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Disambiguating the optic nerve from the surrounding cerebrospinal fluid: Application to MS-related atrophy.
Harrigan, Robert L; Plassard, Andrew J; Bryan, Frederick W; Caires, Gabriela; Mawn, Louise A; Dethrage, Lindsey M; Pawate, Siddharama; Galloway, Robert L; Smith, Seth A; Landman, Bennett A.
Afiliação
  • Harrigan RL; Department of Electrical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • Plassard AJ; Department of Computer Science, Vanderbilt University, Nashville, Tennessee, USA.
  • Bryan FW; Department of Electrical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • Caires G; Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
  • Mawn LA; Biomedical Engineering, Federal University of Rio Grande do Norte, Natal, RN, Brazil.
  • Dethrage LM; Vanderbilt Eye Institute, Vanderbilt University, Nashville, Tennessee, USA.
  • Pawate S; Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
  • Galloway RL; Department of Neurology, Vanderbilt University, Nashville, Tennessee, USA.
  • Smith SA; Department of Biomedical Engineering, Vanderbilt University, Nashville, Tennessee, USA.
  • Landman BA; Institute of Imaging Science, Vanderbilt University, Nashville, Tennessee, USA.
Magn Reson Med ; 75(1): 414-22, 2016 Jan.
Article em En | MEDLINE | ID: mdl-25754412
ABSTRACT

PURPOSE:

Our goal is to develop an accurate, automated tool to characterize the optic nerve (ON) and cerebrospinal fluid (CSF) to better understand ON changes in disease.

METHODS:

Multi-atlas segmentation is used to localize the ON and sheath on T2-weighted MRI (0.6 mm(3) resolution). A sum of Gaussian distributions is fit to coronal slice-wise intensities to extract six descriptive parameters, and a regression forest is used to map the model space to radii. The model is validated for consistency using tenfold cross-validation and for accuracy using a high resolution (0.4 mm(2) reconstructed to 0.15 mm(2)) in vivo sequence. We evaluated this model on 6 controls and 6 patients with multiple sclerosis (MS) and a history of optic neuritis.

RESULTS:

In simulation, the model was found to have an explanatory R-squared for both ON and sheath radii greater than 0.95. The accuracy of the method was within the measurement error on the highest possible in vivo resolution. Comparing healthy controls and patients with MS, significant structural differences were found near the ON head and the chiasm, and structural trends agreed with the literature.

CONCLUSION:

This is a first demonstration that the ON can be exclusively, quantitatively measured and separated from the surrounding CSF using MRI.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Reconhecimento Automatizado de Padrão / Imageamento por Ressonância Magnética / Líquido Cefalorraquidiano / Atrofia Óptica / Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Nervo Óptico / Reconhecimento Automatizado de Padrão / Imageamento por Ressonância Magnética / Líquido Cefalorraquidiano / Atrofia Óptica / Esclerose Múltipla Tipo de estudo: Diagnostic_studies / Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male Idioma: En Ano de publicação: 2016 Tipo de documento: Article