Epidemiology of mutations in superoxide dismutase in amyotrophic lateral sclerosis.

Abstract:

:We registered 366 families in a study of dominantly inherited amyotrophic lateral sclerosis. Two hundred ninety families were screened for mutations in the gene encoding copper-zinc cytosolic superoxide dismutase (SOD1). Mutations were detected in 68 families. The most common SOD1 mutation is an alanine for valine substitution in codon 4 (50%). We present clinical and genetic data concerning 112 families with 395 affected individuals. The clinical characteristics of patients with familial amyotrophic lateral sclerosis arising from SOD1 mutations are similar to those lacking SOD1 defects. Mean age at onset was earlier (Wilcoxon test, p = 0.004) in the SOD1 group (46.9 years [standard deviation, 12.5] vs 50.5 years [11.5] in the non-SOD1 group). Bulbar onset was associated with a later onset age. The presence of either of two mutations, G37R and L38V, predicted an earlier age at onset. Kaplan-Meier plots demonstrated shorter survival in the SOD1 group compared with the non-SOD1 group at early survival times (Wilcoxon test, p = 0.0007). The presence of one mutation, A4V, correlated with shorter survival. G37R, G41D, and G93C mutations predicted longer survival. This information suggests it will be productive to investigate other genetic determinants in amyotrophic lateral sclerosis and to use epidemiological characteristics of the disease to help discern molecular mechanisms of motor neuron cell death.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Cudkowicz ME,McKenna-Yasek D,Sapp PE,Chin W,Geller B,Hayden DL,Schoenfeld DA,Hosler BA,Horvitz HR,Brown RH

doi

10.1002/ana.410410212

subject

Has Abstract

pub_date

1997-02-01 00:00:00

pages

210-21

issue

2

eissn

0364-5134

issn

1531-8249

journal_volume

41

pub_type

杂志文章
  • L-dopa pharmacokinetics in plasma and cisternal and lumbar cerebrospinal fluid of monkeys.

    abstract::The pharmacokinetics of levodopa (L-dopa) in plasma and in cisternal and lumbar cerebrospinal fluid (CSF) were studied in Rhesus monkeys that were given 2- to 3-hour intravenous infusions of L-dopa. Steady-state L-dopa concentrations in cisternal CSF correlated well with plasma levels, and yielded a CSF:plasma ratio o...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410270507

    authors: Hammerstad JP,Woodward WR,Gliessman P,Boucher B,Nutt JG

    更新日期:1990-05-01 00:00:00

  • Quantitative CSF PCR in Epstein-Barr virus infections of the central nervous system.

    abstract::Acute Epstein-Barr virus (EBV) infection of the central nervous system (CNS) is associated with meningoencephalitis and other neurological syndromes and with CNS lymphomas (CNSLs). Diagnosis is based on serological studies and more recently on detection of EBV DNA in cerebrospinal fluid (CSF) by polymerase chain react...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10321

    authors: Weinberg A,Li S,Palmer M,Tyler KL

    更新日期:2002-11-01 00:00:00

  • In vivo butyrylcholinesterase activity is not increased in Alzheimer's disease synapses.

    abstract:OBJECTIVE:We tested the premise that cholinesterase inhibitor therapy should target butyrylcholinesterase (BuChE) in Alzheimer's disease (AD), not acetylcholinesterase (AChE) alone, because both enzymes hydrolyze acetylcholine, and BuChE is increased in AD cerebral cortex. METHODS:To examine this issue in vivo, we qua...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20672

    authors: Kuhl DE,Koeppe RA,Snyder SE,Minoshima S,Frey KA,Kilbourn MR

    更新日期:2006-01-01 00:00:00

  • DNAJC12 and dopa-responsive nonprogressive parkinsonism.

    abstract::Biallelic DNAJC12 mutations were described in children with hyperphenylalaninemia, neurodevelopmental delay, and dystonia. We identified DNAJC12 homozygous null variants (c.187A>T;p.K63* and c.79-2A>G;p.V27Wfs*14) in two kindreds with early-onset parkinsonism. Both probands had mild intellectual disability, mild nonpr...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25048

    authors: Straniero L,Guella I,Cilia R,Parkkinen L,Rimoldi V,Young A,Asselta R,Soldà G,Sossi V,Stoessl AJ,Priori A,Nishioka K,Hattori N,Follett J,Rajput A,Blau N,Pezzoli G,Farrer MJ,Goldwurm S,Rajput AH,Duga S

    更新日期:2017-10-01 00:00:00

  • Intravenous thrombolysis for suspected ischemic stroke with seizure at onset.

    abstract:OBJECTIVE:Seizure at onset (SaO) has been considered a relative contraindication for intravenous thrombolysis (IVT) in patients with acute ischemic stroke, although this appraisal is not evidence based. Here, we investigated the prognostic significance of SaO in patients treated with IVT for suspected ischemic stroke. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1002/ana.25582

    authors: Polymeris AA,Curtze S,Erdur H,Hametner C,Heldner MR,Groot AE,Zini A,Béjot Y,Dietrich A,Martinez-Majander N,von Rennenberg R,Gumbinger C,Schaedelin S,De Marchis GM,Thilemann S,Traenka C,Lyrer PA,Bonati LH,Wegener S,R

    更新日期:2019-11-01 00:00:00

  • Prediction of hemorrhagic transformation after recanalization therapy using T2*-permeability magnetic resonance imaging.

    abstract:OBJECTIVE:Predicting hemorrhagic transformation (HT) is critical in the setting of recanalization therapy for acute stroke. Dedicated magnetic resonance imaging (MRI) sequences for detection of increased blood-brain barrier (BBB) permeability recently have been developed. We evaluated the ability of a novel MRI permeab...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.21174

    authors: Bang OY,Buck BH,Saver JL,Alger JR,Yoon SR,Starkman S,Ovbiagele B,Kim D,Ali LK,Sanossian N,Jahan R,Duckwiler GR,Viñuela F,Salamon N,Villablanca JP,Liebeskind DS

    更新日期:2007-08-01 00:00:00

  • Diffusion-weighted magnetic resonance imaging in boys with neural cell adhesion molecule L1 mutations and congenital hydrocephalus.

    abstract::The phenotype of severe congenital hydrocephalus secondary to neural cell adhesion molecule L1 (L1CAM) gene mutations includes the distinct finding of brainstem corticospinal tract hypoplasia. Using diffusion-weighted imaging (DWI), we failed to demonstrate anisotropy in the corticospinal tracts of the basis pontis in...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Graf WD,Born DE,Shaw DW,Thomas JR,Holloway LW,Michaelis RC

    更新日期:2000-01-01 00:00:00

  • A Novel Autoantibody against Plexin D1 in Patients with Neuropathic Pain.

    abstract:OBJECTIVE:To identify novel autoantibodies for neuropathic pain (NeP). METHODS:We screened autoantibodies that selectively bind to mouse unmyelinated C-fiber type dorsal root ganglion (DRG) neurons using tissue-based indirect immunofluorescence assays (IFA) with sera from 110 NeP patients with various inflammatory and...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25279

    authors: Fujii T,Yamasaki R,Iinuma K,Tsuchimoto D,Hayashi Y,Saitoh BY,Matsushita T,Kido MA,Aishima S,Nakanishi H,Nakabeppu Y,Kira JI

    更新日期:2018-08-01 00:00:00

  • Dopa-responsive parkinsonism phenotype of Machado-Joseph disease: confirmation of 14q CAG expansion.

    abstract::The subtype IV of Machado-Joseph disease (MJD), characterized by parkinsonism variably combined with ataxia, distal atrophy, and sensory loss, has been all but ignored in recent reports of MJD, including those describing the molecular biologic substrate of the disease. We have demonstrated expansion of the CAG trinucl...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410380422

    authors: Tuite PJ,Rogaeva EA,St George-Hyslop PH,Lang AE

    更新日期:1995-10-01 00:00:00

  • Ultrastructural, neurological, and glycosaminoglycan abnormalities in lowe's syndrome.

    abstract::The oculocerebrorenal syndrome (OCRS), Lowe's syndrome, is an X-linked, recessive disease characterized by mental retardation, congenital corneal abnormalities and cataracts, growth failure, rickets, osseous abnormalities, renal dysfunction with periodic acidosis, hypotonia, and areflexia. Ultrastructural studies of s...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410160109

    authors: Wisniewski KE,Kieras FJ,French JH,Houck GE Jr,Ramos PL

    更新日期:1984-07-01 00:00:00

  • Effects of treatment on long-term survivors with malignant astrocytomas.

    abstract::We reviewed the records of 160 consecutive patients with glioblastoma and anaplastic astrocytoma to evaluate the long-term consequences of radiation therapy and chemotherapy. We defined long-term survivors as those patients with glioblastoma or anaplastic astrocytoma who lived at least 100% longer than median survival...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410280614

    authors: Imperato JP,Paleologos NA,Vick NA

    更新日期:1990-12-01 00:00:00

  • Demyelination causes synaptic alterations in hippocampi from multiple sclerosis patients.

    abstract:OBJECTIVE:Multiple Sclerosis (MS) is an inflammatory demyelinating disease of the human central nervous system. Although the clinical impact of gray matter pathology in MS brains is unknown, 30 to 40% of MS patients demonstrate memory impairment. The molecular basis of this memory dysfunction has not yet been investiga...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22337

    authors: Dutta R,Chang A,Doud MK,Kidd GJ,Ribaudo MV,Young EA,Fox RJ,Staugaitis SM,Trapp BD

    更新日期:2011-03-01 00:00:00

  • Enzyme-linked immunosorbent assay for antibody against the nicotinic acetylcholine receptor in human myasthenia gravis.

    abstract::Antibody against acetylcholine receptor (AChR) of human skeletal muscle was measured using enzyme-linked immunosorbent assay and found in 23 (74%) of 31 Japanese patients with generalized myasthenia gravis. In 15 patients with generalized myasthenia gravis who had not undergone thymectomy and who were not receiving ad...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150214

    authors: Kawanami S,Tsuji R,Oda K

    更新日期:1984-02-01 00:00:00

  • Loss and atrophy of layer II entorhinal cortex neurons in elderly people with mild cognitive impairment.

    abstract::Layer II of the entorhinal cortex contains the cells of origin for the perforant path, plays a critical role in memory processing, and consistently degenerates in end-stage Alzheimer's disease. The extent to which neuron loss in layer II of entorhinal cortex is related to mild cognitive impairment without dementia has...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Kordower JH,Chu Y,Stebbins GT,DeKosky ST,Cochran EJ,Bennett D,Mufson EJ

    更新日期:2001-02-01 00:00:00

  • Recovery of hypermetria after a cerebellar stroke occurs as a multistage process.

    abstract::In a prospective study, we repeatedly recorded fast goal-directed wrist movements of 8 patients who had experienced an acute cerebellar hypermetria due to a stroke and who had subsequently recovered clinically. Movements and the associated agonist and antagonist electromyographic (EMG) activities were recorded before ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410380314

    authors: Manto M,Jacquy J,Hildebrand J,Godaux E

    更新日期:1995-09-01 00:00:00

  • Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: dihydrolipoamide acetyltransferase (E2) deficiency.

    abstract::Pyruvate dehydrogenase deficiency is a major cause of primary lactic acidosis and neurological dysfunction in infancy and early childhood. Most cases are caused by mutations in the X-linked gene for the E1alpha subunit of the complex. Mutations in DLAT, the gene encoding dihydrolipoamide acetyltransferase, the E2 core...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20550

    authors: Head RA,Brown RM,Zolkipli Z,Shahdadpuri R,King MD,Clayton PT,Brown GK

    更新日期:2005-08-01 00:00:00

  • Mitochondrial dysfunction in Parkinson's disease.

    abstract::This review discusses the etiology and pathogenesis of Parkinson's disease (PD). Mitochondrial respiratory failure and oxidative stress appear to be two major contributors to nigral neuronal death in PD. Complex I deficiency has been reported by several groups and appears to be one of the basic abnormalities responsib...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410440715

    authors: Mizuno Y,Yoshino H,Ikebe S,Hattori N,Kobayashi T,Shimoda-Matsubayashi S,Matsumine H,Kondo T

    更新日期:1998-09-01 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

  • Progressive loss of cortical acetylcholinesterase activity in association with cognitive decline in Alzheimer's disease: a positron emission tomography study.

    abstract::We measured brain acetylcholinesterase activity in 30 patients with Alzheimer's disease (AD) and 14 age-matched controls by positron emission tomography (PET) and using a carbon 11-labeled acetylcholine analogue. Seven AD patients had repeat PET scans. The k3 values were calculated as an index of acetylcholinesterase ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Shinotoh H,Namba H,Fukushi K,Nagatsuka S,Tanaka N,Aotsuka A,Ota T,Tanada S,Irie T

    更新日期:2000-08-01 00:00:00

  • Sensory discrimination capabilities in patients with focal hand dystonia.

    abstract::To explore the concept that dystonia may result from dysfunction of the sensory system, 14 patients with focal hand dystonia were tested during two somatosensory discrimination tasks. Compared with controls, patients had a higher threshold in a task involving discrimination of two electric stimuli closely related temp...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:

    authors: Bara-Jimenez W,Shelton P,Sanger TD,Hallett M

    更新日期:2000-03-01 00:00:00

  • Cortical activation pattern during saccadic eye movements in humans: localization by focal cerebral blood flow increases.

    abstract::Regional cerebral blood flow (rCBF) was measured in human subjects during saccadic eye movements by a 254-channel dynamic gamma camera. Focal rCBF increases were repeatedly observed in an area within the middle precentral and premotor regions which corresponds to the frontal eye field in humans. Our findings suggest t...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410050112

    authors: Melamed E,Larsen B

    更新日期:1979-01-01 00:00:00

  • Frontoparietal cognitive control of verbal memory recall in Alzheimer's disease.

    abstract:OBJECTIVE:Episodic memory retrieval is reliant upon cognitive control systems, of which 2 have been identified with functional neuroimaging: a cingulo-opercular salience network (SN) and a frontoparietal executive network (EN). In Alzheimer's disease (AD), pathology is distributed throughout higher-order cortices. The ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24199

    authors: Dhanjal NS,Wise RJ

    更新日期:2014-08-01 00:00:00

  • Differential effects of deep brain stimulation target on motor subtypes in Parkinson's disease.

    abstract:OBJECTIVE:The Veterans Administration Cooperative Studies Program #468, a multicenter study that randomized Parkinson's disease (PD) patients to either subthalamic nucleus (STN) or globus pallidus internus (GPi) deep brain stimulation (DBS), found that stimulation at either target provided similar overall motoric benef...

    journal_title:Annals of neurology

    pub_type: 杂志文章,多中心研究,随机对照试验

    doi:10.1002/ana.24374

    authors: Katz M,Luciano MS,Carlson K,Luo P,Marks WJ Jr,Larson PS,Starr PA,Follett KA,Weaver FM,Stern MB,Reda DJ,Ostrem JL,CSP 468 study group.

    更新日期:2015-04-01 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

  • The effect of metrizamide on the electroencephalogram: a prospective study in 61 patients.

    abstract::A prospective study was made of changes in the electroencephalogram after the use of metrizamide for myelography and posterior fossa cisternography in 61 patients (62 studies). The EEG changed in 21 patients (34%); 3 of these had had previously abnormal records, and the abnormalities were accentuated on the second rec...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410060308

    authors: Ropper AH,Chiappa KH,Young RR

    更新日期:1979-09-01 00:00:00

  • Associations between cerebrovascular risk factors and parkinson disease.

    abstract:OBJECTIVE:To determine whether cerebrovascular risk factors are associated with subsequent diagnoses of Parkinson disease, and whether these associations are similar in magnitude to those with subsequent diagnoses of Alzheimer disease. METHODS:This was a retrospective cohort study using claims data from a 5% random sa...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25564

    authors: Kummer BR,Diaz I,Wu X,Aaroe AE,Chen ML,Iadecola C,Kamel H,Navi BB

    更新日期:2019-10-01 00:00:00

  • Juvenile progressive dystonia: a new phenotype of GM2 gangliosidosis.

    abstract::A 10-year-old boy developed progressive dystonia and dementia. His symptoms had begun at age 2 1/2 years, and he had been unable to walk by 8 years. At age 10 he was severely dystonic, unable to use his hands to feed himself, and almost anarthric . He had dysphagia and urinary incontinence, and functioned at a 4-year-...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150408

    authors: Meek D,Wolfe LS,Andermann E,Andermann F

    更新日期:1984-04-01 00:00:00

  • A common pattern of persistent gene activation in human neocortical epileptic foci.

    abstract::Epilepsy is a disease of recurrent seizures that can develop after a wide range of brain insults. Although surgical resection of focal regions of seizure onset can result in clinical improvement, the molecular mechanisms that produce and maintain focal hyperexcitability are not understood. Here, we demonstrate a regio...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20633

    authors: Rakhade SN,Yao B,Ahmed S,Asano E,Beaumont TL,Shah AK,Draghici S,Krauss R,Chugani HT,Sood S,Loeb JA

    更新日期:2005-11-01 00:00:00

  • Stimulus rate determines regional brain blood flow in striate cortex.

    abstract::Intravenous bolus administration of oxygen 15-labeled water and positron emission tomography were used to measure changes in brain blood flow induced by two modes of photic stimuli over a wide range of repetition rates. These stimuli (patterned-flash and reversing checkerboard) were chosen in order to determine whethe...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410170315

    authors: Fox PT,Raichle ME

    更新日期:1985-03-01 00:00:00

  • Expanded disability status scale progression assessment heterogeneity in multiple sclerosis according to geographical areas.

    abstract::Using placebo data from 3 randomized multiple sclerosis (MS) trials with uniform inclusion criteria, we investigated heterogeneity of Expanded Disability Status Scale (EDSS) progression by geographical areas. Our analysis revealed a significantly lower EDSS progression in Eastern European countries (10.8%) compared wi...

    journal_title:Annals of neurology

    pub_type: 杂志文章,meta分析

    doi:10.1002/ana.25323

    authors: Bovis F,Signori A,Carmisciano L,Maietta I,Steinerman JR,Li T,Tansy AP,Sormani MP

    更新日期:2018-10-01 00:00:00