Autopsy validation of 123I-FP-CIT dopaminergic neuroimaging for the diagnosis of DLB.

Abstract:

OBJECTIVE:To conduct a validation study of 123I-N-fluoropropyl-2b-carbomethoxy-3b-(4-iodophenyl) nortropane (123I-FP-CIT) SPECT dopaminergic imaging in the clinical diagnosis of dementia with Lewy bodies (DLB) with autopsy as the gold standard. METHODS:Patients >60 years of age with dementia who had undergone 123I-FP-CIT imaging in research studies and who had donated their brain tissue to the Newcastle Brain Tissue Resource were included. All had structured clinical research assessments, and clinical diagnoses were applied by consensus panels using international diagnostic criteria. All underwent 123I-FP-CIT imaging at baseline, and scans were rated as normal or abnormal by blinded raters. Patients were reviewed in prospective studies and after death underwent detailed autopsy assessment, and neuropathologic diagnoses were applied with the use of standard international criteria. RESULTS:Fifty-five patients (33 with DLB and 22 with Alzheimer disease) were included. Against autopsy diagnosis, 123I-FP-CIT had a balanced diagnostic accuracy of 86% (sensitivity 80%, specificity 92%) compared with clinical diagnosis, which had an accuracy of 79% (sensitivity 87%, specificity 72%). Among patients with DLB, 10% (3 patients) met pathologic criteria for Lewy body disease but had normal 123I-FP-CIT imaging. CONCLUSIONS:This large autopsy analysis of 123I-FP-CIT imaging in dementia demonstrates that it is a valid and accurate biomarker for DLB, and the high specificity compared with clinical diagnosis (20% higher) is clinically important. The results need to be replicated with patients recruited from a wider range of settings, including movement disorder clinics and general practice. While an abnormal 123I-FP-CIT scan strongly supports Lewy body disease, a normal scan does not exclude DLB with minimal brainstem involvement. CLASSIFICATION OF EVIDENCE:This study provides Class I evidence that 123I-FP-CIT dopaminergic neuroimaging accurately identifies patients with DLB.

journal_name

Neurology

journal_title

Neurology

authors

Thomas AJ,Attems J,Colloby SJ,O'Brien JT,McKeith I,Walker R,Lee L,Burn D,Lett DJ,Walker Z

doi

10.1212/WNL.0000000000003512

subject

Has Abstract

pub_date

2017-01-17 00:00:00

pages

276-283

issue

3

eissn

0028-3878

issn

1526-632X

pii

WNL.0000000000003512

journal_volume

88

pub_type

杂志文章
  • Hearing impairment in essential tremor.

    abstract:OBJECTIVE:To assess hearing in patients with essential tremor (ET) vs patients with Parkinson disease (PD) and normal controls. METHODS:The authors assessed demographic and clinical information including use of hearing aids in 250 patients with ET, 127 patients with PD, and 127 normal controls. The authors administere...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000086376.40750.af

    authors: Ondo WG,Sutton L,Dat Vuong K,Lai D,Jankovic J

    更新日期:2003-10-28 00:00:00

  • Lyme neuroborreliosis: central nervous system manifestations.

    abstract::We evaluated 85 patients with serologic evidence of Borrelia burgdorferi infection. Manifestations included encephalopathy (41), neuropathy (27), meningitis (2), multiple sclerosis (MS) (6), and psychiatric disorders (3). We performed lumbar punctures in 53, brain MRI in 33, and evoked potentials (EPs) in 33. Only pat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.39.6.753

    authors: Halperin JJ,Luft BJ,Anand AK,Roque CT,Alvarez O,Volkman DJ,Dattwyler RJ

    更新日期:1989-06-01 00:00:00

  • Effects of breastfeeding in children of women taking antiepileptic drugs.

    abstract:BACKGROUND:Breastfeeding is known to have beneficial effects, but there is concern that breastfeeding during antiepileptic drug (AED) therapy may be harmful to cognitive development. Animal and human studies have demonstrated that some AEDs can adversely affect the immature brain. However, no investigation has examined...

    journal_title:Neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1212/WNL.0b013e3181ffe4a9

    authors: Meador KJ,Baker GA,Browning N,Clayton-Smith J,Combs-Cantrell DT,Cohen M,Kalayjian LA,Kanner A,Liporace JD,Pennell PB,Privitera M,Loring DW,NEAD Study Group.

    更新日期:2010-11-30 00:00:00

  • Plasma exchange and immunosuppressive drug treatment in the Lambert-Eaton myasthenic syndrome.

    abstract::We undertook serial clinical and electromyographic muscle action potential (MAP) amplitude assessments in nine patients with the Lambert-Eaton myasthenic syndrome (LEMS) over 0.5 to 2.5 years who received plasma exchange (PE; 5 to 15 exchanges over 4 to 19 days) and immunosuppressive drug (IS) treatment (prednisolone ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.34.4.480

    authors: Newsom-Davis J,Murray NM

    更新日期:1984-04-01 00:00:00

  • Localization of idiopathic generalized epilepsy on chromosome 6p in families of juvenile myoclonic epilepsy patients.

    abstract::Juvenile myoclonic epilepsy (JME) is a distinct subform of idiopathic generalized epilepsy of adolescence. Linkage studies with Bf and serologic HLA markers in families of JME patients have shown a tight linkage on chromosome 6. We present a linkage analysis with HLA-DQ restriction fragment length polymorphisms on mor...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.41.10.1651

    authors: Durner M,Sander T,Greenberg DA,Johnson K,Beck-Mannagetta G,Janz D

    更新日期:1991-10-01 00:00:00

  • Sturge-Weber syndrome: indications and results of surgery in 20 patients.

    abstract:OBJECTIVE:To discuss the indications and timing for resective surgery in patients with Sturge-Weber syndrome (SWS) and medication-resistant epilepsy. BACKGROUND:SWS that causes epilepsy severe enough to merit surgery is rare. Because of the variable natural history of the disease, it is difficult to establish clear-cu...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.55.10.1472

    authors: Arzimanoglou AA,Andermann F,Aicardi J,Sainte-Rose C,Beaulieu MA,Villemure JG,Olivier A,Rasmussen T

    更新日期:2000-11-28 00:00:00

  • Caffeinated clues and the promise of adenosine A(2A) antagonists in PD.

    abstract::Large prospective epidemiologic studies have linked the consumption of coffee and other caffeinated beverages to a reduced risk of subsequently developing PD. Caffeine as well as more specific antagonists of the adenosine A(2A) receptor have also now been found to attenuate neurotoxicity in a mouse model of PD. The co...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.58.8.1154

    authors: Schwarzschild MA,Chen JF,Ascherio A

    更新日期:2002-04-23 00:00:00

  • Optical coherence tomography is highly sensitive in detecting prior optic neuritis.

    abstract:OBJECTIVE:To explore sensitivity of optical coherence tomography (OCT) in detecting prior unilateral optic neuritis. METHODS:This is a retrospective, observational clinical study of all patients who presented from January 1, 2014, to January 6, 2017, with unilateral optic neuritis and OCT available at least 3 months a...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000006873

    authors: Xu SC,Kardon RH,Leavitt JA,Flanagan EP,Pittock SJ,Chen JJ

    更新日期:2019-02-05 00:00:00

  • Mild cognitive impairment in the oldest old.

    abstract:BACKGROUND:No data exist on whether the syndrome of amnestic mild cognitive impairment occurs in the oldest old, or if the relationships for functional status and neuropsychometric performance based on clinical diagnosis hold true in this age group. DESIGN/METHODS:The authors performed comprehensive neurologic evaluat...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.60.3.477

    authors: Boeve B,McCormick J,Smith G,Ferman T,Rummans T,Carpenter T,Ivnik R,Kokmen E,Tangalos E,Edland S,Knopman D,Petersen R

    更新日期:2003-02-11 00:00:00

  • Episodic paroxysmal hemicrania: two new cases and a literature review.

    abstract::Episodic paroxysmal hemicrania (EPH) is a rare disorder characterized by discrete bouts of hemicranial headache separated by headache-free remissions. Although EPH resembles episodic cluster headache in the location and quality of pain as well as the pattern of associated autonomic features, it is distinguished by the...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/wnl.42.5.964

    authors: Newman LC,Gordon ML,Lipton RB,Kanner R,Solomon S

    更新日期:1992-05-01 00:00:00

  • A novel locus for hereditary spastic paraplegia with thin corpus callosum and epilepsy.

    abstract:BACKGROUND:Hereditary spastic paraplegia (HSP) are classified clinically as pure when progressive spasticity occurs in isolation or complicated when other neurologic abnormalities are present. At least 22 genetic loci have been linked to HSP, 8 of which are autosomal recessive (ARHSP). HSP complicated with the presence...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/01.wnl.0000208501.52849.dd

    authors: Al-Yahyaee S,Al-Gazali LI,De Jonghe P,Al-Barwany H,Al-Kindi M,De Vriendt E,Chand P,Koul R,Jacob PC,Gururaj A,Sztriha L,Parrado A,Van Broeckhoven C,Bayoumi RA

    更新日期:2006-04-25 00:00:00

  • Effects of weight loss on the course of idiopathic intracranial hypertension in women.

    abstract:OBJECTIVE:To determine the role of weight loss in the treatment of idiopathic intracranial hypertension (IIH) in obese women. METHODS:Chart review of 250 patients with suspected IIH revealed 58 women who met our criteria, did not undergo early surgical intervention, and had adequate documentation of visual status, pap...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.50.4.1094

    authors: Kupersmith MJ,Gamell L,Turbin R,Peck V,Spiegel P,Wall M

    更新日期:1998-04-01 00:00:00

  • Serum elements and oxidative status in clinically isolated syndromes: imbalance and predictivity.

    abstract:BACKGROUND:Metals are suspected of being involved in the pathogenesis of various neurologic diseases. We previously found a complex imbalance in serum chemical elements and oxidative status in patients with clinically definite multiple sclerosis (CDMS). OBJECTIVE:To understand whether this imbalance affects people wit...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31820af7de

    authors: Ristori G,Brescianini S,Pino A,Visconti A,Vittori D,Coarelli G,Cotichini R,Bocca B,Forte G,Pozzilli C,Pestalozza I,Stazi MA,Alimonti A,Salvetti M

    更新日期:2011-02-08 00:00:00

  • Fulminant encephalopathy with basal ganglia hyperintensities in HIV-infected drug users.

    abstract:OBJECTIVE:To define a clinical syndrome associated with active drug abuse in HIV-infected individuals. METHODS:We performed a retrospective review to identify individuals treated at the Johns Hopkins Hospital from 1993 to 2008 who were HIV-infected and were actively abusing drugs and had bilateral basal ganglia lesion...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0b013e31820e7b4e

    authors: Newsome SD,Johnson E,Pardo C,McArthur JC,Nath A

    更新日期:2011-03-01 00:00:00

  • The Wernicke area: Modern evidence and a reinterpretation.

    abstract::The term "Wernicke's area" is most often used as an anatomical label for the gyri forming the lower posterior left sylvian fissure. Although traditionally this region was held to support language comprehension, modern imaging and neuropsychological studies converge on the conclusion that this region plays a much large...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:10.1212/WNL.0000000000002219

    authors: Binder JR

    更新日期:2015-12-15 00:00:00

  • Predictors of outcome after anterior temporal lobectomy: the intracarotid amobarbital test.

    abstract::The intracarotid amobarbital test (IAT) examines hemispheric memory and language. We set out to determine whether memory performance on the IAT correlated with seizure relief after anterior temporal lobectomy in 117 patients with refractory epilepsy. The IAT assessed recognition memory performance for nine items with ...

    journal_title:Neurology

    pub_type: 临床试验,杂志文章

    doi:10.1212/wnl.44.12.2325

    authors: Sperling MR,Saykin AJ,Glosser G,Moran M,French JA,Brooks M,O'Connor MJ

    更新日期:1994-12-01 00:00:00

  • Multisequence MRI in clinically isolated syndromes and the early development of MS.

    abstract:OBJECTIVE:To apply multisequence MRI techniques to patients with clinically isolated syndromes, to document the pattern and frequency of abnormalities at baseline and early follow-up, and to determine their predictive values for the early development of clinical MS. BACKGROUND:Disseminated lesions on T2-weighted brain...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.53.6.1184

    authors: Brex PA,O'Riordan JI,Miszkiel KA,Moseley IF,Thompson AJ,Plant GT,Miller DH

    更新日期:1999-10-12 00:00:00

  • Mechanisms of action of anticonvulsant agents.

    abstract::Systematic screening of many compounds in animal models led to identification of the established antiepileptic drugs (AEDs). By contrast, the newer AEDs were specifically designed to enhance an inhibitory process or to inhibit a specific excitatory pathway. However, it was later discovered that some of the designed dr...

    journal_title:Neurology

    pub_type: 杂志文章,评审

    doi:

    authors: Moshé SL

    更新日期:2000-01-01 00:00:00

  • Prospective observational cohort study of early recurrent TIA: Features, frequency, and outcome.

    abstract:OBJECTIVES:To evaluate the frequency, clinical and etiologic features, and short- and long-term outcomes of early recurrent TIA. METHODS:This prospective observational cohort study enrolled all consecutive patients with TIA referred to our emergency department and diagnosed by a vascular neurologist. Expedited assessm...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000010317

    authors: Foschi M,Pavolucci L,Rondelli F,Spinardi L,Favaretto E,Filippini M,Degli Esposti D,Strocchi E,Faggioli G,Cortelli P,Guarino M,Bologna TIA Study-Group.

    更新日期:2020-09-22 00:00:00

  • 18F-FDG-PET correlates of cognitive impairment in ALS.

    abstract:OBJECTIVE:To identify the metabolic signature of the various levels of cognitive deficits in amyotrophic lateral sclerosis (ALS) using 18F-2-fluoro-2-deoxy-d-glucose-PET (18F-FDG-PET). METHODS:A total of 170 ALS cases consecutively enrolled at the ALS Center of Turin underwent brain 18F-FDG-PET and were classified as ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000002242

    authors: Canosa A,Pagani M,Cistaro A,Montuschi A,Iazzolino B,Fania P,Cammarosano S,Ilardi A,Moglia C,Calvo A,Chiò A

    更新日期:2016-01-05 00:00:00

  • Lambert-Eaton myasthenic syndrome: electrodiagnostic findings and response to treatment.

    abstract::The authors reviewed the incidence of cancer, repetitive nerve stimulation findings, and response to treatment in 73 patients with Lambert-Eaton myasthenic syndrome. Thirty-one patients (42%) had lung cancer, 29 small cell. Doubling of the compound motor action potential amplitude in three tested distal muscles was se...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.11.2176

    authors: Tim RW,Massey JM,Sanders DB

    更新日期:2000-06-13 00:00:00

  • Familial 'sleep apnea plus' syndrome: report of a family.

    abstract::We describe a familial disorder consisting of sleep apnea, anosmia, colorblindness, partial complex seizures, and cognitive dysfunction. The phenotypic expression of the syndrome suggests an autosomal dominant inheritance with incomplete penetrance. ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.38.2.190

    authors: Manon-Espaillat R,Gothe B,Adams N,Newman C,Ruff R

    更新日期:1988-02-01 00:00:00

  • Identification of new and common mutations in the EPM2A gene in Lafora disease.

    abstract::Lafora disease is a teenage onset progressive myoclonus epilepsy caused by mutations in the EPM2A gene. In this report, we describe new mutations within EPM2A, review the known mutations to date to identify the most common, and describe three simple tests for prenatal and carrier screening. ...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.54.2.488

    authors: Minassian BA,Ianzano L,Delgado-Escueta AV,Scherer SW

    更新日期:2000-01-25 00:00:00

  • Headache types and panic disorder: directionality and specificity.

    abstract:OBJECTIVE:To examine the relationship of migraine and other severe headaches with panic disorder. METHODS:Representative samples of persons with migraine, non-migrainous severe headaches, and controls with no history of severe headaches, identified by a telephone survey, were interviewed in person, using a standardize...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.3.350

    authors: Breslau N,Schultz LR,Stewart WF,Lipton R,Welch KM

    更新日期:2001-02-13 00:00:00

  • Disease progression in sporadic inclusion body myositis: observations in 78 patients.

    abstract::Functional decline for each decade at symptom onset and need for cane, walker, or wheelchair were assessed in 78 biopsy-proved patients with sporadic inclusion body myositis. Patients with disease onset between 40 and 59 years used a walker after 10.2 +/- 5.8 years, whereas those with disease onset between 60 and 79 y...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.55.2.296

    authors: Peng A,Koffman BM,Malley JD,Dalakas MC

    更新日期:2000-07-25 00:00:00

  • CSF detection of the 14-3-3 protein in unselected patients with dementia.

    abstract:OBJECTIVE:To determine the usefulness of the 14-3-3 test in patients with dementia of various causes. BACKGROUND:Recent reports have suggested that the detection of the 14-3-3 protein in the CSF of patients with Creutzfeldt--Jakob disease is a highly sensitive and specific marker of the disease that might be used as a...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.56.11.1528

    authors: Burkhard PR,Sanchez JC,Landis T,Hochstrasser DF

    更新日期:2001-06-12 00:00:00

  • MRI in patients with suspected vascular parkinsonism.

    abstract::To determine whether MRI can reveal more vascular lesions in patients clinically suspected of having vascular parkinsonism, we compared 15 such patients with 15 patients who had idiopathic Parkinson's disease and 10 hypertensive controls. Patients with suspected vascular parkinsonism had significantly more subcortical...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.45.12.2183

    authors: Zijlmans JC,Thijssen HO,Vogels OJ,Kremer HP,Poels PJ,Schoonderwaldt HC,Merx JL,van 't Hof MA,Thien T,Horstink MW

    更新日期:1995-12-01 00:00:00

  • Sex disparities in access to caregiving in Parkinson disease.

    abstract:OBJECTIVE:To compare access to caregiving between men and women with Parkinson disease (PD). METHODS:This was a cross-sectional and longitudinal study among participants with PD enrolled in the National Parkinson Foundation Parkinson's Outcomes Project from 2009 to 2014 at 21 international sites. The primary outcome m...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/WNL.0000000000004764

    authors: Dahodwala N,Shah K,He Y,Wu SS,Schmidt P,Cubillos F,Willis AW

    更新日期:2018-01-02 00:00:00

  • Hereditary dystonia-parkinsonism syndrome of juvenile onset.

    abstract::We studied a family with an extrapyramidal disorder characterized by childhood onset of lower-limb and axial dystonia, followed by parkinsonism. Dramatic response to levodopa therapy and minimal progression in adult life was seen. The family included five generations of affected members of both sexes in an autosomal d...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.36.11.1424

    authors: Nygaard TG,Duvoisin RC

    更新日期:1986-11-01 00:00:00

  • A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy.

    abstract:OBJECTIVES:Laminin alpha2 deficiency presents at birth with muscle weakness, hypotonia, and usually asymptomatic white matter signal on MRI. Few patients with laminin alpha2 deficiency have been described with seizures and structural brain abnormalities. The reason for the variation in the severity of the clinical phen...

    journal_title:Neurology

    pub_type: 杂志文章

    doi:10.1212/wnl.55.8.1128

    authors: Pegoraro E,Fanin M,Trevisan CP,Angelini C,Hoffman EP

    更新日期:2000-10-24 00:00:00