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1.
Clin Transl Allergy ; 7: 21, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28725346

RESUMO

Diagnostic tests to detect allergic sensitization were introduced at the end of the nineteenth century but only in the late 1990s did the advent of molecular allergology revolutionize the approach to the allergic patient. Personalized Medicine, a medical procedure that separates patients into different groups with different medical decisions, practices and interventions has sanctioned this change. In fact, in the last few years molecular allergology and the observation that not every patient has the same allergic profile, even when allergic to the same allergenic source, has originated the concept "one size does not fit all". This new approach requires the identification of still unknown allergens, but also the more detailed investigation of those already known. In depth studies of the structure-function relationships in allergenic molecules can reveal the structural determinants involved in the IgE-binding. Then, the knowledge of the epitope profile of each allergen and of the environmental/experimental conditions affecting the exposure of IgE-binding epitopes can provide important contributions to the understanding of cross-reaction processes and to the improvement of diagnosis, immunotherapy and the overall patient treatment. The evolution of diagnostic systems cannot ignore these new needs in this field.

2.
Clin Exp Allergy ; 43(1): 128-40, 2013 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-23278887

RESUMO

BACKGROUND: Among the peach-derived allergens which are already known, the lipid transfer protein (Pru p 3) seems to be the one to exert severe allergic reactions. OBJECTIVE: To identify and characterize a new peach allergen causing a clinical picture similar to that of Pru p 3. METHODS: Patients were selected on the basis of their severe clinical reactivity and negative results to a panel of peach allergens available on the ISAC103 microarray. Several in-house and commercial preparations were compared. Several methods were used to characterize the newly identified molecule. Specific IgE and inhibition assays were performed using the Allergen micro-Beads Array (ABA) assay. RESULTS: Negative ISAC results to Pru p 3 were confirmed by additional testing in contrast with the positive results obtained by commercial Pru p 3-enriched peach peel extracts. The analyses of one of these preparations led to the identification of Peamaclein, a new allergenic protein. It is a small, basic, cysteine-rich, heat-stable, digestion-resistant protein, homologous to a potato antimicrobial peptide. Peamaclein was able to trigger positive skin test reactions and to bind IgE in the ABA assay. It displays an electrophoretic mobility and chromatographic behaviour similar to that of Pru p 3; therefore, it can be hidden in Pru p 3 preparations. In fact, Pru p 3-enriched peach peel extracts were found to contain both Pru p 3 and Peamaclein by means of comparative in vivo testing, and by biochemical and immunochemical assays. Commercially available anti-Pru p 3 polyclonal antibodies were found to have a double specificity for the two molecules. CONCLUSIONS AND CLINICAL RELEVANCE: A new allergen from peach belonging to a new family of allergenic proteins has been identified and characterized. This knowledge on Peamaclein will improve our understanding on the clinical aspects of the peach allergy and the quality of diagnostic reagents.


Assuntos
Alérgenos/imunologia , Antígenos de Plantas/imunologia , Hipersensibilidade Alimentar/imunologia , Proteínas de Plantas/imunologia , Prunus/imunologia , Adolescente , Adulto , Alérgenos/efeitos adversos , Alérgenos/química , Antígenos de Plantas/efeitos adversos , Antígenos de Plantas/química , Criança , Pré-Escolar , Método Duplo-Cego , Feminino , Humanos , Imunoglobulina E/biossíntese , Masculino , Pessoa de Meia-Idade , Extratos Vegetais/química , Extratos Vegetais/imunologia , Proteínas de Plantas/efeitos adversos , Proteínas de Plantas/química , Prunus/efeitos adversos , Prunus/química , Adulto Jovem
3.
Br J Dermatol ; 168(6): 1205-14, 2013 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-23252883

RESUMO

BACKGROUND: Bullous pemphigoid (BP) is an autoimmune skin disease in which patient autoantibodies react with BP180 and BP230 proteins. In addition to IgG, IgE has been shown to play a role in the disease. OBJECTIVES: To evaluate the feasibility of detecting IgE and IgG against the immunodominant BP180 NC16A domain (BP180) using a microarray system. METHODS: BP180 was immobilized on an experimental version of the ISAC(®) microarray (Exp96). The BP study group and the controls were all tested on the commercial ISAC 103 version and on the Exp96. IgG and IgE were measured in a single run. BP180 IgG and IgE results were compared with those using an enzyme-linked immunosorbent assay (ELISA). RESULTS: All results obtained using the IgG ELISA on the 31 patients with BP were replicated with the ISAC IgG. Five of eight BP sera tested by ELISA showed similar results with ISAC IgE. Twenty-nine (94%) and 19 (61%) of the 31 patients with BP were IgG and IgE positive to BP180, respectively, whereas four (3%) and six (4%) of 138 normal donors were IgG and IgE positive, respectively. Interestingly, the levels of IgG against BP180 detected using the ISAC system were related to the disease severity. Patients with BP showed a peculiar profile of IgE recognition toward some groups of allergens, which was absent in a group of allergic individuals. A significant, higher prevalence of hen's egg recognition was observed in patients with BP who had specific IgE to BP180. CONCLUSIONS: The present preliminary study indicates that the ISAC microarray system is suitable for detecting IgG and IgE autoantibodies in patients with BP. Notably, this system allows the assessment of IgE and IgG autoantibodies at the same time, could be employed for the detection of autoantibodies to other autoantigens, and allows profiling for specific IgE to allergens.


Assuntos
Autoanticorpos/sangue , Autoantígenos/imunologia , Imunoglobulina E/sangue , Imunoglobulina G/sangue , Colágenos não Fibrilares/imunologia , Penfigoide Bolhoso/imunologia , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Estudos de Casos e Controles , Criança , Pré-Escolar , Ensaio de Imunoadsorção Enzimática/métodos , Feminino , Humanos , Lactente , Masculino , Análise em Microsséries/métodos , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Adulto Jovem , Colágeno Tipo XVII
4.
Clin Exp Allergy ; 42(3): 441-50, 2012 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-22168465

RESUMO

BACKGROUND: Egg allergy is a very common finding in early childhood. Detecting hen's egg (HE) allergy outgrowing and reintroduction of food containing egg is a task for the allergist. OBJECTIVE: We sought to evaluate the suitability of boiled egg food challenge compared with IgE to allergenic molecules from HE white using a microarray system. METHOD: Sixty-eight children referring to our centre by the family paediatricians for a suspected egg allergy were enrolled. Patients underwent double-blind, placebo-controlled food challenge with boiled and raw eggs. Challenge outcomes were compared with skin tests performed using egg white and yolk commercial extracts, to prick-prick test with boiled and raw egg white and yolk, total IgE, egg white specific IgE detected using ImmunoCAP and IgE to egg allergens available on the immunosolid phase allergen chip (ISAC) 103 microarray. RESULT: Nineteen subjects (28%) were reactive to both raw and boiled egg, 14 (20.5%) to raw egg only and 35 (51.4%) tolerated both boiled and raw egg. Efficiency analysis was carried out using both raw and boiled egg challenges as gold standard. Forty four of 47 Gal d 1 negative patients tolerated boiled egg (94%). Conversely, 20 of 21 Gal d 1 positive patients reacted to raw egg (95%). None of the other tests was able to discriminate patients' response to HE challenge. Furthermore, Gal d 1 positivity seems to lead to broader environmental allergen IgE sensitization. CONCLUSION AND CLINICAL RELEVANCE: The Gal d 1 IgE reactivity appears to be a very good predictor of HE clinical allergy. Gal d 1 positive children have a high frequency of HE allergy, whereas Gal d 1 negative children have a high frequency of tolerance to boiled egg. Multiple specific IgE detection by means of ISAC improves the diagnostic approach in HE allergic children, disclosing other food and inhalant allergic sensitizations, anyhow requiring a comprehensive clinical evaluation.


Assuntos
Hipersensibilidade a Ovo/diagnóstico , Testes Imunológicos/métodos , Ovomucina/imunologia , Administração Oral , Alérgenos/administração & dosagem , Alérgenos/imunologia , Animais , Galinhas , Criança , Pré-Escolar , Método Duplo-Cego , Feminino , Humanos , Imunoensaio , Imunoglobulina E/sangue , Imunoglobulina E/imunologia , Lactente , Masculino , Fatores de Risco , Sensibilidade e Especificidade
5.
Clin Exp Immunol ; 167(1): 120-8, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22132891

RESUMO

Immune dysregulation, polyendocrinopathy, enteropathy, X-linked (IPEX) is a rare syndrome due to a mutation in the forkhead box protein 3 gene (FOXP3) leading to an impaired regulatory T cell (T(reg) ) activity associated both with skewed T helper type 2 (Th2) response and autoreactive phenomena. The purpose of this study was to describe a combined proteomics and genomics approach to comprehensively evaluate clinical and immunological phenotypes of patients affected by IPEX. T cell receptor (TCR)-Vß repertoire and peripheral blood lymphocytes phenotype from three brothers affected by IPEX were studied by flow cytometry. Specific immunoglobulin (Ig)E were evaluated by means of an allergenic molecules microarray [immuno solid-phase allergen chip (ISAC)]. Total RNA was extracted and hybridized to Affymetrix oligonucleotide arrays to obtain quantitative gene-expression levels. No FOXP3 protein was detectable within CD127(-) CD25(high) CD4(+) T cells from peripheral blood. A T cell-naive phenotype (CD62L(+) CD45R0(-)) associated with a reduction of both CD26 and CD7 expression and a TCR-Vß 8 and 22 family expansions were found. B lymphocytes were mainly CD5(+) (B1) cells expressing a naive phenotype (tcl1(+) CD27(-)). The three IPEX patients had severe food allergy and specific IgE reactivity to cow's milk allergens, a hen's egg allergen and a wheat allergen. Gene expression profile analysis revealed a dysregulation associated mainly with Th1/Th2 pathways. The multiplexing evaluation reported in this study represents a comprehensive approach in the assessment of genetic conditions affecting the immune system such as the IPEX syndrome, paving the way for the development of diagnostic tools to improve the standard clinical and immunological profiling of the disease.


Assuntos
Doenças do Sistema Endócrino/genética , Hipersensibilidade Alimentar/genética , Fatores de Transcrição Forkhead/deficiência , Genes Ligados ao Cromossomo X , Doenças Genéticas Ligadas ao Cromossomo X/genética , Genômica/métodos , Síndromes de Imunodeficiência/genética , Proteômica/métodos , Adolescente , Adulto , Doenças do Sistema Endócrino/sangue , Doenças do Sistema Endócrino/imunologia , Hipersensibilidade Alimentar/sangue , Hipersensibilidade Alimentar/imunologia , Fatores de Transcrição Forkhead/genética , Perfilação da Expressão Gênica , Doenças Genéticas Ligadas ao Cromossomo X/sangue , Doenças Genéticas Ligadas ao Cromossomo X/imunologia , Humanos , Imunoglobulina E/imunologia , Síndromes de Imunodeficiência/sangue , Imunofenotipagem , Linfoma Difuso de Grandes Células B/genética , Linfoma Difuso de Grandes Células B/patologia , Masculino , Análise de Sequência com Séries de Oligonucleotídeos , Receptores de Antígenos de Linfócitos T alfa-beta/genética , Análise de Sequência de DNA , Subpopulações de Linfócitos T/imunologia , Neoplasias Tonsilares/genética , Neoplasias Tonsilares/patologia , Adulto Jovem
6.
Clin Exp Allergy ; 40(6): 911-21, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20214663

RESUMO

BACKGROUND: The availability of allergenic molecules and high-throughput microtechnologies allow the collection of a large number of IgE results at the same time in a single test. This can be carried out applying the test in the routine diagnostic work-up. OBJECTIVE: The aim of this study was to make a cross-sectional evaluation of the raw prevalence of IgE reactivity to allergenic molecules in serum samples from a cohort of Italian patients using an innovative tool. METHODS: The ISAC, a microarray system, has been used for specific IgE detection using 75 different allergenic molecules. Sera were collected from 23,077 unselected consecutive individuals complaining about any allergic disease. RESULTS: Sixteen thousand four hundred and eight of 23,077 patients had IgE to at least one of 75 allergenic molecules. The top-ranked molecules in this cohort were Cup a 1 (42.7%), Der f 2 (38.7%), and Phl p 1 (37.9%), whereas all the other allergens tested scored in a range between 36.8% and 0.04%, including the first food allergen, Pru p 3, ranked 15th (9.79%). Prevalence varied quite markedly depending on the age range considered, and showing a different behaviour in the lifetime sensitization process. Unsupervised two-way hierarchical clustering analysis generated distinctive patterns of reactivity as the result of IgE recognition of either homologous allergens belonging to different biological sources or non-homologous belonging to the same biological source. CONCLUSIONS: Allergen-based microarray is a tool for the detection of IgE-related sensitization to panels of allergens and gives a more precise and comprehensive evaluation for an IgE-based epidemiology. This insight brings data for better understanding of the sensitization process.


Assuntos
Hipersensibilidade/diagnóstico , Hipersensibilidade/epidemiologia , Imunoglobulina E/sangue , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Adolescente , Adulto , Distribuição por Idade , Alérgenos/genética , Alérgenos/imunologia , Estudos Transversais , Feminino , Humanos , Hipersensibilidade/imunologia , Imunoglobulina E/imunologia , Itália/epidemiologia , Masculino , Pessoa de Meia-Idade , Distribuição por Sexo , Adulto Jovem
7.
Allergy ; 65(5): 597-605, 2010 May.
Artigo em Inglês | MEDLINE | ID: mdl-19958316

RESUMO

BACKGROUND: Mulberry (Morus spp.) is a genus comprising several species of deciduous trees whose fruits are commonly eaten in southern Europe. Subjects with severe systemic reaction have been described. The aim of this study was to isolate the allergens of this species. METHODS: A nonspecific lipid transfer protein 1 (ns-LTP1) was purified from black mulberry by ion exchange and reverse phase high-performance liquid chromatography, and the primary structure was elucidated by direct protein sequencing. Its allergenic activity was evaluated in vivo by skin prick test and in vitro by Western Blot, CD203c basophil activation assay and high throughput multiplex inhibition method on immunosolid-phase allergen chip (ISAC). RESULTS: Mulberry ns-LTP (Mor n 3) comprises 91 amino acids producing a molecular mass of 9246 Da. This protein shows high sequence identity with several allergenic ns-LTP1. Immunoblot analysis and CD203c activation assay demonstrated its allergenic activity in symptomatic subjects and in ns-LTP allergic patients who are not mulberry consumers. Immunological co-recognition was studied in vivo on a selected group of well-characterized ns-LTP allergic patients showing a high percentage of nMor n 3(+) subjects (88.46%) even in patients who have never eaten mulberry before. IgE inhibition on ISAC micro-array demonstrated an almost complete cross-reactivity to nArt v 3, rCor a 8 and a very high percentage of inhibition to nPru p 3. CONCLUSIONS: Mor n 3 is the first allergen isolated in black mulberry and immunologically characterized. It displayed allergenic activity among symptomatic and nonconsumer patients and a pattern of cross-reactivity to other plant-derived LTPs.


Assuntos
Antígenos de Plantas/imunologia , Proteínas de Transporte/imunologia , Morus/imunologia , Proteínas de Plantas/imunologia , Adolescente , Adulto , Sequência de Aminoácidos , Antígenos de Plantas/química , Teste de Degranulação de Basófilos , Proteínas de Transporte/química , Criança , Pré-Escolar , Cromatografia Líquida de Alta Pressão , Cromatografia por Troca Iônica , Reações Cruzadas/imunologia , Feminino , Humanos , Immunoblotting , Imunoglobulina E/imunologia , Masculino , Dados de Sequência Molecular , Proteínas de Plantas/química , Homologia de Sequência de Aminoácidos , Testes Cutâneos , Espectrometria de Massas por Ionização e Dessorção a Laser Assistida por Matriz , Adulto Jovem
8.
Int J Immunopathol Pharmacol ; 21(3): 659-67, 2008.
Artigo em Inglês | MEDLINE | ID: mdl-18831934

RESUMO

The aim of this study is to evaluate the presence of antibodies to carbonic anhydrase I and/or II (ACAI and ACAII) in patients affected by connective tissue diseases (CTD) and to investigate their association with lung involvement evaluated by High resolution CT scan (HRCT). Ninety-six patients affected by CTD were studied, i.e. 33 rheumatoid arthritis (RA), 8 psoriatic arthritis (PA), 8 ankylosing spondilitis (AS), 23 Systemic Lupus Erythematosus (SLE), 10 Sjogren Syndrome (SS), and 14 Systemic Sclerosis (SSc). ACA were detected by ELISA. The lung involvement was evaluated by means of a previously described HRCT score. According to a receiver operator characteristic curve, patients were divided into those with HRCT score > or = 10 and those with HRCT score < 10, where HRCT score > or = 10 was predictive of interstitial lung disease. ACAI and/or ACAII were detected in 30/96 patients (31.2%) (P < 0.0001 in comparison with controls). In particular, the prevalence of ACAI and/or ACAII was significantly higher in patients with RA (P = 0.002), PA (P < 0.0001), SLE (P = 0.0003) and SSc (P < 0.0001). A positive correlation was found between HRCT scores and CRP or ACAI levels (P = < 0.0001 and P = 0.004, respectively). Thirty-nine of 96 patients (40.6%) showed a HRCT score > or = 10 and both their CRP and ACAI levels were significantly higher when compared with patients showing a HRCT score less than 10 (P < 0.0006 and P = 0.0009, respectively). Moreover, C3 and C4 complement fractions inversely correlated with HRCT scores (P = 0.0004 and P < 0.0001, respectively) and lower values of C3 and C4 complement fractions were found in patients with HRCT score > or = 10 than in those with HRCT score less than 10 (P = 0.014 and P = 0.007, respectively). Due to the lower levels of complement fractions detected in patients with HRCT score > or = 10, a possible immune-complex-mediated pathogenic mechanism of lung involvement could be suggested.


Assuntos
Autoanticorpos/sangue , Anidrases Carbônicas/imunologia , Doenças do Tecido Conjuntivo/imunologia , Pneumopatias/etiologia , Adulto , Idoso , Proteína C-Reativa/análise , Complemento C3/análise , Complemento C4/análise , Doenças do Tecido Conjuntivo/complicações , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X
9.
Lupus ; 16(1): 56-8, 2007.
Artigo em Inglês | MEDLINE | ID: mdl-17283587

RESUMO

The antiphospholipid syndrome (APS) is an autoimmune disorder, characterized by a wide spectrum of clinical manifestations. Thromboembolic events, with a greater involvement of extremities veins, are the most common features, and obstruction of abdominal vessels are sporadically reported. We present a singular case of a patient with primary APS (PAPS) that developed a spontaneous splenorenal shunt, secondary to a total portal, mesenteric and splenic vein thrombosis. Spontaneous splenorenal shunt, an uncommon circumstance reported in cirrhotic disease, to the best of our knowledge, has not been previously described in PAPS.


Assuntos
Síndrome Antifosfolipídica/complicações , Fístula/etiologia , Oclusão Vascular Mesentérica/etiologia , Veia Porta/patologia , Veias Renais/patologia , Veia Esplênica/patologia , Trombose Venosa/etiologia , Feminino , Fístula/diagnóstico por imagem , Predisposição Genética para Doença , Heterozigoto , Humanos , Metilenotetra-Hidrofolato Redutase (NADPH2)/deficiência , Metilenotetra-Hidrofolato Redutase (NADPH2)/genética , Pessoa de Meia-Idade , Deficiência de Proteína C/complicações , Deficiência de Proteína S/complicações , Veias Renais/diagnóstico por imagem , Veia Esplênica/diagnóstico por imagem , Trombofilia/etiologia , Trombofilia/genética , Ultrassonografia Doppler em Cores
10.
Scand J Rheumatol ; 35(5): 388-94, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-17062440

RESUMO

OBJECTIVES: To assess the prevalence of interstitial lung disease (ILD) in patients with different forms of connective tissue disease (CTD) using non-invasive procedures including high-resolution computed tomography (HRCT) and to evaluate the relationship between the imaging and functional status of the patients. METHODS: Eighty-one subjects with CTD (47 inpatients and 34 outpatients) were evaluated with pulmonary function tests (PFT) and radiological investigations. The extent and severity of lung disease was quantified with an HRCT scoring system previously used in patients with systemic sclerosis (SSc). Interstitial lung involvement was defined as predominantly fibrotic or inflammatory based on HRCT abnormalities. RESULTS: HRCT abnormalities suggestive of ILD were observed in 69 patients (85.1%), whereas PFT and plain radiograph alterations occurred less frequently (40.7%). The most frequent HRCT abnormalities were septal/subpleural lines and ground-glass appearance whereas lesions consistent with advanced fibrosis were observed in a minority of patients. The HRCT score was higher in patients with abnormal PFT (p<0.001). Thirty-five patients had predominant fibrosis and 34 patients predominantly inflammatory abnormalities. A score of 10 points represented the best compromise between sensitivity and specificity in predicting functional impairment. CONCLUSIONS: A high prevalence of ILD was found based on HRCT abnormalities. However, HRCT scans characterized by minor abnormalities have poor specificity for clinically significant disease and functional findings should also be considered. The large number of patients with predominantly inflammatory HRCT abnormalities suggests that many cases of ILD may be diagnosed in a relatively early stage of the disease.


Assuntos
Doenças do Tecido Conjuntivo/complicações , Doenças Pulmonares Intersticiais/diagnóstico por imagem , Doenças Pulmonares Intersticiais/etiologia , Tomografia Computadorizada por Raios X , Adulto , Idoso , Doenças do Tecido Conjuntivo/patologia , Feminino , Humanos , Pulmão/diagnóstico por imagem , Pulmão/patologia , Pulmão/fisiopatologia , Doenças Pulmonares Intersticiais/epidemiologia , Masculino , Pessoa de Meia-Idade , Prevalência , Fibrose Pulmonar/diagnóstico por imagem , Fibrose Pulmonar/patologia , Testes de Função Respiratória , Índice de Gravidade de Doença
12.
G Ital Med Lav Ergon ; 27(1): 88-95, 2005.
Artigo em Italiano | MEDLINE | ID: mdl-15915680

RESUMO

Neuromuscular problems reduce working ability of aging workers, and increase cases of work loss and accidents. For this reason, elderly people throughout Europe are forced into early retirement, and fail to be self-supporting. There is a need to identify and monitor work related neuromuscular disorders in order to reduce their consequences by monitoring the most vulnerable individuals, identify the determinants of neuromuscular aging related to occupational conditions, prevent pathologies and their evolution. Preliminary results show the possibility of identification of neuromuscular problems through non invasive techniques, some of which, recently developed within the SENIAM and PROCID Concerted Actions, can provide quantitative indices of neuromuscular performance. Substantial field tests and training initiatives are required to demonstrate if these techniques can be used outside the research labs, if there may be a European market in the fields of ergonomics and occupational health, and if they can be routinely used with standardized methodology to monitor the relationship between occupational and neuromuscular system conditions in the working environment. The objective of the European Project Neuromuscular assessment in the Elderly Worker (NEW) is to answer these questions.


Assuntos
Avaliação Geriátrica , Doenças Neuromusculares/diagnóstico , Doenças Profissionais/diagnóstico , Idoso , Desenho de Equipamento , Ergonomia/instrumentação , Europa (Continente) , Humanos
13.
J Electromyogr Kinesiol ; 13(2): 113-24, 2003 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-12586517

RESUMO

The Cinderella hypothesis postulates the continuous activity of specific motor units (MUs) during low-level muscle contraction. The MUs may become metabolically overloaded, with the subject developing muscle pain and strain. The hypothesis requires MUs that are active for a time long enough to actually damage muscle fibers. The aim of this study was to determine if there are continuously active MUs in the right trapezius muscle during normal computer work using a computer mouse. Fourteen healthy subjects executed an interactive computer-learning program (ErgoLight) for 30 min. Six-channel intramuscular EMG and two-channel surface EMG signals were recorded from two positions of the trapezius muscle. Decomposition was achieved with automated, multi-channel, long-term decomposition software (EMG-LODEC). In two out of the 14 subjects, three MUs were continuously active throughout the 30 min. Although the majority of the MUs were active during only part of the experimental session, an ordered on-off behavior (e.g. substitution) pattern was not observed. As long-lasting activity was verified in some subjects, the results support the Cinderella hypothesis. However, it cannot be concluded here how long the MUs could stay active. If continuous activity overloads low threshold MUs, the potential exists for selective fibre injuries in low threshold MUs of the trapezius muscle in subjects exposed to long-term computer work.


Assuntos
Periféricos de Computador , Antebraço/fisiologia , Neurônios Motores/fisiologia , Contração Muscular/fisiologia , Músculo Esquelético/fisiologia , Adulto , Algoritmos , Análise por Conglomerados , Eletromiografia , Feminino , Humanos , Masculino , Movimento/fisiologia , Músculo Esquelético/inervação , Recrutamento Neurofisiológico/fisiologia , Software
14.
Eur Rev Med Pharmacol Sci ; 7(5): 139-45, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-15214589

RESUMO

While initial researches documented that Rheumatoid Arthritis (RA) patients who took biologic agents had decreased symptoms with those receiving traditional treatment, safety of the drugs remains a concern. The authors in this paper review the safety of the RA new therapeutic approach utilizing biological agents and compare it with the safety of conventional disease-modifying anti-rheumatic drugs (DMARDs).


Assuntos
Anti-Inflamatórios não Esteroides/efeitos adversos , Artrite Reumatoide/tratamento farmacológico , Fatores Imunológicos/efeitos adversos , Anti-Inflamatórios não Esteroides/uso terapêutico , Artrite Reumatoide/fisiopatologia , Ensaios Clínicos Fase III como Assunto , Humanos , Fatores Imunológicos/uso terapêutico , Vigilância de Produtos Comercializados/métodos , Ensaios Clínicos Controlados Aleatórios como Assunto , Estudos Retrospectivos
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