4.7 Article

Reproducibility of fMRI in the clinical setting: Implications for trial designs

期刊

NEUROIMAGE
卷 42, 期 2, 页码 603-610

出版社

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.neuroimage.2008.05.005

关键词

multiple sclerosis; functional magnetic resonance imaging; clinical trial; plasticity

资金

  1. Medical Research Council [G9409531, G0601943, G9901399] Funding Source: researchfish
  2. Medical Research Council [G9901399, G0601943, G9409531] Funding Source: Medline
  3. Multiple Sclerosis Society [748] Funding Source: Medline
  4. Wellcome Trust [078204] Funding Source: Medline
  5. MRC [G0601943, G9901399, G9409531] Funding Source: UKRI

向作者/读者索取更多资源

With expanding potential clinical applications of functional magnetic resonance imaging (fMRI) it is important to test how reliable different measures of fMRI activation are between subjects and sessions and between centres. This study compared variability across 17 patients with multiple sclerosis (MS) and 22 age-matched healthy controls (HC) in 5 European centres performing an fMRI block design with hand tapping. We recruited subjects from sites using 1.5 T scanners from different manufacturers. 5 healthy volunteers also were studied at each of 4 of the centres. We found that reproducibility between runs and sessions for single individuals was consistently much greater than between individuals. There was greater run-to-run variability for MS patients than for HC. Measurements of maximum signal change (MSC) appeared to provide higher reproducibility within individuals and greater sensitivity to differences between individuals than region of interest (ROI) suprathreshold voxel Counts. The variability in measurements between centres was not as great as that between individuals. Consistent with these observations, we estimated that power should not be reduced substantially with use of multi-, as opposed to single-, centre study designs with similar numbers of subjects. Multi-centre interventional studies in which fMRI is used as an outcome measure thus appear practical even when implemented in conventional clinical environments. (C) 2008 Elsevier Inc. All rights reserved.

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