Peripapillary atrophy detection by sparse biologically inspired feature manifold.

Published

Journal Article

Peripapillary atrophy (PPA) is an atrophy of pre-existing retina tissue. Because of its association with eye diseases such as myopia and glaucoma, PPA is an important indicator for diagnosis of these diseases. Experienced ophthalmologists are able to determine the presence of PPA using visual information from the retinal images. However, it is tedious, time consuming and subjective to examine all images especially in a screening program. This paper presents biologically inspired feature (BIF) for the automatic detection of PPA. BIF mimics the process of cortex for visual perception. In the proposed method, a focal region is segmented from the retinal image and the BIF is extracted. As BIF is an intrinsically low dimensional feature embedded in a high dimensional space, it is not suitable to measure the similarity between two BIFs directly based on the Euclidean distance. Therefore, it is necessary to obtain a suitable mapping to reduce the dimensionality. In this paper, we explore sparse transfer learning to transfer the label information from ophthalmologists to the sample distribution knowledge contained in all samples. Selective pair-wise discriminant analysis is used to define two strategies of sparse transfer learning: negative and positive sparse transfer learning. Experimental results show that negative sparse transfer learning is superior to the positive one for this task. The proposed BIF based approach achieves an accuracy of more than 90% in detecting PPA, much better than previous methods. It can be used to save the workload of ophthalmologists and thus reduce the diagnosis costs.

Full Text

Duke Authors

Cited Authors

  • Cheng, J; Tao, D; Liu, J; Wong, DWK; Tan, N-M; Wong, TY; Saw, SM

Published Date

  • December 2012

Published In

Volume / Issue

  • 31 / 12

Start / End Page

  • 2355 - 2365

PubMed ID

  • 22987511

Pubmed Central ID

  • 22987511

Electronic International Standard Serial Number (EISSN)

  • 1558-254X

Digital Object Identifier (DOI)

  • 10.1109/TMI.2012.2218118

Language

  • eng

Conference Location

  • United States