Differential changes in neurochemical markers of striatal dopamine nerve terminals in idiopathic Parkinson's disease.

Abstract:

:To determine the extent that different dopamine (DA) neuronal markers provide similar estimates of striatal (caudate and putamen) DA nerve terminal loss in idiopathic Parkinson's disease (PD), we compared, in postmortem striatum of 12 patients with PD and 10 matched controls, levels of five different DA neuronal markers. These markers included DA itself, three different estimates of the density of the DA transporter (DAT) ([3H])GBR 12,935 and [3H]WIN 35,428 binding; DAT protein immunoreactivity), and one estimate of the vesicular monoamine transporter (VMAT2; [3H]DTBZ binding). Striatal levels of all examined DA markers in PD were significantly intercorrelated. However, the magnitude of loss relative to controls was unequal (DAT protein = DA > [3H]WIN 35,428 > [3H]DTBZ > [3H]GBR 12, 935), with the differences more marked in the severely affected putamen. The less severe reduction of binding of the DAT/VMAT2 radioligands relative to DA and DAT protein could be explained by differential regulation/degeneration of different DA nerve terminal components or lack of specificity of the radioligands for the DA neuron. These postmortem data may help in interpretation of in vivo neuroimaging studies in PD in which only one radioligand is routinely employed.

journal_name

Neurology

journal_title

Neurology

authors

Wilson JM,Levey AI,Rajput A,Ang L,Guttman M,Shannak K,Niznik HB,Hornykiewicz O,Pifl C,Kish SJ

doi

10.1212/wnl.47.3.718

subject

Has Abstract

pub_date

1996-09-01 00:00:00

pages

718-26

issue

3

eissn

0028-3878

issn

1526-632X

journal_volume

47

pub_type

杂志文章
  • Myasthenia gravis activities of daily living profile.

    abstract::The authors have developed an MG activities of daily living (ADL) profile (MG-ADL)-a simple eight-question survey of MG symptoms. In 254 consecutive encounters with established MG patients, the authors compared scores from the MG-ADL to the quantitative MG score (QMG)-a standardized, reliable scale used in clinical tr...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.52.7.1487

    authors: Wolfe GI,Herbelin L,Nations SP,Foster B,Bryan WW,Barohn RJ

    更新日期:1999-04-22 00:00:00

  • Muscle acid protease activity in amyotrophic lateral sclerosis: correlation with clinical and pathologic features.

    abstract::Acid protease activity was increased in skeletal muscle of patients with ALS. The highest levels of activity were found in individuals with the clinically and histologically most affected muscle. High levels of proteolytic activity correlated with the extent of muscle atrophy, the presence of target fibers and the ove...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.32.8.901

    authors: Antel JP,Chelmicka-Schorr E,Sportiello M,Stefansson K,Wollmann RL,Arnason BG

    更新日期:1982-08-01 00:00:00

  • A family with different clinical forms of acid maltase deficiency (glycogenosis type II): biochemical and genetic studies.

    abstract::In the same family, the generalized or infantile form of acid maltase deficiency (glycogenosis type II, Pompe disease) and the muscular or adult-onset form affected different individuals. Autosomal-recessive inheritance for the two clinical forms was demonstrated in this family by assay of acid alpha-glucosidase in mu...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.31.10.1209

    authors: Loonen MC,Busch HF,Koster JF,Martin JJ,Niermeijer MF,Schram AW,Brouwer-Kelder B,Mekes W,Slee RG,Tager JM

    更新日期:1981-10-01 00:00:00

  • Risk factors for Alzheimer's disease: a case-control study.

    abstract::A case-control study was conducted to assess personal and family medical history and the appearance of Alzheimer's disease. We compared 98 men with clinically diagnosed Alzheimer's disease and 162 controls, matched by sex, year of birth, and town of residence. Family history of dementia and personal history of depress...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.37.10.1630

    authors: Shalat SL,Seltzer B,Pidcock C,Baker EL Jr

    更新日期:1987-10-01 00:00:00

  • Crossed cerebellar and uncrossed basal ganglia and thalamic diaschisis in Alzheimer's disease.

    abstract::We detected crossed cerebellar as well as uncrossed basal ganglia and thalamic diaschisis in Alzheimer's disease by positron emission tomography (PET) using 18F-fluorodeoxyglucose. We studied a series of 26 consecutive, clinically diagnosed Alzheimer cases, including 6 proven by later autopsy, and compared them with 9...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.39.4.541

    authors: Akiyama H,Harrop R,McGeer PL,Peppard R,McGeer EG

    更新日期:1989-04-01 00:00:00

  • Vestibular perception in patients with acquired ophthalmoplegia.

    abstract::Using a perceptual technique it is shown that patients with chronic external ophthalmoplegia have shortened vestibular responses. It is postulated that this is secondary to the retinal image slip experienced by these patients during head movements and a useful compensatory mechanism to suppress motion-induced sickness...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000067992.17185.60

    authors: Grunfeld EA,Shallo-Hoffmann JA,Cassidy L,Okada T,Faldon M,Acheson JF,Bronstein AM

    更新日期:2003-06-24 00:00:00

  • Influenza and myoglobinuria in brothers.

    abstract::Two adult brothers became ill within 48 hours of each other, and both had severe myoglobinuria. One brother died of oliguric renal failure. The other did not have renal failure and survived. Acute influenza A infection was documented serologically and from throat washings in the surviving brother, and by isolation of ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.29.3.340

    authors: Zamkoff K,Rosen N

    更新日期:1979-03-01 00:00:00

  • A family with Machado-Joseph disease, previously diagnosed as dentatorubral-pallidoluysian atrophy.

    abstract::We report a family with Machado-Joseph disease (MJD) that was previously diagnosed with dentatorubral-pallidoluysian atrophy (DRPLA), on the basis of the neuropathologic findings. Because the clinical and pathologic reevaluation strongly suggested a diagnosis of MJD, we conducted a genetic study in the family. Two pat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.46.4.1154

    authors: Sakai T,Antoku Y,Kawakami H,Maruyama H,Nakamura S,Tanaka K

    更新日期:1996-04-01 00:00:00

  • Brain functional connectivity network breakdown and restoration in blindness.

    abstract:OBJECTIVE:To characterize brain functional connectivity in subjects with prechiasmatic visual system damage and relate functional connectivity features to extent of vision loss. METHODS:In this case-control study, resting-state, eyes-closed EEG activity was recorded in patients with partial optic nerve damage (n = 15)...

    journal_title:Neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1212/WNL.0000000000000672

    authors: Bola M,Gall C,Moewes C,Fedorov A,Hinrichs H,Sabel BA

    更新日期:2014-08-05 00:00:00

  • Ophthalmologic features of Parkinson's disease.

    abstract::Patients with Parkinson's disease (PD) commonly complain of impaired visual function and difficulty reading, despite normal visual acuity. Although previous studies have evaluated contrast sensitivity, color vision, visuospatial processing, visual hallucinations, and ocular movements, none has systematically evaluated...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000103444.45882.d8

    authors: Biousse V,Skibell BC,Watts RL,Loupe DN,Drews-Botsch C,Newman NJ

    更新日期:2004-01-27 00:00:00

  • Sensory neuronopathy and Sjögren's syndrome: clinical and immunologic study of two patients.

    abstract::In two patients, a sensory neuronopathy was the initial presentation of Sjögren's syndrome. There was no systemic or peripheral nerve vasculitis. Immunochemical studies failed to demonstrate specific antibodies against the nervous system. These features suggest that the damage to the sensory neurons might not be media...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.38.10.1637

    authors: Graus F,Pou A,Kanterewicz E,Anderson NE

    更新日期:1988-10-01 00:00:00

  • Central nervous system disease in patients with systemic lupus erythematosus.

    abstract::Central nervous system (CNS) dysfunction in patients with systemic lupus erythematosus (SLE) is highly variable, although it is often described under a single heading of "neuropsychiatric" or "CNS" SLE. To clarify these CNS abnormalities, we studied 91 lupus patients, 63 of whom had CNS symptoms or signs, over 599 pat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.42.9.1649

    authors: Futrell N,Schultz LR,Millikan C

    更新日期:1992-09-01 00:00:00

  • Age-associated leukoaraiosis and cortical cholinergic deafferentation.

    abstract:OBJECTIVE:To investigate the relationship between age-associated MRI leukoaraiosis or white matter hyperintensities (WMH) and cortical acetylcholinesterase (AChE) activity. BACKGROUND:One possible mechanism of cognitive decline in elderly individuals with leukoaraiosis is disruption of cholinergic fibers by strategica...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181a187c6

    authors: Bohnen NI,Müller ML,Kuwabara H,Constantine GM,Studenski SA

    更新日期:2009-04-21 00:00:00

  • Absence of IgG1 response in the cerebrospinal fluid of relapsing neuromyelitis optica.

    abstract::The authors studied immunoglobulin (Ig) G subclasses in the CSF and sera of patients with relapsing neuromyelitis optica (RNMO) and typical multiple sclerosis (MS). Although the total IgG concentrations were elevated in the CSF of patients with RNMO and MS, IgG1% and IgG1 index were significantly elevated only in pati...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.62.1.144

    authors: Nakashima I,Fujihara K,Fujimori J,Narikawa K,Misu T,Itoyama Y

    更新日期:2004-01-13 00:00:00

  • Severity of REM atonia loss in idiopathic REM sleep behavior disorder predicts Parkinson disease.

    abstract:BACKGROUND:Over 50% of persons with idiopathic REM sleep behavior disorder (RBD) will develop Parkinson disease (PD) or dementia. At present, there is no way to predict who will develop disease. Since polysomnography is performed in all patients with idiopathic RBD at diagnosis, there is an opportunity to analyze if ba...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181ca0166

    authors: Postuma RB,Gagnon JF,Rompré S,Montplaisir JY

    更新日期:2010-01-19 00:00:00

  • Prevalence of mild cognitive impairment is higher in men. The Mayo Clinic Study of Aging.

    abstract:OBJECTIVE:We investigated the prevalence of mild cognitive impairment (MCI) in Olmsted County, MN, using in-person evaluations and published criteria. METHODS:We evaluated an age- and sex-stratified random sample of Olmsted County residents who were 70-89 years old on October 1, 2004, using the Clinical Dementia Ratin...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181f11d85

    authors: Petersen RC,Roberts RO,Knopman DS,Geda YE,Cha RH,Pankratz VS,Boeve BF,Tangalos EG,Ivnik RJ,Rocca WA

    更新日期:2010-09-07 00:00:00

  • Isoniazid for tremor in multiple sclerosis: a controlled trial.

    abstract::We evaluated the effects of isoniazid on tremor in 13 patients with MS. Patients were evaluated before treatment, after 1 month of therapy (1,000 mg daily), and 1 month after the last dose. Ten patients improved on at least one of three methods of evaluation. Transient side effects were common, possibly because there ...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章

    doi:10.1212/wnl.35.12.1772

    authors: Duquette P,Pleines J,du Souich P

    更新日期:1985-12-01 00:00:00

  • Obstacles in the diagnosis and treatment of syphilitic amyotrophy.

    abstract::The authors describe a case of syphilitic amyotrophy in a 37-year-old man presenting with subacute progressive painless weakness in the right arm. Syphilitic amyotrophy is still an existing differential diagnosis of painless and progressive weakness. The authors explore potential obstacles in the diagnostic workup and...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000046584.72672.d3

    authors: Etgen T,Bischoff C,Resch M,Winbeck K,Conrad B,Sander D

    更新日期:2003-02-11 00:00:00

  • Prevalence and patterns of cognitive impairment in sporadic ALS.

    abstract:OBJECTIVE:To investigate the prevalence and nature of cognitive changes associated with sporadic amyotrophic lateral sclerosis (ALS) using a large scale study. METHODS:Consecutive patients with sporadic ALS (n = 279) underwent comprehensive neurologic evaluation and neuropsychological testing. Testing data from normal...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000172911.39167.b6

    authors: Ringholz GM,Appel SH,Bradshaw M,Cooke NA,Mosnik DM,Schulz PE

    更新日期:2005-08-23 00:00:00

  • Utilization of unconventional treatments by persons with MS: is it alternative or complementary?

    abstract::This cross-sectional mail survey evaluated the prevalence and predictors of unconventional therapy (UT) utilization among 569 community-based people with MS. One-third reported having visited a UT practitioner in the last 6 months. Utilizers tended to report at least one medical comorbidity, earn at least $50,000 a ye...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.52.3.626

    authors: Schwartz CE,Laitin E,Brotman S,LaRocca N

    更新日期:1999-02-01 00:00:00

  • Altered functional connectivity in the motor network after traumatic brain injury.

    abstract:BACKGROUND:A large proportion of survivors of traumatic brain injury (TBI) have persistent cognitive impairments, the profile of which does not always correspond to the size and location of injuries. One possible explanation could be that TBI-induced damage extends beyond obvious lesion sites to affect remote brain net...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e3181e7ca58

    authors: Kasahara M,Menon DK,Salmond CH,Outtrim JG,Taylor Tavares JV,Carpenter TA,Pickard JD,Sahakian BJ,Stamatakis EA

    更新日期:2010-07-13 00:00:00

  • The use of "clinic room" presentation as an educational tool in the ambulatory care setting.

    abstract:OBJECTIVE:To evaluate the utility of "clinic room" case presentation in the ambulatory care setting. BACKGROUND:Neurology is increasingly an outpatient specialty. The transition from ward to clinic presents challenges for student and resident education. Interaction between attending physician and trainee is limited by...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:

    authors: Smith AG,Bromberg MB,Singleton JR,Forshew DA

    更新日期:1999-01-15 00:00:00

  • Incidence and prevalence of intracranial vascular malformations in Olmsted County, Minnesota, 1965 to 1992.

    abstract::We used the Mayo Clinic medical records linkage system to detect all cases of intracranial vascular malformation (IVM) among residents of Olmsted County, Minnesota from 1965 to 1992 and found 48 IVMs over the 27-year period, including four patients with IVM detected at autopsy, without prior symptoms. Twenty-nine of 4...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.46.4.949

    authors: Brown RD Jr,Wiebers DO,Torner JC,O'Fallon WM

    更新日期:1996-04-01 00:00:00

  • Prevalence and severity of dementia among northern Italian centenarians.

    abstract::Using diagnostic criteria from the fourth edition of the Diagnostic and Statistical Manual of Mental Disorders, dementia was clinically diagnosed in 57 (62%) of 92 centenarians living in two northern Italian provinces. The condition was severely disabling in approximately 70% of the demented patients. Although clinica...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.53.2.416

    authors: Ravaglia G,Forti P,De Ronchi D,Maioli F,Nesi B,Cucinotta D,Bernardi M,Cavalli G

    更新日期:1999-07-22 00:00:00

  • Treatment of pseudobulbar affect in ALS with dextromethorphan/quinidine: a randomized trial.

    abstract:BACKGROUND:Patients with ALS commonly exhibit pseudobulbar affect. METHODS:The authors conducted a multicenter, randomized, double-blind, controlled, parallel, three-arm study to test a defined combination of dextromethorphan hydrobromide (DM) and quinidine sulfate (Q) (AVP-923) for the treatment of pseudobulbar affec...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章,多中心研究,随机对照试验

    doi:10.1212/01.wnl.0000142042.50528.2f

    authors: Brooks BR,Thisted RA,Appel SH,Bradley WG,Olney RK,Berg JE,Pope LE,Smith RA,AVP-923 ALS Study Group.

    更新日期:2004-10-26 00:00:00

  • Bioavailability of interferon beta 1b in MS patients with and without neutralizing antibodies.

    abstract:BACKGROUND:Neutralizing antibodies (NAB) to interferon beta (IFNbeta) occur in about one-third of MS patients treated with IFNbeta-1b and there is an association with a loss of clinical and MRI efficacy. However, there are no data regarding the bioavailability of IFNbeta-1b in patients with and without NAB. METHODS:Th...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.52.6.1239

    authors: Deisenhammer F,Reindl M,Harvey J,Gasse T,Dilitz E,Berger T

    更新日期:1999-04-12 00:00:00

  • Relative effect of APOE ε4 on neuroimaging biomarker changes across the lifespan.

    abstract:OBJECTIVE:To provide a comprehensive understanding of APOE ε4 effects across the lifespan on the 3 main neuroimaging biomarkers. METHODS:Two hundred seven community-dwelling, cognitively normal APOE ε4 carriers and noncarriers aged 20-87 years were involved in this study. They underwent structural MRI, fluorodeoxygluc...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章

    doi:10.1212/WNL.0000000000003234

    authors: Gonneaud J,Arenaza-Urquijo EM,Fouquet M,Perrotin A,Fradin S,de La Sayette V,Eustache F,Chételat G

    更新日期:2016-10-18 00:00:00

  • Electroclinical features of absence seizures in childhood absence epilepsy.

    abstract:OBJECTIVE:To accurately define the electroclinical features of absence seizures in children with newly diagnosed, untreated childhood absence epilepsy (CAE). METHODS:The authors searched an EEG database for absence seizures in normal children with new onset untreated absence epilepsy. Seventy consecutive children were...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000228257.60184.82

    authors: Sadleir LG,Farrell K,Smith S,Connolly MB,Scheffer IE

    更新日期:2006-08-08 00:00:00

  • The lower hippocampus global connectivity, the higher its local metabolism in Alzheimer disease.

    abstract:OBJECTIVES:Based on the hippocampus disconnection hypothesis in Alzheimer disease (AD), which postulates that uncoupling from cortical inputs contributes to disinhibition-like changes in hippocampus activity, we suggested that in patients with AD, the more the intrinsic functional connectivity between hippocampus and p...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000001575

    authors: Tahmasian M,Pasquini L,Scherr M,Meng C,Förster S,Mulej Bratec S,Shi K,Yakushev I,Schwaiger M,Grimmer T,Diehl-Schmid J,Riedl V,Sorg C,Drzezga A

    更新日期:2015-05-12 00:00:00

  • Frequency and risk factors of antibody-induced secondary failure of botulinum neurotoxin therapy.

    abstract:OBJECTIVE:To investigate the risk factors of neutralizing antibody (NAB)-induced complete secondary treatment failure (cSTF) during long-term botulinum neurotoxin (BoNT) treatment in various neurologic indications. METHODS:This monocenter retrospective cohort study analyzed the data of 471 patients started on BoNT the...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000009444

    authors: Walter U,Mühlenhoff C,Benecke R,Dressler D,Mix E,Alt J,Wittstock M,Dudesek A,Storch A,Kamm C

    更新日期:2020-05-19 00:00:00