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1.
Environ Entomol ; 39(4): 1359-68, 2010 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22127188

RESUMO

As part of an investigation into the potential unintended ecological impacts of transgenic trees, invertebrates were sampled from a field trial of transgenic Pinus radiata D. Don carrying the expressed antibiotic resistance marker gene neomycin phosphotransferase II (nptII) along with other genes known to affect reproductive development in plants and from nontransformed control trees. Invertebrate species abundance, richness, diversity, and composition were measured and compared among trees of five different transclones and nontransformed isogenic control trees. Invertebrates were sampled at six-monthly intervals over a period of 2 yr. In total, 19,162 individuals were collected comprising 279 invertebrate recognizable taxonomic units. Total invertebrate populations as well as populations of herbivorous lepidopteran larvae and Hemiptera were compared among transgenic and control trees. The results show that the transclones had no significant unintended influence on species abundance, richness, diversity, or composition for all populations investigated.


Assuntos
Biodiversidade , Hemípteros , Lepidópteros , Pinus/parasitologia , Plantas Geneticamente Modificadas/parasitologia , Animais
2.
Gut ; 58(12): 1612-9, 2009 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-19700435

RESUMO

BACKGROUND AND AIMS: Infliximab is an effective treatment for ulcerative colitis with over 60% of patients responding to treatment and up to 30% reaching remission. The mechanism of resistance to anti-tumour necrosis factor alpha (anti-TNFalpha) is unknown. This study used colonic mucosal gene expression to provide a predictive response signature for infliximab treatment in ulcerative colitis. METHODS: Two cohorts of patients who received their first treatment with infliximab for refractory ulcerative colitis were studied. Response to infliximab was defined as endoscopic and histological healing. Total RNA from pre-treatment colonic mucosal biopsies was analysed with Affymetrix Human Genome U133 Plus 2.0 Arrays. Quantitative RT-PCR was used to confirm microarray data. RESULTS: For predicting response to infliximab treatment, pre-treatment colonic mucosal expression profiles were compared for responders and non-responders. Comparative analysis identified 179 differentially expressed probe sets in cohort A and 361 in cohort B with an overlap of 74 probe sets, representing 53 known genes, between both analyses. Comparative analysis of both cohorts combined, yielded 212 differentially expressed probe sets. The top five differentially expressed genes in a combined analysis of both cohorts were osteoprotegerin, stanniocalcin-1, prostaglandin-endoperoxide synthase 2, interleukin 13 receptor alpha 2 and interleukin 11. All proteins encoded by these genes are involved in the adaptive immune response. These markers separated responders from non-responders with 95% sensitivity and 85% specificity. CONCLUSION: Gene array studies of ulcerative colitis mucosal biopsies identified predictive panels of genes for (non-)response to infliximab. Further study of the pathways involved should allow a better understanding of the mechanisms of resistance to infliximab therapy in ulcerative colitis. ClinicalTrials.gov number, NCT00639821.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Colite Ulcerativa/tratamento farmacológico , Fármacos Gastrointestinais/uso terapêutico , Mucosa Intestinal/metabolismo , Adulto , Estudos de Coortes , Colite Ulcerativa/genética , Colite Ulcerativa/metabolismo , Colo/metabolismo , Resistência a Medicamentos/genética , Feminino , Perfilação da Expressão Gênica/métodos , Humanos , Infliximab , Masculino , Pessoa de Meia-Idade , Análise de Sequência com Séries de Oligonucleotídeos/métodos , Prognóstico , Reprodutibilidade dos Testes , Reação em Cadeia da Polimerase Via Transcriptase Reversa/métodos , Resultado do Tratamento , Fator de Necrose Tumoral alfa/imunologia , Adulto Jovem
3.
Gut ; 58(4): 492-500, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18832518

RESUMO

BACKGROUND AND AIMS: This observational study assessed the long-term clinical benefit of infliximab (IFX) in 614 consecutive patients with Crohn's disease (CD) from a single centre during a median follow-up of 55 months (interquartile range (IQR) 27-83). METHODS: The primary analysis looked at the proportion of patients with initial response to IFX who had sustained clinical benefit at the end of follow-up. The long-term effects of IFX on the course of CD as reflected by the rate of surgery and hospitalisations and need for corticosteroids were also analysed. RESULTS: 10.9% of patients were primary non-responders to IFX. Sustained benefit was observed in 347 of the 547 patients (63.4%) receiving long-term treatment. In 68.3% of these, treatment with IFX was ongoing and in 31.7% IFX was stopped, with the patient being in remission. Seventy patients (12.8%) had to stop IFX due to side effects and 118 (21.6%) due to loss of response. Although the yearly drop-out rates of IFX in patients with episodic (10.7%) and scheduled treatment (7.1%) were similar, the need for hospitalisations and surgery decreased less in the episodic than in the scheduled group. Steroid discontinuation also occurred in a higher proportion of patients in the scheduled group than in the episodic group. CONCLUSIONS: In this large real-life cohort of patients with CD, long-term treatment with IFX was very efficacious to maintain improvement during a median follow-up of almost 5 years and changed disease outcome by decreasing the rate of hospitalisations and surgery.


Assuntos
Anticorpos Monoclonais/uso terapêutico , Doença de Crohn/tratamento farmacológico , Fármacos Gastrointestinais/uso terapêutico , Adulto , Idoso , Idoso de 80 Anos ou mais , Anticorpos Monoclonais/efeitos adversos , Doença de Crohn/cirurgia , Esquema de Medicação , Quimioterapia Combinada , Tolerância a Medicamentos , Feminino , Seguimentos , Fármacos Gastrointestinais/efeitos adversos , Glucocorticoides/administração & dosagem , Glucocorticoides/uso terapêutico , Hospitalização/estatística & dados numéricos , Humanos , Imunossupressores/efeitos adversos , Imunossupressores/uso terapêutico , Infliximab , Masculino , Pessoa de Meia-Idade , Prognóstico , Estudos Prospectivos , Resultado do Tratamento , Fator de Necrose Tumoral alfa/antagonistas & inibidores
4.
Gut ; 58(4): 501-8, 2009 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18832524

RESUMO

BACKGROUND AND AIMS: This study evaluates the long-term safety of infliximab in patients with inflammatory bowel disease (IBD) treated with the drug over a 14-year period. METHODS: The medical records of 734 patients with IBD treated with infliximab and 666 control patients not treated with infliximab were reviewed for adverse events. The time of onset and outcome, severity and concomitant medication were recorded. RESULTS: Patients and controls were followed up for serious adverse events for a median time of 58 months (IQR 33-88) and 144 months (IQR 83-163), respectively. 112 severe adverse events occurred in 93 patients (13%) treated with infliximab and 157 occurred in 126 (19%) control patients (OR 1.33 (95% CI 0.56 to 3.00, p = 0.45). There was no difference between the two groups in mortality, malignancies and infection rate. Tuberculosis was diagnosed in two patients receiving infliximab who had negative skin tests at baseline whereas none of 16 patients with positive skin tests who received prophylaxis developed tuberculosis. Concomitant treatment with steroids was the only independent risk factor for infections in patients treated with infliximab (OR 2.69 (95% CI 1.18 to 6.12), p = 0.018). The most commonly observed systemic side effects were skin eruptions including psoriasiform eruptions in 150 patients (20%). CONCLUSIONS: Long-term infliximab treatment had a good overall safety profile in the patient cohort studied.


Assuntos
Anticorpos Monoclonais/efeitos adversos , Fármacos Gastrointestinais/efeitos adversos , Doenças Inflamatórias Intestinais/tratamento farmacológico , Adolescente , Adulto , Anticorpos Monoclonais/uso terapêutico , Doenças Autoimunes/induzido quimicamente , Toxidermias/etiologia , Avaliação de Medicamentos , Feminino , Seguimentos , Fármacos Gastrointestinais/uso terapêutico , Humanos , Imunossupressores/efeitos adversos , Imunossupressores/uso terapêutico , Infliximab , Masculino , Neoplasias/induzido quimicamente , Infecções Oportunistas/induzido quimicamente , Estudos Retrospectivos , Fator de Necrose Tumoral alfa/antagonistas & inibidores , Adulto Jovem
5.
Environ Pollut ; 154(2): 330-7, 2008 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-18023948

RESUMO

The influence of two vermicomposts from winery and distillery wastes on the distribution of diuron in agricultural soil was studied. Physical soil fractionations at 0, 9, 27, 49 and 77 days, allowed the quantification of pesticide residues in different particle-size fractions, coarse waste (WF), sand-sized (SF), silt-sized (SiF), clay-sized (CF) and dissolved organic matter-sized fraction (DOM). The SiF made a greater contribution to the formation of non-extractable residues in unamended soil, but when vermicomposts were added, new sorption sites in WF appeared, being higher for the more humified vermicompost V2. The dissolved organic carbon (DOC) increased with the addition of vermicompost, but the concentration of the desorbed 14C-radiochemical did not increase. Non-significant increment was observed with time for the non-extractable fraction with amendments. Diuron was transformed in all samples, although less than 0.5% was mineralized. The main effect caused by vermicomposts was a reduction in the availability of diuron in soil.


Assuntos
Cerveja , Diurona/análise , Recuperação e Remediação Ambiental/métodos , Resíduos Industriais , Praguicidas/análise , Poluentes do Solo/análise , Solo/análise , Vinho , Adsorção , Agricultura , Carbono , Ecossistema , Monitoramento Ambiental/métodos , Substâncias Húmicas , Tamanho da Partícula , Solubilidade
6.
Rev. chil. ultrason ; 10(1): 30-36, 2007. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-467663

RESUMO

Introducción: Los prematuros extremos (PE) tienen alto riesgo de morbilidad y secuelas neurológicas. La leucomalacia periventricular (LMPV) y hemorragia intraventricular (HIV) extensa son patologías típicas de la prematurez que se asocian al desarrollo de parálisis cerebral (PC) y fácilmente pesquisables por ultrasonografía cerebral (USC). El objetivo es predecir PC a los dos años de edad corregida en todos los PE dados de alta en base a la presencia e intensidad del daño cerebral diagnosticado por USC. Pacientes y métodos: Se constituyó un equipo neuropediátrico y se protocoliza un plan de seguimiento clínico, neurológico y ultrasonográfico para todos los PE dados de alta nacidos en los años 2001 al 2003. Los resultados de la USC se dividieron en: grupo A (USC normal), grupo B (con lesiones cerebrales favorables) y grupo C (lesiones desfavorables), y se registra el diagnóstico de PC a los dos años de edad corregida. Resultados: 247 niños fueron dados de alta pero sólo 171 (69,2 por ciento) completaron el seguimiento. En el grupo A hubo 3 de 78 niños que presentaron PC (3, 8 por ciento), no se registraron casos en los 45 niños del grupo B, y en el grupo C presentaron PC 15 de 48 niños (31,2 por ciento). En total se registraron 18 casos de PC (10, 5 por ciento), 13 de ellos de carácter invalidante (7,6 por ciento) y 10 casos fueron asociados a HIV. Al juntar los grupos de USC normal y favorable (A y B) y confrontarlos con el grupo de USC desfavorable (C) se observa que la USC para predecir PC tiene sensibilidad de 83,3 por ciento, especificidad de 78,4 por ciento, valor predictivo positivo 31,3 por ciento y negativo 97,6 por ciento. Conclusiones: La prevalencia de PC fue similar a otras publicaciones. La USC demostró utilidad en seleccionar pacientes de mayor riesgo neuromotor aunque no predice PC a largo plazo y no determina el manejo neuro-kinésico posterior. Dado lo trascendente del diagnóstico de PC resulta importante saber que 1 de 3 niños con USC desfav...


Assuntos
Humanos , Feminino , Gravidez , Recém-Nascido , Lactente , Ecoencefalografia , Hemorragia Cerebral , Recém-Nascido Prematuro , Leucomalácia Periventricular , Paralisia Cerebral/etiologia , Paralisia Cerebral/prevenção & controle , Hemorragia Cerebral/complicações , Leucomalácia Periventricular/complicações , Valor Preditivo dos Testes , Prevalência , Paralisia Cerebral/epidemiologia , Sensibilidade e Especificidade , Ultrassonografia Pré-Natal
8.
Med Vet Entomol ; 19(3): 251-62, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16134973

RESUMO

Blowflies (Diptera: Calliphoridae) and flesh flies (Diptera: Sarcophagidae) are potential vectors of rabbit haemorrhagic disease virus (RHDV) in New Zealand. The associations between habitat and weather factors on the abundance of these flies were investigated. Between October 1999 and June 2001, flies were trapped on open pasture and in dense vegetation patches on farmland in the Himatangi area of the North Island. Five calliphorid species were trapped commonly at scrub edges and the most abundant sarcophagid, Oxysarcodexia varia Walker, was trapped mainly on open pasture. An abundance peak of O. varia was probably associated with the occurrence of a rabbit haemorrhagic disease (RHD) outbreak in the study area. Overall abundance of flies varied according to habitat and species, and species numbers differed between seasons and years. The all-day minimum temperature 3 weeks before trapping was a significant variable in all models of fly abundance, whereas average rainfall did not affect fly abundance. The all-day temperature range was significant only for O. varia. The influence of other climatic factors varied between fly species. Climate dependent variations in fly abundance may contribute to the risk of transmission of RHD, which occurred intermittently on the site during the study period.


Assuntos
Infecções por Caliciviridae/veterinária , Dípteros , Vírus da Doença Hemorrágica de Coelhos , Insetos Vetores , Coelhos/virologia , Tempo (Meteorologia) , Animais , Infecções por Caliciviridae/transmissão , Nova Zelândia , Estações do Ano
9.
Gut ; 54(10): 1421-7, 2005 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-15955786

RESUMO

BACKGROUND AND AIMS: Recent data suggest identification of causal genetic variants for inflammatory bowel disease in the DLG5 gene and in the organic cation transporter (OCTN) cluster, both situated in previously described linkage regions. PATIENTS AND METHODS: The polymorphisms in DLG5 (113 G-->A, 4136 C-->A, and DLG5_e26), SLC22A4 (1672 C-->T), and SLC22A5 (-207 G-->C) were assessed in 625 patients with Crohn's disease (CD), 363 patients with ulcerative colitis (UC), and 1012 healthy controls. Association with disease susceptibility, clinical phenotypes, and possible genetic interactions of these polymorphisms with disease associated CARD15/NOD2 mutations was analysed. RESULTS: No significant association of DLG5 polymorphisms with CD or UC was observed. Homozygosity for the OCTN-TC haplotype was associated with an increased CD risk (OR = 1.65), which was even greater in the presence of CARD15 mutations. Genotype-phenotype analysis revealed that this association was particularly strong in patients with colonic disease. The TC haplotype was associated with non-fistulising non-fibrostenotic disease, an earlier age of disease onset, and reduced need for surgery. CONCLUSION: Our observations argue against a role of DLG5 polymorphisms in the susceptibility for inflammatory bowel disease, whereas the OCTN polymorphisms are associated with CD. However, due to the comparable weak association observed herein, extended linkage disequilibrium analyses of these variants with the IBD5 haplotype tagged single nucleotide polymorphims might be advisable before definitive conclusions about their causative role in CD can be drawn.


Assuntos
Doença de Crohn/genética , Proteínas de Membrana/genética , Proteínas de Transporte de Cátions Orgânicos/genética , Polimorfismo Genético/genética , Proteínas Supressoras de Tumor/genética , Adolescente , Adulto , Idoso , Criança , Colite Ulcerativa/genética , Feminino , Marcadores Genéticos/genética , Predisposição Genética para Doença/genética , Genótipo , Haplótipos , Humanos , Peptídeos e Proteínas de Sinalização Intracelular/genética , Desequilíbrio de Ligação/genética , Masculino , Pessoa de Meia-Idade , Mutação , Proteína Adaptadora de Sinalização NOD2 , Fenótipo
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