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Published online before print April 15, 2005, 10.1148/radiol.2353032071
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235/3/1036    most recent
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(Radiology 2005;235:1036-1044.)
© RSNA, 2005


Technical Developments

Assessment of Multiple Sclerosis Lesions with Spherical Harmonics: Comparison of MR Imaging and Pathologic Findings1

Daniel Goldberg-Zimring, PhD, Bruria Shalmon, MD, Kelly H. Zou, PhD, Haim Azhari, DSc, Dvora Nass, MD and Anat Achiron, MD, PhD

1 From the Department of Biomedical Engineering, Technion, Israel Institute of Technology, Haifa, Israel (D.G.Z., H.A.); Department of Radiology, Brigham and Women’s Hospital, Harvard Medical School, 75 Francis St, Boston, MA 02115 (D.G.Z., K.H.Z.); Department of Pathology (B.S., D.N.) and Multiple Sclerosis Center (A.A.), Sheba Medical Center, Tel Hashomer, Israel; Department of Health Care Policy, Harvard Medical School, Boston, Mass (K.H.Z.); and Department of Neurology, Tel Aviv University, Sackler Faculty of Medicine, Tel Aviv, Israel (A.A.). Received December 19, 2003; revision requested February 25, 2004; final revision received August 30; accepted September 17. D.G.Z. supported by the "Sociedad Venezolana Amigos del Technion" and in part by NIH grant R21MH67054 and grant RG3478AZ/Z from the National Multiple Sclerosis Society, U.S. D.G.Z. and K.H.Z. supported in part by NIH grant R01LM007861–01A1. Address correspondence to D.G.Z. (e-mail: daniel@bwh.harvard.edu).

Spherical harmonics (SH) were used to approximate the volume and three-dimensional geometry of multiple sclerosis (MS) lesions in deceased patients. The institutional ethical committee does not require its approval for studies involving pathologic specimens. Pathologic findings were used as the reference standard. In addition, lesion volume was measured with cylindrical approximation (CA). Volumetric comparisons of biases were based on summary statistics, Spearman correlation, Wilcoxon test, and two-way analysis of variance. Shape comparison metrics included mean distance and Dice similarity coefficient (DSC). Eight of 11 lesions had smaller biases with SH method (P < .001). Median biases with SH and CA did not differ significantly, as compared with pathologic findings (r = 1.00 vs 0.99, respectively). Variances of the biases were significantly smaller for SH (P = .04). Ranges of normalized distance and DSC were 0.1%–2.5% and 75%–96%, respectively. Mean DSC was significantly higher than 70% (P < .001). SH method provided unbiased lesion volume and added geometric information that may enable a better understanding of the pathogenesis and lesion evolution over time.

© RSNA, 2005







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