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1.
Sci Rep ; 12(1): 4777, 2022 03 21.
Artigo em Inglês | MEDLINE | ID: mdl-35314720

RESUMO

Improved risk stratification of patients suspected of prostate cancer prior to biopsy continues to be an unmet clinical need. ExoDx Prostate (IntelliScore) "EPI" is a non-invasive urine test utilizing RNA from exosomes to provide a risk score that correlates with the likelihood of finding high grade prostate cancer at biopsy. Here, we present the results from a prospective clinical validation study of EPI-CE, a CE-marked in-vitro diagnostic (IVD) assay, specifically developed for use in European clinical laboratories. The study (NCT04720599) enrolled patients with ≥ 50 years, PSA 2-10 ng/mL, prior to MRI, who were scheduled for initial biopsy. First catch urine samples were collected from participants without prior digital rectal examination or prostate massage. Exosomal RNA was isolated and expression levels of three biomarkers ERG, PCA3 and SPDEF were analyzed according to the EPI-CE Instructions For Use. In the study cohort of N = 109 patients, EPI-CE was validated to have a Negative Predictive Value of 89%, a Sensitivity of 92% and a superior performance to two commonly used multiparametric risk calculators (PCPT and ERSPC) in both Receiver Operating Characteristics with a higher Area Under the Curve for EPI-CE 0.67 (95% CI 0.56-0.77) versus PCPT 0.59 (95% CI 0.47-0.71) and ERSPC 0.60 (95% CI 0.49-0.72) and higher Net Benefits analysis across a wide range of risk acceptance levels. This is the first clinical study reporting on the performance of EPI-CE. We demonstrate that EPI-CE provides information beyond standard clinical parameters and provides a better risk assessment prior to MRI, of patients suspected of prostate cancer, than the commonly used multiparametric risk calculators.


Assuntos
Antígeno Prostático Específico , Neoplasias da Próstata , Biópsia , Humanos , Masculino , Gradação de Tumores , Estudos Prospectivos , Neoplasias da Próstata/diagnóstico , Neoplasias da Próstata/genética , Neoplasias da Próstata/patologia , RNA , Medição de Risco/métodos
2.
PLoS One ; 11(6): e0157774, 2016.
Artigo em Inglês | MEDLINE | ID: mdl-27310007

RESUMO

Negative energy balance and ketosis are thought to cause impaired immune function and to increase the risk of clinical mastitis in dairy cows. The present in vitro study aimed to investigate the effect of elevated levels of the predominant ketone body ß-hydroxybutyrate on the innate defense capability of primary bovine mammary epithelial cells (pbMEC) challenged with the mastitis pathogen Escherichia coli (E. coli). Therefore, pbMEC of healthy dairy cows in mid- lactation were isolated from milk and challenged in culture with 3 mM BHBA and E. coli. pbMEC stimulated with E. coli for 6 h or 30 h showed an up-regulation of several innate immune genes, whereas co-stimulation of pbMEC with 3 mM BHBA and E. coli resulted in the down-regulation of CCL2, SAA3, LF and C3 gene expression compared to the challenge with solely the bacterial stimulus. These results indicated that increased BHBA concentrations may be partially responsible for the higher mastitis susceptibility of dairy cows in early lactation. Elevated levels of BHBA in blood and milk during negative energy balance and ketosis are likely to impair innate immune function in the bovine mammary gland by attenuating the expression of a broad range of innate immune genes.


Assuntos
Ácido 3-Hidroxibutírico/farmacologia , Complemento C3/genética , Células Epiteliais/imunologia , Escherichia coli/crescimento & desenvolvimento , Imunidade Inata , Receptores Toll-Like/genética , Animais , Bovinos , Quimiocina CCL2/genética , Quimiocina CCL2/imunologia , Complemento C3/metabolismo , Metabolismo Energético/efeitos dos fármacos , Metabolismo Energético/imunologia , Células Epiteliais/efeitos dos fármacos , Células Epiteliais/microbiologia , Feminino , Perfilação da Expressão Gênica , Regulação da Expressão Gênica , Lactoferrina/genética , Lactoferrina/imunologia , Glândulas Mamárias Animais/imunologia , Glândulas Mamárias Animais/microbiologia , Proteína Amiloide A Sérica/genética , Proteína Amiloide A Sérica/imunologia , Transdução de Sinais , Receptores Toll-Like/imunologia
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