Cutaneous allodynia in the migraine population.

Abstract:

OBJECTIVE:To develop and validate a questionnaire for assessing cutaneous allodynia (CA), and to estimate the prevalence and severity of CA in the migraine population. METHODS:Migraineurs (n = 11,388) completed the Allodynia Symptom Checklist, assessing the frequency of allodynia symptoms during headache. Response options were never (0), rarely (0), less than 50% of the time (1), > or = 50% of the time (2), and none (0). We used item response theory to explore how well each item discriminated CA. The relations of CA to headache features were examined. RESULTS:All 12 questions had excellent item properties. The greatest discrimination occurred with CA during "taking a shower" (discrimination = 2.54), wearing a necklace (2.39) or ring (2.31), and exposure to heat (2.1) or cold (2.0). The factor analysis demonstrated three factors: thermal, mechanical static, and mechanical dynamic. Based on the psychometrics, we developed a scale distinguishing no CA (scores 0-2), mild (3-5), moderate (6-8), and severe (> or = 9). The prevalence of allodynia among migraineurs was 63.2%. Severe CA occurred in 20.4% of migraineurs. CA was associated with migraine defining features (eg, unilateral pain: odds ratio, 2.3; 95% confidence interval, 2.0-2.4; throbbing pain: odds ratio, 2.3; 95% confidence interval, 2.1-2.6; nausea: odds ratio, 2.3; 95% confidence interval, 2.1-2.6), as well as illness duration, attack frequency, and disability. INTERPRETATION:The Allodynia Symptom Checklist measures overall allodynia and subtypes. CA affects 63% of migraineurs in the population and is associated with frequency, severity, disability, and associated symptoms of migraine. CA maps onto migraine biology.

journal_name

Ann Neurol

journal_title

Annals of neurology

authors

Lipton RB,Bigal ME,Ashina S,Burstein R,Silberstein S,Reed ML,Serrano D,Stewart WF,American Migraine Prevalence Prevention Advisory Group.

doi

10.1002/ana.21211

subject

Has Abstract

pub_date

2008-02-01 00:00:00

pages

148-58

issue

2

eissn

0364-5134

issn

1531-8249

journal_volume

63

pub_type

杂志文章
  • Reconstruction magnetic resonance neurography in chronic inflammatory demyelinating polyneuropathy.

    abstract::To study distribution and patterns of nerve hypertrophy in chronic inflammatory demyelinating polyneuropathy (CIDP), magnetic resonance neurography with 3-dimensional reconstruction of short tau inversion recovery images was performed in 33 patients. This technique clearly showed longitudinal morphological changes fro...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.24314

    authors: Shibuya K,Sugiyama A,Ito S,Misawa S,Sekiguchi Y,Mitsuma S,Iwai Y,Watanabe K,Shimada H,Kawaguchi H,Suhara T,Yokota H,Matsumoto H,Kuwabara S

    更新日期:2015-02-01 00:00:00

  • Epileptogenic mineralization: pathological variants with good prognosis.

    abstract::Four examples of grossly mineralized lesions of the brain, causing seizures, are described; they include 2 hamartomas, a choristoma (novel associations), and an idiopathic "brain stone." Each was detectable with routine roentgenograms, and the seizures were ameliorated by surgical therapy. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410020413

    authors: Averback P

    更新日期:1977-10-01 00:00:00

  • Diffuse axonal injury in children: clinical correlation with hemorrhagic lesions.

    abstract::An inception cohort of 40 children and adolescents with traumatic brain injury and suspected diffuse axonal injury were studied using a new high-resolution magnetic resonance imaging susceptibility-weighted technique that is very sensitive for hemorrhage. A blinded comparison was performed between the extent of parenc...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20123

    authors: Tong KA,Ashwal S,Holshouser BA,Nickerson JP,Wall CJ,Shutter LA,Osterdock RJ,Haacke EM,Kido D

    更新日期:2004-07-01 00:00:00

  • Development of a functional magnetic resonance imaging protocol for intraoperative localization of critical temporoparietal language areas.

    abstract::The aim of this study was to evaluate the use of functional magnetic resonance imaging as an alternative to intraoperative electrocortical stimulation mapping for the localization of critical language areas in the temporoparietal region. We investigated several requirements that functional magnetic resonance imaging m...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10117

    authors: Rutten GJ,Ramsey NF,van Rijen PC,Noordmans HJ,van Veelen CW

    更新日期:2002-03-01 00:00:00

  • Spreading depolarizations trigger caveolin-1-dependent endothelial transcytosis.

    abstract:OBJECTIVE:Cortical spreading depolarizations (CSDs) are intense and ubiquitous depolarization waves relevant for the pathophysiology of migraine and brain injury. CSDs disrupt the blood-brain barrier (BBB), but the mechanisms are unknown. METHODS:A total of six CSDs were evoked over 1 hour by topical application of 30...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25298

    authors: Sadeghian H,Lacoste B,Qin T,Toussay X,Rosa R,Oka F,Chung DY,Takizawa T,Gu C,Ayata C

    更新日期:2018-09-01 00:00:00

  • Toward the development of rational therapies in multiple sclerosis: what is on the horizon?

    abstract::Although the cause of multiple sclerosis (MS) has remained obscure, many findings support an autoimmune pathogenesis on the background of a complex interaction between multiple genes and environmental factors. Accordingly, targeting the immune system has been a rational approach for the treatment of MS. The developmen...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.21289

    authors: Hemmer B,Hartung HP

    更新日期:2007-10-01 00:00:00

  • New innovations: therapeutic opportunities for intellectual disabilities.

    abstract::Intellectual disability is common and is associated with significant morbidity. Until the latter half of the 20th century, there were no efficacious treatments. Following initial breakthroughs associated with newborn screening and metabolic corrections, little progress was made until recently. With improved understand...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.24002

    authors: Picker JD,Walsh CA

    更新日期:2013-09-01 00:00:00

  • Natural history of multiple sclerosis.

    abstract::Multiple sclerosis (MS) is the most common idiopathic inflammatory disease of the central nervous system. The distinction between MS and other benign or fulminant inflammatory demyelinating disorders is based on quantitative, rather than qualitative, differences in chronicity and severity. Primary progressive MS may d...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410360704

    authors: Weinshenker BG

    更新日期:1994-01-01 00:00:00

  • Oxidative damage to mitochondrial DNA is increased in Alzheimer's disease.

    abstract::Oxidative damage to DNA may play a role in both normal aging and in neurodegenerative diseases. We examined whether Alzheimer's disease (AD) is associated with increased oxidative damage to nDNA and mtDNA in postmortem brain tissue. We measured the oxidized nucleoside, 8-hydroxy-2'-deoxyguanosine (OH8dG), in DNA isola...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410360510

    authors: Mecocci P,MacGarvey U,Beal MF

    更新日期:1994-11-01 00:00:00

  • Neurophysiological identification of the subthalamic nucleus in surgery for Parkinson's disease.

    abstract::Microelectrode recording methods for stereotactic localization of the subthalamic nucleus (STN) and surrounding structures are described. These methods accurately define targets for chronic deep brain stimulation in the treatment of Parkinson's disease. Mean firing rates and a burst index were determined for all recor...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410440407

    authors: Hutchison WD,Allan RJ,Opitz H,Levy R,Dostrovsky JO,Lang AE,Lozano AM

    更新日期:1998-10-01 00:00:00

  • Interleukin 9 alterations linked to alzheimer disease in african americans.

    abstract:OBJECTIVE:Compared to older Caucasians, older African Americans have higher risks of developing Alzheimer disease (AD) and lower cerebrospinal fluid (CSF) tau biomarker levels. It is not known whether tau-related differences begin earlier in life or whether race modifies other AD-related biomarkers such as inflammatory...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.25543

    authors: Wharton W,Kollhoff AL,Gangishetti U,Verble DD,Upadhya S,Zetterberg H,Kumar V,Watts KD,Kippels AJ,Gearing M,Howell JC,Parker MW,Hu WT

    更新日期:2019-09-01 00:00:00

  • Disease mechanisms revealed by transcription profiling in SOD1-G93A transgenic mouse spinal cord.

    abstract::Mutations of copper,zinc-superoxide dismutase (cu,zn SOD) are found in patients with a familial form of amyotrophic lateral sclerosis. When expressed in transgenic mice, mutant human cu,zn SOD causes progressive loss of motor neurons with consequent paralysis and death. Expression profiling of gene expression in SOD1-...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.1252

    authors: Olsen MK,Roberds SL,Ellerbrock BR,Fleck TJ,McKinley DK,Gurney ME

    更新日期:2001-12-01 00:00:00

  • Blood expression profiles for tuberous sclerosis complex 2, neurofibromatosis type 1, and Down's syndrome.

    abstract::Blood gene expression profiling has been applied to a variety of hematological malignancies, autoimmune disorders, and infectious diseases. This study applies this approach to genetic diseases without obvious blood phenotypes. Three genetic diseases including tuberous sclerosis complex 2, neurofibromatosis type 1, and...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20291

    authors: Tang Y,Schapiro MB,Franz DN,Patterson BJ,Hickey FJ,Schorry EK,Hopkin RJ,Wylie M,Narayan T,Glauser TA,Gilbert DL,Hershey AD,Sharp FR

    更新日期:2004-12-01 00:00:00

  • Successful treatment with tocainide of recessive generalized congenital myotonia.

    abstract::A patient with recessive generalized congenital myotonia and severe, disabling weakness underwent various forms of treatment while being monitored electrophysiologically. Phenytoin, verapamil, and acetazolamide were ineffective, but tocainide yielded good results. Improvement was dose-dependent, and was limited by irr...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410190515

    authors: Streib EW

    更新日期:1986-05-01 00:00:00

  • A randomized trial of plasma exchange in acute central nervous system inflammatory demyelinating disease.

    abstract::There are no established treatments for patients with acute, severe neurological deficits caused by multiple sclerosis or other inflammatory demyelinating diseases of the central nervous system who fail to recover after treatment with high-dose corticosteroids. We conducted a randomized, sham-controlled, double-masked...

    journal_title:Annals of neurology

    pub_type: 临床试验,杂志文章,随机对照试验

    doi:10.1002/1531-8249(199912)46:6<878::aid-ana10>3.0.c

    authors: Weinshenker BG,O'Brien PC,Petterson TM,Noseworthy JH,Lucchinetti CF,Dodick DW,Pineda AA,Stevens LN,Rodriguez M

    更新日期:1999-12-01 00:00:00

  • White matter lesions defined by diffusion tensor imaging in older adults.

    abstract:OBJECTIVE:The cellular and molecular mechanisms underlying magnetic resonance imaging-defined white matter (WM) changes associated with age-related cognitive decline remain poorly defined. We tested the hypothesis that WM lesions in older adults, defined by diffusion tensor imaging (DTI), arise in the setting of vascul...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.22484

    authors: Back SA,Kroenke CD,Sherman LS,Lawrence G,Gong X,Taber EN,Sonnen JA,Larson EB,Montine TJ

    更新日期:2011-09-01 00:00:00

  • Phase 2 trial of a DNA vaccine encoding myelin basic protein for multiple sclerosis.

    abstract:OBJECTIVE:To evaluate the efficacy and safety of BHT-3009 in relapsing-remitting multiple sclerosis (MS) and to confirm that BHT-3009 causes immune tolerance. METHODS:BHT-3009 is a tolerizing DNA vaccine for MS, encoding full-length human myelin basic protein. Relapsing-remitting MS patients were randomized 1:1:1 into...

    journal_title:Annals of neurology

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/ana.21370

    authors: Garren H,Robinson WH,Krasulová E,Havrdová E,Nadj C,Selmaj K,Losy J,Nadj I,Radue EW,Kidd BA,Gianettoni J,Tersini K,Utz PJ,Valone F,Steinman L,BHT-3009 Study Group.

    更新日期:2008-05-01 00:00:00

  • Neuronal migration abnormality in peroxisomal bifunctional enzyme defect.

    abstract::Patterns of brain dysgenesis that resemble those in the Zellweger syndrome were demonstrated in a boy with an isolated defect of the peroxisomal bifunctional enzyme. There was bilateral centrosylvian pachygyria and polymicrogyria, diffuse hemispheric hypomyelination with heterotopic neurons, Purkinje cell heterotopias...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410390218

    authors: Kaufmann WE,Theda C,Naidu S,Watkins PA,Moser AB,Moser HW

    更新日期:1996-02-01 00:00:00

  • Shortening reaction in patients with cerebellar ataxia.

    abstract::During passive extension of the elbow, the triceps muscle normally shows a burst of electromyographic activity. This shortening reaction (SR) is known to be exaggerated in extrapyramidal disease states, but the effects of cerebellar disease are unknown. The SR was measured in both arms of a patient with hemiataxia, th...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410110307

    authors: Angel RW

    更新日期:1982-03-01 00:00:00

  • Animal models and therapeutic prospects for Charcot-Marie-Tooth disease.

    abstract::Charcot-Marie-Tooth (CMT) neuropathies are inherited neuromuscular disorders caused by a length-dependent neurodegeneration of peripheral nerves. More than 900 mutations in 60 different genes are causative of the neuropathy. Despite significant progress in therapeutic strategies, the disease remains incurable. The inc...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.23987

    authors: Bouhy D,Timmerman V

    更新日期:2013-09-01 00:00:00

  • Electroconvulsive therapy treatment of depression in a patient with adult GM2 gangliosidosis.

    abstract::Adult GM2 gangliosidosis is a rare disorder that often presents with both neurological and psychiatric syndromes. Effective treatment of the psychotic and affective symptoms associated with this disorder has been complicated by poor treatment response and the concern that many psychotropic agents may worsen the underl...

    journal_title:Annals of neurology

    pub_type: 杂志文章,评审

    doi:10.1002/ana.410310320

    authors: Renshaw PF,Stern TA,Welch C,Schouten R,Kolodny EH

    更新日期:1992-03-01 00:00:00

  • Quinolinic acid catabolism is increased in cerebellum of patients with dominantly inherited olivopontocerebellar atrophy.

    abstract::We measured the activities of the enzymes responsible for the metabolism of the excitotoxin quinolinic acid, 3-hydroxyanthranilate oxygenase and quinolinic acid phosphoribosyltransferase, in autopsied brain of 11 patients with olivopontocerebellar atrophy. In cerebellar cortex, severe Purkinje cell loss was evident bu...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410290119

    authors: Kish SJ,Du F,Parks DA,Robitaille Y,Ball MJ,Schut L,Hornykiewicz O,Schwarcz R

    更新日期:1991-01-01 00:00:00

  • Somatotopical organization of striatal activation during finger and toe movement: a 3-T functional magnetic resonance imaging study.

    abstract::The present study aimed at determining the distribution and somatotopical organization of striatal activation during performance of simple motor tasks. Ten right-handed healthy volunteers were studied by using a 3-T whole-body magnetic resonance unit and echo planar imaging. The tasks consisted of self-paced flexion/e...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410440319

    authors: Lehéricy S,van de Moortele PF,Lobel E,Paradis AL,Vidailhet M,Frouin V,Neveu P,Agid Y,Marsault C,Le Bihan D

    更新日期:1998-09-01 00:00:00

  • N-methyl-D-aspartate receptor antibodies in herpes simplex encephalitis.

    abstract:OBJECTIVE:To determine the presence and kinetics of antibodies against synaptic proteins in patients with herpes simplex virus encephalitis (HSE). METHODS:Retrospective analysis of 44 patients with polymerase chain reaction-proven HSE for the presence of a large panel of onconeuronal and synaptic receptor antibodies. ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.23689

    authors: Prüss H,Finke C,Höltje M,Hofmann J,Klingbeil C,Probst C,Borowski K,Ahnert-Hilger G,Harms L,Schwab JM,Ploner CJ,Komorowski L,Stoecker W,Dalmau J,Wandinger KP

    更新日期:2012-12-01 00:00:00

  • Rapid alterations of the axon membrane in antibody-mediated demyelination.

    abstract::Alterations of nodal and paranodal axolemma of the rat sciatic nerve were investigated in antigalactocerebroside serum-induced demyelination. A ferric ion-ferrocyanide (FeFCN) stain that appears to stain the regions with a high sodium channel density in nerve fibers was applied. When acute conduction block was initiat...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410150611

    authors: Saida K,Saida T,Kayama H,Nishitani H

    更新日期:1984-06-01 00:00:00

  • Assessment of reliability and biological significance of glutamate levels in cerebrospinal fluid.

    abstract::The published information on glutamate levels in cerebrospinal fluid (CSF) and modifications in neurological disorders is controversial. In the present study, we demonstrated a metabolic instability of glutamate in untreated CSF and a spurious elevation of its levels by the current methods of CSF acidification. These ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410330316

    authors: Ferrarese C,Pecora N,Frigo M,Appollonio I,Frattola L

    更新日期:1993-03-01 00:00:00

  • Clinical and magnetic resonance imaging findings in Batten disease: analysis of the major mutation (1.02-kb deletion).

    abstract::A total of 36 patients with Batten disease (juvenile-onset neuronal ceroid lipofuscinosis), homozygous or heterozygous for the major mutation, a 1.02-kb deletion, in the CLN3 gene, were studied to relate their genotype to their clinical phenotype. The onset of visual failure and epilepsy was highly concordant in both ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.410420517

    authors: Järvelä I,Autti T,Lamminranta S,Aberg L,Raininko R,Santavuori P

    更新日期:1997-11-01 00:00:00

  • Retrograde reactions of Clarke's nucleus neurons after human spinal cord injury.

    abstract::Successful axon regeneration depends on the expression of regeneration-associated genes by axotomized neurons. Here, we demonstrate, for the first time to our knowledge, the expression of regeneration-associated genes by axotomized human CNS neurons. In situ hybridization and immunohistochemistry showed a transient in...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10724

    authors: Schmitt AB,Breuer S,Polat L,Pech K,Kakulas B,Love S,Martin D,Schoenen J,Noth J,Brook GA

    更新日期:2003-10-01 00:00:00

  • Prolongation of levodopa responses by glycineB antagonists in parkinsonian primates.

    abstract::To examine the antiparkinsonian effects of blocking glycineB receptors, we designed a pilot study testing the potent and selective antagonist, PAMQX, in 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine-treated primates. PAMQX had no intrinsic effects but markedly potentiated the antiparkinsonian action of levodopa. In a d...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.20279

    authors: Papa SM,Auberson YP,Greenamyre JT

    更新日期:2004-11-01 00:00:00

  • Comparison of kindreds with parkinsonism and alpha-synuclein genomic multiplications.

    abstract::Genomic triplication of the alpha-synuclein gene recently has been associated with familial Parkinson's disease in the Spellman-Muenter kindred. Here, we present an independent family, of Swedish-American descent, with hereditary early-onset parkinsonism with dementia due to alpha-synuclein triplication. Brain tissue ...

    journal_title:Annals of neurology

    pub_type: 杂志文章

    doi:10.1002/ana.10846

    authors: Farrer M,Kachergus J,Forno L,Lincoln S,Wang DS,Hulihan M,Maraganore D,Gwinn-Hardy K,Wszolek Z,Dickson D,Langston JW

    更新日期:2004-02-01 00:00:00