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1.
J Mater Chem B ; 10(34): 6472-6482, 2022 08 31.
Artigo em Inglês | MEDLINE | ID: mdl-35968772

RESUMO

Cardiac tissue regeneration strategies are increasingly taking advantage of electroactive scaffolds to actively recreate the tissue microenvironment. In this context, this work reports on advanced materials based on two different ionic liquids (ILs), 2-hydroxyethyl-trimethylammonium dihydrogen phosphate ([Ch][DHP]) and choline bis(trifluoromethylsulfonyl)imide ([Ch][TFSI]), combined with poly(vinylidene fluoride-co-trifluoroethylene) (P(VDF-TrFE)) for the development of ionic electroactive IL/polymer hybrid materials for cardiac tissue engineering (TE). The morphological, physico-chemical, thermal and electrical properties of the hybrid materials, as well as their potential use as scaffolds for cardiac TE applications, were evaluated. Besides inducing changes in surface topography, roughness and wettability of the composites, the incorporation of [Ch][DHP] and [Ch][TFSI] leads to the increase in surface (σsurface) and volume (σvolume) electrical conductivities. Furthermore, washing the hybrid samples with phosphate-buffered saline solution strongly decreases the σsurface, whereas σsurface and σvolume of the composites remain almost unaltered after exposure to ultraviolet sterilization treatment. Additionally, it is verified that the incorporation of IL influences the P(VDF-TrFE) microstructure and crystallization process, acting as a defect during its crystallization. Cytotoxicity assays revealed that hybrid films based on [Ch][DHP] alone are not cytotoxic. These films also support H9c2 myoblast cell adhesion and proliferation, demonstrating their suitability for cardiac TE strategies based on electroactive microenvironments.


Assuntos
Líquidos Iônicos , Engenharia Tecidual , Condutividade Elétrica , Líquidos Iônicos/química , Fosfatos , Polímeros
2.
Actas dermo-sifiliogr. (Ed. impr.) ; 106(6): 470-476, jul.-ago. 2015. tab
Artigo em Espanhol | IBECS | ID: ibc-139453

RESUMO

INTRODUCCIÓN: Los pacientes con psoriasis y hepatopatías son un reto terapéutico dado el mayor riesgo de efectos adversos que presentan con el tratamiento sistémico clásico y a que, aunque los fármacos anti-TNF-α son considerados más seguros, también se han descrito reactivaciones de hepatitis vírica y hepatitis tóxica en relación con los mismos. El ustekinumab (UTK) tiene un mecanismo de acción diferente y se sabe poco de sus efectos en el hígado, sobre todo a partir de los estudios pivotales. Nuestro objetivo ha sido estimar la incidencia de toxicidad hepática en los pacientes tratados con UTK en la práctica clínica habitual, y examinar los cambios hepáticos en aquellos pacientes tratados que tenían hepatopatía de base. MÉTODO: Se incluyeron todos los pacientes tratados con UTK según pauta habitual. Se analizaron la edad, el género, el tipo de psoriasis, la afectación ungueal, la artritis, los tratamientos previos, la hepatopatía previa, las serologías virales y el PASI (basal y a las 12, 16 y 52 semanas). Se analizaron también las transaminasas, los signos y síntomas de hepatopatía y los factores como el índice de masa corporal, el hábito enólico, la ferritina y la ecografía hepática. RESULTADOS: Se observaron hipertransaminasemias de grado 1 en solo 6 pacientes. Ninguno presentó hipertransaminasemias graves. Ninguno de los pacientes con hipertransaminasemia basal tuvo problemas durante el tratamiento. CONCLUSIONES: La hepatotoxicidad asociada a UTK es poco frecuente y grave, y parece seguro a nivel hepático, incluso en pacientes con hepatopatía basal o que habían presentado con anterioridad alteraciones hepáticas con otros fármacos


INTRODUCTION: The therapy of patients with psoriasis and liver disease can be a challenge due to the increased risk of adverse effects from traditional systemic treatments; in addition, although the anti-tumor necrosis factor agents are considered safer, they have also been associated with drug-induced liver injury and reactivation of viral hepatitis. Ustekinumab has a different mechanism of action and the little that is known of its effects on the liver comes from pivotal studies. The objectives of this study were to estimate the incidence of drug-induced liver injury in patients treated with ustekinumab in daily clinical practice and to analyze liver alterations in those patients with pre-existing liver disease. METHOD: All patients treated with the standard regimen of ustekinumab were included in the study. Variables gathered included age, sex, type of psoriasis, nail involvement, arthritis, previous treatments, history of liver disease, viral serology, Psoriasis Area Severity Index (at baseline and at 12, 16, and 52 weeks), transaminase levels, manifestations of liver disease, liver ultrasound, and factors such as body mass index, alcohol consumption, and ferritin levels. RESULTS: Grade 1 elevation of the transaminases was only observed in 6 patients; no cases of severe hypertransaminasemia were observed. None of the patients with elevation of the transaminases at baseline developed problems during treatment. CONCLUSIONS: Ustekinumab-related liver injury is uncommon and mild. From a hepatic point of view, the drug appears safe, even in patients with pre-existing liver disease and those who have developed altered liver function previously with other drugs


Assuntos
Humanos , Psoríase/tratamento farmacológico , Doença Hepática Induzida por Substâncias e Drogas/diagnóstico , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Estudos Retrospectivos , Anticorpos Monoclonais/efeitos adversos
3.
Actas Dermosifiliogr ; 106(6): 470-6, 2015.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-25912374

RESUMO

INTRODUCTION: The therapy of patients with psoriasis and liver disease can be a challenge due to the increased risk of adverse effects from traditional systemic treatments; in addition, although the anti-tumor necrosis factor agents are considered safer, they have also been associated with drug-induced liver injury and reactivation of viral hepatitis. Ustekinumab has a different mechanism of action and the little that is known of its effects on the liver comes from pivotal studies. The objectives of this study were to estimate the incidence of drug-induced liver injury in patients treated with ustekinumab in daily clinical practice and to analyze liver alterations in those patients with pre-existing liver disease. METHOD: All patients treated with the standard regimen of ustekinumab were included in the study. Variables gathered included age, sex, type of psoriasis, nail involvement, arthritis, previous treatments, history of liver disease, viral serology, Psoriasis Area Severity Index (at baseline and at 12, 16, and 52 weeks), transaminase levels, manifestations of liver disease, liver ultrasound, and factors such as body mass index, alcohol consumption, and ferritin levels. RESULTS: Grade 1 elevation of the transaminases was only observed in 6 patients; no cases of severe hypertransaminasemia were observed. None of the patients with elevation of the transaminases at baseline developed problems during treatment. CONCLUSIONS: Ustekinumab-related liver injury is uncommon and mild. From a hepatic point of view, the drug appears safe, even in patients with pre-existing liver disease and those who have developed altered liver function previously with other drugs.


Assuntos
Doença Hepática Induzida por Substâncias e Drogas/etiologia , Fármacos Dermatológicos/efeitos adversos , Psoríase/tratamento farmacológico , Ustekinumab/efeitos adversos , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Alanina Transaminase/sangue , Aspartato Aminotransferases/sangue , Doença Hepática Induzida por Substâncias e Drogas/diagnóstico , Doença Hepática Induzida por Substâncias e Drogas/epidemiologia , Comorbidade , Fármacos Dermatológicos/uso terapêutico , Feminino , Humanos , Subunidade p40 da Interleucina-12/antagonistas & inibidores , Hepatopatias/sangue , Hepatopatias/complicações , Masculino , Pessoa de Meia-Idade , Psoríase/complicações , Estudos Retrospectivos , Espanha/epidemiologia , Ustekinumab/uso terapêutico , Adulto Jovem
5.
Arthritis Rheumatol ; 66(11): 3178-89, 2014 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-25132671

RESUMO

OBJECTIVE: To define and characterize the progression of the spontaneous autoimmune disease that develops in mice in the absence of the leukocyte adhesion receptor P-selectin glycoprotein ligand 1 (PSGL-1). METHODS: Skin-resident immune cells from PSGL-1-deficient mice and C57BL/6 control mice of different ages were isolated and analyzed by flow cytometry. Biochemical parameters were analyzed in mouse serum and urine, and the presence of serum autoantibodies was investigated. Skin and internal organs were extracted, and their structure was analyzed histologically. RESULTS: Skin-resident innate and adaptive immune cells from PSGL-1(-/-) mice had a proinflammatory phenotype with an imbalanced T effector cell:Treg cell ratio. Sera from PSGL-1(-/-) mice had circulating autoantibodies commonly detected in connective tissue-related human autoimmune diseases. Biochemical and histologic analysis of skin and internal organs revealed skin fibrosis and structural and functional abnormalities in the lungs and kidneys. Furthermore, PSGL-1(-/-) mice exhibited vascular alterations, showing loss of dermal vessels, small vessel medial layer remodeling in the lungs and kidneys, and ischemic processes in the kidney that promote renal infarcts. CONCLUSION: Our study demonstrates that immune system overactivation due to PSGL-1 deficiency triggers an autoimmune syndrome with characteristics similar to systemic sclerosis, including skin fibrosis, vascular alterations, and systemic organ involvement. These results suggest that PSGL-1 expression contributes to the maintenance of the homeostasis of the immune system and could act as a barrier for autoimmunity in mice.


Assuntos
Doenças Autoimunes/fisiopatologia , Rim/fisiopatologia , Pulmão/fisiopatologia , Glicoproteínas de Membrana/deficiência , Glicoproteínas de Membrana/fisiologia , Escleroderma Sistêmico/fisiopatologia , Pele/fisiopatologia , Animais , Autoanticorpos/metabolismo , Doenças Autoimunes/patologia , Doenças do Tecido Conjuntivo/epidemiologia , Doenças do Tecido Conjuntivo/fisiopatologia , Modelos Animais de Doenças , Feminino , Fibrose/epidemiologia , Fibrose/fisiopatologia , Rim/patologia , Nefropatias/epidemiologia , Nefropatias/fisiopatologia , Pulmão/patologia , Doenças Pulmonares Intersticiais/epidemiologia , Doenças Pulmonares Intersticiais/fisiopatologia , Masculino , Glicoproteínas de Membrana/genética , Camundongos , Camundongos Endogâmicos C57BL , Camundongos Knockout , Prevalência , Escleroderma Sistêmico/patologia , Pele/patologia , Dermatopatias/epidemiologia , Dermatopatias/fisiopatologia
6.
Actas dermo-sifiliogr. (Ed. impr.) ; 105(4): 378-393, mayo 2014. tab, graf
Artigo em Espanhol | IBECS | ID: ibc-122010

RESUMO

Las características de nuestro entorno sugieren que enfermedades como la queratosis actínica (QA) aumentarán su prevalencia y, en consecuencia, la demanda asistencial en los próximos años. Deben tenerse en cuenta una extensa lista de características clínicas en el abordaje terapéutico de la QA, hasta hace poco compuesto únicamente por técnicas ablativas y exclusivamente dirigidas a las lesiones, sin considerar el campo de cancerización. El incremento del arsenal terapéutico de los últimos años hace necesaria la homogenización de criterios que faciliten la elección de la mejor opción para cada paciente. La formulación de recomendaciones de consenso entre expertos a partir de la revisión de las evidencias científicas en cuanto a diagnóstico y tratamiento disponibles, permite aportar conocimiento dirigido a la mayor calidad en la atención de los pacientes, facilita una mayor homogeneidad en la toma de decisiones y promueve la sensibilización necesaria de todos los agentes sanitarios involucrados


Current trends in our setting indicate that the prevalence of actinic keratosis and similar diseases will increase in coming years and impose a greater burden on health care resources. A long list of clinical features must be taken into account when approaching the treatment of actinic keratosis. Until recently, therapeutic approaches focused solely on ablative procedures and the treatment of individual lesions and did not take into account areas of field cancerization. Now that the therapeutic arsenal has grown, standardized criteria are needed to guide the optimal choice of treatment for each patient. The elaboration of evidence-based consensus recommendations for the diagnosis and treatment of actinic keratosis generates knowledge that will help clinicians to deliver the highest level of care possible, standardizing decision-making processes and enhancing awareness among all the health professionals involved in the care pathway


Assuntos
Humanos , Ceratose Actínica/diagnóstico , Ceratose Actínica/terapia , Padrões de Prática Médica
7.
Actas Dermosifiliogr ; 105(4): 378-93, 2014 May.
Artigo em Inglês | MEDLINE | ID: mdl-24725552

RESUMO

Current trends in our setting indicate that the prevalence of actinic keratosis and similar diseases will increase in coming years and impose a greater burden on health care resources. A long list of clinical features must be taken into account when approaching the treatment of actinic keratosis. Until recently, therapeutic approaches focused solely on ablative procedures and the treatment of individual lesions and did not take into account areas of field cancerization. Now that the therapeutic arsenal has grown, standardized criteria are needed to guide the optimal choice of treatment for each patient. The elaboration of evidence-based consensus recommendations for the diagnosis and treatment of actinic keratosis generates knowledge that will help clinicians to deliver the highest level of care possible, standardizing decision-making processes and enhancing awareness among all the health professionals involved in the care pathway.


Assuntos
Ceratose Actínica/diagnóstico , Ceratose Actínica/terapia , Guias de Prática Clínica como Assunto , Algoritmos , Europa (Continente) , Humanos , Espanha
8.
Actas dermo-sifiliogr. (Ed. impr.) ; 105(3): 233-242, abr. 2014. ilus, tab
Artigo em Espanhol | IBECS | ID: ibc-121151

RESUMO

En esta segunda parte se describen las características de los 3 tipos de estudios fotobiológicos: el fototest, la fotoprovocación y la prueba del fotoparche. Se detalla la metodología, los resultados esperados y la utilidad clínica de estos métodos en las distintas fotodermatosis estudiadas. Estos estudios son esenciales para la inducción de fotoadaptación o fototolerancia que se emplea para los casos más invalidantes


The second of this series describes the characteristics of 3 types of photobiologic studies: the light test, the photochallenge test, and the photopatch test. We explain how the tests are carried out, the expected results, and their clinical usefulness in various photodermatoses. These tests are needed before attempting to induce adaptation (skin hardening or light tolerance) in the most debilitating cases


Assuntos
Humanos , Fotobiologia/métodos , Transtornos de Fotossensibilidade/fisiopatologia , Dermatite Fotoalérgica , Luz Solar/efeitos adversos
9.
Actas Dermosifiliogr ; 105(3): 233-42, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24661955

RESUMO

The second of this series describes the characteristics of 3 types of photobiologic studies: the light test, the photochallenge test, and the photopatch test. We explain how the tests are carried out, the expected results, and their clinical usefulness in various photodermatoses. These tests are needed before attempting to induce adaptation (skin hardening or light tolerance) in the most debilitating cases.


Assuntos
Transtornos de Fotossensibilidade/diagnóstico , Humanos , Luz , Fotobiologia , Testes Cutâneos/métodos
10.
Clin Exp Dermatol ; 39(3): 323-6, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24635070

RESUMO

Paraneoplastic pemphigus (PNP) is an autoimmune blistering disease associated with neoplasms, typically lymphoproliferative disorders. PNP is characterized clinically by painful erosive stomatitis and polymorphous skin lesions. Histopathological findings are also very varied, and include lichen planus-like and pemphigus-like changes. These polymorphic clinicopathological findings are probably due to the complex pathogenic mechanism, in which both cellular and humoral immunity are implicated. Eosinophilic spongiosis, although infrequent, can be found with pemphigus herpetiformis and bullous pemphigoid, although this association has not been established in PNP. The presence of autoantibodies against envoplakin and periplakin in PNP has been reported, but autoantibodies against desmocollins (Dscs) have been found in only a very few cases of PNP, probably due to the lack of studies on such associations. We report the first case, to our knowledge, of PNP with eosinophilic spongiosis as the initial histopathological finding, and presence of autoantibodies to Dsc2 and Dsc3.


Assuntos
Desmocolinas/imunologia , Eosinofilia/patologia , Síndromes Paraneoplásicas/imunologia , Penfigoide Bolhoso/imunologia , Idoso de 80 Anos ou mais , Autoanticorpos/imunologia , Feminino , Humanos
12.
Actas dermo-sifiliogr. (Ed. impr.) ; 105(2): 112-121, mar. 2014. tab, ilus, graf
Artigo em Espanhol | IBECS | ID: ibc-120247

RESUMO

Las fotodermatosis son enfermedades de la piel inducidas o exacerbadas por la radiación electromagnética (que incluye la radiación ultravioleta, la luz visible y la radiación infrarroja) emitida por el sol o por fuentes artificiales. En la primera parte de esta revisión expondremos los conocimientos actuales sobre la fisiopatología de estos procesos y su clasificación. Además, realizaremos una serie de consideraciones técnicas acerca de las bases físicas de los estudios fotobiológicos y, finalmente, se detallarán los equipos necesarios para su realización (fuentes de luz, instrumentos de medición y sistemas de calibración)


Photodermatoses are skin conditions that are induced or exacerbated by electromagnetic radiation (including visible light, UV light, and infrared radiation) from the sun or artificial light sources. In Part 1 of this series we review current understanding of the pathophysiology of these processes and their classification. We also discuss technical aspects and the basic physics of photobiology and describe the equipment required for photobiologic testing and calibration (light sources and measurement instruments)


Assuntos
Humanos , Transtornos de Fotossensibilidade/fisiopatologia , Fotobiologia/métodos , Lesões por Radiação/diagnóstico , Radiação Solar/efeitos adversos
16.
Actas Dermosifiliogr ; 105(2): 112-21, 2014 Mar.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-23183156

RESUMO

Photodermatoses are skin conditions that are induced or exacerbated by electromagnetic radiation (including visible light, UV light, and infrared radiation) from the sun or artificial light sources. In Part 1 of this series we review current understanding of the pathophysiology of these processes and their classification. We also discuss technical aspects and the basic physics of photobiology and describe the equipment required for photobiologic testing and calibration (light sources and measurement instruments).


Assuntos
Transtornos de Fotossensibilidade/diagnóstico , Transtornos de Fotossensibilidade/fisiopatologia , Doença Crônica , Desenho de Equipamento , Humanos , Fotobiologia/instrumentação , Transtornos de Fotossensibilidade/etiologia
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