Aphasia outcome: the interactions between initial severity, lesion size and location.

Abstract:

OBJECTIVES:The outcome of aphasia at 3 months is variable in patients with moderate/severe stroke. The aim was to predict 3-month aphasia outcome using prediction models including initial severity in addition to the interaction between lesion size and location at the acute phase. METHODS:Patients with post-stroke aphasia (assessed by the Aphasia Rapid Test at day 7-ART D7) and MRI performed at day 1 were enrolled (n = 73). Good outcome at 3-months was defined by an Aphasia Handicap Score of 0-2. Each infarct lesion was overlapped with an area of interest in the left temporo-parietal region to compute an intersection index (proportion of the critical region damaged by the infarct). We tested ART D7, age, lesion volume, and intersection index as well as a combined variable lesion volume*intersection in a univariate analysis. Then, we performed a multivariate analysis to investigate which variables were independent predictors of good outcome. RESULTS:ART at D7, infarct volume, and the intersection index were univariate predictors of good outcome. In the multivariate analysis, ART D7 and "volume ≥ 50 ml or intersection index ≥ 20%" correctly classified 89% of the patients (p < 0.0001). When added to the model, the interaction between both variables was significant indicating that the impact of the size or site variable depends on the initial severity of aphasia. CONCLUSION:In patients with initially severe aphasia, large infarct size or critical damage in left temporoparietal junction is associated with poor language outcome at 3 months.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Benghanem S,Rosso C,Arbizu C,Moulton E,Dormont D,Leger A,Pires C,Samson Y

doi

10.1007/s00415-019-09259-3

subject

Has Abstract

pub_date

2019-06-01 00:00:00

pages

1303-1309

issue

6

eissn

0340-5354

issn

1432-1459

pii

10.1007/s00415-019-09259-3

journal_volume

266

pub_type

杂志文章
  • Diagnostic yield of external loop recording in patients with acute ischemic stroke or TIA.

    abstract::Atrial fibrillation (AF) is a strong risk factor for first-ever stroke and stroke recurrence. The detection rate is low and detection is often costly and time-consuming. We evaluated the diagnostic yield of an external loop recorder (ELR) in patients with acute ischemic stroke or TIA, and assessed factors that are ass...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-014-7621-3

    authors: Plas GJ,Bos J,Velthuis BO,Scholten MF,den Hertog HM,Brouwers PJ

    更新日期:2015-03-01 00:00:00

  • Dementia and assisted suicide and euthanasia.

    abstract::The number of dementia patients requesting euthanasia in the Netherlands has increased over the past five years. The issue is highly controversial. In this contribution we discuss some of the main arguments: the nature of suffering, the voluntariness of the request and the role of the physician. We argue that society ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-016-8095-2

    authors: de Beaufort ID,van de Vathorst S

    更新日期:2016-07-01 00:00:00

  • Clinical phenotypic heterogeneity of Alzheimer's disease associated with mutations of the presenilin-1 gene.

    abstract::It is now 10 years since the first report of mutations in the presenilin genes that were deterministic for familial autosomal dominant Alzheimer's disease. The most common of these mutations occurs in the presenilin-1 gene (PSEN1) located on chromosome 14. In the ensuing decade, more than 100 PSEN1 mutations have been...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-005-0019-5

    authors: Larner AJ,Doran M

    更新日期:2006-02-01 00:00:00

  • Predictors of weight loss in early treated Parkinson's disease from the NET-PD LS-1 cohort.

    abstract::Weight loss is a common symptom of Parkinson's disease and is associated with impaired quality of life. Predictors of weight loss have not been studied in large clinical cohorts. We previously observed an association between change in body mass index and change in Unified Parkinson's Disease Rating Scale (UPDRS) motor...

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1007/s00415-017-8562-4

    authors: Wills AM,Li R,Pérez A,Ren X,Boyd J,NINDS NET-PD Investigators.

    更新日期:2017-08-01 00:00:00

  • Stroke in younger patients: the heart of the matter.

    abstract::Stroke in young adults is not a rare entity, and often provides difficult management decisions for neurologists. The knowledge gained from stroke in older adults does not transfer easily to this younger group given the different causes of stroke observed. Cardiac causes of stroke are common in this group, but often co...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-010-5647-8

    authors: Cotter PE,Belham M,Martin PJ

    更新日期:2010-11-01 00:00:00

  • Right temporal cerebral dysfunction heralds symptoms of acute mountain sickness.

    abstract::Acute mountain sickness (AMS) can occur during climbs to high altitudes and may seriously disturb the behavioral and intellectual capacities of susceptible subjects. During a Himalayan expedition 32 mountaineers were examined with electroencephalography (EEG) and transcranial doppler sonography (TCD) to assess relativ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-006-0376-8

    authors: Feddersen B,Ausserer H,Neupane P,Thanbichler F,Depaulis A,Waanders R,Noachtar S

    更新日期:2007-03-01 00:00:00

  • The relationship among restless legs syndrome (Willis-Ekbom Disease), hypertension, cardiovascular disease, and cerebrovascular disease.

    abstract::Untreated sleep disorders may contribute to secondary causes of uncontrolled hypertension, cardiovascular disease (CVD), and stroke. Restless legs syndrome, or Willis-Ekbom Disease (RLS/WED), is a common sensorimotor disorder with a circadian rhythmicity defined by an uncontrollable urge to move the legs that worsens ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-013-7065-1

    authors: Ferini-Strambi L,Walters AS,Sica D

    更新日期:2014-06-01 00:00:00

  • T4, T3 and rT3 levels in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

    abstract::Thyronine (T4), triiodothyronine (T3), and reverse-triiodothyronine (rT3) levels were evaluated in cerebrospinal fluid (CSF) and in serum of 12 patients with definite amyotrophic lateral sclerosis (ALS) by specific radioimmunoassays. Circulating microsomal and thyroglobulin antibodies were also evaluated. In all patie...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314221

    authors: Malin JP,Ködding R,Fuhrmann H,von zur Mühlen A

    更新日期:1989-01-01 00:00:00

  • Stroke and Fabry disease.

    abstract::Fabry disease (FD) is a rare inherited disorder of the metabolism, associated with renal, cardiac, and cerebrovascular complications. Ischemic and hemorrhagic stroke in FD present with a similar proportion to that observed in the general population, but usually at an early age. Ischemic stroke may result from cardiac ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-011-6278-4

    authors: Viana-Baptista M

    更新日期:2012-06-01 00:00:00

  • REM sleep behaviour disorder and visuoperceptive dysfunction: a disorder of the ventral visual stream?

    abstract::In idiopathic rapid eye movement sleep behaviour disorder (RBD), an association with visuoperceptive disorders has been described. However, such an association has not been clearly established in RBD secondary to Parkinson's disease (PD). We compared visuoperceptive function in four groups of non-demented patients (pa...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5328-7

    authors: Marques A,Dujardin K,Boucart M,Pins D,Delliaux M,Defebvre L,Derambure P,Monaca C

    更新日期:2010-03-01 00:00:00

  • Early diagnosis of dementia: which tests are indicated? What are their costs?

    abstract::Dementia is reversible in a minority of patients, and these should be diagnosed but without subjecting the majority with irreversible disease to an excessive set of investigations. Should a battery of ancillary investigations be performed routinely in dementia? Or can these tests be carried out as clinically indicated...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s004150050311

    authors: van Crevel H,van Gool WA,Walstra GJ

    更新日期:1999-02-01 00:00:00

  • How well do we recognise non-motor symptoms in a British Parkinson's disease population?

    abstract::Although awareness of non-motor symptoms in Parkinson's disease (PD) has recently increased, little is known about their recognition and treatment in routine clinical practice. We therefore applied non-motor rating scales for dementia, depression, anxiety and excessive daytime sleepiness to a community-ascertained coh...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-011-5972-6

    authors: Hu M,Cooper J,Beamish R,Jones E,Butterworth R,Catterall L,Ben-Shlomo Y

    更新日期:2011-08-01 00:00:00

  • Spinal cord atrophy in spinocerebellar ataxia type 3 and 6 : impact on clinical disability.

    abstract:OBJECTIVE:To quantify spinal cord atrophy and its impact on clinical disability in spinocerebellar ataxia (SCA) type 3 and 6. METHODS:Atrophy of the upper spinal cord was assessed by high resolution T1-weighted MRI of patients with SCA3 (n = 14) and SCA6 (n = 10). Furthermore, two groups of age- and sex-matched health...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0907-6

    authors: Lukas C,Hahn HK,Bellenberg B,Hellwig K,Globas C,Schimrigk SK,Köster O,Schöls L

    更新日期:2008-08-01 00:00:00

  • T2*-weighted MRI in diagnosis of multiple system atrophy. A practical approach for clinicians.

    abstract:BACKGROUND:Putaminal iron deposition is a histopathological feature of multiple system atrophy (MSA), which is not observed in patients with idiopathic Parkinson's disease (PD). T2*-weighted magnetic resonance imaging (MRI) gradient echo (GE) sequences are sensitive for paramagnetic susceptibility changes and therefore...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-006-0496-1

    authors: von Lewinski F,Werner C,Jörn T,Mohr A,Sixel-Döring F,Trenkwalder C

    更新日期:2007-09-01 00:00:00

  • Wallenberg's lateral medullary syndrome with loss of pain and temperature sensation on the contralateral face: clinical, MRI and electrophysiological studies.

    abstract::Thirteen patients with Wallenberg's lateral medullary syndrome (WLMS) were studied. Clinical and magnetic resonance imaging (MRI) evidence demonstrated infarction in the dorsolateral medulla which produced loss of pain and temperature sensation on one side of the face ipsilateral to the lesion in seven patients. Howev...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00874113

    authors: Chia LG,Shen WC

    更新日期:1993-09-01 00:00:00

  • Dopamine transporter binding in chronic manganese intoxication.

    abstract::Chronic exposure to manganese may induce parkinsonism similar to idiopathic Parkinson's disease (PD). However, clinical manifestations of manganism also have some features different from PD. The mechanisms of manganese-induced parkinsonism remain not fully understood. (99m)Tc-TRODAT-1 is a cocaine analogue that can bi...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-003-0214-1

    authors: Huang CC,Weng YH,Lu CS,Chu NS,Yen TC

    更新日期:2003-11-01 00:00:00

  • Disturbed benzodiazepine receptor function at the onset of temporal lobe epilepsy--lomanzenil-binding in de-novo TLE.

    abstract:PURPOSE:Epileptogenic foci exhibit disturbed function at the level of the benzodiazepine receptor. The aim of our study was to investigate the incidence of focal reductions of temporal benzodiazepine receptor binding (BRB) as assessed by scintigraphy with 123I-iomazenil in patients with denovo temporal lobe epilepsy (T...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150170136

    authors: Matheja P,Lüdemann P,Kuwert T,Weckesser M,Kellinghaus C,Weitemeyer L,Diehl B,Schuierer G,Ringelstein EB,Schober O

    更新日期:2001-07-01 00:00:00

  • Fixation instability and oculomotor abnormalities in Friedreich's ataxia.

    abstract::Eye movements were studied in 13 patients with Friedreich's ataxia and correlated with MRI findings to investigate whether oculomotor abnormalities can be traced to cerebellar disturbances in this disease. One of the most prominent eye signs was fixation instability (square-wave jerks, SWJ.). Besides SWJ the patients ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00867423

    authors: Spieker S,Schulz JB,Petersen D,Fetter M,Klockgether T,Dichgans J

    更新日期:1995-08-01 00:00:00

  • Optic neuritis presenting with amaurosis fugax.

    abstract::Optic neuritis usually presents with rapid and gradual loss of vision that is either complete or incomplete, and typically associated with retro-orbital pain. To our knowledge there have been no documented reports of optic neuritis presenting with multiple episodes of amaurosis fugax, the sudden and transient loss of ...

    journal_title:Journal of neurology

    pub_type: 信件

    doi:10.1007/s00415-009-5302-4

    authors: Awad AM,Estephan B,Warnack W,Stüve O

    更新日期:2009-12-01 00:00:00

  • Reorientation to vertical modulated by combined support surface tilt and virtual visual flow in healthy elders and adults with stroke.

    abstract::We explored how changes in visual attention impacted postural motor performance in healthy elders and adults post-stroke within a virtual reality environment, including when vestibular information was not perceptible. Visual dependence in 13 healthy (50-80 years) and 13 adults post-stroke (49-70 years) was assessed wi...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-012-6566-7

    authors: Slaboda JC,Keshner EA

    更新日期:2012-12-01 00:00:00

  • Clinical features of CIS of the brainstem/cerebellum of the kind seen in MS.

    abstract::Recognition of multiple sclerosis (MS) attacks relies mostly on clinical assessment. However, their definition based on McDonald criteria refers mostly to timing and when dealing with clinical features is rather ambiguous: "...of the kind seen in multiple sclerosis." This is heightened in clinically isolated syndromes...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5403-0

    authors: Sastre-Garriga J,Tintoré M,Nos C,Tur C,Río J,Téllez N,Castilló J,Horga A,Perkal H,Comabella M,Rovira A,Montalban X

    更新日期:2010-05-01 00:00:00

  • Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland.

    abstract::Charcot-Marie-Tooth disease (CMT) is the most common inherited neuropathy with heterogeneous clinical presentation and genetic background. The axonal form (CMT2) is characterised by decreased action potentials indicating primary axonal damage. The underlying pathology involves axonal degeneration which is supposed to ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-015-7778-4

    authors: Bansagi B,Antoniadi T,Burton-Jones S,Murphy SM,McHugh J,Alexander M,Wells R,Davies J,Hilton-Jones D,Lochmüller H,Chinnery P,Horvath R

    更新日期:2015-08-01 00:00:00

  • Psychosocial aspects in patients with myasthenia gravis.

    abstract::Myasthenia gravis patients usually present with fluctuating, asymmetrical stress-dependent weakness in the absence of other neurological disturbances. In weak patients psychopathological disturbances are frequently reported and misdiagnosed as a psychiatric disorder. The question to what extent psychiatric symptoms ar...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-007-2022-5

    authors: Köhler W

    更新日期:2007-05-01 00:00:00

  • Myoclonus and adult coeliac disease.

    abstract::A 56-year-old woman with coeliac disease developed myoclonus of cortical origin and palatal myoclonus with lesions of subcortical white matter on magnetic resonance imaging. Myoclonus can thus be a prominent feature of coeliac disease encephalopathy. A slight vitamin E deficiency was found but does not satisfactorily ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314464

    authors: Tison F,Arne P,Henry P

    更新日期:1989-07-01 00:00:00

  • Magnesium deficiency as a cause of acute intractable seizures.

    abstract::Clinical and experimental investigations have shown that magnesium depletion causes a marked irritability of the nervous system, eventually resulting in epileptic seizures. Although magnesium deficiency as a cause of epilepsy is uncommon, its recognition and correction may prove life-saving. Two case reports are prese...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00319737

    authors: Nuytten D,Van Hees J,Meulemans A,Carton H

    更新日期:1991-08-01 00:00:00

  • Emotional responding in amyotrophic lateral sclerosis.

    abstract::Amyotrophic lateral sclerosis (ALS) is a fatal disease, leaving the patient in a partially or completely deafferented state. In an explorative study, we investigated responses to visual socio-emotional stimuli in ALS patients. Pictures from the International Affective Picture System (IAPS) were verbally judged by 12 m...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-005-0907-8

    authors: Lulé D,Kurt A,Jürgens R,Kassubek J,Diekmann V,Kraft E,Neumann N,Ludolph AC,Birbaumer N,Anders S

    更新日期:2005-12-01 00:00:00

  • ANO10 mutational screening in recessive ataxia: genetic findings and refinement of the clinical phenotype.

    abstract::Autosomal recessive cerebellar ataxia type 3 (ARCA3) is a rare inherited disorder caused by mutations in the ANO10 gene. The disease is characterized by slowly progressive spastic ataxia variably associated with motor neuron involvement, epilepsy, and cognitive decline. We performed mutational screening in 80 patients...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-018-9141-z

    authors: Nanetti L,Sarto E,Castaldo A,Magri S,Mongelli A,Rossi Sebastiano D,Canafoglia L,Grisoli M,Malaguti C,Rivieri F,D'Amico MC,Di Bella D,Franceschetti S,Mariotti C,Taroni F

    更新日期:2019-02-01 00:00:00

  • Chorea and polycythaemia.

    abstract::Two patients with chorea and polycythaemia vera are described. The literature on this rare association is reviewed and its pathophysiology discussed. ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313895

    authors: Mas JL,Gueguen B,Bouche P,Derouesné C,Varet B,Castaigne P

    更新日期:1985-01-01 00:00:00

  • Low prevalence of ataxic polyneuropathy in a community with high exposure to cyanide from cassava foods.

    abstract:INTRODUCTION:Ataxic polyneuropathy, which occurs in endemic form in an area in southwest Nigeria, is attributed to exposure to cyanide from cassava foods. Exposure to cyanide from cassava is, however, not exclusive to this endemic area. In this study, the occurrence of ataxic polyneuropathy was compared in two communit...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-002-0779-0

    authors: Oluwole OS,Onabolu AO,Cotgreave IA,Rosling H,Persson A,Link H

    更新日期:2002-08-01 00:00:00

  • Rare association of motor neuron disease and spinocerebellar ataxia type 2 (SCA2): a new case and review of the literature.

    abstract::We report a rare association of spinocerebellar ataxia and motor neuron disease (MND) in a woman with genetically confirmed SCA2 who subsequently developed a rapidly progressive and fatal form of MND. Considering the rarity of these two neurological conditions, it is interesting to note that the concomitant occurrence...

    journal_title:Journal of neurology

    pub_type: 信件,评审

    doi:10.1007/s00415-009-5237-9

    authors: Nanetti L,Fancellu R,Tomasello C,Gellera C,Pareyson D,Mariotti C

    更新日期:2009-11-01 00:00:00