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1.
Artigo em Inglês | MEDLINE | ID: mdl-27012012

RESUMO

BACKGROUND: Lipoxins could be potential modulators of inflammation in the lungs. To our knowledge, the role of exhaled breath condensate (EBC) lipoxin A4 (LXA4) in asthmatic children with exercise-induced bronchoconstriction (EIB) has not been investigated. OBJECTIVE: The aim of our study was to determine the involvement of EBC LXA4 in EIB. METHODS: Forty-five patients aged between 5 and 17 years were included in the study. Patients were divided into 2 groups: asthmatic children with a positive response to exercise (n = 17) and asthmatic children with a negative response to exercise (n = 28). Levels of LXA4 were determined in EBC before and immediately after the exercise challenge using ELISA. RESULTS: EBC LXA4 levels were significantly increased immediately after exercise in asthmatic children with a positive response to the exercise challenge (P = .05). No significant differences were observed in children with a negative response to exercise (P > .05). There was an inverse correlation between LXA4 levels and the percent degree of reduction in forced expiratory volume in the first second (FEV1%) postexercise in children with a positive exercise challenge (P = .05, r = -0.50). No significant differences were observed in LXA4 levels between atopic and nonatopic asthmatics (P > .05, Mann-Whitney U test). CONCLUSIONS: Levels of EBC LXA4 increased immediately after exercise in asthmatic children with a positive exercise challenge response. We hypothesize that airway LXA4 levels increase to compensate bronchoconstriction and suppress acute inflammation, and that spontaneous bronchodilatation after EIB may be due to LXA4.


Assuntos
Asma Induzida por Exercício/metabolismo , Testes Respiratórios , Broncoconstrição , Expiração , Mediadores da Inflamação/metabolismo , Lipoxinas/metabolismo , Pulmão/metabolismo , Adolescente , Fatores Etários , Asma Induzida por Exercício/diagnóstico , Asma Induzida por Exercício/fisiopatologia , Biomarcadores/metabolismo , Estudos de Casos e Controles , Criança , Pré-Escolar , Ensaio de Imunoadsorção Enzimática , Teste de Esforço , Feminino , Volume Expiratório Forçado , Humanos , Pulmão/fisiopatologia , Masculino , Valor Preditivo dos Testes , Estudos Prospectivos , Regulação para Cima
2.
Eur Ann Allergy Clin Immunol ; 48(4): 149-52, 2016 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-27425172

RESUMO

Immediate reactions against contact to raw potato has been reported in adults with generally being in the form of an oral contact dermatitis or contact urticaria, but it may also manifest as rhinitis symptoms, wheezing or even anaphylaxis. Cooked or raw potato allergy has been rarely reported in children as some is being immediate and others being late reactions, and it usually results from ingestion. Herein, we report two cases with a background of allergic diseases developed anaphylaxis one with cooked potato and the other one with raw potato.


Assuntos
Anafilaxia/imunologia , Hipersensibilidade Alimentar/imunologia , Solanum tuberosum/imunologia , Anafilaxia/diagnóstico , Anafilaxia/dietoterapia , Pré-Escolar , Culinária , Hipersensibilidade Alimentar/diagnóstico , Hipersensibilidade Alimentar/dietoterapia , Humanos , Lactente , Testes Intradérmicos , Masculino , Raízes de Plantas , Valor Preditivo dos Testes , Fatores de Risco , Solanum tuberosum/efeitos adversos
3.
Genet Couns ; 23(1): 9-12, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22611636

RESUMO

Canavan disease (CD) is an autosomal recessive inherited disorder characterized by spongy degeneration of the brain. The deficiency of aspartoacylase (ASPA), resulting in the accumulation of N-acetyl aspartic acid (NAA) in the brain, plays an important role in the pathogenesis of the disease. The cardinal features of this neurodegenerative disease are macrocephaly, mental retardation, and hypotonia. Magnetic resonance imaging (MRI) of the brain generally shows diffuse white matter degeneration and also elevated excretion of urinary NAA is usually seen. A large number of mutations were identified to date. We report here a 9 months old girl with Canavan Disease and a homozygous c.79G>A mutation in the ASPA gene, detected for the first time in Turkish population.


Assuntos
Amidoidrolases/genética , Encéfalo/patologia , Doença de Canavan/genética , Doença de Canavan/patologia , Feminino , Humanos , Imageamento por Ressonância Magnética , Mutação
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