Automated brain tumor segmentation using spatial accuracy-weighted hidden Markov Random Field. Academic Article uri icon

Overview

abstract

  • A variety of algorithms have been proposed for brain tumor segmentation from multi-channel sequences, however, most of them require isotropic or pseudo-isotropic resolution of the MR images. Although co-registration and interpolation of low-resolution sequences, such as T2-weighted images, onto the space of the high-resolution image, such as T1-weighted image, can be performed prior to the segmentation, the results are usually limited by partial volume effects due to interpolation of low-resolution images. To improve the quality of tumor segmentation in clinical applications where low-resolution sequences are commonly used together with high-resolution images, we propose the algorithm based on Spatial accuracy-weighted Hidden Markov random field and Expectation maximization (SHE) approach for both automated tumor and enhanced-tumor segmentation. SHE incorporates the spatial interpolation accuracy of low-resolution images into the optimization procedure of the Hidden Markov Random Field (HMRF) to segment tumor using multi-channel MR images with different resolutions, e.g., high-resolution T1-weighted and low-resolution T2-weighted images. In experiments, we evaluated this algorithm using a set of simulated multi-channel brain MR images with known ground-truth tissue segmentation and also applied it to a dataset of MR images obtained during clinical trials of brain tumor chemotherapy. The results show that more accurate tumor segmentation results can be obtained by comparing with conventional multi-channel segmentation algorithms.

publication date

  • May 14, 2009

Research

keywords

  • Algorithms
  • Brain Neoplasms
  • Image Processing, Computer-Assisted
  • Magnetic Resonance Imaging
  • Pattern Recognition, Automated

Identity

PubMed Central ID

  • PMC2739047

Scopus Document Identifier

  • 67349168722

Digital Object Identifier (DOI)

  • 10.1016/j.compmedimag.2009.04.006

PubMed ID

  • 19446435

Additional Document Info

volume

  • 33

issue

  • 6