Logo Logo
Help
Contact
Switch Language to German
De Guio, Francois; Jouvent, Eric; Biessels, Geert Jan; Black, Sandra E.; Brayne, Carol; Chen, Christopher; Cordonnier, Charlotte; De Leeuw, Frank-Eric; Dichgans, Martin; Doubal, Fergus; Duering, Marco; Dufouil, Carole; Duzel, Emrah; Fazekas, Franz; Hachinski, Vladimir; Ikram, M. Arfan; Linn, Jennifer; Matthews, Paul M.; Mazoyer, Bernard; Mok, Vincent; Norrving, Bo; O'Brien, John T.; Pantoni, Leonardo; Ropele, Stefan; Sachdev, Perminder; Schmidt, Reinhold; Seshadri, Sudha; Smith, Eric E.; Sposato, Luciano A.; Stephan, Blossom; Swartz, Richard H.; Tzourio, Christophe; Buchem, Mark van; Lugt, Aad van der; Oostenbrugge, Robert van; Vernooij, Meike W.; Viswanathan, Anand; Werring, David; Wollenweber, Frank; Wardlaw, Joanna M.; Chabriat, Hugues (2016): Reproducibility and variability of quantitative magnetic resonance imaging markers in cerebral small vessel disease. In: Journal of Cerebral Blood Flow and Metabolism, Vol. 36, No. 8: pp. 1319-1337
Full text not available from 'Open Access LMU'.

Abstract

Brain imaging is essential for the diagnosis and characterization of cerebral small vessel disease. Several magnetic resonance imaging markers have therefore emerged, providing new information on the diagnosis, progression, and mechanisms of small vessel disease. Yet, the reproducibility of these small vessel disease markers has received little attention despite being widely used in cross-sectional and longitudinal studies. This review focuses on the main small vessel disease-related markers on magnetic resonance imaging including: white matter hyperintensities, lacunes, dilated perivascular spaces, microbleeds, and brain volume. The aim is to summarize, for each marker, what is currently known about: (1) its reproducibility in studies with a scan-rescan procedure either in single or multicenter settings;(2) the acquisition-related sources of variability;and, (3) the techniques used to minimize this variability. Based on the results, we discuss technical and other challenges that need to be overcome in order for these markers to be reliably used as outcome measures in future clinical trials. We also highlight the key points that need to be considered when designing multicenter magnetic resonance imaging studies of small vessel disease.