Impact of aging on the progression of neuropathy after liver transplantation in transthyretin Val30Met amyloidosis.

Abstract:

INTRODUCTION:Information related to the long-term follow-up of neuropathy in patients with familial amyloid polyneuropathy after liver transplantation is still scarce. METHODS:We describe the neuropathic features of 3 patients with the transthyretin Val30Met mutation. Each patient underwent liver transplantation at an early stage of neuropathy, as indicated by the absence of motor dysfunction and relative preservation of myelinated fibers in sural nerve biopsy specimens. RESULTS:Although the patient with late-onset disease (at age 60 years) presented with the least amount of amyloid deposition, he had neuropathic progression after liver transplantation. An older early-onset (at age 40 years) patient reported a slight exacerbation of both somatic and autonomic neuropathic symptoms 10 years after transplantation. However, the younger early-onset (at age 28 years) patient did not exhibit characteristics suggestive of neuropathy 7 years after transplantation. CONCLUSION:Aging may determine the progression of neuropathy after liver transplantation.

journal_name

Muscle Nerve

journal_title

Muscle & nerve

authors

Koike H,Hashimoto R,Tomita M,Kawagashira Y,Iijima M,Nakamura T,Watanabe H,Kamei H,Kiuchi T,Sobue G

doi

10.1002/mus.23480

subject

Has Abstract

pub_date

2012-12-01 00:00:00

pages

964-70

issue

6

eissn

0148-639X

issn

1097-4598

journal_volume

46

pub_type

杂志文章
  • Calcium paradox in skeletal muscles: physiologic and microscopic observations.

    abstract::Immersion of rat hemidiaphragms in Ca2+-free Krebs solution (KS) containing Ca2+ chelator in vitro leads to separation of basal lamina from the plasma membrane, as well as transient contracture and rapid loss of twitch response [calcium paradox (CP) phase 1]. Subsequent immersion in regular KS results in necrosis of m...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090306

    authors: Soza M,Karpati G,Carpenter S

    更新日期:1986-03-01 00:00:00

  • Magnetic resonance imaging in Duchenne muscular dystrophy: longitudinal assessment of natural history over 18 months.

    abstract:INTRODUCTION:In Duchenne muscular dystrophy (DMD), fat replacement of muscle may be a useful endpoint in trials of therapy, although progression in different muscle groups is uneven. In this study we assessed the progression of fat replacement with T(1) -weighted imaging over 2 9-month periods. METHODS:Eight ambulant,...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.23879

    authors: Hollingsworth KG,Garrood P,Eagle M,Bushby K,Straub V

    更新日期:2013-10-01 00:00:00

  • Isometric contractions of normal and spastic human skeletal muscle.

    abstract::Isometric contractile properties of human elbow flexor muscles were examined in 27 normal subjects (7 females and 20 males). Contractions of elbow flexors were elicited by application of electrical pulses to the biceps motor points. The tension development was recorded at the wrist with the elbow angle fixed at 90 deg...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880040307

    authors: Ismail HM,Ranatunga KW

    更新日期:1981-05-01 00:00:00

  • Protection of human muscle acetylcholinesterase from soman by pyridostigmine bromide.

    abstract:INTRODUCTION:Pretreatment with pyridostigmine bromide (PB) of human intercostal muscle fibers exposed to the irreversible acetylcholinesterase (AChE) inhibitor soman was investigated. METHODS:Muscles were pretreated with 3 × 10(-6) M PB or saline for 20 minutes, then exposed to 10(-7) M soman for 10 minutes. RESULTS:...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21922

    authors: Maselli RA,Henderson JD,Ng J,Follette D,Graves G,Wilson BW

    更新日期:2011-04-01 00:00:00

  • Consideration of repetitive nerve stimulation of the median nerve in patients being evaluated for myasthenia gravis.

    abstract::Repetitive nerve stimulation (RNS) of the median nerve is rarely studied in myasthenia gravis (MG). We performed a retrospective analysis of RNS studies performed on 448 patients at our center between 2010 and 2016. Among 95 patients with MG, an abnormal decrement of the compound muscle action potential amplitude was ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.26713

    authors: Lee TH,Li Y

    更新日期:2019-12-01 00:00:00

  • Does impaired glucose metabolism cause polyneuropathy? Review of previous studies and design of a prospective controlled population-based study.

    abstract::In spite of extensive studies it is unclear whether impaired fasting glucose (IFG) or impaired glucose tolerance (IGT), i.e., impaired glucose metabolism (IGM), causes diabetic sensorimotor polyneuropathy (DSPN) or chronic idiopathic axonal polyneuropathy (CIAP); the results and conclusions vary considerably in differ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.20846

    authors: Dyck PJ,Dyck PJ,Klein CJ,Weigand SD

    更新日期:2007-10-01 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

  • Differential response of heat shock proteins to hindlimb unloading and reloading in the soleus.

    abstract::Hindlimb unloading (HU) results in oxidative stress, skeletal muscle atrophy, and increased damage upon reloading. Heat shock proteins (HSPs) protect against oxidative stress. However, it is unknown whether HSPs are depressed with long-term unloading (28 days) or reloading. We tested the hypotheses that long-term HU w...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20454

    authors: Lawler JM,Song W,Kwak HB

    更新日期:2006-02-01 00:00:00

  • Skin-derived precursor Schwann cell myelination capacity in focal tibial demyelination.

    abstract:INTRODUCTION:Skin-derived precursor cells (SKPs) are neural crest progenitor cells that can attain a Schwann cell-like phenotype through in vitro techniques (SKP-SCs). We hypothesized that SKP-SCs could produce mature myelin and, in doing so, facilitate the recovery of a focal demyelination injury. METHODS:We unilater...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24136

    authors: Grochmal J,Dhaliwal S,Stys PK,van Minnen J,Midha R

    更新日期:2014-08-01 00:00:00

  • Physical function and mobility in children with congenital myotonic dystrophy.

    abstract:INTRODUCTION:Congenital myotonic dystrophy (CDM) occurs when symptoms of myotonic dystrophy present at birth. In this study we evaluated the relationship between physical function, muscle mass, and age to provide an assessment of the disease and help prepare for therapeutic trials. METHODS:CDM participants performed t...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.25482

    authors: Pucillo EM,Dibella DL,Hung M,Bounsanga J,Crockett B,Dixon M,Butterfield RJ,Campbell C,Johnson NE

    更新日期:2017-08-01 00:00:00

  • Sensory physiology assessed by evoked potentials in survivors of poliomyelitis.

    abstract::Evidence suggests that sensory loss may occur in a proportion of patients affected by poliomyelitis. We hypothesize that sensory problems may be a lasting sequela in some polio survivors. Sensory pathways in polio survivors were evaluated clinically and electrophysiologically using sensory evoked potentials (SEPs). Pa...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.21093

    authors: Prokhorenko OA,Vasconcelos OM,Lupu VD,Campbell WW,Jabbari B

    更新日期:2008-10-01 00:00:00

  • Dystrophin gene transcripts skipping the mdx mutation.

    abstract::The mdx mouse, an animal model used to study Duchenne muscular dystrophy, has a nonsense mutation in exon 23 of the dystrophin gene which should result in a truncated protein that cannot be correctly localized at the sarcolemma of the muscle fibers. Immunohistochemical staining with antidystrophin antibodies has shown...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199706)20:6<728::aid-mus10

    authors: Wilton SD,Dye DE,Laing NG

    更新日期:1997-06-01 00:00:00

  • Skeletal muscle ultrastructure and function in statin-tolerant individuals.

    abstract:INTRODUCTION:Statins have well-known benefits on cardiovascular mortality, though up to 15% of patients experience side effects. With guidelines from the American Heart Association, American College of Cardiology, and American Diabetes Association expected to double the number of statin users, the overall incidence of ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24722

    authors: Rengo JL,Callahan DM,Savage PD,Ades PA,Toth MJ

    更新日期:2016-02-01 00:00:00

  • Minimal clinically important difference in myasthenia gravis: outcomes from a randomized trial.

    abstract:INTRODUCTION:The minimal clinically important difference (MCID) is the smallest outcome change that has clinical significance. Its use has not been established in the study of myasthenia gravis (MG). METHODS:Patients from a published intravenous immunoglobulin (IVIg) vs. placebo study were studied. One anchor-based an...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,随机对照试验

    doi:10.1002/mus.23988

    authors: Katzberg HD,Barnett C,Merkies IS,Bril V

    更新日期:2014-05-01 00:00:00

  • Clinical utility of reflex studies in assessing cervical radiculopathy.

    abstract::We prospectively studied the diagnostic utility of upper limb segmental reflexes in patients with suspected cervical radiculopathy (CR). Fifty-three patients (29 men and 24 women), referred for electrodiagnostic testing, were positive for at least one of four clinical criteria for CR: abnormal (1) history, (2) motor (...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199908)22:8<1075::aid-mus1

    authors: Miller TA,Pardo R,Yaworski R

    更新日期:1999-08-01 00:00:00

  • A freeze-fracture analysis of intramembrane particle densities on dystrophic hamster heart sarcolemma.

    abstract::The intramembrane particle (IMP) profile of control and dystrophic (Bio 14.6) hamster cardiac muscle plasma membrane was assessed in freeze-fracture replicas to determine whether this animal model of muscular dystrophy exhibits the same membrane characteristics found in skeletal muscle from other more thoroughly studi...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880070702

    authors: Graham KA,Shivers RR,Atkinson BG

    更新日期:1984-09-01 00:00:00

  • The temperature dependence of halothane-induced contractures of skeletal muscle.

    abstract::Frog muscles bathed in solutions equilibrated with 0.5%-2.0% halothane develop large contractures when cooled to 2-4 degrees C. These halothane-cooling contractures (HCC) are dose dependent and reproducible; they are potentiated by lidocaine (5 mM), abolished by procaine (5 mM), and partially inhibited by procainamide...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880090107

    authors: Suarez-Kurtz G,Sudo RT

    更新日期:1986-01-01 00:00:00

  • Asymptomatic vasculitic neuropathy.

    abstract:INTRODUCTION:We performed a retrospective analysis of the clinical, pathological, and electrophysiological features of 21 cases of Asymptomatic vasculitic neuropathy (AsVN). METHODS:Among 270 patients with biopsy-proven vasculitic neuropathy, we identified 21 (7.8%) who had asymptomatic neuropathy. RESULTS:Of the 21 ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24494

    authors: Kurt S,Alsharabati M,Lu L,Claussen GC,Oh SJ

    更新日期:2015-07-01 00:00:00

  • Central fatigue assessed by transcranial magnetic stimulation.

    abstract::Central fatigue is a subjective phenomenon which can be examined using transcranial magnetic stimulation (TMS). To assess central fatigue, we compared TMS and peripheral electrical stimulations in patients with central nervous system (CNS) lesions and controls before and after an exhaustive task. The recovery times of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(SICI)1097-4598(199611)19:11<1429::AID-MUS

    authors: Liepert J,Kotterba S,Tegenthoff M,Malin JP

    更新日期:1996-11-01 00:00:00

  • Persistent and transient "conduction block" in motor neuron diseases.

    abstract::Although conduction block indicates dysfunction of peripheral nerve, it may occur in patients with clinically typical motor neuron disease. There are no universally accepted criteria to identify conduction block, so diagnosis may be difficult. In some peripheral neuropathies, conduction block persists over long period...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880160903

    authors: Lange DJ,Trojaborg W,McDonald TD,Blake DM

    更新日期:1993-09-01 00:00:00

  • Advancements in magnetic resonance imaging-based biomarkers for muscular dystrophy.

    abstract::Recent years have seen steady progress in the identification of genetic muscle diseases as well as efforts to develop treatment for these diseases. Consequently, sensitive and objective new methods are required to identify and monitor muscle pathology. Magnetic resonance imaging offers multiple potential biomarkers of...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.26497

    authors: Leung DG

    更新日期:2019-10-01 00:00:00

  • Acute exercise causes mitochondrial DNA deletion in rat skeletal muscle.

    abstract::The present study was conducted to determine the effects of acute overload exercise on mitochondrial DNA and the structure of skeletal muscles. Rats were forced to run for 20 min until reaching complete exhaustion. We detected the large-scale deletion (7052 bp) of mitochondrial DNA by the nested polymerase chain react...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/(sici)1097-4598(199902)22:2<258::aid-mus15

    authors: Sakai Y,Iwamura Y,Hayashi J,Yamamoto N,Ohkoshi N,Nagata H

    更新日期:1999-02-01 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

  • Anodal sensory nerve action potentials: From physiological understanding to potential clinical applicability.

    abstract:INTRODUCTION:Low-intensity electrical stimuli of digital nerves may generate a double peak potential (DPp), composed of a cathodal (caAP) and an anodal (anAP) potential in orthodromic recordings. METHODS:We studied the effects on caAP and anAP of stimuli of variable intensity, duration, and frequency. We also applied ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.24957

    authors: Leote J,Pereira P,Cabib C,Cipullo F,Valls-Sole J

    更新日期:2016-06-01 00:00:00

  • Motor neuron firing range, axonal conduction velocity, and muscle fiber histochemistry in neuromuscular diseases.

    abstract::The voluntary discharge properties and axonal conduction velocity of single motor units were studied in patients with neuromuscular diseases with retained differentiation of the muscle fibers into type 1 and type 2, and in patients with late-onset hereditary distal myopathy in which muscle fibers have only intermediat...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880020603

    authors: Borg J,Grimby L,Hannerz J

    更新日期:1979-11-01 00:00:00

  • Three-dimensional topography of the motor endplates of the rat gastrocnemius muscle.

    abstract::Spatial distribution of motor endplates affects the shape of the electrical activity recorded from muscle. In order to provide information for realistic models of action potential propagation within muscles, we assembled three-dimensional maps of the motor endplates of the rat medial gastrocnemius (MGM) and lateral ga...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20378

    authors: Prodanov D,Thil MA,Marani E,Delbeke J,Holsheimer J

    更新日期:2005-09-01 00:00:00

  • The tarsal tunnel syndrome.

    abstract::Tarsal tunnel syndrome is relatively rare and the diagnosis may be difficult even though the etiologies for the syndrome are multiple. The symptoms are often vague but are usually burning pain and paresthesias in the toes and soles of the feet with nocturnal exacerbations. The physical examination may elicit a sensory...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.880060908

    authors: DeLisa JA,Saeed MA

    更新日期:1983-11-01 00:00:00

  • COVID-19-associated Guillain-Barré syndrome: The early pandemic experience.

    abstract::Guillain-Barré syndrome (GBS) is an inflammatory polyradiculoneuropathy associated with numerous viral infections. Recently, there have been many case reports describing the association between coronavirus disease-2019 (COVID-19) and GBS, but much remains unknown about the strength of the association and the features ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章,评审

    doi:10.1002/mus.27024

    authors: Caress JB,Castoro RJ,Simmons Z,Scelsa SN,Lewis RA,Ahlawat A,Narayanaswami P

    更新日期:2020-10-01 00:00:00

  • Diabetic neuropathies.

    abstract::Diabetic neuropathies are the most common type of neuropathies seen in clinical practice. These neuropathies can range clinically from asymptomatic to manifesting symptoms caused by motor, sensory, and autonomic nerve dysfunction. These neuropathies can affect the peripheral nervous system, pain receptors, cardiovascu...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.27014

    authors: Patel K,Horak H,Tiryaki E

    更新日期:2021-01-01 00:00:00

  • Medullary infarcts may cause ipsilateral masseter reflex abnormalities.

    abstract::There is a suprasegmental influence on the masseter reflex (MassR) in animals, which is mediated via the fifth nerve spinal nucleus (5SpN). Corresponding data in humans are lacking. Out of 268 prospectively recruited patients with clinical signs of acute brainstem infarctions, we identified 38 with magnetic resonance ...

    journal_title:Muscle & nerve

    pub_type: 杂志文章

    doi:10.1002/mus.20829

    authors: Thömke F,Marx JJ,Cruccu G,Stoeter P,Hopf HC

    更新日期:2007-10-01 00:00:00