4.7 Article

Age-related changes in conventional, magnetization transfer, and diffusion-tensor MR imaging findings: Study with whole-brain tissue histogram analysis

Journal

RADIOLOGY
Volume 227, Issue 3, Pages 731-738

Publisher

RADIOLOGICAL SOC NORTH AMERICA
DOI: 10.1148/radiol.2273020721

Keywords

aging; brain, atrophy; brain, MR; magnetic resonance (MR), diffusion tensor; magnetic resonance (MR), magnetization transfer

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PURPOSE: To investigate the influence of aging on conventional magnetic resonance (MR) imaging-, magnetization transfer MR imaging-, and diffusion-tensor MR imaging-derived measurements. MATERIALS AND METHODS: Dual-echo T-weighted magnetization transfer and diffusion-tensor MR images of the brain were obtained in 89 healthy subjects. Normalized brain parenchymal volume (NBV) was measured by using a fully automated technique. Magnetization transfer ratio (MTR), apparent diffusion coefficient (ADC), and fractional anisotropy (FA) histograms were created for the whole brain (MTR values) or for a large representative portion of it (ADC and FA values). Bivariate correlations were assessed by using the Spearman rank correlation coefficient. A stepwise selection procedure was used to identify the combination of variables that were most influenced by subject age in a multivariate regression model. RESULTS: Significant correlations were found between subject age and the following variables: number of hyperintense areas in the brain at T2-weighted MR imaging (r = 0.63, P <.001), NBV (r = -0.79, P <.001), mean ADC (r = 0.34, P =.001), ADC peak height (r= -0.34, P =.001), and FA peak height (r = -0.57, P<.001). NBV correlated significantly with number of hyperintense areas (P <.001), MTR peak height (P <.001), mean ADC (P =.001), ADC peak height (P =.001), and FA peak height (P <.001). The final multivariable regression model included NBV and number of hyperintense areas at T2-weighted MR imaging as independent predictors of subject age. CONCLUSION: In addition to the extent of T2-weighted MR imaging hyperintense areas and the measurement of NBV, diffusion-tensor MR imaging provides additional in vivo information about microstructural age-related brain tissue changes. (C) RSNA, 2003.

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