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2.
Nervenarzt ; 95(6): 553-559, 2024 Jun.
Artigo em Alemão | MEDLINE | ID: mdl-38193935

RESUMO

The type, distribution pattern and time course of spontaneous muscular activity are important for the diagnostics of neuromuscular diseases in the clinical practice. In neurogenic lesions with motor axonal involvement, pathologic spontaneous activity (PSA) is usually reliably detectable by needle electromyography (EMG) 2-4 weeks after occurrence of the lesion. The distribution pattern correlates with the lesion location. The focus of the present work is the description of the different forms of PSA in myogenic diseases.


Assuntos
Eletromiografia , Músculo Esquelético , Humanos , Músculo Esquelético/fisiopatologia , Doenças Neuromusculares/fisiopatologia , Doenças Neuromusculares/diagnóstico , Contração Muscular/fisiologia
3.
Klin Monbl Augenheilkd ; 241(1): 110-118, 2024 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-36581053

RESUMO

PURPOSE: Dry eye syndrome (DES) is one of the most common diseases of the ocular surface. Affected persons suffer from different subjective complaints, with sometimes severe impairment in the quality of life. The aetiology and pathogenesis are multifactorial, multifaceted, and not yet fully understood. The present study is intended to provide deeper insights into possible triggering factors and correlating comorbidities. MATERIALS AND METHODS: In German ophthalmological practices, 306 persons (174 women, 132 men, age: 18 - 87 years) were interviewed by questionnaire on concomitant diseases and possible further triggering factors. DES was diagnosed by an ophthalmologist in 170 cases. The statistical comparative analysis between persons with and without DES was carried out using the chi-squared test (SPSS statistical software). RESULTS: DES occurred with significantly (p < 0.05) increased frequency in women over 40 years of age, as well as in persons exposed to screen work, air conditioning, persons with chronic ocular inflammation, myomas (hysterectomy), dry skin, arterial hypertonicity in need of medication, cardiac arrhythmias, fatty liver, gastric ulcer, appendicitis, cholecystectomy, depression, hyperlipidaemia, hyperuricaemia, osteoporosis, and nephrolithiasis. CONCLUSION: Some of the known comorbidities and DES risk factors, e.g., computer work or depression, were confirmed. In contrast, the higher prevalence of hyperlipidaemia, hyperuricaemia, osteoporosis, nephrolithiasis, and fibroids among DES patients has not previously been reported. Additional studies should be performed on causal connections between DES and specific comorbidities.


Assuntos
Síndromes do Olho Seco , Hiperlipidemias , Hiperuricemia , Nefrolitíase , Osteoporose , Masculino , Humanos , Feminino , Adulto , Pessoa de Meia-Idade , Adolescente , Adulto Jovem , Idoso , Idoso de 80 Anos ou mais , Qualidade de Vida , Hiperuricemia/complicações , Síndromes do Olho Seco/diagnóstico , Síndromes do Olho Seco/epidemiologia , Fatores de Risco , Hiperlipidemias/complicações , Osteoporose/complicações , Nefrolitíase/complicações
4.
Muscle Nerve ; 62(5): 593-596, 2020 11.
Artigo em Inglês | MEDLINE | ID: mdl-33180362

RESUMO

BACKGROUND: The time interval between two potential components of the same motor unit potential (MUP) is measured for jitter analysis. Enhanced jitter is generally thought to result from impaired neuromuscular transmission as occurs in myasthenia gravis or during reinnervation. METHODS: Within a database of conventional video-electromyography (EMG) recordings 4 MUP with peculiar jitter patterns were identified. In 1 spontaneously discharging MUP, massive and chaotic jitter was seen with a mean consecutive difference (MCD) of 9.3 ms. In 2 spontaneously discharging MUP a certain potential subgroup jittered relative to the other part(s) of the MUP (MCD 2.0 and 3.3 ms). A jittering satellite was detected in a fourth voluntarily recruited MUP (MCD 0.6 ms). RESULTS: These different jitter patterns recorded with conventional EMG technique may mainly result from dysmyelination. CONCLUSIONS: A new look at the contribution of dysmyelination to abnormal jitter is also warranted in single fiber EMG recordings.


Assuntos
Eletromiografia/métodos , Neurônios Motores/fisiologia , Fibras Musculares Esqueléticas/fisiologia , Idoso , Neuropatias do Plexo Braquial/fisiopatologia , Feminino , Humanos , Masculino , Paralisia/fisiopatologia
5.
Brain Sci ; 10(6)2020 Jun 05.
Artigo em Inglês | MEDLINE | ID: mdl-32517058

RESUMO

Complex repetitive discharges (CRDs) are poorly understood phenomena in needle electromyography (EMG) recordings. The data presented here suggest that CRDs may mainly be a sign of motor unit reinnervation. EMG "video" data of 108 CRDs from neurogenic (ND, n = 39) and myogenic (MD, n = 14) disorders were retrospectively analyzed for cycle duration, potential-free time intervals, spike components (SC), maximum amplitudes, blockade, and increased jitter. CRD-SC in ND disorders (9.3 ± 7.8) outnumbered those in MD disorders (6.3 ± 6.2). The CRD cycle duration was correlated with SC and silent periods (p each < 0.000001). Blockade was observed in 36% and increased jitter in 27% of the CRDs. A higher number of CRD-SC in ND vs. MD fits the known differences in motor unit dimensions. Blockade and increased jitter are known features of diseased neuromuscular junctions, such as during reinnervation. The SC patterns of single CRD cycles resemble reinnervation potentials. Thus, CRDs may result from myo-axonal re-excitation in sprouting motor units. The purpose of this investigation was to better understand the circumstances under which CRDs may occur and eventually to contribute to the understanding of their pathogenesis.

6.
Heliyon ; 6(6): e04230, 2020 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-32596526

RESUMO

Chronic inflammatory demyelinating polyneuropathy (CIDP) is a relatively rare disease with progressive limb weakness and sensory loss. A few patients show a severely progressing course without major response to intravenous immunoglobulin or plasma exchange therapy. CIDP-MGUS (monoclonal gammopathy of undetermined significance) is a seldom CIDP variant that has been rarely addressed in therapeutic studies. In the presented CIDP-MGUS case, B cell depletion with rituximab had a favourable effect on the disease course, clinically and in nerve conduction studies.

7.
J Clin Neurosci ; 74: 238-240, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31982277

RESUMO

An ischemic stroke during sexual intercourse is very rare. A basilar artery thrombosis during sexual intercourse has not been described previously. We report a young woman with a life-threatening basilar artery thrombosis during sexual intercourse, with a resulting locked-in syndrome. The positive high intensity transient signals (HITS) diagnosis showed a right-to-left shunt and is in line with paradoxic embolism. The molecular genetics revealed a homozygosity 4G/4G in the region PAI1, -675 (promoter polymorphism) as a risk factor for ischemic stroke. Sexual intercourse is a possible, albeit unusual stroke cause, especially in young people.


Assuntos
Artéria Basilar/patologia , Coito , Acidente Vascular Cerebral/etiologia , Trombose/complicações , Adolescente , Adulto , Encéfalo/patologia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Trombose/patologia
8.
Muscle Nerve ; 61(3): 387-390, 2020 03.
Artigo em Inglês | MEDLINE | ID: mdl-31875989

RESUMO

INTRODUCTION: Motor unit hyperexcitability (MUH) may become manifest in needle electromyography (EMG) recordings as fasciculation potentials, myokymic discharges, or neuromyotonic discharges. Here, we describe a further MUH phenomenon. METHODS: Needle EMG recordings of the Neurology Hospital of Halle (Saale) stored in a video mode as .wav data between 2000 and 2015 were screened for spontaneous continuous motor unit single discharges (SCMUSD). RESULTS: We identified 23 video needle EMG waveforms from 14 patients with SCMUSD. The corresponding motor units discharged at a rate of about 6 H Z (6.3 ± 4.0; range, 1.3-18.1). The coefficient of variation of the discharge rate was 3.5% ± 1.7%. Neurogenic disorders were diagnosed in 12 patients, limb girdle muscle dystrophy was diagnosed in one patient, and stiff-limb syndrome was diagnosed in one patient. DISCUSSION: Spontaneous continuous motor unit single discharge, as described here, widens the spectrum of MUH phenomena.


Assuntos
Potenciais de Ação , Neurônios Motores/fisiologia , Doenças Neuromusculares/fisiopatologia , Adulto , Idoso , Idoso de 80 Anos ou mais , Eletrodos , Eletromiografia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Doença dos Neurônios Motores , Músculo Esquelético/inervação , Doenças Neuromusculares/diagnóstico
9.
Mol Biol Rep ; 46(4): 4085-4094, 2019 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-31087247

RESUMO

The aetiology of inflammatory myopathies is not clearly known. A predominance of activated Cd8+ T lymphocytes in inflammatory infiltrates has already been detected. Superantigens activate lymphocytes in an oligoclonal manner. In the present investigation, we investigated local effects after injection of the superantigen (Sag) Staphylococcus enterotoxin A (SEA) in the quadriceps femoris muscle of Lewis rats. Histopathology and gene expression profiling was performed after injection of SEA or saline (control group) after one, three and 10 days. Histology revealed focal myositis predominated by Cd8+ T lymphocytes with a perimysial, endomysial and perivascular distribution, peaking 3 days after SEA injection. Using DNA microarray analysis (Affymetrix Rat Genome 230 2.0) genes that were differentially over-expressed at least 15 times at days one, three or ten after SEA injection were further analysed. One day after SEA injection over-expressed genes were related to the immune response (e.g. Fcnb, CD8a) but also to cell proliferation, differentiation and migration (e.g. Mpp2). Three days after SEA injection, differentially overexpressed genes were mainly related to the immune reaction with a clear signature for a Cd8+ T lymphocyte response (e.g. Cd3d, Cd8, Prf1, Gzmb). Ten days after SEA injection, the differentially overexpressed genes were again associated with the immune reaction (e.g. Cd3d, Il2) but also with regenerative processes and wound healing (e.g. Tgfa, Tpm1, Ripply1). The inflammatory response induced by SEA in Lewis rats shares histological and molecular similarities to polymyositis in humans. Therefore, SEA induced myositis can be taken as a new and apt model for polymyositis.


Assuntos
Enterotoxinas/imunologia , Miosite/imunologia , Superantígenos/imunologia , Animais , Linfócitos T CD8-Positivos/efeitos dos fármacos , Antígenos de Histocompatibilidade Classe II , Peptídeos e Proteínas de Sinalização Intracelular , Ativação Linfocitária , Masculino , Proteínas de Membrana , Modelos Animais , Ratos , Ratos Endogâmicos Lew , Superantígenos/metabolismo
11.
Ann Anat ; 216: 90-94, 2018 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-29278744

RESUMO

PURPOSE: To quantify and compare the amounts of surfactant proteins SP-A, SP-B, SP-C and SP-D in the tear fluid collected from patients with dry eye syndrome and from individuals with a healthy ocular surface. METHODS: Schirmer strips were used to collect tear fluid from both eyes of 241 volunteers (99 men, 142 women; age range: 18-87 years). Dry eye syndrome was diagnosed by ophthalmologists in 125 patients, whereas the healthy control group comprised 116 individuals. The total protein concentration was determined via Bradford assay. The relative concentration of surfactant proteins SP-A through -D was measured by enzyme-linked immuno-sorbent assay (ELISA). RESULTS: The mean relative concentrations of SP-A, SP-C and SP-D were significantly higher in the dry eye group as compared to the healthy controls (p<0.05, one-way ANOVA). SP-B was also detected at a higher concentration in the dry eye group, but the difference to the control group was not statistically significant. CONCLUSIONS: The upregulation of SP-A and SP-D in the dry eye group is probably related to these proteins' known antimicrobial and immunomodulatory effects at the ocular surface. It may represent a pathophysiological response to the inflammatory condition of the ocular surface in dry eye. The upregulation of SP-B and SP-C may represent an effort of the lacrimal system to reduce surface tension and thus to counteract the increased tendency of the tear film to tear in dry eye.


Assuntos
Síndromes do Olho Seco/metabolismo , Surfactantes Pulmonares/análise , Lágrimas/química , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Ensaio de Imunoadsorção Enzimática , Feminino , Voluntários Saudáveis , Humanos , Masculino , Pessoa de Meia-Idade , Regulação para Cima , Adulto Jovem
12.
Brain Behav ; 7(3): e00627, 2017 03.
Artigo em Inglês | MEDLINE | ID: mdl-28293469

RESUMO

INTRODUCTION: The needle electromyography (EMG) serves to supply additional information in patients with suspected neuromuscular disorders. We aimed to provide motor unit potential (MUP) data by concentric needle EMG in the erector spinae (ES) in comparison with biceps brachii (BB) and lateral vastus (LV). METHODS: Electromyography MUP data (n) were obtained in ES (517), BB (539), and LV (627) in 32 healthy volunteers (16f). RESULTS: Motor unit potential data: amplitude (µV) 393 ± 174 (ES), 375 ± 162 (BB), and 577 ± 304 (LV); duration (ms) 10.4 ± 2.4 (ES), 10.1 ± 2.1 (BB), and 11.1 ± 2.3 (LV), area (µV × ms) 585 ± 327 (ES), 538 ± 267 (BB), and 881 ± 492 (LV); phase number 3.23 ± 0.94 (ES), 2.98 ± 0.76 (BB), and 3.19 ± 0.81 (LV); size index 0.60 ± 0.56 (ES), 0.51 ± 0.53 (BB), and 0.96 ± 0.55 (LV). LV displayed higher values (p at least <.001) for MUP amplitude, duration, area, and size index as compared to both, BB and ES. CONCLUSION: Concentric needle EMG investigations in healthy adult human subjects revealed similar MUP parameters in the ES and BB muscles, while in the LV muscle MUP amplitude, duration, area, and size index were significantly larger. Different neuromuscular disorders display a predominant involvement of proximally located muscles such as truncal muscles. The present results given here may facilitate the diagnosis of neuromuscular disorders.


Assuntos
Eletromiografia/métodos , Músculo Esquelético/fisiologia , Músculos Paraespinais/fisiologia , Recrutamento Neurofisiológico/fisiologia , Adulto , Eletromiografia/instrumentação , Feminino , Humanos , Masculino , Agulhas , Adulto Jovem
13.
Clin Auton Res ; 26(4): 303-5, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-27379500

RESUMO

This report describes the clinical course over almost one decade of a male patient presenting with immune-mediated pure autonomic neuropathy resembling a distinct variant of chronic dysimmune polyneuropathies. We suppose autoantibodies directed against epitopes on autonomic axons or neurons causative for the symptoms.


Assuntos
Doenças do Sistema Nervoso Autônomo/fisiopatologia , Doenças Autoimunes Desmielinizantes do Sistema Nervoso Central/fisiopatologia , Polineuropatias/fisiopatologia , Doenças do Sistema Nervoso Autônomo/patologia , Vasos Sanguíneos/patologia , Doenças Autoimunes Desmielinizantes do Sistema Nervoso Central/patologia , Progressão da Doença , Resposta Galvânica da Pele , Frequência Cardíaca , Humanos , Masculino , Pessoa de Meia-Idade , Polineuropatias/patologia , Teste da Mesa Inclinada
14.
Dtsch Med Wochenschr ; 141(12): 895-6, 2016 Jun.
Artigo em Alemão | MEDLINE | ID: mdl-27305308

RESUMO

Since November 2015, businesslike assisted suicide is punishable in Germany. But who acts businesslike? The majority of the German population prefers to make own decisions about the circumstances of their arriving death, and many of them would also accept (physician) assisted suicide if necessary. Only a minority of physicians plead for prohibiting assisted suicide in general. In the end everyone should be able to take position on his own. No one is obliged to use or execute assisted suicide.


Assuntos
Tomada de Decisões , Suicídio Assistido/legislação & jurisprudência , Suicídio Assistido/psicologia , Alemanha , Humanos , Testamentos Quanto à Vida/legislação & jurisprudência , Testamentos Quanto à Vida/psicologia , Autonomia Pessoal , Relações Médico-Paciente , Suspensão de Tratamento/legislação & jurisprudência
15.
Ann Anat ; 195(2): 137-42, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23357333

RESUMO

Human tear fluid is a complex mixture containing over 500 solute proteins, lipids, electrolytes, mucins, metabolites, hormones and desquamated epithelial cells as well as foreign substances from the ambient air. Little is known to date about the function of most tear components. The efficient and gentle collection of tear fluid facilitates closer investigation of these matters. The objective of the present paper was to compare two commonly used methods of obtaining tear fluid, the capillary tube and Schirmer strip methods, in terms of usefulness in molecular biological investigation of tear film. The comparative protein identification methods Bradford and Western Blot were used in the analyses to this end. The surfactant proteins (SP) A-D recently described as present on the eye surface were selected as the model proteins. Both methods feature sufficient uptake efficiency for proteins in or extraction from the sampling means used (capillary tube/Schirmer strip). The total protein concentration can be determined and the proteins in the tears can be detected - besides the hydrophilic SP-A and D also the non-water-soluble proteins of smaller size such as SP-B and C. Thus both methods afford a suitable basis for comparative analysis of the physiological processes in the tear fluid of healthy and diseased subjects. On the whole, the Schirmer strip has several advantages over the capillary tube.


Assuntos
Western Blotting/instrumentação , Tubo Capilar , Técnicas de Diagnóstico Oftalmológico , Proteoma/análise , Manejo de Espécimes/instrumentação , Tensoativos/análise , Lágrimas/química , Adulto , Desenho de Equipamento , Feminino , Humanos , Masculino , Manejo de Espécimes/métodos , Adulto Jovem
16.
Ann Anat ; 192(2): 65-9, 2010 Apr 20.
Artigo em Inglês | MEDLINE | ID: mdl-20307963

RESUMO

The ocular surface, constantly exposed to environmental pathogens, is particularly vulnerable to infection. Hence an advanced immune defence system is essential to protect the eye from microbial attack. Antimicrobial peptides, such as beta-defensins, are essential components of the innate immune system and are the first line of defence against invaders of the eye. High concentrations of L-arginine and L-lysine are necessary for the expression of beta-defensins. These are supplied by epithelial cells in inflammatory processes. The limiting factor for initiation of beta-defensin production is the transport of L-arginine and L-lysine into the cell. This transport is performed to 80% by only one transporter system in the human, the y(+)-transporter. This group of proteins exclusively transports the cationic amino acids L-arginine, L-lysine and L-ornithine and is also known under the term cationic amino acid transporter proteins (CAT-proteins). Various infections associated with L-arginine deficiency (for example psoriasis, keratoconjuctivitis sicca) are also associated with an increase in beta-defensin production. For the first time, preliminary work has shown the expression of human CATs in ocular surface epithelia and tissues of the lacrimal apparatus indicating their relevance for diseases of the ocular surface. In this review, we summarize current knowledge on the human CATs that appear to be integrated in causal regulation cascades of beta-defensins, thereby offering novel concepts for therapeutic perspectives.


Assuntos
Sistemas de Transporte de Aminoácidos Básicos/metabolismo , Síndromes do Olho Seco/tratamento farmacológico , Dermatopatias/tratamento farmacológico , beta-Defensinas/metabolismo , beta-Defensinas/uso terapêutico , Sistemas de Transporte de Aminoácidos Básicos/genética , Arginina/metabolismo , Transporte Biológico , Pré-Escolar , Defensinas/metabolismo , Síndromes do Olho Seco/complicações , Humanos , Lisina/metabolismo , Psoríase/metabolismo , Erros de Refração/tratamento farmacológico , Dermatopatias/complicações , Ureia/metabolismo , Transtornos da Visão/epidemiologia , Acuidade Visual , beta-Defensinas/genética
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