Pain in patients with myotonic dystrophy type 2: a postal survey in Finland.

Abstract:

INTRODUCTION:Widespread musculoskeletal pain is a well-known symptom of myotonic dystrophy type 2 (DM2), but so far it has been addressed in only a few studies. METHODS:A postal survey for all traceable DM2 patients (n = 132) was conducted. A specific questionnaire, and severity and interference subscales of the Brief Pain Inventory, quality of life (RAND-36), and modified Beck Depression Inventory were completed. RESULTS:The response rate was 70%. The mean age of respondents was 53 years, 59% of whom were women. Current pain was reported by 54%. Lifetime prevalence of pain was 76%. The mean intensity of pain at its highest in the last week was 5.9, and 2.3 at its lowest (on a numerical rating scale of 0-10). Quality of life was lower in DM2 patients who reported pain. In 18%, the depression score was noticeably different. CONCLUSIONS:Pain of moderate severity and unpleasant muscular symptoms are common in DM2. DM2 should be taken into consideration in the differential diagnosis of musculoskeletal pain.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Suokas KI,Haanpää M,Kautiainen H,Udd B,Hietaharju AJ

doi

10.1002/mus.22249

subject

Has Abstract

pub_date

2012-01-01 00:00:00

pages

70-4

issue

1

eissn

0148-639X

issn

1097-4598

journal_volume

45

pub_type

杂志文章
  • Serum CK, calcium, magnesium, and oxidative phosphorylation in mdx mouse muscular dystrophy.

    abstract::Serum creatine kinase (CK) activity, calcium (Ca) and magnesium (Mg) contents of skeletal muscle and isolated mitochondria, as well as oxidative phosphorylation of X-linked muscular dystrophic (mdx) mice were compared with normal control animals at ages 5, 10, and 23 weeks. Serum CK is elevated in mdx mice at all ages...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880110809

    authors: Glesby MJ,Rosenmann E,Nylen EG,Wrogemann K

    更新日期:1988-08-01 00:00:00

  • Needle electromyography of the frontalis muscle in patients with amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:We sought to determine which muscles to choose for better assessment of the craniobulbar region in establishing the diagnosis of amyotrophic lateral sclerosis (ALS). METHODS:We studied the frontalis muscle in 83 controls and compared it with the tongue, sternocleidomastoid (SCM), and trapezius muscles in ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25236

    authors: Pan H,Jian F,Lin J,Chen N,Zhang Z,Wang Y,Cui L,Kimura J

    更新日期:2016-12-01 00:00:00

  • Amyotrophic lateral sclerosis-Evolutionary and other perspectives.

    abstract::In this study some particular and puzzling aspects of amyotrophic lateral sclerosis (ALS) are discussed, with an emphasis on the role of neocortical evolution. Other issues explored include the nature of the clinical deficit in ALS; anatomical and evolutionary aspects of the neocortex, motor cortex, and corpus callosu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21404

    authors: Eisen A

    更新日期:2009-08-01 00:00:00

  • Sensory group Ia proximal conduction velocity.

    abstract::The fastest median and ulnar velocities derived by recording motor and mixed nerve action potentials, F waves, H-reflexes, and somatosensory evoked potentials (SEPs) were compared. H-reflex recording was facilitated by employing selective group Ia excitation during voluntary muscular contraction. Mixed nerve, SEP, and...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880070807

    authors: Eisen A,Hoirch M,White J,Calne D

    更新日期:1984-10-01 00:00:00

  • Ultrasound elastography assessment of the median nerve in leprosy patients.

    abstract:INTRODUCTION:We sought to compare median nerve elasticity between leprosy patients (LPs) and healthy volunteers (HVs) using ultrasound elastography (UE). METHODS:Two radiologists independently measured the strain ratio of the median nerve/flexor digitorum superficialis muscle (MN/FDSM) of 18 LP and 18 HV using real-ti...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25510

    authors: Nogueira-Barbosa MH,Lugão HB,Gregio-Júnior E,Crema MD,Kobayashi MTT,Frade MAC,Pavan TZ,Carneiro AAO

    更新日期:2017-09-01 00:00:00

  • Single fiber EMG in the frontalis muscle in ocular myasthenia: specificity and sensitivity.

    abstract::Patients (n = 41) with isolated weakness of the eyelids or extraocular muscles, who had been referred for single fiber electromyography (SFEMG), were followed up after 4 to 24 months, At follow-up the patients were classified as "definite ocular myasthenia gravis" (MG), "definite other diagnosis," or "no definite diag...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150322

    authors: Rouseev R,Ashby P,Basinski A,Sharpe JA

    更新日期:1992-03-01 00:00:00

  • A prognostic model for the patient-reported outcome of surgical treatment of carpal tunnel syndrome.

    abstract:INTRODUCTION:Many prognostic factors have been studied in carpal tunnel decompression, but most studies consider only a subset of variables. METHODS:Three thousand three hundred thirty-two operations were used to develop prognostic models, and 885 operations were used for validation. Outcome recorded on a Likert scale...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26297

    authors: Bowman A,Rudolfer S,Weller P,Bland JDP

    更新日期:2018-12-01 00:00:00

  • Fatigue trends in and the diagnosis of myasthenia gravis by frequency analysis of EMG interference patterns.

    abstract::Twenty patients with myasthenia gravis were studied. Needle interference patterns at maximal isometric contractions were recorded from the biceps brachii muscles. Each recording lasted for 30 seconds and induced some fatigue. The EMG signals were transformed into power spectra and were analyzed for differences between...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880080410

    authors: Yaar I,Mitz AR,Pottala EW

    更新日期:1985-05-01 00:00:00

  • Clinical and molecular aspects of the myotonic dystrophies: a review.

    abstract::Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in adults, has intrigued physicians for over a century. Unusual features, compared with other dystrophies, include myotonia, anticipation, and involvement of other organs, notably the brain, eyes, smooth muscle, cardiac co...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20301

    authors: Machuca-Tzili L,Brook D,Hilton-Jones D

    更新日期:2005-07-01 00:00:00

  • Congenital myasthenia: further evidence of disease heterogeneity.

    abstract::The findings in two cases of congenital myasthenia investigated by intercostal muscle biopsy are presented. The first case, a 16-year-old boy, showed reduced miniature endplate potential amplitude and normal 125I-alpha-bungarotoxin binding to postsynaptic acetylcholine receptors. Muscle biopsy and endplate ultrastruct...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090307

    authors: Lecky BR,Morgan-Hughes JA,Murray NM,Landon DN,Wray D,Prior C

    更新日期:1986-03-01 00:00:00

  • Effect of gender and obesity on electrical current thresholds.

    abstract:INTRODUCTION:In this study we investigated the influence of gender and obesity on electrical current thresholds in an attempt to optimize the application of skeletal muscle electrical stimulation (ES) in clinical practice. METHODS:Thirty-two obese and 35 age-matched, non-obese men and women received graded ES to the q...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.22050

    authors: Maffiuletti NA,Morelli A,Martin A,Duclay J,Billot M,Jubeau M,Agosti F,Sartorio A

    更新日期:2011-08-01 00:00:00

  • Adjustments in the force-frequency relationship during passive and exercise-induced hyperthermia.

    abstract:INTRODUCTION:We examined the extent to which fatiguing cycling exercise in the heat influences contractile function in modulating the force-frequency relationship. METHODS:Before (∽37.0 °C) and after (∽38.5 °C) exercise (ExH) and passive (PaH) hyperthermia, an 8-s train of stimulation at 10, 20, 50, and 100 Hz (2 s pe...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24228

    authors: Périard JD,Racinais S,Thompson MW

    更新日期:2014-11-01 00:00:00

  • Analysis of crosstalk in the mechanomyographic signals generated by forearm muscles during different wrist postures.

    abstract:INTRODUCTION:In this study, we analyzed the crosstalk in mechanomyographic (MMG) signals generated by the extensor digitorum (ED), extensor carpi ulnaris (ECU), and flexor carpi ulnaris (FCU) muscles of the forearm during wrist flexion (WF) and extension (WE) and radial (RD) and ulnar (UD) deviations. METHODS:Twenty r...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24454

    authors: Islam A,Sundaraj K,Ahmad RB,Sundaraj S,Ahamed NU,Ali MA

    更新日期:2015-06-01 00:00:00

  • Chronic inflammatory demyelinating polyradiculoneuropathy in children: II. Long-term follow-up, with comparison to adults.

    abstract::We previously reviewed the presentation, initial clinical course, and electrodiagnostic features of children with chronic inflammatory demyelinating polyradiculoneuropathy (CIDP). We now report the long-term follow-up of 12 children with idiopathic CIDP, and compare these to 62 adults with idiopathic CIDP. Children of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199712)20:12<1569::aid-mus

    authors: Simmons Z,Wald JJ,Albers JW

    更新日期:1997-12-01 00:00:00

  • Coexistent autoimmune autonomic ganglionopathy and myasthenia gravis associated with non-small-cell lung cancer.

    abstract::We report the case of a 55-year-old man with non-small-cell lung cancer who underwent radiation, chemotherapy with carbotaxol and paclitaxel, and left upper lobe removal 2 years prior to evaluation. He was referred for disabling orthostatic hypotension (113/69 mm Hg supine and 66/47 mm Hg standing after 10 minutes) wi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21528

    authors: Peltier AC,Black BK,Raj SR,Donofrio P,Robertson D,Biaggioni I

    更新日期:2010-03-01 00:00:00

  • Novel mutations in the gene encoding very long-chain acyl-CoA dehydrogenase identified in patients with partial carnitine palmitoyltransferase II deficiency.

    abstract:INTRODUCTION:Twenty-six patients with clinical symptoms of adult onset carnitine palmitoyltransferase II (CPTII) deficiency were examined. All patients had skeletal muscle CPTII enzyme activity levels indicative of heterozygosity for CPT2 mutations, however sequence analysis identified no pathogenic mutations within th...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23498

    authors: Isackson PJ,Sutton KA,Hostetler KY,Vladutiu GD

    更新日期:2013-02-01 00:00:00

  • Failure to detect HTLV-I by in situ hybridization in the biopsied muscles of viral carriers with polymyositis.

    abstract::Direct infection of muscle fibers by human T-lymphotropic virus type I (HTLV-I) has recently been reported in a patient with polymyositis infected with both HTLV-I and human immunodeficiency virus (HIV). Coinfections of these viruses are frequently found in the United States. In Kagoshima, Japan, patients with polymyo...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880150108

    authors: Higuchi I,Nerenberg M,Yoshimine K,Yoshida M,Fukunaga H,Tajima K,Osame M

    更新日期:1992-01-01 00:00:00

  • Myasthenia gravis associated with HTLV-I infection and atypical brain lesions.

    abstract::We report a patient who experienced progressive diplopia and distal weakness of the upper limbs. Magnetic resonance imaging of the brain showed extensive white matter lesions and analysis of cerebrospinal fluid revealed acute human T-lymphotropic virus type I (HTLV-I) infection. Myasthenia gravis (MG) was evidenced by...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20694

    authors: Lalive PH,Allali G,Truffert A

    更新日期:2007-04-01 00:00:00

  • Effect of static stretch training on neural and mechanical properties of the human plantar-flexor muscles.

    abstract::To determine the contributions of neural and mechanical mechanisms to the limits in the range of motion (ROM) about a joint, we studied the effects of 30 sessions of static stretch training on the characteristics of the plantar-flexor muscles in 12 subjects. Changes in the maximal ankle dorsiflexion and the torque pro...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10549

    authors: Guissard N,Duchateau J

    更新日期:2004-02-01 00:00:00

  • Peripheral axon caliber and conduction velocity are decreased after burn injury in mice.

    abstract::Peripheral neuropathies are reported to arise as a result of the systemic inflammatory response produced by a full-thickness cutaneous burn injury. This study was designed to characterize the magnitude and time course of functional and morphological changes in peripheral axons that arise after a full-thickness dermal ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20306

    authors: Higashimori H,Whetzel TP,Mahmood T,Carlsen RC

    更新日期:2005-05-01 00:00:00

  • Detecting fasciculations in cranial nerve innervated muscles with ultrasound in amyotrophic lateral sclerosis.

    abstract:INTRODUCTION:Cranial muscle fasciculations may be difficult to detect in amyotrophic lateral sclerosis (ALS). Ultrasound (US) detection of fasciculations in these muscles may have clinical utility. METHODS:Patients with suspected ALS were prospectively enrolled. Nerve conduction studies, needle electromyography (EMG),...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,多中心研究

    doi:10.1002/mus.25676

    authors: O'gorman CM,Weikamp JG,Baria M,Van Den Engel-Hoek L,Kassardjian C,Van Alfen N,Boon AJ

    更新日期:2017-12-01 00:00:00

  • A novel CLCN1 mutation: P480T in a Japanese family with Thomsen's myotonia congenita.

    abstract::At least 50 disease-causing mutations in the skeletal muscle voltage-gated chloride channel gene (CLCN1), almost all of which originate from Caucasian families, have been identified. We investigated a Japanese family with Thomsen's myotonia congenita that included 16 affected individuals (8 men and 8 women) through fi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/1097-4598(200103)24:3<357::aid-mus1006>3.0

    authors: Sasaki R,Ito N,Shimamura M,Murakami T,Kuzuhara S,Uchino M,Uyama E

    更新日期:2001-03-01 00:00:00

  • A large German kindred with cold-aggravated myotonia and a heterozygous A1481D mutation in the SCN4A gene.

    abstract::Muscle sodium-channel disorders cover a spectrum of rare myotonic diseases. In a German family with 17 affected individuals in four generations, we identified a heterozygous missense mutation in exon 24 A1481D (c.4442 C>A) of the voltage-gated sodium channel gene (SCN4A) alpha subunit. Phenotypes of 12 family members ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20733

    authors: Schoser BG,Schröder JM,Grimm T,Sternberg D,Kress W

    更新日期:2007-05-01 00:00:00

  • Transthyretin amyloidosis presenting with multifocal demyelinating mononeuropathies.

    abstract::We describe a patient with transthyretin amyloidosis who presented with multifocal mononeuropathies with features of demyelination on nerve conduction studies, a constellation of findings not previously described in amyloid polyneuropathy. Genetic testing revealed a valine122isoleucine mutation in the coding region of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.10614

    authors: Briemberg HR,Amato AA

    更新日期:2004-02-01 00:00:00

  • Involvement of PI3K/Akt/TOR pathway in stretch-induced hypertrophy of myotubes.

    abstract::Skeletal muscle cells are hypertrophied by mechanical stresses, but the underlying molecular mechanisms are not fully understood. Two signaling pathways, phosphatidylinositol 3-kinase (PI3K)/Akt to target of rapamycin (TOR) and extracellular signal-regulated kinase kinase (MEK) to extracellular signal-regulated kinase...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21473

    authors: Sasai N,Agata N,Inoue-Miyazu M,Kawakami K,Kobayashi K,Sokabe M,Hayakawa K

    更新日期:2010-01-01 00:00:00

  • Yields of muscle from myogenic cells implanted into young and old mdx hosts.

    abstract::Implantation of normal muscle precursor cells (mpc) for treatment for inherited myopathies such as Duchenne muscular dystrophy is in clear need of improvement to become practicable, but few variables have been studied comparatively. Here, we report the first quantitative estimate of the effectiveness of implanting mpc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(SICI)1097-4598(199602)19:2<132::AID-MUS2>

    authors: Morgan JE,Fletcher RM,Partridge TA

    更新日期:1996-02-01 00:00:00

  • Sources of error in the diagnosis of Guillain-Barre syndrome.

    abstract::A careful monitoring of the accuracy of diagnosis in six cases of Guillain-Barre syndrome has shown that a substantial proportion of these patients initially diagnosed as having Guillain-Barre syndrome on the basis of characteristic clinical findings and an elevated level of protein in the spinal fluid had a neuropath...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880050206

    authors: Feit H,Tindall RS,Glasberg M

    更新日期:1982-02-01 00:00:00

  • Acquired neuromyotonia and peripheral neuropathy in a patient with Hodgkin's disease.

    abstract::Acquired neuromyotonia is characterized by hyperexcitability of motor nerves resulting in continuous muscle fiber activity. It occurs most often as a paraneoplastic syndrome in patients with cancers of the immune system. Antibodies against voltage-gated potassium channels (VGKCs) have been detected in some patients. P...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.1078

    authors: Lahrmann H,Albrecht G,Drlicek M,Oberndorfer S,Urbanits S,Wanschitz J,Zifko UA,Grisold W

    更新日期:2001-06-01 00:00:00

  • Probabilistic muscle characterization using QEMG: application to neuropathic muscle.

    abstract::Clinicians who use electromyographic (EMG) signals to help determine the presence or absence of abnormality in a muscle often, with varying degrees of success, evaluate sets of motor unit potentials (MUPs) qualitatively and/or quantitatively to characterize the muscle in a clinically meaningful way. The resulting musc...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21456

    authors: Pino LJ,Stashuk DW,Boe SG,Doherty TJ

    更新日期:2010-01-01 00:00:00

  • Optimal location for eliciting the tibial H-reflex and motor response.

    abstract:INTRODUCTION:Although there are numerous protocols to adjust the amplitude of the Hoffmann reflex (H-reflex) relative to the size of the direct motor response (M-response), the optimal stimulating location has not been described. We sought to determine the optimal positioning of the stimulating cathode when evoking the...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26308

    authors: Özyurt MG,Shabsog M,Dursun M,Türker KS

    更新日期:2018-12-01 00:00:00