Back to Search Start Over

Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study

Authors :
Jayne Ness
Tanuja Chitnis
Robert Zivadinov
Lauren B. Krupp
Alexander Zaitsev
Dorothee Chabas
Mark P. Gorman
Brian C. Healy
Bianca Weinstock-Guttman
Jonathan B. Strober
Nancy L. Kuntz
Charles R.G. Guttmann
Niels Bergsland
Alexander Musallam
Moses Rodriguez
Emmanuelle Waubant
Daniel Pelletier
Bradley J. Erickson
Ann Yeh
Source :
BMC Neurology, Chitnis, Tanuja; Guttmann, Charles R; Zaitsev, Alexander; Musallam, Alexander; Weinstock-Guttmann, Bianca; Yeh, Ann; et al.(2013). Quantitative MRI analysis in children with multiple sclerosis: a multicenter feasibility pilot study. BMC Neurology, 13(1), 173. doi: http://dx.doi.org/10.1186/1471-2377-13-173. Retrieved from: http://www.escholarship.org/uc/item/97w1p62z
Publication Year :
2013
Publisher :
BioMed Central, 2013.

Abstract

Background: Pediatric multiple sclerosis (MS) is a rare disorder with significant consequences. Quantitative MRI measurements may provide significant insights, however multicenter collaborative studies are needed given the small numbers of subjects. The goal of this study is to demonstrate feasibility and evaluate lesion volume (LV) characteristics in a multicenter cohort of children with MS. Methods: A common MRI-scanning guideline was implemented at six member sites of the U.S. Network of Pediatric MS Centers of Excellence. We included in this study the first ten scans performed at each site on patients meeting the following inclusion criteria: pediatric RRMS within 3 years of disease onset, examination within 1 month of MRI and no steroids 1 month prior to MRI. We quantified T2 number, T2-LV and individual lesion size in a total of 53 MRIs passing quality control procedures and assessed gadolinium-enhancing lesion number and LV in 55 scans. We studied MRI measures according to demographic features including age, race, ethnicity and disability scores, controlling for disease duration and treatment duration using negative binomial regression and linear regression. Results: The mean number of T2 lesions was 24.30 ± 19.68 (range:1–113) and mean gadolinium-enhancing lesion count was 1.85 ± 5.84, (range:0–32). Individual lesion size ranged from 14.31 to 55750.60 mm 3 . Non-white subjects had higher T2–LV (unadjusted pT2-LV= 0.028; adjusted pT2-LV= 0.044), and maximal individual T2-LV (unadjusted pMax = 0.007; adjusted pMax = 0.011) than white patients. We also found a trend toward larger mean lesion size in males than females (p = 0.07). Conclusion: Assessment of MRI lesion LV characteristics is feasible in a multicenter cohort of children with MS. Background Multiple sclerosis (MS) is an increasingly recognized disorder in children and adolescents. The onset of MS prior to the age of 18 occurs in 3-5% of the total MS population [1-3]. Children and adolescents with MS have higher relapse rates than adults with the disease [4], suggesting inflammation as a prominent feature. Children also demonstrate considerable cognitive disability early in the disease course [5-7] but relatively less

Details

Language :
English
ISSN :
14712377
Volume :
13
Database :
OpenAIRE
Journal :
BMC Neurology
Accession number :
edsair.doi.dedup.....79cd71d5581fa2dbeeab94ae1c2492e7
Full Text :
https://doi.org/10.1186/1471-2377-13-173.