You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT ARCHIVES
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 65 No. 9, September 2008 TABLE OF CONTENTS
  Archives
  •  Online Features
  Original Contribution
 This Article
 •Full text
 •PDF
 • Reply to article
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citation map
 •Citing articles on HighWire
 •Contact me when this article is cited
 Related Content
 •Related article
 •Similar articles in this journal
 Topic Collections
 •Multiple Sclerosis/ Demyelinating Disease
 •Ophthalmology
 •Ophthalmological Disorders, Other
 •Immunologic Disorders
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati
What's this?

A Preliminary Validation Study of Diffusion Tensor Imaging as a Measure of Functional Brain Injury

Robert J. Fox, MD; Roderick W. McColl, PhD; Jar-Chi Lee, MS; Teresa Frohman, BA; Ken Sakaie, PhD; Elliot Frohman, MD, PhD

Arch Neurol. 2008;65(9):1179-1184.

Background  Diffusion tensor imaging (DTI) characterizes multiple sclerosis (MS) tissue injury, although it has remained unproven whether DTI changes in disease have functional consequences. The medial longitudinal fasciculus (MLF) is a key brainstem pathway for ocular adduction and is commonly injured in patients with MS, typically resulting in internuclear ophthalmoparesis.

Objective  To validate DTI as a physiologically relevant measure of brain tissue integrity.

Design  A correlation study of ocular dysmotility and DTI conducted between January 2004 and September 2004.

Setting  Multiple Sclerosis Center, University of Texas Southwestern Medical Center, Dallas.

Patients  Six patients with chronic, unilateral, or bilateral internuclear ophthalmoparesis and 10 healthy control subjects.

Main Outcome Measure  We used infrared oculography to correlate the velocity versional dysconjugacy index, defined as the ratio of the velocity of the abducting to adducting eye movements during horizontal saccades, and DTI measures within the MLF as measured through an anatomical overlay. Overall diffusion was measured by mean diffusivity, and anisotropy was measured by the lattice index.

Results  Within the pontine MLF, the mean diffusivity was increased compared with healthy controls (P < .005), whereas the pontine lattice index was decreased (P < .03). Correlations were observed between the velocity versional dysconjugacy index and the mean diffusivity (left: r = 0.65, P < .01; right: r = 0.46, P = .07). Similar correlations were found between the versional dysconjugacy index and the lattice index (left: r = –0.43, P = .09; right: r = –0.65, P <.01).

Conclusions  We identified DTI evidence of pathologic disruption of a small brainstem fiber pathway, which is crucial for accurate horizontal eye movements. In this small study, we observed correlations between the DTI changes and oculomotor dysfunction. Our preliminary observations provide criterion validity of DTI as a surrogate marker of brain tissue integrity.


Author Affiliations: Mellen Center for Multiple Sclerosis, Department of Neurology (Dr Fox), Department of Quantitative Health Sciences (Ms Lee), and Department of Radiology (Dr Sakaie), Cleveland Clinic Foundation, Cleveland, Ohio; and Departments of Radiology (Dr McColl) and Neurology (Ms Frohman and Dr Frohman), University of Texas Southwestern Medical Center, Dallas.



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati     What's this?

RELATED ARTICLE

This Month in Archives of Neurology
Arch Neurol. 2008;65(9):1152-1153.
FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Picturing injury and recovery with diffusion tensor imaging: The eyes have it
Bermel and Fox
Neurology 2009;72:584-585.
FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2008 American Medical Association. All Rights Reserved.