Spatial analysis of amyotrophic lateral sclerosis in Northern New England, USA, 1997-2009.

Abstract:

INTRODUCTION:An environmental trigger of sporadic amyotrophic lateral sclerosis (ALS) is supported by geographic disparities in ALS incidence and development of the disease in conjugal couples. This study aims to investigate the incidence of ALS in the Northern New England states of New Hampshire (NH), Vermont (VT), and Maine (ME). METHODS:We reviewed medical records and community databases to identify dwelling addresses of 688 patients diagnosed with ALS in 1997-2009 in NH, VT, and ME. We used spatial analysis to identify clusters of census block groups with statistically significant high incidence. RESULTS:We identified 11 clusters of statistically significant high incidence, each containing 6 or more cases of ALS. These 11 clusters are grouped in 4 distinct regions. CONCLUSIONS:There appear to be areas of significant spatial clustering within Northern New England. Further analysis will be needed to confirm whether there is any correlation between these areas and potential environmental risk factors.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Caller TA,Chipman JW,Field NC,Stommel EW

doi

10.1002/mus.23761

subject

Has Abstract

pub_date

2013-08-01 00:00:00

pages

235-41

issue

2

eissn

0148-639X

issn

1097-4598

journal_volume

48

pub_type

杂志文章
  • Health services received by individuals with duchenne/becker muscular dystrophy.

    abstract:INTRODUCTION:Anecdotal reports from families and care providers suggest a wide variation in services received by individuals with Duchenne/Becker muscular dystrophy (DBMD). METHODS:We documented the type and frequency of health services received by individuals with DBMD using the Muscular Dystrophy Surveillance Tracki...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24727

    authors: Pandya SK,Campbell KA,Andrews JG,Meaney FJ,Ciafaloni E

    更新日期:2016-02-01 00:00:00

  • Stem cell route to neuromuscular therapies.

    abstract::As applied to skeletal muscle, stem cell therapy is a reincarnation of myoblast transfer therapy that has resulted from recent advances in the cell biology of skeletal muscle. Both strategies envisage the reconstruction of damaged muscle from its precursors, but stem cell therapy employs precursors that are earlier in...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.10243

    authors: Partridge TA

    更新日期:2003-02-01 00:00:00

  • Analysis of motor unit firing patterns in patients with central or peripheral lesions using singular-value decomposition.

    abstract::We applied the singular value decomposition (SVD) method to study single motor unit firing patterns. Two projects were carried out: (1) a computer simulation study to confirm the meanings of two SVD parameters, the eigenvalue corresponding to the positive-slope eigenvector (PEV) and that corresponding to the negative-...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/1097-4598(200007)23:7<1057::aid-mus8>3.0.c

    authors: Sun TY,Chen JJ,Lin TS

    更新日期:2000-07-01 00:00:00

  • Do A-waves help predict intravenous immunoglobulin response in multifocal motor neuropathy without block?

    abstract:INTRODUCTION:Are there electrophysiological findings that predict response to intravenous immunoglobulin (IVIg) in patients with lower motor neuron (LMN) syndromes without multifocal conduction block (MCB)? METHODS:We enrolled 9 patients with LMN syndromes without MCB to receive 18 weeks of IVIg therapy. Response was ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21914

    authors: Lange DJ,Nijjar R,Voustianiouk A,Seidel G,Panchal J,Wang AK

    更新日期:2011-04-01 00:00:00

  • Anatomic variation of the innervation of the flexor digitorum profundus muscle and its clinical implications.

    abstract::In anterior interosseous nerve syndrome and ulnar neuropathy, paralysis or weakness of the flexor digitorum profundus (FDP) muscles has been shown to vary according to the degree of involvement of the median and ulnar nerves, respectively. We traced these nerves in 50 cadaveric specimens in which each FDP was complete...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21281

    authors: Oh CS,Won HS,Lee KS,Chung IH,Kim SM

    更新日期:2009-04-01 00:00:00

  • Activity of 2'3'-cyclic-nucleotide 3'-phosphodiesterase and content of PO protein in the peripheral nervous system of the dystrophic mouse and chicken.

    abstract::To investigate whether various myelin markers could detect pathological changes in myelination, the activity of 2'-3'-cyclic nucleotide 3'-phosphodiesterase (CNP) and the level of PO protein were compared in the peripheral nervous system (PNS) of the dystrophic mouse and chicken and their phenotypically normal sibling...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080207

    authors: Lewis LN,Mezei C

    更新日期:1985-02-01 00:00:00

  • Chronic idiopathic axonal polyneuropathy: Electrophysiological progression and human leukocyte antigen associations.

    abstract:BACKGROUND:We aimed to describe the electrophysiological progression rate of chronic idiopathic axonal polyneuropathy (CIAP) and look into the potential role of human leukocyte antigen (HLA) genetic susceptibility in its development. METHODS:We recruited 57 patients with CIAP (mean age at diagnosis 67, mean follow-up ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27164

    authors: Zis P,Sarrigiannis PG,Artemiadis A,Skarlatou V,Hadjivassiliou M

    更新日期:2021-01-13 00:00:00

  • The effects of chronic muscular activity on age-related changes in single fiber electromyography.

    abstract::Single fiber electromyography ( SFEMG ) of the extensor digitorum communis (EDC) muscle and nerve conduction studies were performed on healthy, active elderly men (66-77 years old) to assess age-related changes in neuromuscular physiology and the effect of long-term increased muscular activity on these changes. The fo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880070403

    authors: Shields RW Jr,Robbins N,Verrilli AA 3rd

    更新日期:1984-05-01 00:00:00

  • Pain location and intensity impacts function in persons with myotonic dystrophy type 1 and facioscapulohumeral dystrophy with chronic pain.

    abstract:INTRODUCTION:We examined the effects of pain site and intensity on function in patients with myotonic dystrophy type 1 (DM1) and facioscapulohumeral muscular dystrophy (FSHD) and chronic pain. METHODS:Questionnaires assessing pain sites, pain extent (number of sites), pain intensity, and pain interference were complet...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24079

    authors: Miró J,Gertz KJ,Carter GT,Jensen MP

    更新日期:2014-06-01 00:00:00

  • Further observations on forearm flexor weakness in inclusion body myositis.

    abstract::In order to further characterize and provide a possible mechanism for the asymmetrical involvement of forearm muscles in inclusion body myositis (IBM), we measured isometric hand and pinch grip strength, and forearm muscle girth on 15 IBM patients. Forearm muscle strength and girth were significantly greater on the do...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199805)21:5<659::aid-mus17

    authors: Felice KJ,Relva GM,Conway SR

    更新日期:1998-05-01 00:00:00

  • Changes in Na(+) channel expression and nodal persistent Na(+) currents associated with peripheral nerve regeneration in mice.

    abstract::Patients with peripheral neuropathy frequently suffer from positive sensory (pain and paresthesias) and motor (muscle cramping) symptoms even in the recovery phase of the disease. To investigate the pathophysiology of increased axonal excitability in peripheral nerve regeneration, we assessed the temporal and spatial ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21031

    authors: Nakata M,Baba H,Kanai K,Hoshi T,Sawai S,Hattori T,Kuwabara S

    更新日期:2008-06-01 00:00:00

  • Polymyositis--an immunofluorescence study on the distribution of collagen types.

    abstract::Type-specific antibodies to the polymorphic types of collagen have been used to study their distribution in polymyositis. Dramatic increases were observed in the staining with antibodies to Type III collagen and, to a lesser extent, with antibodies to Types I, IV, and V. The changes in capillary and endomysial basemen...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880030605

    authors: Duance VC,Black CM,Dubowitz V,Hughes GR,Bailey AJ

    更新日期:1980-11-01 00:00:00

  • Electromyographic and morphological functional compensation in late poliomyelitis.

    abstract::Patients with prior poliomyelitis may experience muscle function deterioration decades after onset of disease. The present study is aimed at describing electromyographic and morphometric evidence of muscular compensation and of on-going muscular instability. Ten subjects 42-62 years of age with onset of polio 25-52 ye...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/mus.880130214

    authors: Einarsson G,Grimby G,Stålberg E

    更新日期:1990-02-01 00:00:00

  • Load-controlled moderate and high-intensity resistance training programs provoke similar strength gains in young women.

    abstract:INTRODUCTION:While current exercise guidelines recommend progressive, high-intensity resistance training (RT) to promote muscle hypertrophy and strength gains, controversy exists regarding the efficacy of lighter-load RT. We compared 2 work-matched RT interventions that differed in training intensity. METHODS:Fifteen ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24271

    authors: Alegre LM,Aguado X,Rojas-Martín D,Martín-García M,Ara I,Csapo R

    更新日期:2015-01-01 00:00:00

  • Bcl-2 and bax immunohistochemistry in denervation-reinnervation and necrosis-regeneration of rat skeletal muscles.

    abstract::Bcl-2 and Bax immunohistochemistry was examined in the skeletal muscle of rats after cutting the sciatic nerve, as a model of denervation and reinnervation, and in the anterior tibialis muscle of rats after an intramuscular injection of metoclopramide, as a model of necrosis and regeneration of muscle fibers, to bette...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/1097-4598(200012)23:12<1862::aid-mus10>3.0

    authors: Olivé M,Ferrer I

    更新日期:2000-12-01 00:00:00

  • Statistical motor unit number estimation: reproducibility and sources of error in patients with amyotrophic lateral sclerosis.

    abstract::The reliability of motor unit number estimation (MUNE) for assessment of the long-term course of ALS is dependent on the reproducibility of the technique. We report our results with the statistical method of MUNE on the ulnar nerve/hypothenar muscle in 16 ALS patients who were studied on 52 occasions. On each occasion...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/(sici)1097-4598(200002)23:2<193::aid-mus8>

    authors: Olney RK,Yuen EC,Engstrom JW

    更新日期:2000-02-01 00:00:00

  • Real-time ultrasound imaging of muscles.

    abstract::A prospective study was done on 222 consecutive new patients referred to our pediatric muscle clinic to assess the diagnostic value of ultrasound imaging. Ultrasound scans were interpreted without knowledge of clinical presentation or results of other tests. Muscular dystrophy produced a brightly speckled pattern of i...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110110

    authors: Heckmatt JZ,Pier N,Dubowitz V

    更新日期:1988-01-01 00:00:00

  • Quantitative analysis of reflex inhibition in single motor units in human masseter muscle: effects of stimulus intensity.

    abstract::Inhibitory reflex responses to electrical stimulation of the mental nerve were studied in recordings from single motor units (SMU) in the human masseter muscle. A new analytical technique for spike train data was used. Electrical stimuli were delivered to the mental nerve when the SMU fired with two consecutive inter-...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/(sici)1097-4598(200002)23:2<259::aid-mus18

    authors: Graven-Nielsen T,Svensson P,McMillan AS,Arendt-Nielsen L

    更新日期:2000-02-01 00:00:00

  • Short-term aerobic training response in chronic myopathies.

    abstract::We have previously demonstrated that patients with mitochondrial myopathies can benefit from short-term aerobic exercise training. In this study, we compared the responses to short-term aerobic training of patients with mitochondrial myopathies, patients with nonmetabolic myopathies, and sedentary normal subjects. Tra...

    journal_title:Muscle & nerve

    pub_type: 临床试验,杂志文章

    doi:10.1002/(sici)1097-4598(199909)22:9<1239::aid-mus1

    authors: Taivassalo T,De Stefano N,Chen J,Karpati G,Arnold DL,Argov Z

    更新日期:1999-09-01 00:00:00

  • Thymus imaging in myasthenia gravis: The relevance in clinical practice.

    abstract:INTRODUCTION:The ability to distinguish between normal thymus, thymic hyperplasia, and thymoma should aid clinical management and decision making in patients with myasthenia gravis (MG). We sought to determine the accuracy of routine imaging in predicting thymic pathology. METHODS:We retrospectively analyzed records o...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26096

    authors: Klimiec E,Quirke M,Leite MI,Hilton-Jones D

    更新日期:2018-02-09 00:00:00

  • Charcot-Marie-Tooth disease with intermediate conduction velocities caused by a novel mutation in the MPZ gene.

    abstract::Charcot-Marie-Tooth (CMT) disease is a heterogeneous group of inherited sensory and motor neuropathies. Mutations in the gene that encodes for myelin protein zero (MPZ) can produce different phenotypes: CMT1 (with low conduction velocities), CMT2 (less frequent and with unaffected conduction velocities), and CMTID (wi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21643

    authors: Banchs I,Casasnovas C,Montero J,Volpini V,Martínez-Matos JA

    更新日期:2010-08-01 00:00:00

  • Peripheral neuropathy in glycogen storage disease type III: Fact or myth?

    abstract:INTRODUCTION:The aim of this study was to assess whether peripheral neuropathy is a feature of glycogen storage disease type IIIa (GSD IIIa) in adult patients. METHODS:Medical records of a cohort of adult GSD IIIa patients who underwent electromyography (EMG) and nerve conduction studies (NCS) were reviewed, and the r...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24977

    authors: Herlin B,Laforět P,Labrune P,Fournier E,Stojkovic T

    更新日期:2016-02-01 00:00:00

  • Proteins of muscle subcellular fractions in Duchenne progressive muscular dystrophy stained with "stains-all" cationic carbocyanine dye and with Coomassie Blue.

    abstract::The protein compositions of subcellular fractions of muscle obtained from 17 Duchenne dystrophy patients, 15 disease controls (10 different primary myopathies, 5 spinal muscular atrophy patients), and 10 normals were examined by polyacrylamide gel electrophoresis. The gels were stained with Coomassie Brilliant Blue an...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880120404

    authors: Niebroj-Dobosz I,Kornguth S,Schutta H,Siegel FL,Hausmanowa-Petrusewicz I

    更新日期:1989-04-01 00:00:00

  • What does chronic electrical stimulation teach us about muscle plasticity?

    abstract::The model of chronic low-frequency stimulation for the study of muscle plasticity was developed over 30 years ago. This protocol leads to a transformation of fast, fatigable muscles toward slower, fatigue-resistant ones. It involves qualitative and quantitative changes of all elements of the muscle fiber studied so fa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/(sici)1097-4598(199906)22:6<666::aid-mus3>

    authors: Pette D,Vrbová G

    更新日期:1999-06-01 00:00:00

  • Within-train neuromuscular propagation varies with torque in paralyzed human muscle.

    abstract::Electromyographic (EMG) recordings may serve an important role in predicting torque during repetitive activation of paralyzed muscle. We compared the initial M-wave to the subsequent M-waves of the same train under fatigued and recovered conditions in the paralyzed human soleus muscle. Sixteen individuals with chronic...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10245

    authors: Chang YJ,Shields RK

    更新日期:2002-11-01 00:00:00

  • Effects of extracorporeal shock-wave lithotripsy directed at the parotid gland on oxidative stress parameters and some trace element levels in facial nerve of rats.

    abstract:INTRODUCTION:This study was designed to assess the effect of extracorporeal shock-wave lithotripsy (ESWL) exposure of the parotid gland on oxidative stress and some trace element levels in the facial nerves of rats. METHODS:Twelve male Wistar albino rats were divided into two groups, each consisting of 6 animals. The ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22326

    authors: Kavak S,Garca MF,Gecit I,Meral I,Cengiz N,Demir H

    更新日期:2012-04-01 00:00:00

  • Neuroimaging of classic neuralgic amyotrophy.

    abstract:INTRODUCTION:Neuralgic amyotrophy (NA) often imposes diagnostic problems. Recently, MRI and high-resolution ultrasound (HRUS) have proven useful in diagnosing peripheral nerve disorders. METHODS:We performed a chart and imaging review of patients who were examined using neuroimaging and who were referred because of cl...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25147

    authors: Lieba-Samal D,Jengojan S,Kasprian G,Wöber C,Bodner G

    更新日期:2016-12-01 00:00:00

  • Painful cramps and giant myotonic discharges in a family with the Nav1.4-G1306A mutation.

    abstract:INTRODUCTION:Two previously reported Norwegian patients with painful muscle cramps and giant myotonic discharges were genotyped and compared with those of members of 21 families harboring the same mutation. METHODS:Using primers specific for SCN4A and CLCN1, the DNA of the Norwegian family members was amplified and bi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24672

    authors: Torbergsen T,Jurkat-Rott K,Stålberg EV,Løseth S,Hødneø A,Lehmann-Horn F

    更新日期:2015-10-01 00:00:00

  • Continuous motor unit activity confined to the upper extremities.

    abstract::We report a patient with clinical vermiform motor activity, muscle cramps, delayed relaxation of grip, and continuous motor unit discharges who developed mild symmetric symptoms in the upper extremities following a viral infection. Treatment with carbamazepine produced considerable symptomatic improvement. Needle elec...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110310

    authors: Tandan R,Fries TJ

    更新日期:1988-03-01 00:00:00

  • Inflammatory processes in amyotrophic lateral sclerosis.

    abstract::Neuroinflammation is a characteristic of pathologically affected tissue in several neurodegenerative disorders. These changes can be observed in the brainstem and spinal cord of amyotrophic lateral sclerosis (ALS) cases and in mouse models of the disease. They include an accumulation of large numbers of activated micr...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.10191

    authors: McGeer PL,McGeer EG

    更新日期:2002-10-01 00:00:00