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J Magn Reson Imaging ; 42(2): 477-87, 2015 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-25410482

RESUMO

BACKGROUND: To introduce a segmentation method to calculate an automatic arterial input function (AIF) based on principal component analysis (PCA) of dynamic contrast enhanced MR (DCE-MR) imaging and compare it with individual manually selected and population-averaged AIFs using calculated pharmacokinetic parameters. METHODS: The study included 65 individuals with prostate examinations (27 tumors and 38 controls). Manual AIFs were individually extracted and also averaged to obtain a population AIF. Automatic AIFs were individually obtained by applying PCA to volumetric DCE-MR imaging data and finding the highest correlation of the PCs with a reference AIF. Variability was assessed using coefficients of variation and repeated measures tests. The different AIFs were used as inputs to the pharmacokinetic model and correlation coefficients, Bland-Altman plots and analysis of variance tests were obtained to compare the results. RESULTS: Automatic PCA-based AIFs were successfully extracted in all cases. The manual and PCA-based AIFs showed good correlation (r between pharmacokinetic parameters ranging from 0.74 to 0.95), with differences below the manual individual variability (RMSCV up to 27.3%). The population-averaged AIF showed larger differences (r from 0.30 to 0.61). CONCLUSION: The automatic PCA-based approach minimizes the variability associated to obtaining individual volume-based AIFs in DCE-MR studies of the prostate.


Assuntos
Velocidade do Fluxo Sanguíneo , Angiografia por Ressonância Magnética/métodos , Meglumina/farmacocinética , Modelos Biológicos , Neovascularização Patológica/fisiopatologia , Compostos Organometálicos/farmacocinética , Neoplasias da Próstata/fisiopatologia , Simulação por Computador , Meios de Contraste/farmacocinética , Humanos , Aumento da Imagem/métodos , Interpretação de Imagem Assistida por Computador/métodos , Masculino , Pessoa de Meia-Idade , Modelos Estatísticos , Neovascularização Patológica/diagnóstico , Análise de Componente Principal , Neoplasias da Próstata/diagnóstico , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
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