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1.
PeerJ ; 2: e309, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-24688883

RESUMO

Background. Pacifier use decreases the risk of sudden infant death syndrome (SIDS). An emergency department (ED) visit may provide an opportunistic 'teachable moment' for parents. Objectives. To test the hypotheses (1) that caregivers were less familiar with the role of pacifiers in sudden infant death (SIDS) prevention than other recommendations, and (2) that an ED educational intervention would increase pacifier use in infants younger than six months, and (3) that otitis media would not occur more frequently in pacifier users. Methods. We did an intervention-group-only longitudinal study in a county hospital ED. We measured pacifier use infants and baseline knowledge of SIDs prevention recommendations in caregivers. We followed up three months later to determine pacifier use, and 12 months later to determine episodes of otitis media. Results. We analyzed data for 780 infants. Parents knew of advice against co-sleeping in 469/780 (60%), smoking in 660/776 (85%), and prone sleeping in 613/780 (79%). Only 268/777 (35%) knew the recommendation to offer a pacifier at bedtime. At enrollment 449/780 (58%) did not use a pacifier. Of 210/338 infants aged less than 6 months followed up 41/112 (37%) non-users had started using a pacifier at bedtime (NNT 3). Over the same period, 37/98 (38%) users had discontinued their pacifier. Otitis media did not differ between users and non-users at 12 months. Conclusion. Caregiver knowledge of the role of pacifiers in SIDS prevention was less than for other recommendations. Our educational intervention appeared to increase pacifier use. Pacifier use was not associated with increased otitis media.

2.
Mol Immunol ; 46(8-9): 1688-95, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19297025

RESUMO

To accurately measure the relative expression of a target gene, mRNA expression data is routinely normalized with reference to an internal control gene. We examined the transcriptional stability of four internal control genes, beta-actin, glyceraldehyde-3 phosphate dehydrogenase (GAPDH), elongation factor1-alpha (EF1-alpha), and 18S ribosomal RNA (18S rRNA) while measuring the mRNA expression of a gene encoding a pattern recognition protein, lipopolysaccharide and glucan binding protein (LGBP) gene, in healthy and white spot syndrome virus (WSSV) infected shrimp (Penaeus stylirostris) before and after (4, 8, 16 and 32 h) challenge using real-time RT-PCR. Here, we describe a method to rank the internal control genes based on a linear regression analysis. This analysis enables us to analyze the multivariate data set, e.g. time course study samples with control and treatment groups. Using the linear regression analysis and the WSSV-challenged time course samples, GAPDH was found to be the most stable internal control gene followed by the genes EF1-alpha, 18S rRNA and beta-actin. Using the program geNorm, GAPDH was also found to be the most stable gene followed by the genes EF1-alpha, beta-actin and 18S rRNA. Using the program NormFinder, the ranking of the internal control genes were in the order of EF1-alpha>GAPDH>18S rRNA>beta-actin. The ability to compare the healthy and WSSV infected samples in parallel by the regression analysis makes this method a very useful approach while identifying the optimal reference gene for gene expression analysis.


Assuntos
Perfilação da Expressão Gênica/métodos , Genes MHC da Classe II , Penaeidae/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa/normas , Actinas/análise , Actinas/genética , Animais , Clonagem Molecular , Gliceraldeído-3-Fosfato Desidrogenase (Fosforiladora)/análise , Gliceraldeído-3-Fosfato Desidrogenase (Fosforiladora)/genética , Hepatopâncreas/imunologia , Hepatopâncreas/metabolismo , Modelos Lineares , Penaeidae/imunologia , Fator 1 de Elongação de Peptídeos/análise , Fator 1 de Elongação de Peptídeos/genética , Estabilidade de RNA/fisiologia , RNA Ribossômico 18S/análise , RNA Ribossômico 18S/genética , Padrões de Referência , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Transcrição Gênica
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