학술논문

Reliability and validity of the Wolfram Unified Rating Scale (WURS)
Document Type
Academic Journal
Source
Orphanet Journal of Rare Diseases. November 14, 2012, Vol. 7
Subject
Children -- Diseases
Medical research
Medicine, Experimental
Nervous system diseases -- Development and progression -- Research
Diabetes -- Development and progression -- Research
Medical colleges -- Research
Deafness -- Development and progression -- Research
Language
English
ISSN
1750-1172
Abstract
Background Wolfram syndrome (WFS) is a rare, neurodegenerative disease that typically presents with childhood onset insulin dependent diabetes mellitus, followed by optic atrophy, diabetes insipidus, deafness, and neurological and psychiatric dysfunction. There is no cure for the disease, but recent advances in research have improved understanding of the disease course. Measuring disease severity and progression with reliable and validated tools is a prerequisite for clinical trials of any new intervention for neurodegenerative conditions. To this end, we developed the Wolfram Unified Rating Scale (WURS) to measure the severity and individual variability of WFS symptoms. The aim of this study is to develop and test the reliability and validity of the Wolfram Unified Rating Scale (WURS). Methods A rating scale of disease severity in WFS was developed by modifying a standardized assessment for another neurodegenerative condition (Batten disease). WFS experts scored the representativeness of WURS items for the disease. The WURS was administered to 13 individuals with WFS (6-25 years of age). Motor, balance, mood and quality of life were also evaluated with standard instruments. Inter-rater reliability, internal consistency reliability, concurrent, predictive and content validity of the WURS were calculated. Results The WURS had high inter-rater reliability (ICCs>.93), moderate to high internal consistency reliability (Cronbach's [alpha] = 0.78-0.91) and demonstrated good concurrent and predictive validity. There were significant correlations between the WURS Physical Assessment and motor and balance tests (r.sub.s.67, p Conclusions These preliminary findings demonstrate that the WURS has acceptable reliability and validity and captures individual differences in disease severity in children and young adults with WFS.
Author(s): Chau Nguyen[sup.1] , Erin R Foster[sup.1,3] , Alexander R Paciorkowski[sup.6] , Amy Viehoever[sup.3] , Colleen Considine[sup.2] , Aidena Bondurant[sup.2] , Bess A Marshall[sup.4] , Tamara Hershey[sup.2,3,5] and [sup.] Background [...]