Subjects at risk of Parkinson's disease in health checkup examinees: cross-sectional analysis of baseline data of the NaT-PROBE study.

Abstract:

INTRODUCTION:The present study aimed to survey the prevalence of prodromal symptoms of Parkinson's disease (PD) in Japanese health checkup examinees, for identifying at-risk subjects. METHODS:We conducted a questionnaire survey of annual health checkup examinees without neurological symptoms using the following self-reported questionnaires: Japanese version of the Scale for Outcomes in Parkinson's disease for Autonomic Symptoms (SCOPA-AUT); Self-administered Odor Question (SAOQ); REM Sleep Behavior Disorder Screening Scale (RBDSQ); Beck Depression Inventory-Second Edition (BDI-II); Epworth Sleepiness Scale (ESS); and Physical Activity Scale for the Elderly (PASE). The presence of prodromal symptoms was determined using the 90th percentile threshold of each questionnaire. Subjects ≥ 50 years of age with ≥ 2 core prodromal symptoms (dysautonomia, hyposmia, and RBD), were classified as at risk. RESULTS:Between March 2017 and March 2018, 4,953 participants sufficiently answered the questionnaires. Among 2,726 subjects ≥ 50 years of age, 155 were classified as at risk. These subjects had worse values of BDI-II (12.0 ± 8.3 vs. 4.4 ± 3.8, p < 0.001) and ESS (9.6 ± 5.0 vs. 6.3 ± 3.2, p < 0.001), in addition to SCOPA-AUT, SAOQ, and RBDSQ. Male at-risk subjects showed lower values of hemoglobin (14.8 ± 1.3 vs. 15.0 ± 1.1, p = 0.032) and low density lipoprotein cholesterol (114.5 ± 30.3 vs. 123.0 ± 28.9, p = 0.004) than the examinees reporting no prodromal symptoms. CONCLUSION:Approximately 6% of the population aged 50 years or older was at risk for PD. Male at-risk subjects had mild hematological and metabolic changes relevant to PD.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Hattori M,Tsuboi T,Yokoi K,Tanaka Y,Sato M,Suzuki K,Arahata Y,Hori A,Kawashima M,Hirakawa A,Washimi Y,Watanabe H,Katsuno M

doi

10.1007/s00415-020-09714-6

subject

Has Abstract

pub_date

2020-05-01 00:00:00

pages

1516-1526

issue

5

eissn

0340-5354

issn

1432-1459

pii

10.1007/s00415-020-09714-6

journal_volume

267

pub_type

杂志文章
  • Dissections after childbirth.

    abstract::The occurrence of spontaneous internal carotid or vertebral artery dissection after childbirth remains rare. To our knowledge, seven cases of arterial dissection in the postpartum period have been described in the literature as single case reports. We report four additional cases of internal carotid and vertebral arte...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s004150050437

    authors: Gasecki AP,Kwiecinski H,Lyrer PA,Lynch TG,Baxter T

    更新日期:1999-08-01 00:00:00

  • The neurological update: therapies for cerebellar ataxias in 2020.

    abstract::Cerebellar ataxias (CAs) represent a heterogeneous group of sporadic or inherited disorders. The clinical spectrum of CAs is continuously expanding. Our understanding of the mechanisms leading to the clinical deficits has improved over these last decades, in particular thanks to progress in genetics, neuroimaging and ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-020-09717-3

    authors: Gandini J,Manto M,Bremova-Ertl T,Feil K,Strupp M

    更新日期:2020-04-01 00:00:00

  • Normalized grip strength is a sensitive outcome measure through all stages of Duchenne muscular dystrophy.

    abstract:OBJECTIVE:The main aim was to explore the changes in hand-grip strength in patients with Duchenne muscular dystrophy (DMD) aged 5-29 years. Secondary aims were to test the effect of mutation, ambulatory status and glucocorticoid use on grip strength and its changes over time and to compute the number of subjects needed...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-09800-9

    authors: Hogrel JY,Decostre V,Ledoux I,de Antonio M,Niks EH,de Groot I,Straub V,Muntoni F,Ricotti V,Voit T,Seferian A,Gidaro T,Servais L

    更新日期:2020-07-01 00:00:00

  • A morphological and chemical study of calcification of the pineal gland.

    abstract::A general scheme of analysis for the investigation of minute calcification is presented. After low temperature ashing, the samples are subjected to chemical, structural and morphological study, using atomic absorption spectrometry, infrared spectrometry, X-ray diffraction and scanning electron microscopy. Details abou...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00312479

    authors: Michotte Y,Lowenthal A,Knaepen L,Collard M,Massart DL

    更新日期:1977-06-13 00:00:00

  • Neutral lipid and sphingolipid composition of the brain of a patient with membranous lipodystrophy.

    abstract::Lipids were extracted from brains of a patient with membranous lipodystrophy (ML) and three normal patients and the neutral lipid and sphingolipid constituents were investigated. The storage of a large amount of free fatty acid was observed in the ML brain, but no cholesterol ester was found. Total lipid, cholesterol ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313947

    authors: Ohtani Y,Miura S,Tamai Y,Kojima H,Kashima H

    更新日期:1979-03-22 00:00:00

  • Cerebrospinal fluid proteins and cells in normal-pressure hydrocephalus.

    abstract::A total of 21 patients with normal-pressure hydrocephalus were examined. Cerebrospinal fluid (CSF) was collected before and after operation with a ventriculoperitoneal shunt. A slight plasma-like protein pattern indicating a blood-brain barrier (BBB) dysfunction was seen in 38% of the patients before operation. No cha...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313729

    authors: Wikkelsø C,Blomstrand C

    更新日期:1982-01-01 00:00:00

  • A role for cannabinoids in the treatment of myotonia? Report of compassionate use in a small cohort of patients.

    abstract:BACKGROUND:The symptomatic treatment of myotonia and myalgia in patients with dystrophic and non-dystrophic myotonias is often not satisfactory. Some patients anecdotally report symptoms' relief through consumption of cannabis. METHODS:A combination of cannabidiol and tetrahydrocannabinol (CBD/THC) was prescribed as c...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-019-09593-6

    authors: Montagnese F,Stahl K,Wenninger S,Schoser B

    更新日期:2020-02-01 00:00:00

  • Reversible abnormal functional neuroimaging presentations in polycythemia vera with chorea.

    abstract::We report a case of polycythemia vera with chorea in which the brain metabolism and dopamine system were investigated using 2-[(18)F]fluoro-2-deoxy-D-glucose positron emission tomography (FDG PET) and (99m)Tc-labeled tropane dopamine transporter ((99m)Tc-TRODAT-1) single photon emission computed tomography (SPECT). Al...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-011-6069-y

    authors: Huang HC,Wu YC,Shih LY,Lo WC,Tsai CH,Shyu WC

    更新日期:2011-11-01 00:00:00

  • The primary motor area for voluntary diaphragmatic motion identified by high field fMRI.

    abstract::In order to identify the precise location of the primary motor area for the diaphragm with respect to the classical motor homunculus, functional magnetic resonance imaging (fMRI) experiments were performed utilizing independent component-cross correlation- sequential epoch (ICS) analysis on a high-field (3.0 Tesla) sy...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-004-0413-4

    authors: Nakayama T,Fujii Y,Suzuki K,Kanazawa I,Nakada T

    更新日期:2004-06-01 00:00:00

  • Cognitive and social cognitive functioning in spinocerebellar ataxia : a preliminary characterization.

    abstract:INTRODUCTION:The spinocerebellar ataxias (SCAs), are rare neurodegenerative disorders caused by distinct genetic mutations. Clinically, the SCAs are characterised by progressive ataxia and a variety of other features, including cognitive dysfunction. The latter is consistent with a growing body of evidence supporting a...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0680-6

    authors: Garrard P,Martin NH,Giunti P,Cipolotti L

    更新日期:2008-03-01 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

  • Rehabilitation for patients with multiple sclerosis?

    abstract::In the epidemiological area of Southern Lower Saxony 92 patients with clinically definite or probable diagnosis of multiple sclerosis (MS) were interviewed and examined. This group contained a remarkably high percentage of benign cases (52%) in comparison with a sample of hospitalized patients. Neurological examinatio...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313292

    authors: Poser S,Bauer HJ,Ritter G,Friedrich H,Beland H,Denecke P

    更新日期:1981-01-01 00:00:00

  • Comparative efficacy and acceptability of disease-modifying therapies in patients with relapsing-remitting multiple sclerosis: a systematic review and network meta-analysis.

    abstract:BACKGROUND:Multiple sclerosis (MS) is an autoimmune, demyelinating disease of the central nervous system. The treatment of MS has always been a focus of neurological research. To date, the US Food and Drug Administration has approved 15 medications for modifying the course of multiple sclerosis. In this study, we exami...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-019-09395-w

    authors: Li H,Hu F,Zhang Y,Li K

    更新日期:2020-12-01 00:00:00

  • Systemic risk score evaluation in ischemic stroke patients (SCALA): a prospective cross sectional study in 85 German stroke units.

    abstract:BACKGROUND AND PURPOSE:Stratification of patients with transient ischemic attack (TIA) or ischemic stroke (IS) by risk of recurrent stroke can contribute to optimized secondary prevention. We therefore aimed to assess cardiovascular risk factor profiles of consecutive patients hospitalized with TIA/IS to stratify the r...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-007-0590-z

    authors: Weimar C,Goertler M,Röther J,Ringelstein EB,Darius H,Nabavi DG,Kim IH,Theobald K,Diener HC,SCALA Study Group.

    更新日期:2007-11-01 00:00:00

  • Spatial correlation and segregation of multimodal MRI abnormalities in multiple system atrophy.

    abstract:OBJECTIVE:The variability of the severity and regional distribution of pathological process in basal ganglia (BG) and brainstem-cerebellar systems results in clinical heterogeneity and represents the motor subtype of multiple system atrophy (MSA). This study aimed to quantify spatial patterns of multimodal MRI abnormal...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-018-8874-z

    authors: Lee MJ,Kim TH,Mun CW,Shin HK,Son J,Lee JH

    更新日期:2018-07-01 00:00:00

  • Muscle glucose-6-phosphate dehydrogenase deficiency.

    abstract::Muscle glucose-6-phosphate dehydrogenase (G6PD) deficiency is described in four clinically heterogeneous patients: an athlete who developed myoglobinuria after physical exercise; a 7-year-old, mildly mentally retarded boy, who had episodes of dark urine and high creatine kinase; and two brothers of Sardinian origin, t...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314498

    authors: Bresolin N,Bet L,Moggio M,Meola G,Fortunato F,Comi G,Adobbati L,Geremia L,Pittalis S,Scarlato G

    更新日期:1989-05-01 00:00:00

  • An exploratory study of serum urate levels in patients with amyotrophic lateral sclerosis.

    abstract::Urate is a natural antioxidant, and high serum urate levels could be protective against the development of amyotrophic lateral sclerosis (ALS). To determine if serum urate concentrations were lower in ALS patients than in healthy controls, we compared serum urate levels in 132 ALS patients and 337 age/sex-matched cont...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-010-5735-9

    authors: Zoccolella S,Simone IL,Capozzo R,Tortelli R,Leo A,D'Errico E,Logroscino G

    更新日期:2011-02-01 00:00:00

  • Neurological complications in liver transplantation.

    abstract::To define the incidence and type of neurological complications and associated factors, we reviewed 41 consecutive patients who had 45 procedures for liver transplantation. Encephalopathy occurred after 28 procedures (62%) with immediate onset and no significant recovery before death or re-transplantation in 11 (24%), ...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s004150170023

    authors: Ghaus N,Bohlega S,Rezeig M

    更新日期:2001-12-01 00:00:00

  • Disease reactivation after switching from natalizumab to daclizumab.

    abstract::Discontinuation of natalizumab can lead to severe rebound of disease activity in patients with relapsing-remitting multiple sclerosis (RRMS); nevertheless, the treatment regimen in this clinical situation remains controversial. We report the case of a 25-year-old male patient with RRMS who was clinically stable under ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-017-8622-9

    authors: Uphaus T,Oberwittler C,Groppa S,Zipp F,Bittner S

    更新日期:2017-12-01 00:00:00

  • Herpes simplex virus type 2 meningitis without genital lesions: an immunoblot study.

    abstract::Two sexually active female patients presented with acute meningitis. The CSF abnormalities were severe and persistent. In spite of the absence of genital lesions, serological studies revealed a primary infection by herpes simplex virus type 2. An immunoblot study revealed intrathecal synthesis of anti-herpes antibodie...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314743

    authors: Boucquey D,Chalon MP,Sindic CJ,Lamy ME,Laterre C

    更新日期:1990-08-01 00:00:00

  • Intrathecal IgG synthesis in multiple sclerosis and other neurological diseases: a comparative evaluation by IgG-index and isoelectric focusing.

    abstract::Intrathecal IgG synthesis has been investigated by determining the IgG index and by isoelectric focusing in 30 cases of definite multiple sclerosis, in 15 cases of probable multiple sclerosis and in 128 patients affected by other neurological diseases. The blood-brain barrier function was evaluated at the same time by...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314641

    authors: Poloni M,Rocchelli B,Scelsi R,Pinelli P

    更新日期:1979-10-01 00:00:00

  • The role of IVIg in autoimmune neuropathies: the latest evidence.

    abstract::Guillain-Barré syndrome (GBS), chronic inflammatory demyelinating polyradiculoneuropathy (CIDP) and multifocal motor neuropathy (MMN) are the major immune neuropathies. Although a detailed understanding of the pathogenesis of these conditions is not yet available, the multiple effects of IVIg on the immune and inflamm...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-008-3003-z

    authors: Hughes R

    更新日期:2008-07-01 00:00:00

  • Updates in the management of high-grade glioma.

    abstract::The management of high-grade glioma (HGG) has evolved significantly over the last decade. Patients are managed in a multidisciplinary team setting in order to ensure their care is guided by the most current evidenced based treatments. The outcome in patients with HGG, while still poor, has improved in terms of both su...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-013-7032-x

    authors: Bradley D,Rees J

    更新日期:2014-04-01 00:00:00

  • Key emerging issues in progressive supranuclear palsy and corticobasal degeneration.

    abstract::It has been approximately 50 years since neurologists were introduced to the entities, "progressive supranuclear palsy" and "corticobasal degeneration". Since the two seminal publications, there have been significant advancements in our understanding of these two neurodegenerative diseases, particularly the fact that ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-015-7682-y

    authors: Josephs KA

    更新日期:2015-03-01 00:00:00

  • MRI-visible perivascular spaces as an imaging biomarker in Fabry disease.

    abstract:INTRODUCTION:Fabry disease (FD) is an X-linked lysosomal storage disorder resulting in vascular glycosphingolipid accumulation and increased stroke risk. MRI findings associated with FD include white matter hyperintensities (WMH) and cerebral microbleeds (CMBs), suggesting the presence of cerebral small vessel disease....

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-10209-7

    authors: Lyndon D,Davagnanam I,Wilson D,Jichi F,Merwick A,Bolsover F,Jager HR,Cipolotti L,Wheeler-Kingshott C,Hughes D,Murphy E,Lachmann R,Werring DJ

    更新日期:2020-10-19 00:00:00

  • Diagnostic and prognostic power of CSF Tau in amyotrophic lateral sclerosis.

    abstract:BACKGROUND:Amyotrophic lateral sclerosis (ALS) is a fatal neurodegenerative disease that still lacks reliable diagnostic biomarkers. This study aims to evaluate the diagnostic and prognostic potential of CSF total Tau (t-Tau), phospho-Tau (p-Tau) and p-Tau/t-Tau ratio in ALS patients using CSF neurofilament light (NFL)...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-018-9008-3

    authors: Scarafino A,D'Errico E,Introna A,Fraddosio A,Distaso E,Tempesta I,Morea A,Mastronardi A,Leante R,Ruggieri M,Mastrapasqua M,Simone IL

    更新日期:2018-10-01 00:00:00

  • Plasma levels of nitric oxide and stroke outcome.

    abstract::Production of reactive oxygen species after cerebral blood flow disruption may enhance tissue damage through multiple molecular pathways. Changes in nitric oxide (NO) metabolism and oxidative stress status were investigated in 47 patients with ischemic stroke by measuring plasma nitric oxide (NO) and peroxynitrite (ON...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-007-0700-y

    authors: Taffi R,Nanetti L,Mazzanti L,Bartolini M,Vignini A,Raffaelli F,Pasqualetti P,Vernieri F,Provinciali L,Silvestrini M

    更新日期:2008-01-01 00:00:00

  • Late-onset Pompe disease: a genetic-radiological correlation on cerebral vascular anomalies.

    abstract::Pompe disease is an autosomal recessive disorder in which deficiency of the lysosomal enzyme acid alpha-glucosidase results in the accumulation of glycogen mostly in muscle tissues. Several reports suggest a higher incidence of intracranial vascular abnormalities (IVAs) in this condition, as well as brain microbleeds ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-017-8601-1

    authors: Pichiecchio A,Sacco S,De Filippi P,Caverzasi E,Ravaglia S,Bastianello S,Danesino C

    更新日期:2017-10-01 00:00:00

  • Compound heterozygous PNPLA6 mutations cause Boucher-Neuhäuser syndrome with late-onset ataxia.

    abstract::PNPLA6 mutations, known to be associated with the development of motor neuron phenotypes, have recently been identified in families with Boucher-Neuhäuser syndrome. Boucher-Neuhäuser is a rare autosomal recessive syndrome characterized by the co-occurrence of cerebellar ataxia, hypogonadotropic hypogonadism, and chori...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-014-7516-3

    authors: Deik A,Johannes B,Rucker JC,Sánchez E,Brodie SE,Deegan E,Landy K,Kajiwara Y,Scelsa S,Saunders-Pullman R,Paisán-Ruiz C

    更新日期:2014-12-01 00:00:00

  • Copper deficiency myelopathy.

    abstract::Acquired copper deficiency has been recognised as a rare cause of anaemia and neutropenia for over half a century. Copper deficiency myelopathy (CDM) was only described within the last decade, and represents a treatable cause of non-compressive myelopathy which closely mimics subacute combined degeneration due to vita...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-010-5511-x

    authors: Jaiser SR,Winston GP

    更新日期:2010-06-01 00:00:00