stroke is a no-no even if it is true. 

Politeness will never solve anything in stroke. Yes, I'm a bomb thrower and proud of it. Someday a stroke 'leader' will try to ream me out for making them look bad by being truthful , I look forward to that day.

Leukoaraiosis Mediates the Association of Total White Blood Cell Count With Post-Stroke Cognitive Impairment

Wanying Shan1, Liang Xu2, Yuan Xu1, Zhuoyin Qiu1, Jie Feng1, Jie Zhao3* and Jingwen Wang1*
  • 1Department of Neurology, Suzhou Ninth People's Hospital, Soochow University, Suzhou, China
  • 2Department of Anesthesiology, The First Affiliated Hospital of Soochow University, Suzhou, China
  • 3Department of Gerontology, Suzhou Ninth People's Hospital, Soochow University, Suzhou, China

Background and Purpose: The inflammatory response could play a key role in cognitive impairment. However, there has been limited research into the association between total white blood cell (WBC) count and post-stroke cognitive impairment (PSCI), and the significance of leukoaraiosis (LA) in this relationship is unknown. We aimed to examine the total WBC count in relation to PSCI and whether this association was mediated by LA.

Methods: Consecutive patients with first-ever ischemic stroke were prospectively enrolled from October 2020 to June 2021. The total WBC count was measured after admission. Cognitive function evaluations were performed at the 3-month follow-up using Mini-mental State Examination (MMSE). We defined the PSCI as an MMSE score <27.

Results: A total of 276 patients (mean age, 66.5 years; 54.7% male) were included in this analysis. Among them, 137 (49.6%) patients experienced PSCI. After adjustment for potential confounders, higher total WBC count was significantly correlated with an increased risk of LA [per 1-SD increase, odds ratio (OR), 1.39; 95% CI 1.06–1.82; p = 0.017] and PSCI (per 1-SD increase, OR, 1.51; 95% CI 1.12–2.04; p = 0.006). Furthermore, mediation analysis demonstrated that the association between total WBC count and PSCI was partly mediated by LA (the regression coefficient was changed by 9.7% for PSCI, and 12.4% for PSCI severity, respectively).

Conclusion: Increased total WBC count is a risk factor for PSCI. The presence of LA was partially responsible for the PSCI in patients who had a higher total WBC count.

Introduction

In China, ischemic stroke has been ranked as the first leading cause of major disability and death (1). Post-stroke cognitive impairment (PSCI) is the most common complication with a prevalence ranging from 20 to 80% (2). It involves deficits in the ability to think and remember, language, and attention that are significant enough to greatly impact daily life (3). PSCI is reported to influence the performance in daily life and at work (4) and increase the risk of long-term mortality (5). Many clinical characteristics have been linked to the advancement of cognitive impairment following a stroke, such as advanced age, female gender, education, and vascular comorbidities (2). However, the underlying mechanisms of PSCI are still unclear. Determining the exact biomarkers and potential mechanisms for PSCI is of vital importance for continuously improving the prognosis of patients with ischemic stroke.

The inflammatory response has been linked to cognitive impairment after ischemic stroke (69). Increased total WBC count is associated with adverse clinical outcomes in patients with acute ischemic stroke (10). In addition, a higher WBC count, even within the normal range, was found to be related to the worse psychomotor cognitive performance in the elderly (11). However, the influence of total WBC count on PSCI has not yet been clarified. Leukoaraiosis (LA) is one of the leading risk factors for vascular cognitive impairment (12), and multiple lines of evidence from clinical trials and animal studies indicated that inflammatory response may contribute to the presence and development of LA (1317). Therefore, LA may be a mediator in the pathway between inflammation and the presence of PSCI.

We, therefore, performed this prospective study to examine: (1) the cross-sectional relationship between increased total WBC count and risk of 90-day PSCI among Chinese patients with ischemic stroke; (2) the mediating effect of LA on this potential relationship.

More at link.

 

Friday, June 11, 2021

Brain Atrophy and Leukoaraiosis Correlate with Futile Stroke Thrombectomy

If you fall into this futile category you are totally fucking screwed. Your doctor has NOTHING even close to any protocols to get you 100% recovery.

Brain Atrophy and Leukoaraiosis Correlate with Futile Stroke Thrombectomy

Abstract

Introduction

Although mechanical thrombectomy (MT) is a proven therapy for acute large vessel occlusion strokes, futile recanalization in the elderly is common and costly. Strategies to minimize futile recanalization may reduce unnecessary thrombectomy transfers and procedures. We evaluated whether a simple and rapid visual assessment of brain atrophy and leukoaraiosis on a plain head CT correlates with futile stroke recanalization in the elderly.

Methods

Consecutive stroke patients admitted for thrombectomy, older than 65 years of age, all with TICI 2b/3 recanalization rates were retrospectively studied from multiple comprehensive stroke centers. Brain atrophy and leukoaraiosis were visually analyzed from pre-intervention plain head CTs using a simplified scheme based on validated scales. Baseline demographics were collected and the primary outcome measure was 90-day modified Rankin score (mRS). Cochran-Armitage trend test was applied in analyzing the association of the severity of brain atrophy and leukoaraiosis with 90-day mRS.

Results

Between 2017 and 2019, 175 patients > 65 years who underwent thrombectomy with TICI 2b/3 recanalization from two comprehensive stroke centers were evaluated. The median age was 77 years. IV-tPA was given in 59% of patients, average initial NIHSS was 19, average baseline mRS was 0.77 and median time to recanalization was 300 minutes. Age and severity of atrophy/leukoaraiosis was categorized into three groups of increasing severity and associated with 90 day mRS 0-3 rates of 62%, 49% and 41% (p=0.037) respectively.

Conclusions

A simplified, visual assessment of the degree of brain atrophy and leukoaraiosis measured on plain head CT correlates with futile recanalization in patients age >65 years. Although additional validation is needed, these findings suggest that brain atrophy and leukoaraiosis may have value as a surrogate marker of prestroke functional status. In doing so, simplified visual plain head CT grading scales may minimize elderly futile recanalization.

 

Thursday, March 13, 2014

Correlation between Leukoaraiosis Volume and Circle of Willis Variants

Your doctor should be able to tell you if you have a normal Circle of Willis and prevention measures to stop Leukoaraiosis.
http://onlinelibrary.wiley.com/doi/10.1111/jon.12103/abstract?
  1. Luca Saba MD1,*,
  2. Eytan Raz MD2,3,
  3. Girish Fatterpekar MD2,
  4. Roberto Montisci MD4,
  5. Michele di Martino MD5,
  6. Pier Paolo Bassareo MD6,
  7. Mario Piga MD1
Article first published online: 5 MAR 2014
DOI: 10.1111/jon.12103

Keywords:

  • Leukoaraiosis;
  • Circle Of Willis;
  • MRA

ABSTRACT

BACKGROUND AND PURPOSE

The Circle of Willis (COW) is the main collateral system between the bilateral carotid systems and the posterior circulation. COW normal variants are encountered in up to 62% of subjects. We hypothesize that, in patients with carotid artery stenosis, the presence of COW variants is a risk factor for leukoaraiosis.

MATERIALS AND METHODS

Forty-seven patients (mean age 72.1 ± 9 years, males = 39) with carotid artery stenosis admitted for carotid endarterectomy were included and underwent an admission brain MRI/MRA. Two neuroradiologists evaluated the COW variants. FLAIR-leukoaraiosis lesion-volume was performed using a semiautomated segmentation technique. Mann–Whitney and Pearson correlations were conducted to identify the correlation between the FLAIR-leukoaraiosis lesion-volume and the COW variants. ROC analysis was performed to evaluate the AUC of FLAIR-leukoaraiosis lesion-volume and presence/absence of COW variants.

RESULTS

Pearson correlation demonstrated that the leukoaraiosis lesion-volume is significantly associated with the COW variants number (rho = .358, P = .0215). When patients were dicotomized in two subgroups, with and without COW variants, the lesion-volume was significantly higher in the variants group (P = .0405). The ROC curve analysis showed an AUC of .688 (SE = .083, 95%CI = .525-.823) with a statistically significant P = .0225, between the presence of COW variants and the FLAIR-leukoaraiosis lesion-volume.

CONCLUSION

The presence and the number of COW variants are associated with a higher leukoaraiosis volume in patients with significant internal carotid artery stenosis.

Friday, October 25, 2013

C-reactive protein and cognition are unrelated to leukoaraiosis

My doctor just threw off a comment to me that I had had some earlier infarcts, so I'm assuming it was some white matter hyperintensities, obviously not important since I didn't get to see a picture of them or any explanation of what to do about them. My doctor told me nothing and as far as I could tell knew nothing, did nothing and should have never been paid for his non-efforts. So even though I have leukoaraiosis I think my cognition is still damn good, better than my doctors.
http://scholar.google.com/scholar_url?hl=en&q=http://downloads.hindawi.com/journals/tswj/aip/121679.pdf&sa=X&scisig=AAGBfm1sH0XbW4TGUMjDn5PEQgJ5eR3ILA&oi=scholaralrt
Introduction
Inflammation has been increasingly recognized as component in cerebrovascular (1) and neurodegenerative diseases (2, 3). In addition, biological aging of the brain is partly attributable to aging of the cerebrovascular circulation and the effects of vascular changes on the brain (4). Inflammation has been linked to the pathogenesis of cardiovascular disease, obesity and insulin resistance, which are so related to cognitive impairment (5). The hypothesis that inflammation is related to cognitive impairment, although new, is consistent (2). Therefore, few studies evaluated that circulating inflammatory proteins are associated with increased risk of dementia (6), cognitive impairment (7) and cerebral white matter lesions (WML), common referred to leukoaraiosis (8-10).
CRP, composed of five 23 kDa subunits, is a hepatically derived pentraxin that has important role in the human immune system (11). That protein is a sensitive nonspecific marker of systemic low-grade inflammation (5) and increased serum concentrations of CRP have been associated with impaired cognition, stroke and depression (2, 6, 8).

Beyond pro-inflammatory response, that causes neuronal damage directly, increased concentrations of CRP acting as cardiovascular risk factor - approved predictor by Food and Drug Administration - or causing brain atherosclerosis can result in cerebral macro or microangiopathies. Both lesions can disrupt the integrity of frontal-subcortical circuits and are responsible for the development of cognitive impairment, dementia or depressive disorders (12). There are some evidences that elevated serum CRP levels may be a useful biomarker to identify individuals at an increased risk for cognitive impairment (7).

Monday, August 26, 2013

Regional Low Cerebral Blood Flow Predicts Leukoaraiosis Development at 18 Months in Patients with TIA and Minor Stroke

What is your doctor doing to identify this and prevent its occurrence? ANYTHING AT ALL?
Shouldn't your doctor know more than this graduate student?
http://theses.ucalgary.ca/handle/11023/884
Author: Bernbaum, Manya
Supervisor: Coutts, Shelagh
Submission Date: 2013
Institution: University of Calgary
Faculty: Graduate Studies
Graduate Program: Medicine, Neuroscience
URI: http://hdl.handle.net/11023/884
Subject Area: Neuroscience
Keywords: Minor Stroke
Leukoaraiosis
Cerebral Blood Flow
TIA
MR Perfusion
White Matter Disease
White Matter Hyperintensity
Type: Thesis
Degree: MSc
Abstract: The purpose of this study was to investigate whether low cerebral blood flow (CBF) is associated with subsequent white matter hyperintensity (WMH) development in minor stroke and transient ischemic attack (TIA) patients. New WMH at 18 months were identified by comparing follow-up with baseline FLAIR, and regions of interest (ROI) were placed in normal appearing and hyperintense white matter. Co-registered CBF maps were used to quantify relative CBF. Forty patients were evaluated, where mean age was 62+/-12 years, 78% male and 9% diabetic. A mixed effects logistic regression accounting for “within patient” clustering, showed that as CBF increases by 1mL/100g/min, the odds of having a new WMH decrease by 0.61. Results suggest that regions of white matter that develop WMH at 18 months have low baseline CBF. Future studies aiming to improve cerebral perfusion in normal appearing white matter might provide a target for arresting the development of WMH.

Tuesday, February 26, 2013

Leukoaraiosis, a Common Brain Magnetic Resonance Imaging Finding, as a Predictor of Traffic Crashes

Diffuse white matter abnormalities, possibly from silent strokes.

Leukoaraiosis, a Common Brain Magnetic Resonance Imaging Finding, as a Predictor of Traffic Crashes

Abstract

Background

There are no reported studies on the relationship between traffic crashes and brain tissue changes in healthy drivers. The relationship between traffic crashes and leukoaraiosis, a common magnetic resonance imaging finding, was investigated in this study.

Methods

A total of 3,930 automobile drivers (2,037 men and 1,893 women; age, 21–87 years) who underwent brain magnetic resonance imaging as part of total health check-ups and answered a road traffic questionnaire were examined to determine whether asymptomatic leukoaraiosis was associated with various types of traffic crashes. Multiple logistic regression analysis was performed to elucidate the relationship between leukoaraiosis and various types of traffic crashes.

Results

Subcortical leukoaraiosis was diagnosed in 28.52% of all subjects, whereas periventricular leukoaraiosis was diagnosed in 9.57% of all subjects. Adjusted odds ratios for involvement in all types of traffic crashes were not significant for subjects with periventricular leukoaraiosis; however, they were significant for subjects with multiple and large multiple subcortical leukoaraiosis. Adjusted odds ratios for involvement in crashes at crossroads were 1.09 (95% confidence interval [CI], 0.60–2.00) for subjects with single subcortical leukoaraiosis, 3.35 (95% CI, 2.36–4.77) for subjects with multiple subcortical leukoaraiosis, and 2.45 (95% CI, 2.36–4.98) for subjects with large multiple subcortical leukoaraiosis. Periventricular leukoaraiosis was not significantly associated with crossroad crashes. Involvement in crashes of any type, parking lot crashes, and rear-end collisions showed no significant association with either subcortical or periventricular leukoaraiosis.

Conclusions

Multiple subcortical leukoaraiosis, but not periventricular leukoaraiosis, is significantly associated with traffic crashes, in particular, crossroad crashes. This association is independent of sex, age, and driving exposure. To our knowledge, this is the first evidence describing the relationship between brain tissue changes and traffic crashes.

Tuesday, September 25, 2012

Saturday, January 21, 2012

Association between serum total bilirubin level and leukoaraiosis in Korean adults.

leukoaraiosis - white matter disease is a term for changes in the cerebral white matter that can be detected with high frequency by CT and MRI in aged individuals.
It is also commonly referred to as white matter hyperintensities (WMH) due to its bright white appearance on T2 MRI scans.
http://www.ncbi.nlm.nih.gov/pubmed/22245549

Abstract

OBJECTIVES:

Leukoaraiosis is associated with cerebrovascular microangiopathy. Increasing evidence suggests that bilirubin is a potent cytoprotectant in the development of cardiovascular diseases. This study aimed to determine whether total bilirubin is related to leukoaraiosis.

METHODS:

We examined the relationship of total bilirubin with leukoaraiosis in 1331 Korean adults. The odds ratios for leukoaraiosis were calculated using multivariate logistic regression across serum total bilirubin tertiles.

RESULTS:

In comparison with the subjects in the reference group (total bilirubin: 15-26μmol/L), the odds ratio (95% CI) for leukoaraiosis in the 3rd tertile (total bilirubin ≤10μmol/L) was 5.50 (1.24-24.40) in women after adjusting for confounding variables. However, this inverse association between serum total bilirubin and the prevalence of leukoaraiosis was not found in men after adjusting for the same co-variables.

CONCLUSION:

Total bilirubin level was inversely associated with leukoaraiosis regardless of classical cardiovascular risk factors in Korean women.

Ok, so what should we research next? Raising the bilirubin level?

Thursday, October 27, 2011

Leukoaraiosis is associated with arterial wall thickness: A quantitative analysis

Leukoaraiosis or periventricular white matter disease is a term for changes in the cerebral white matter that can be detected with high frequency by CT and MRI in aged individuals.
http://onlinelibrary.wiley.com/doi/10.1111/j.1440-1789.2011.01262.x/full

Keywords:

  • blood vessels;
  • leukoaraiosis;
  • stroke;
  • white matter changes

Leukoaraiosis refers to an age-related, abnormal appearance of the brain white matter on neuroimaging. The association between leukoaraiosis and cerebrovascular disease suggests that ischemia may be an important contributing factor; however, the pathogenesis of the condition remains controversial. We hypothesized that physical abnormalities of blood vessels might be culpable and compared the external and internal measurements of blood vessel walls between brains that demonstrated leukoaraiosis on imaging and normal control brains. Fourteen brains of individuals who had been diagnosed as having severe leukoaraiosis and five non-leukoaraiosis control brains were studied. Arterial cross-sections were evaluated by length measurements with an image analysis device. Arterial wall thickness and the ratio of the outer and inner diameters of the vessel were measured. We measured a total of 108 vessels in the leukoaraiosis group and 95 vessels in the control group. The vessel walls of the leukoaraiosis patients were an average of 5.5 µm thicker than the walls of control vessels of the same inside diameter (P = 0.0000, 95% CI 3.01–8.08) and an average of 2.3 µm thicker than walls of control vessels of the same outside diameter (P = 0.016, 95% CI 0.48–4.17). Our data provide evidence that leukoaraiosis is associated with vessel wall thickening in an additive fashion and indicate that structural vascular abnormalities are associated with leukoaraiosis.

Saturday, September 24, 2011

Stroke: 30 Years of Progress

I look at this and say that unless the ASA gets survivors on their strategy and planning commissions they will have wasted the next thirty years.
http://stroke.ahajournals.org/content/33/1/1.full

The only safe prediction about stroke in the next three decades is that it will be very different. Progress largely depends on discovery, and discovery cannot be predicted. However, understanding from where we are coming may help guide where we are going. Each of the previous editors of Stroke has given his view of stroke and the journal during his tenure, providing a concise and unique chronicle of our field by those who helped shape it.1–5 Several trends will likely affect the field and the journal.

The Field

The Growing Burden of Stroke

Stroke is the second-leading cause of death in the world6 and rising. In the developed world, the proportion of the population over the age of 65 years is growing. In the developing world, where most strokes occur, the population over 60 will double in the next 2 decades.7 These trends portend sharp increases in stroke incidence. The shift from traditional, rural ways of life to urbanization and Westernization often means less exercise, more calories, and bad habits, such as smoking. If we are serious about prevention, much can be done to lessen this burden.8

The Changing Pathophysiology of Stroke

Most attention has been paid to extracranial disease. However, in the developing world and in American minorities, intracranial disease prevails, about which we know little. Moreover, imaging has unveiled the common occurrence of leukoaraiosis and of “silent” infarcts, both of which can be associated with cognitive decline. Increasingly we are becoming aware of not only large strokes that cripple the body, but little strokes that undermine the mind. Cerebral vascular disease and Alzheimer’s disease often coincide and may interact in the brains of elderly individuals. New avenues need to be pursued to see whether stroke precipitates Alzheimer’s disease, and if so, whether this can be prevented, delayed, or mitigated.9
When hypertension is treated, intracerebral hemorrhage declines, but as people survive longer they become more prone to hemorrhages from amyloid angiopathy and cerebral infarcts from atrial fibrillation.10
The genetics of atherosclerosis, intracerebral hemorrhage, and small-vessel brain disease are just beginning to be unraveled.
Vladimir Hachinski, MD, FRCPC, DSc, is professor of neurology and past Richard and Beryl Ivey Chair of the Department of Clinical Neurological Sciences, University of Western Ontario, London, Canada. He graduated with an MD from the University of Toronto and trained in internal medicine and neurology in Montreal and Toronto and in research in London, U.K., and Copenhagen.
Dr. Hachinski’s contributions include pioneering with Dr. John W. Norris the establishment of acute stroke units, discovering the key role of the insula of the brain in cardiac complications of stroke including sudden death; crystallizing the concepts and coining the terms multi-infarct dementia, leukoaraiosis, vascular cognitive impairment, and brain attack; and devising the ischemic score that bears his name. He was the principal neurological investigator of the Canadian American Ticlopidine Study, the EC/IC Bypass Study, and the North American Symptomatic Carotid Endarterectomy Trial. He was the first recipient of the Trillium Award for outstanding research accomplishments and more recently received a Doctor honoris causa from the University of Salamanca, Spain, the Award of Excellence of the Canadian Stroke Consortium, and the Mihara Award of the International Stroke Society. Currently he is researching the question: Can strokes trigger Alzheimer’s disease?

The Escalating Sophistication of Diagnosis

Imaging
Some of the most spectacular advances in stroke have been in the application of imaging techniques, such as computerized axial tomography, MRI, and ultrasonography of the extracranial and intracranial vessels. It is likely that imaging will be refined to the point that it can also give physiological information and can replace conventional contrast angiography.
Genetics and Gene Function
Some of the most dramatic advances in diagnosis will come from structural genetics and gene physiology—initially in the identification of individuals who may have adverse reaction to drugs, and eventually in the genetic profiling of individuals in terms of estimating their risk for vascular disease, targeting treatment and assessing prognosis. Studies of the mutants of the low-density lipoprotein receptor have already been highly informative about the genetics of atherosclerosis vascular disease. Comparable research into the functional impact of mutations in the structures of genes affecting vascular tone may likewise be expected to advance the understanding of the pathogenesis diagnosis and treatment of vascular disease.
Gene Imaging
Technology is already being developed to image genes and their impact on cellular function in laboratory animals.11 Eventually this may also be possible in humans.
One of the paradoxes of advances in diagnostic technology is the neglect of clinical skills. Too often the attitude is to shoot a picture first and ask questions later. Not all that matters can be imaged, and not everything that can be imaged matters—a lesson that some have learned to their patients’ sorrow. Ironically, the more advanced the diagnostic technology, the greater the need for refined clinical skills, since the easy diagnoses will be made by the technological aids, leaving the most difficult cases to be resolved by clinical approaches and judgment.

The Stumbling Steps to Better Treatment

Failed Neuroprotectant Trials

The effectiveness of thrombolysis in acute stroke and of preventive interventions contrast starkly with the long list of failed neuroprotective trials in acute stroke. Many reasons account for this.
Extrapolation From Animal Models to Patients
The problem stems not so much from the animal models but from the failure to pay enough attention to them and to the conditions under which the results were obtained. Most clinical trials comprise patients with strokes of different types, causes, extent, and duration and who have a range of comorbidities. These conditions seldom resemble the standardized animal models and circumstances yielding the promising results.
Selection of Drugs and Time Window
Thus far, all trials have been of one drug at a time, often with a single purported mechanism. The ischemic cascade, even if it could be stopped by a single step, would require exquisite interventional timing, which is almost impossible to achieve in the human situation, where timing and extent of the ischemia vary widely. Neuroprotectant trials have typically been with a time window of 6 hours or more; such timing may be beyond the ability of the drug to salvage ischemic brain. Moreover, however powerful a neuroprotectant may be in preserving ischemic tissue, ultimately it will fail, unless blood perfusion is restored, naturally or through treatment.
Selection of Outcomes and Sample Size
Current methods of evaluating outcome are coarse and heavily weighted toward motor function. Coupled with this has been an overoptimism about the degree to which a drug could affect outcome, resulting in inadequate sample sizes.
Self-Preservation of the Clinical Trial Team
Typically, by the time a team is appointed, following expert external advice not to proceed with the trial would mean dissolution of the team and embarrassment for those who led its formation. So the trial goes on, with predictable results.
Patients need to be selected or characterized more carefully, and ideally, imaging the volume of viable tissue at the time of the intervention. Outcome measures need to be refined, expectations diminished, sample sizes amplified, and combination therapies tried, allowing thrombolysis to reestablish perfusion and neuroprotectants to act at multiple steps in the ischemic cascade.
Despite trial shortcomings and exaggerated expectations, a rationale remains for carrying out trials of neuroprotectants in stroke. Stroke is so common and devastating that a little difference in salvaged tissue may make a big difference in the ultimate quality of life.

The Future

Molecular genetics will play a growing role. The unraveling of the human genome will lead to the identification of new proteins and novel therapeutic targets. Genotyping individuals will allow not only earlier but more appropriate interventions. Drugs will be tailored to individual responses and side effects. Along with better drugs will come better delivery systems, including means of breaching the blood brain barrier and improving gene therapy.
Models will include virtual chemistry, where promising molecules will be fitted atom by atom to their therapeutic target, the drug will then be tested on transgenic animals, and treatment responses and side effects will be modeled on virtual patients created from clinical trial databases.
Globalization and the convergence of industry, academia, and government will create more uniform international standards and accelerate drug development and approval. Progress will come at a price. The increasing commercialization of science will skew development toward large-market, large-profit therapeutic agents and will leave little incentive for developing treatments for rare diseases or testing further drugs of great therapeutic power but limited profit potential, such as acetylsalicylic acid.
Individuals will play an increasingly important role in their own treatment. From surfing the Internet to being the subject of direct advertising, more and more individuals will make their own choices, including alternative medicine.
The next 30 years will transform stroke from a field of diagnostic precision and therapeutic impotence of 30 years ago into the most exciting area of treatment opportunities.

Brain Repair and Recovery

Neurologists have been mainly interested in the location, causes, and acute treatment of brain lesions, whereas rehabilitation specialists have focused on the generic management of the consequences of these lesions. Their respective approaches need to be reconciled and integrated, because it matters to patients.
It has long been established that organized stroke care as delivered in stroke units has a favorable and lasting effect on outcomes.12 We need to learn which of the many components of diagnosis, evaluation, treatment, avoidance of complications, and rehabilitation contribute to this beneficial effect.
The rehabilitation literature has suffered from lack of interest in the brain. What reliable clinical trials exist have largely focused on global evaluations and not on identifiable pathophysiological mechanisms. Moreover, much of what is done is based on tradition and belief. As recently as 1997, 66% of the recommendations of the guidelines for poststroke management had no basis in research.13,14 However, imaging, genetics, and experimental work in brain reorganization and grafting offer real hope of progress. If neuroscientists, trialists, and clinicians converge their efforts, we will begin to understand why strokes are remarkable, not because of the damage that they inflict but because of the recovery that they allow.
Even before joining forces to advance our understanding of brain injury and repair, a number of relatively simple trials can be carried out. There is now excellent evidence that an enriched environment enhances functional outcome and that the environment interacts with more direct measures such as drugs or neocortical grafting.15 Although much stock is put on stem cells, the 2 fundamental steps toward their clinical application have not yet been taken—to show that embryonic cells can integrate and replace lost function in damaged brain and that stem cells can be engineered to perform as well as embryonic cells.

Prevention: The Hope and the Disappointment

The hope is that up to 75% of cardiac and cerebrovascular disease can be prevented by the successful management of the known risk factors.16 The disappointment is that only about 25% of those with known risk factors have them controlled.17,18
The fact that this gap between knowledge and application has been observed in different countries and in different health care systems suggests that the problem goes beyond accessibility and economics. Almost certainly ignorance, different risk perceptions, and attitudes to their management play a role.
An intervention can be not only underused but also overused and misused, as exemplified by carotid endarterectomy, the most effective surgical procedure for stroke prevention.19
Open surgery is increasingly being replaced by less invasive procedures, such as angioplasty, stenting, infusion, ballooning, and coiling. We trust that the pioneers of innovation will work closely with trialists seeking proof for effectiveness of these procedures.

Between the Ideal and the Affordable

The price of improvements often exceeds their value. Better methods of diagnosis, treatment, prevention, and rehabilitation will become available, but at increasing cost. We need to develop a common currency of evaluation or a Relative Return Ratio (RRR) (my term). Such a common unit would allow ranking of treatments according to their effectiveness and return for investment in comparison with some health outcome measures such as a quality-adjusted life year (QALY) or another measure depending on the purpose. Knowing what it costs to attain a QALY by treatment A would give a direct comparison with what it would cost to attain a QALY by treatment B. Choices could then be made by the individual and/or society in comparison with other health measures or in comparison with competing demands, such as education. The price of implementing an intervention will vary from country to country, eg, staffing a stroke unit, but the value per measure or the RRR will be similar.
The RRR can be calculated, the costs computed, and informed decisions made regarding yield per effort and what that is worth to an individual or a health care system. Sophisticated consumers of the future may ask their doctors not only about the latest drug that they see advertised in the media but also about its RRR.

The Journal

In 30 years, Stroke may not be a paper journal. There are strong trends toward electronic publishing, linking and creating a customized learning environment. However, the demand for wisely selected and evaluated new, valid, and important information will remain. While the Internet has made every author into a potential editor and publisher,20 the need for quality assurance has not diminished. If the peer review system were to be abolished, it would have to be reinvented.21
The magnitude of the problem of stroke along with the increasing ability to do something about it have created an unprecedented demand for stroke experts. Special training programs need to be devised, the door opened to a wider range of individuals to train and retrain, and the great potential of online education should be fully exploited. Stroke can play a role as a major source of relevant and reliable information.
In addition to publishing results of original research, journals can provide systematic reviews, meta-analyses, and guidelines that can make knowledge more tractable, accessible, and relevant. However, systematizing information cannot provide guidance in areas where the state of the art is ignorance, nor where knowledge is meager but the physician has to act. Moreover, by their nature, the results from clinical trials are averages, while the real need is for individual profiles of risk, response to treatment, and rehabilitation. The individual phenotype, genotype, and persontype need to be understood and considered in diagnosis, treatment, and rehabilitation. Perhaps a new discipline of integrated approaches will emerge from the proliferating fragments of subspecialization.
Stroke could play an increasing role in setting standards, providing the means for education of professionals, the public, and policy makers, and become a forum for the advocacy of measures that may advance the field, and a clearing house and synergizer of new ideas.

Conclusion

Seldom has a field in medicine been transformed so radically from pessimism to the beginnings of hope as stroke. However, many challenges remain, particularly in the developing world, where stroke numbers continue to mount. Genetics, proteinomics imaging, and informatics offer unlimited possibilities of progress but pose unprecedented issues in ethics, funding, ownership, and accessibility. We need not only to make further discoveries but to ensure that what we learn is applied for the benefit of humankind.
Stroke can play a role by publishing, facilitating, and highlighting the best work to address these challenges. The journal itself will be challenged by contemporary trends, including speed. Everything is accelerating so much that speed is threatening to overtake quality. We believe with Augustus in festina lente (make haste slowly). We will aim to be comprehensive, succinct, credible, accessible, and attractive but will focus on the one irreplaceable quality: quality.