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Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates.

Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates. Research Abstract Details 

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  • Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates. Abstract Text:

    v m andersonV M Anderson,j w bartlettJ W Bartlett,n c foxN C Fox,l fisnikuL Fisniku,d h millerD H Miller,valerie m andersonValerie M Anderson,jonathan w bartlettJonathan W Bartlett,nick c foxNick C Fox,leonora fisnikuLeonora Fisniku,david h millerDavid H Miller,valerie m andersonValerie M Anderson,jonathan w bartlettJonathan W Bartlett,nick c foxNick C Fox,leonora fisnikuLeonora Fisniku,david h millerDavid H Miller,

    Brain atrophy, thought to reflect neuroaxonal degeneration, may be considered an objective marker of disease progression in multiple sclerosis (MS). Our objective was to estimate sample sizes required for parallel group placebo-controlled trials of disease-modifying treatments in relapsing remitting MS (RRMS), using brain atrophy on MRI as the outcome measure. In addition, we investigated how brain atrophy measurement method and trial duration affect sample sizes. Thirtythree patients with RRMS and 16 controls had T1-weighted volumetric MR imaging acquired at baseline and up to six repeat timepoints (six monthly intervals). Brain atrophy was quantified between baseline and each repeat image using four methods: segmented brain volume difference, BBSI, SIENA and ventricular enlargement. Linear mixed models were fitted to data from each subject group and method. Sample size calculations were performed using mean and variance estimates from these models. For a 2 year trial, a treatment slowing atrophy rate by 30% required 123 subjects in each treatment arm if using SIENA to measure atrophy, 157 for the BBSI, 140 for ventricular enlargement and 763 for segmented brain volume difference. For a given effect size and method, sample sizes were statistically significantly reduced the longer the trial duration. Our estimations suggest that brain atrophy could provide an additional outcome measure to clinical assessment for monitoring treatment effects in RRMS although the relationship between atrophy and subsequent disability, and potential confounding factors to atrophy measurement must be further investigated.

    Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates. Publishing Authors By Initials

    vm andersonVM Anderson,jw bartlettJW Bartlett,nc foxNC Fox,l fisnikuL Fisniku,dh millerDH Miller,vm andersonVM Anderson,jw bartlettJW Bartlett,nc foxNC Fox,l fisnikuL Fisniku,dh millerDH Miller,vm andersonVM Anderson,jw bartlettJW Bartlett,nc foxNC Fox,l fisnikuL Fisniku,dh millerDH Miller,

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    Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates. Journal Published:

    PUBLICATION TYPE: Journal Article

    Journal: Journal of neurology

    VOLUME: 254

    Page Numbers: 1588-94

    Journal Abbreviation: J. Neurol.

    ISSN: 0340-5354

    DAY: 25

    MONTH: 10

    YEAR: 2007

    Detecting treatment effects on brain atrophy in relapsing remitting multiple sclerosis: Sample size estimates. Information

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    LANGUAGE: eng

    NlmUniqueID: 423161

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    AFFILIATION: MS NMR Research Unit, University College London Institute of Neurology, Queen Square, London, WC1N 3BG, UK.

    Country: Germany

    Germany Research PublicationGermany Research Publication

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    MEDLINETA: J Neurol

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