Positron emission tomography studies on the dopaminergic system and striatal opioid binding in the olivopontocerebellar atrophy variant of multiple system atrophy.

Abstract:

:Ten patients with sporadic olivopontocerebellar atrophy and autonomic failure were studied with positron emission tomography. Subjects underwent both an [11C]diprenorphine and an [18F]fluorodopa scan. The mean caudate-occipital uptake ratio for [11C]diprenorphine was significantly reduced to 88% and the putamen-occipital uptake ratio to 85% of the control values. Individually, 4 of the 10 patients had significantly reduced opioid binding in the putamen. Mean putamen [18F]fluorodopa uptake was significantly diminished (to 71% of the control mean); individually 7 patients had significantly reduced uptake. There was a significant positive correlation between putamen-occipital uptake ratios for [11C]diprenorphine and putamen uptake of [18F]fluorodopa. Our results suggest that subclinical nigrostriatal dysfunction is present in the majority of patients with sporadic olivopontocerebellar atrophy, in accordance with it being part of the spectrum of multiple system atrophy.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Rinne JO,Burn DJ,Mathias CJ,Quinn NP,Marsden CD,Brooks DJ

doi

10.1002/ana.410370505

subject

Has Abstract

pub_date

1995-05-01 00:00:00

pages

568-73

issue

5

eissn

0364-5134

issn

1531-8249

journal_volume

37

pub_type

杂志文章
  • JC virus granule cell neuronopathy and GCN-IRIS under natalizumab treatment.

    abstract::Progressive multifocal leukoencephalopathy is the most common clinical presentation of JC virus (JCV)-associated central nervous system (CNS) disease and has emerged as a major safety concern in multiple sclerosis patients treated with the monoclonal antibody natalizumab. Here we report clinical, radiological, and his...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.23973

    authors: Schippling S,Kempf C,Büchele F,Jelcic I,Bozinov O,Bont A,Linnebank M,Sospedra M,Weller M,Budka H,Martin R

    更新日期:2013-10-01 00:00:00

  • Hyperexcitability of motor and sensory neurons in neuromyotonia.

    abstract::Two members of a family with a neuropathy resembling Charcot-Marie-Tooth disease were unable to relax their muscles after voluntary contraction. Muscle spasm often outlasted voluntary contraction by 30 seconds or more before subsiding into myokymia and fasciculations. The posture of the hand during muscle spasm resemb...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410050605

    authors: Lance JW,Burke D,Pollard J

    更新日期:1979-06-01 00:00:00

  • Left thalamic infarction and disturbance of verbal memory: a clinicoanatomical study with a new method of computed tomographic stereotaxic lesion localization.

    abstract::A 41-year-old right-handed man developed disturbances of language and memory after a discrete thalamic infarction. Detailed neuropsychological assessment revealed deficits in verbal fluency, word finding, confrontation naming, and anterograde memory for verbal material. High-resolution computed tomography with stereot...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410200604

    authors: Mori E,Yamadori A,Mitani Y

    更新日期:1986-12-01 00:00:00

  • Correlation of phasic muscle strength and corticomotoneuron conduction time in multiple sclerosis.

    abstract::Central motor conduction times for the adductor pollicis muscle, the twitch force of that muscle to scalp magnetic motor cortex stimulation, and the maximum force of phasic voluntary contraction of the same muscle were measured in 15 patients with multiple sclerosis. Two tests of manual dexterity of the same hand also...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290104

    authors: van der Kamp W,Maertens de Noordhout A,Thompson PD,Rothwell JC,Day BL,Marsden CD

    更新日期:1991-01-01 00:00:00

  • Dichloroacetate exerts therapeutic effects in transgenic mouse models of Huntington's disease.

    abstract::Dichloroacetate (DCA) stimulates pyruvate dehydrogenase complex (PDHC) activity and lowers cerebral lactate concentrations. In the R6/2 and N171-82Q transgenic mouse models of Huntington's disease (HD), DCA significantly increased survival, improved motor function, delayed loss of body weight, attenuated the developme...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.1085

    authors: Andreassen OA,Ferrante RJ,Huang HM,Dedeoglu A,Park L,Ferrante KL,Kwon J,Borchelt DR,Ross CA,Gibson GE,Beal MF

    更新日期:2001-07-01 00:00:00

  • Point-of-care reversal treatment in phenprocoumon-related intracerebral hemorrhage.

    abstract:OBJECTIVE:Rapid reversal of the anticoagulatory effect of vitamin K antagonists represents the primary emergency treatment for oral anticoagulant-related intracerebral hemorrhage (OAC-ICH). Predicting the amount of prothrombin complex concentrate (PCC) needed to reverse OAC in individual patients is difficult, and repe...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1002/ana.21965

    authors: Rizos T,Jenetzky E,Herweh C,Hug A,Hacke W,Steiner T,Veltkamp R

    更新日期:2010-06-01 00:00:00

  • Weakness in malignancy: evidence for a remote effect of tumor on distal axons.

    abstract::Malignant tumors are known to have a "remote" or nonmetastatic effect on the central and peripheral nervous systems. Eight patients were seen with proximal muscle weakness in association with bronchogenic carcinoma (5), carcinoma of breast (2), and leukemia (1). Electromyography demonstrated small polyphasic motor uni...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410040314

    authors: Barron SA,Heffner RR Jr

    更新日期:1978-09-01 00:00:00

  • Proteolytic activity in amyotrophic lateral sclerosis IgG preparations.

    abstract::Sporadic amyotrophic lateral sclerosis is a motor neuron disease of unknown origin. Autoimmunity against voltage-gated calcium channels is one mechanism hypothesized to be the cause of the disease. In support of this hypothesis, it was previously reported that amyotrophic lateral sclerosis IgG specifically blocked the...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410400505

    authors: Nyormoi O

    更新日期:1996-11-01 00:00:00

  • Neonatal vitamin D status and risk of multiple sclerosis.

    abstract:OBJECTIVE:Low vitamin D status at birth may be associated with risk of adult onset multiple sclerosis, but this link has not been studied directly. We assessed the relation between neonatal vitamin D concentrations, measured in stored blood samples, and risk of multiple sclerosis. METHODS:This was a population-based c...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24210

    authors: Ueda P,Rafatnia F,Bäärnhielm M,Fröbom R,Korzunowicz G,Lönnerbro R,Hedström AK,Eyles D,Olsson T,Alfredsson L

    更新日期:2014-09-01 00:00:00

  • Benzodiazepine receptors in focal epilepsy with cortical dysgenesis: an 11C-flumazenil PET study.

    abstract::Previous imaging studies using 11C-flumazenil in patients with mesial temporal lobe epilepsy and neocortical partial seizure disorders have found focal decreases in gamma-aminobutyric acid type A/benzodiazepine receptor binding. These studies used subjective visual assessment and a region of interest approach to quant...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410400210

    authors: Richardson MP,Koepp MJ,Brooks DJ,Fish DR,Duncan JS

    更新日期:1996-08-01 00:00:00

  • Evidence for mitochondrial dysfunction in patients with alternating hemiplegia of childhood.

    abstract::Phosphorus magnetic resonance spectra of resting muscle were obtained from 4 patients with alternating hemiplegia of childhood. All patients had abnormally high resonance intensities from inorganic phosphate and an abnormally low calculated cytosolic phosphorylation potential. Two of the 4 patients had abnormally low ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410330608

    authors: Arnold DL,Silver K,Andermann F

    更新日期:1993-06-01 00:00:00

  • Soluble ST2 links inflammation to outcome after subarachnoid hemorrhage.

    abstract:OBJECTIVE:To investigate whether soluble growth stimulation expressed gene 2 (sST2), a prognostic marker in cardiovascular and inflammatory disorders, is associated with neurological injury after aneurysmal subarachnoid hemorrhage (SAH). METHODS:We studied SAH patients from 2 independent cohorts. Outcome assessments i...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1002/ana.25545

    authors: Bevers MB,Wolcott Z,Bache S,Hansen C,Sastre C,Mylvaganam R,Koch MJ,Patel AB,Møller K,Kimberly WT

    更新日期:2019-09-01 00:00:00

  • Chronic levodopa is not toxic for remaining dopamine neurons, but instead promotes their recovery, in rats with moderate nigrostriatal lesions.

    abstract::Orally administered levodopa remains the most effective symptomatic treatment for Parkinson's disease (PD). The introduction of levodopa therapy is often delayed, however, because of the fear that it might be toxic for the remaining dopaminergic neurons and, thus, accelerate the deterioration of patients. However, in ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410430504

    authors: Murer MG,Dziewczapolski G,Menalled LB,García MC,Agid Y,Gershanik O,Raisman-Vozari R

    更新日期:1998-05-01 00:00:00

  • Quinolinic acid catabolism is increased in cerebellum of patients with dominantly inherited olivopontocerebellar atrophy.

    abstract::We measured the activities of the enzymes responsible for the metabolism of the excitotoxin quinolinic acid, 3-hydroxyanthranilate oxygenase and quinolinic acid phosphoribosyltransferase, in autopsied brain of 11 patients with olivopontocerebellar atrophy. In cerebellar cortex, severe Purkinje cell loss was evident bu...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290119

    authors: Kish SJ,Du F,Parks DA,Robitaille Y,Ball MJ,Schut L,Hornykiewicz O,Schwarcz R

    更新日期:1991-01-01 00:00:00

  • The pathophysiology of myotonia produced by aromatic carboxylic acids.

    abstract::A series of nine related aromatic monocarboxylic acids (ACAs) previously shown to inhibit muscle membrane chloride conductance (GCl) selectively in the rat were studied for their ability to produce myotonia. All nine induced characteristic repetitive electrical activity and delayed relaxation in isolated muscle, altho...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410040411

    authors: Furman RE,Barchi RL

    更新日期:1978-10-01 00:00:00

  • Neonatal myasthenia gravis in the infant of a myasthenic mother in remission.

    abstract::A 26-year-old woman was in spontaneous clinical remission from myasthenia gravis (MG) for six months, yet gave birth to a full-term infant with typical neonatal MG. It is believed that transplacental transfer of anti-acetylcholine (ACh) receptor antibodies is responsible for neonatal MG; therefore, neonatal MG represe...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410060119

    authors: Elias SB,Butler I,Appel SH

    更新日期:1979-07-01 00:00:00

  • Sequence variants in human neurofilament proteins: absence of linkage to familial amyotrophic lateral sclerosis.

    abstract::Neurofilaments, assembled from NF-L (68 kd), NF-M (95 kd), and NF-H (115 kd), are the most abundant structural components in large myelinated axons, particularly those of motor neurons. Aberrant neurofilament accumulation in cell bodies and axons of motor neurons is a prominent pathological feature of several motor ne...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410400410

    authors: Vechio JD,Bruijn LI,Xu Z,Brown RH Jr,Cleveland DW

    更新日期:1996-10-01 00:00:00

  • Antioxidants halt axonal degeneration in a mouse model of X-adrenoleukodystrophy.

    abstract:OBJECTIVE:Axonal degeneration is a main contributor to disability in progressive neurodegenerative diseases in which oxidative stress is often identified as a pathogenic factor. We aim to demonstrate that antioxidants are able to improve axonal degeneration and locomotor deficits in a mouse model of X-adrenoleukodystro...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22363

    authors: López-Erauskin J,Fourcade S,Galino J,Ruiz M,Schlüter A,Naudi A,Jove M,Portero-Otin M,Pamplona R,Ferrer I,Pujol A

    更新日期:2011-07-01 00:00:00

  • Glucose metabolism and serotonin receptors in the frontotemporal lobe degeneration.

    abstract::In patients with the frontal variant of frontotemporal lobar degeneration (fv-FTLD), behavioral abnormalities may vary from apathy with motor slowness (apathetic form) to disinhibition with agitation (disinhibited form). These clinical presentations may be related to specific regional cerebral dysfunction and to defic...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20365

    authors: Franceschi M,Anchisi D,Pelati O,Zuffi M,Matarrese M,Moresco RM,Fazio F,Perani D

    更新日期:2005-02-01 00:00:00

  • Sequence heterogeneity of HTLV-I proviral DNA in the central nervous system of patients with HTLV-I-associated myelopathy.

    abstract::The nucleotide sequence of human T-lymphotropic virus type I (HTLV-I) in central nervous system tissue was determined in 3 autopsy cases with HTLV-I-associated myelopathy (HAM)/tropical spastic paraparesis (TSP) and 1 seropositive carrier without HAM/TSP but with multiple sclerosis. All HAM/TSP samples (3 spinal cords...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410360206

    authors: Kira J,Koyanagi Y,Yamada T,Itoyama Y,Tateishi J,Akizuki S,Kishikawa M,Baba E,Nakamura M,Suzuki J

    更新日期:1994-08-01 00:00:00

  • Selective vulnerability in Huntington's disease: preferential loss of cannabinoid receptors in lateral globus pallidus.

    abstract::Selective neuronal vulnerability is a key feature of the neuropathology of Huntington's disease. We used [3H]CP-55,940, a synthetic cannabinoid, to label cannabinoid receptors in tissue sections from individuals dying with Huntington's disease and from normal control subjects. The density of cannabinoid receptors in s...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410360406

    authors: Richfield EK,Herkenham M

    更新日期:1994-10-01 00:00:00

  • Confusing placebo effect with natural history in epilepsy: A big data approach.

    abstract::For unknown reasons, placebos reduce seizures in clinical trials in many patients. It is also unclear why some drugs showing statistical superiority to placebo in one trial may fail to do so in another. Using Seizuretracker.com, a patient-centered database of 684,825 seizures, we simulated "placebo" and "drug" trials....

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24470

    authors: Goldenholz DM,Moss R,Scott J,Auh S,Theodore WH

    更新日期:2015-09-01 00:00:00

  • Blood biomarkers of carbohydrate, lipid, and apolipoprotein metabolisms and risk of amyotrophic lateral sclerosis: A more than 20-year follow-up of the Swedish AMORIS cohort.

    abstract:OBJECTIVE:To assess the associations of blood biomarkers of carbohydrate, lipid, and apolipoprotein metabolisms with the future risk of amyotrophic lateral sclerosis (ALS). METHODS:In the Apolipoprotein-related MOrtality RISk study, we enrolled 636,132 men and women during 1985-1996 in Stockholm, Sweden, with measurem...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24936

    authors: Mariosa D,Hammar N,Malmström H,Ingre C,Jungner I,Ye W,Fang F,Walldius G

    更新日期:2017-05-01 00:00:00

  • Upregulation of Bcl-2 protein in the myasthenic thymus.

    abstract::We examined the expression of Fas antigen and Bcl-2 protein in thymic tissue surgically resected from 10 patients with myasthenia gravis, using immunocytochemical techniques. Histologically, thymic tissues from 7 myasthenia gravis patients showed hyperplasia, while 3 other patients had thymomas. In hyperplastic thymic...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410390414

    authors: Onodera J,Nakamura S,Nagano I,tobita M,Yoshioka M,Takeda A,Oouchi M,Itoyama Y

    更新日期:1996-04-01 00:00:00

  • New anatomical and functional imaging methods.

    abstract::Powerful new methods for imaging both brain anatomy and brain function are appearing at an increasing rate. The modern era of minimally invasive, highly informative, neurological diagnostic imaging methods began with the introduction of x-ray computed tomography in the 1970s. More recently, positron emission tomograph...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410320316

    authors: Prichard JW,Brass LM

    更新日期:1992-09-01 00:00:00

  • Diffuse axonal injury in children: clinical correlation with hemorrhagic lesions.

    abstract::An inception cohort of 40 children and adolescents with traumatic brain injury and suspected diffuse axonal injury were studied using a new high-resolution magnetic resonance imaging susceptibility-weighted technique that is very sensitive for hemorrhage. A blinded comparison was performed between the extent of parenc...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20123

    authors: Tong KA,Ashwal S,Holshouser BA,Nickerson JP,Wall CJ,Shutter LA,Osterdock RJ,Haacke EM,Kido D

    更新日期:2004-07-01 00:00:00

  • Effect of subthalamic deep brain stimulation on the function of the urinary bladder.

    abstract::Detrusor hyperreflexia is a relevant clinical symptom for patients suffering from Parkinson's disease. In a series of 16 patients, we demonstrated that subthalamic deep brain stimulation has a significant and urodynamically recordable effect leading to a normalization of pathologically increased bladder sensibility. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10806

    authors: Seif C,Herzog J,van der Horst C,Schrader B,Volkmann J,Deuschl G,Juenemann KP,Braun PM

    更新日期:2004-01-01 00:00:00

  • Adult polyglucosan body disease in Ashkenazi Jewish patients carrying the Tyr329Ser mutation in the glycogen-branching enzyme gene.

    abstract::Adult polyglucosan body disease (APBD) is a late-onset, slowly progressive disorder of the nervous system caused by glycogen branching enzyme (GBE) deficiency in a subgroup of patients of Ashkenazi Jewish origin. Similar biochemical finding is shared by glycogen storage disease type IV (GSD IV) that, in contrast to AP...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410440604

    authors: Lossos A,Meiner Z,Barash V,Soffer D,Schlesinger I,Abramsky O,Argov Z,Shpitzen S,Meiner V

    更新日期:1998-12-01 00:00:00

  • Linking MRI postprocessing with magnetic source imaging in MRI-negative epilepsy.

    abstract:OBJECTIVE:MRI-negative (MRI-) pharmacoresistant focal epilepsy (PFE) patients are most challenging for epilepsy surgical management. This study utilizes a voxel-based MRI postprocessing technique, implemented using a morphometric analysis program (MAP), aiming to facilitate detection of subtle focal cortical dysplasia ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24169

    authors: Wang ZI,Alexopoulos AV,Jones SE,Najm IM,Ristic A,Wong C,Prayson R,Schneider F,Kakisaka Y,Wang S,Bingaman W,Gonzalez-Martinez JA,Burgess RC

    更新日期:2014-05-01 00:00:00

  • Stroke prevention in nonvalvular atrial fibrillation: a review of prospective randomized trials.

    abstract::Patients with atrial fibrillation are at risk for cerebral embolism; however, the roles of chronic anticoagulation or antiplatelet therapy for stroke prevention in patients with nonvalvular atrial fibrillation have been controversial. Recently, the results of three large prospective randomized trials that examined the...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410300402

    authors: Albers GW,Sherman DG,Gress DR,Paulseth JE,Petersen P

    更新日期:1991-10-01 00:00:00