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1.
Orv Hetil ; 152(43): 1739-44, 2011 Oct 23.
Artigo em Húngaro | MEDLINE | ID: mdl-21983400

RESUMO

UNLABELLED: Psychoneuroimmunologic studies on positive emotions are few, and their clinical relevance is limited. AIMS: This "SHoRT" (Smiling Hospital Research Team) study evaluates the effects that Smiling Hospital artists have on hospitalized children. METHODS: Blood samples were taken in a non-painful way through branules in an accredited Infectology Ward, 30 minutes before and 1 hour after a visit of tale tellers, puppeteers and handicraft artists. 24 children were visited and 9 were included in the control group. Blood lymphocyte counts and Th1/Th2 cytokine levels were determined. Artists evaluated their effect on a subjective scale. RESULTS: In the visited group, the increase of lymphocytes was 8.43% higher, the decrease was 12.45% lower, and the proportion of children showing increased lymphocyte counts was more increased. Changes were more marked after more successful visits. Authors found non-significant, still considerable changes in interferon-γ level (p < 0.055) and in Th1/Th2 cytokine ratios. CONCLUSIONS: This pediatric study suggests that immunological changes may develop when more attention is given to hospitalized children.


Assuntos
Criança Hospitalizada , Citocinas/imunologia , Felicidade , Sorriso , Células Th1/imunologia , Células Th2/imunologia , Adolescente , Criança , Criança Hospitalizada/psicologia , Criança Hospitalizada/estatística & dados numéricos , Pré-Escolar , Citocinas/sangue , Feminino , Citometria de Fluxo , Fundações , Hospitais de Ensino , Humanos , Hungria , Lactente , Interferon gama/sangue , Interleucinas/sangue , Linfotoxina-alfa/sangue , Masculino , Fatores de Tempo
2.
PLoS One ; 7(3): e33573, 2012.
Artigo em Inglês | MEDLINE | ID: mdl-22432035

RESUMO

Genetic studies indicate high number of potential factors related to asthma. Based on earlier linkage analyses we selected the 11q13 and 14q22 asthma susceptibility regions, for which we designed a partial genome screening study using 145 SNPs in 1201 individuals (436 asthmatic children and 765 controls). The results were evaluated with traditional frequentist methods and we applied a new statistical method, called bayesian network based bayesian multilevel analysis of relevance (BN-BMLA). This method uses bayesian network representation to provide detailed characterization of the relevance of factors, such as joint significance, the type of dependency, and multi-target aspects. We estimated posteriors for these relations within the bayesian statistical framework, in order to estimate the posteriors whether a variable is directly relevant or its association is only mediated.With frequentist methods one SNP (rs3751464 in the FRMD6 gene) provided evidence for an association with asthma (OR = 1.43(1.2-1.8); p = 3×10(-4)). The possible role of the FRMD6 gene in asthma was also confirmed in an animal model and human asthmatics.In the BN-BMLA analysis altogether 5 SNPs in 4 genes were found relevant in connection with asthma phenotype: PRPF19 on chromosome 11, and FRMD6, PTGER2 and PTGDR on chromosome 14. In a subsequent step a partial dataset containing rhinitis and further clinical parameters was used, which allowed the analysis of relevance of SNPs for asthma and multiple targets. These analyses suggested that SNPs in the AHNAK and MS4A2 genes were indirectly associated with asthma. This paper indicates that BN-BMLA explores the relevant factors more comprehensively than traditional statistical methods and extends the scope of strong relevance based methods to include partial relevance, global characterization of relevance and multi-target relevance.


Assuntos
Asma/genética , Predisposição Genética para Doença , Testes Genéticos , Genoma Humano/genética , Análise Multinível , Adolescente , Asma/complicações , Teorema de Bayes , Criança , Pré-Escolar , Bases de Dados Genéticas , Epistasia Genética , Feminino , Humanos , Masculino , Modelos Genéticos , Polimorfismo de Nucleotídeo Único/genética , Rinite/complicações , Rinite/genética , Transdução de Sinais/genética , Adulto Jovem
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