Levels of HVA, 5-HIAA, and MHPG in the CSF of vascular parkinsonism compared to Parkinson's disease and controls.

Abstract:

:The neurochemical abnormalities underlying vascular parkinsonism (VP) have not been well characterised. A better understanding may help to optimize pharmacological interventions. Since VP patients generally have a poorer response to l-Dopa than Parkinson's disease (PD) patients, we investigated whether levels of relevant CSF neurotransmitter metabolites may be differentially altered in VP and PD and assessed the potential of neurotransmitter metabolites as biomarkers. We compared CSF levels of homovanillic acid (HVA), 5-hydroxyindolacetic acid, and 3-methoxy-4-hydroxyphenylethyleneglycol, in 16 VP patients, 57 PD patients and 60 non-neurological controls. We found that levels of HVA were reduced in PD compared with both VP and controls but did not differ significantly between VP and controls indicating that dopamine deficiency was less pronounced in VP.

journal_name

J Neurol

journal_title

Journal of neurology

authors

Herbert MK,Kuiperij H,Bloem BR,Verbeek MM

doi

10.1007/s00415-013-7126-5

subject

Has Abstract

pub_date

2013-12-01 00:00:00

pages

3129-33

issue

12

eissn

0340-5354

issn

1432-1459

journal_volume

260

pub_type

杂志文章
  • The detection of activated cerebrospinal fluid B lymphocytes by peroxidase conjugated antibodies.

    abstract::A method for the preparation of a potent and specific peroxidase-labelled antihuman IgG antibody is described. CSF cells from patients with various neurological diseases were stained. Only in cases of inflammatory diseases was IgG detectable. The stained cells were so-called lymphoid cells. As the demonstrable IgG can...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313346

    authors: Schädlich HJ,Nekić M,Felgenhauer K

    更新日期:1980-01-01 00:00:00

  • Primary DQ effect in the association between HLA and neurological syndromes with anti-GAD65 antibodies.

    abstract::The primary cause of neurological syndromes with antibodies against glutamic acid decarboxylase 65 (GAD65-Ab) is unknown, but genetic predisposition may exist as it is suggested by the co-occurrence in patients and their relatives of other organ-specific autoimmune diseases, notably type 1 diabetes mellitus (T1DM), an...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-020-09782-8

    authors: Muñiz-Castrillo S,Ambati A,Dubois V,Vogrig A,Joubert B,Rogemond V,Picard G,Lin L,Fabien N,Mignot E,Honnorat J

    更新日期:2020-07-01 00:00:00

  • Is there a difference in gastric emptying between Parkinson's disease patients under long-term L-dopa therapy with and without motor fluctuations? An analysis using the 13C-acetate breath test.

    abstract::The mechanism underlying the motor fluctuations that develop after long-term L-dopa therapy is not fully known. It has been speculated that malabsorption of L-dopa from the small intestine occurs. It was reported that gastric retention in Parkinson's disease (PD) patients with motor fluctuations is increased as compar...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5220-5

    authors: Tanaka Y,Kato T,Nishida H,Araki H,Murase M,Nagaki M,Moriwaki H,Inuzuka T

    更新日期:2009-12-01 00:00:00

  • Parvalbumin-immunoreactive neurons in the cortex in Pick's disease.

    abstract::Parvalbumin (a calcium-binding protein)-immunoreactive (PV-Ir) neurons in the cerebral cortex were examined in 20 postmortem brains obtained from elderly controls and patients with Pick's disease (PD). The type of PV-Ir neurons and their distribution in control and PD brains were similar. The number of PV-Ir neurons i...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00314780

    authors: Arai H,Noguchi I,Makino Y,Kosaka K,Heizmann CW,Iizuka R

    更新日期:1991-07-01 00:00:00

  • Cerebral disseminated coagulation. An encephalitis-like syndrome in a boy with dissecting aortic aneurysm.

    abstract::A boy was suspected of having meningoencephalitis probably of viral origin, although all microbiological, including virological, tests were negative. Postmortem examination revealed a dissecting aortic aneurysm and disseminated intravascular coagulation involving the central nervous system exclusively. The clinical ev...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313465

    authors: Hens L,Dom R,Goddeeris P,van den Bergh R

    更新日期:1981-01-01 00:00:00

  • Clinicopathological features of multiple mononeuropathy associated with systemic lupus erythematosus: a multicenter study.

    abstract::Multiple mononeuropathy (MM) occurs rarely during systemic lupus erythematosus (SLE) but may lead to major disability. The aim of this study was to investigate the clinic-pathological presentations of MM during SLE, as well as long-term outcomes. We conducted a multicentric retrospective study that included patients r...

    journal_title:Journal of neurology

    pub_type: 杂志文章,多中心研究

    doi:10.1007/s00415-017-8519-7

    authors: Rivière E,Cohen Aubart F,Maisonobe T,Maurier F,Richez C,Gombert B,Gousseff M,Adoue D,Mathian A,Hié M,Haroche J,Amoura Z

    更新日期:2017-06-01 00:00:00

  • Apolipoprotein E genotype and concomitant clinical features in early-onset Alzheimer's disease.

    abstract::We have studied the relationship between the apolipoprotein E gene (APOE) and the development of myoclonus, tremors, rigidity and seizures in 168 patients with probable early-onset Alzheimer's disease (AD). There was a statistically significantly lower risk of tremor for carriers of the epsilon 4 allele of APOE. This ...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00900501

    authors: Bronzova J,van Duijn CM,Havekes LM,de Knijff P,Van Broeckhoven C,Hofman A

    更新日期:1996-06-01 00:00:00

  • Copy number variations are a rare cause of non-CMT1A Charcot-Marie-Tooth disease.

    abstract::Hereditary peripheral neuropathies present a group of clinically and genetically heterogeneous entities. All known forms, including the various forms of Charcot-Marie-Tooth disease (CMT) are characterized as Mendelian traits and over 35 genes have been identified thus far. The mutational mechanism of the most common C...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-009-5401-2

    authors: Huang J,Wu X,Montenegro G,Price J,Wang G,Vance JM,Shy ME,Züchner S

    更新日期:2010-05-01 00:00:00

  • Quantification of the heterogeneity of cerebral blood flow in vascular dementia.

    abstract:BACKGROUND:In vascular dementia (VaD), assessment of cerebral blood flow by single photon emission computed tomography (CBF SPECT) has been used to detect a patchy decrease of blood flow or a frontal reduction. In addition to reduced blood flow, the heterogeneous distribution of cerebral blood flow is often observed in...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章

    doi:10.1007/s00415-003-0972-9

    authors: Yoshikawa T,Murase K,Oku N,Kitagawa K,Imaizumi M,Takasawa M,Rishu P,Hashikawa K,Nishikawa T,Hori M,Matsumoto M

    更新日期:2003-02-01 00:00:00

  • Botulinum toxin in multiple sclerosis.

    abstract::Local administration of botulinum toxin (BoTx) inhibits presynaptic acetylcholine release. All cholinergically innervated muscles and glands can be paralyzed accordingly. Studies on the application of BoTx in multiple sclerosis have shown good results for focal spasticity, in particular, of the extremities. The first ...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-006-1104-0

    authors: Jost WH

    更新日期:2006-02-01 00:00:00

  • Myasthenia gravis associated with adrenocortical insufficiency. Report of two cases.

    abstract::Two cases of Addison's disease associated with myasthenia gravis are reported. This association has been described only rarely in the literature. In the first case, there were marked immunological abnormalities. It is most likely that the origin of the adrenocortical insufficiency in the second case is tuberculous. Th...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313835

    authors: Dumas P,Archambeaud-Mouveroux F,Vallat JM,Barussaud D,Hugon J,Dumas M

    更新日期:1985-01-01 00:00:00

  • Subthalamic nucleus stimulation and levodopa-resistant postural instability in Parkinson's disease.

    abstract::We examined the effect of bilateral subthalamic nucleus stimulation on levodopa-resistant balance impairment in 14 patients with Parkinson's disease and 18 matched controls. Instability was quantitatively assessed using standardized multidirectional dynamic posturography. Patients were tested after taking a suprathres...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-008-0636-x

    authors: Visser JE,Allum JH,Carpenter MG,Esselink RA,Speelman JD,Borm GF,Bloem BR

    更新日期:2008-02-01 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

  • Prevalence of non-motor symptoms in young-onset versus late-onset Parkinson's disease.

    abstract::Non-motor symptoms (NMS) of Parkinson's disease (PD) have only recently been increasingly recognized for their impact on a patient's quality of life. In this study, we applied the validated, comprehensive self-completed NMS questionnaire for PD (NMS Quest) to 101 patients with young-onset PD (onset between 21 and 45 y...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-012-6600-9

    authors: Spica V,Pekmezović T,Svetel M,Kostić VS

    更新日期:2013-01-01 00:00:00

  • ALS and MMN mimics in patients with BSCL2 mutations: the expanding clinical spectrum of SPG17 hereditary spastic paraplegia.

    abstract::Silver syndrome/SPG17 is a motor manifestation of mutations in the BSCL2 gene and usually presents as a complicated form of hereditary spastic paraplegia (HSP). We present clinical data, follow-up, and genetic results of seven patients with Silver syndrome/SPG17 including a family with a variable intrafamilial phenoty...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-016-8301-2

    authors: Musacchio T,Zaum AK,Üçeyler N,Sommer C,Pfeifroth N,Reiners K,Kunstmann E,Volkmann J,Rost S,Klebe S

    更新日期:2017-01-01 00:00:00

  • Classic ataxia-telangiectasia: the phenotype of long-term survivors.

    abstract:OBJECTIVE:Patients with classic ataxia-telangiectasia (A-T) generally die in the second or third decade of life. Clinical descriptions of A-T tend to focus on the symptoms at presentation. However, during the course of the disease, other symptoms and complications emerge. As long-term survivors with classic A-T develop...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-019-09641-1

    authors: van Os NJH,van Deuren M,Weemaes CMR,van Gaalen J,Hijdra H,Taylor AMR,van de Warrenburg BPC,Willemsen MAAP

    更新日期:2020-03-01 00:00:00

  • MRI findings of small subcortical "lacunar-like" infarction resulting from large vessel disease.

    abstract::Small subcortical infarctions resulting from large-vessel disease are often observed. It is important to distinguish these from pure lacunar infarction resulting from small-vessel disease because the investigations and examinations differ. We investigated the differences on brain magnetic resonance imaging (MRI) betwe...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150050584

    authors: Adachi T,Kobayashi S,Yamaguchi S,Okada K

    更新日期:2000-04-01 00:00:00

  • Nerve conduction and electromyography studies.

    abstract::Nerve conduction studies (NCS) and electromyography (EMG), often shortened to 'EMGs', are a useful adjunct to clinical examination of the peripheral nervous system and striated skeletal muscle. NCS provide an efficient and rapid method of quantifying nerve conduction velocity (CV) and the amplitude of both sensory ner...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-012-6497-3

    authors: Kane NM,Oware A

    更新日期:2012-07-01 00:00:00

  • Levodopa, bromocriptine and selegiline modify cardiovascular responses in Parkinson's disease.

    abstract::Autonomic nervous system (ANS) involvement is frequently found in Parkinson's disease (PD), but its causal relationship to the disease itself and its medication is unclear. We evaluated the effects of PD medications on cardiovascular ANS functions. Heart rate (HR) responses to normal and deep breathing, the Valsalva m...

    journal_title:Journal of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1007/s004150070075

    authors: Haapaniemi TH,Kallio MA,Korpelainen JT,Suominen K,Tolonen U,Sotaniemi KA,Myllylä VV

    更新日期:2000-11-01 00:00:00

  • Cerebral microdialysis as a monitoring method in subarachnoid hemorrhage patients, and correlation with clinical events--a systematic review.

    abstract:BACKGROUND:One of the goals in treating subarachnoid hemorrhage patients is to prevent or minimize vasospasm-induced ischemia. Intracerebral microdialysis is a rapidly developing tool to monitor physiological and pathophysiological changes in chemical processes associated with ischemia. OBJECTIVE:To determine the diag...

    journal_title:Journal of neurology

    pub_type: 杂志文章,评审

    doi:10.1007/s00415-003-1079-z

    authors: Peerdeman SM,van Tulder MW,Vandertop WP

    更新日期:2003-07-01 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

  • Diagnosis of asymptomatic natalizumab-associated PML: are we between a rock and a hard place?

    abstract::The diagnosis of natalizumab-associated progressive multifocal leukoencephalopathy (PML) in multiple sclerosis patients in an asymptomatic stage is crucial since it is associated with better clinical outcome measures. Current diagnostic criteria on PML diagnosis in asymptomatic patients require the detection of JC vir...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-014-7336-5

    authors: Wattjes MP,Vennegoor A,Mostert J,van Oosten BW,Barkhof F,Killestein J

    更新日期:2014-06-01 00:00:00

  • Differentiation of the humoral immune response in inflammatory diseases of the central nervous system.

    abstract::The three main immunoglobulin classes obey the basic principles of passive protein transfer at the blood-CSF barrier and the serum-derived portions could therefore be quantified with the help of the permeability marker albumin. The Ig fractions secreted into the CSF by sessile plasma cell clones have been determined i...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313413

    authors: Felgenhauer K

    更新日期:1982-01-01 00:00:00

  • Utility of measuring vitamin B12 and its active fraction, holotranscobalamin, in neurological vitamin B12 deficiency syndromes.

    abstract::Vitamin B(12) (VitB(12), cobalamin) deficiency has been associated with various neuropsychiatric conditions, such as peripheral neuropathy, subacute combined degeneration, affective disorders, and cognitive impairment. Current assays analyze vitamin B(12), of which only a small percentage is metabolically active. Meas...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-010-5764-4

    authors: Schrempf W,Eulitz M,Neumeister V,Siegert G,Koch R,Reichmann H,Storch A

    更新日期:2011-03-01 00:00:00

  • Elevated inflammatory laboratory parameters in spontaneous cervical artery dissection as compared to traumatic dissection: a retrospective case-control study.

    abstract::Several studies have reported infection as a possible risk factor for cervical artery dissection (CAD). We retrospectively analyzed several inflammatory parameters of CAD patients with the aim of detecting differences between spontaneous (n = 25) and traumatic (n = 18) CAD. In this case-control study, we observed sign...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-006-0109-z

    authors: Forster K,Poppert H,Conrad B,Sander D

    更新日期:2006-06-01 00:00:00

  • Prognostic significance of body weight variation after diagnosis in ALS: a single-centre prospective cohort study.

    abstract:BACKGROUND:Body weight reduction after disease onset is an independent predictor of survival in amyotrophic lateral sclerosis (ALS), but significance of weight variation after diagnosis remains to be established. OBJECTIVE:To investigate weight variation after diagnosis and its prognostic significance in patients with...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-019-09276-2

    authors: Shimizu T,Nakayama Y,Matsuda C,Haraguchi M,Bokuda K,Ishikawa-Takata K,Kawata A,Isozaki E

    更新日期:2019-06-01 00:00:00

  • Cerebellar ataxia and congenital disorder of glycosylation Ia (CDG-Ia) with normal routine CDG screening.

    abstract::Cerebellar ataxia can have many genetic causes among which are the congenital disorders of glycosylation type I (CDG-I). In this group of disorders, a multisystem phenotype is generally observed including the involvement of many organs, the endocrine, hematologic and central nervous systems. A few cases of CDG-Ia have...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s00415-007-0546-3

    authors: Vermeer S,Kremer HP,Leijten QH,Scheffer H,Matthijs G,Wevers RA,Knoers NA,Morava E,Lefeber DJ

    更新日期:2007-10-01 00:00:00

  • MRI findings in Hirayama's disease: flexion-induced cervical myelopathy or intrinsic motor neuron disease?

    abstract::Hirayama's disease is a benign juvenile form of focal amyotrophy affecting the upper limbs. Previous studies have suggested that the disorder is a neck flexion induced cervical myelopathy. We report clinical and magnetic resonance imaging findings in nine patients with Hirayama's disease. Cervical imaging of seven pat...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/s004150050514

    authors: Schröder R,Keller E,Flacke S,Schmidt S,Pohl C,Klockgether T,Schlegel U

    更新日期:1999-11-01 00:00:00

  • Saccadic intrusions in Alzheimer-type dementia.

    abstract::Horizontal eye-movement responses of four patients with Alzheimer-type dementia were recorded using the infrared oculographic technique. Abnormally frequent saccadic intrusions occurred during the fixation and slow, smooth pursuit tasks in all four patients. Saccadic intrusions have previously been reported in the lit...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313742

    authors: Jones A,Friedland RP,Koss B,Stark L,Thompkins-Ober BA

    更新日期:1983-01-01 00:00:00

  • Idiopathic dystonia: neuropharmacological study.

    abstract::A total of 15 patients affected by idiopathic dystonia (7 with generalized and 8 with focal or segmental dystonia) were subjected to therapy with bromocriptine at low doses, pimozide and trihexyphenidyl. The symptoms were evaluated by giving a progressive score in relation to the intensity of the dystonic symptom to e...

    journal_title:Journal of neurology

    pub_type: 杂志文章

    doi:10.1007/BF00313391

    authors: Girotti F,Scigliano G,Nardocci N,Angelini L,Broggi G,Giovannini P,Caraceni T

    更新日期:1982-01-01 00:00:00