Disorders

Research Grant - 2009

Research Category: Multiple Sclerosis Award

Associate Professor Simon Broadley was the recipient of Brain Foundation grant funding in 2009

Multiple Sclerosis Award

Multiple Sclerosis Award
Prevalence and incidence study of neuromyelitis optica in Australia and New Zealand with population-based sensitivity and specificity of NMO IgG antibody positivity.
Associate Professor Simon Broadley
School of Medicine, Griffith University
Funded By Kathleen Toy Estate and Christopher Warren Hallam Bequest
Co-Investigators : Dr John Parratt, Associate Professor Robert Heard, Professor Bruce Brew, Dr Jeannette Lechner Scott, Professor Allan Kermode, Dr Pam McCombe, Dr Helmut Butzkuven, Associate Professor Bruce Taylor, Emeritus Professor John Pollard, Dr Mark Slee and Associate Professor Ernie Willoughby

Project Summary:

Neuromyelitis optica is a rare variant of multiple sclerosis which tends to be more severe and particularly affects vision and walking. Recently an unusual antibody to a water channel molecule (aquaporin-4) has been described in association with this condition supporting the long held clinical view that it may be a separate disease or is at least a distinct variant of multiple sclerosis. However, because of overlap in clinical features and a lack of precision in testing for this antibody considerable doubt remains regarding both the status of neurolmyelitis optica as a separate entity and the role of the aquaporin-4 antibody plays in diagnosis. Through a combination of extensive population-based collection of clinical data and systematic testing with MRI and antibodies this study hopes to clearly define the true spectrum of this disease and the value of aquaporin-4 antibodies play in diagnosis. The study will involve a nationwide survey of neuromyelitis optica in Australia and New Zealand and will provide accurate data on the sensitivity and specificity of various components of the diagnostic criteria including the aquaporin-4 antibody test. It is hoped that this study will advance our knowledge of how to diagnose this condition and shed light upon its cause. It is also hoped that the study will provide a platform for future study including clinical trials to improve the treatment of this condition.

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