摘要

PurposeThe longitudinal relaxation rate (R-1) measured in vivo depends on the local microstructural properties of the tissue, such as macromolecular, iron, and water content. Here, we use whole brain multiparametric in vivo data and a general linear relaxometry model to describe the dependence of R-1 on these components. We explore a) the validity of having a single fixed set of model coefficients for the whole brain and b) the stability of the model coefficients in a large cohort. MethodsMaps of magnetization transfer (MT) and effective transverse relaxation rate (R-2*) were used as surrogates for macromolecular and iron content, respectively. Spatial variations in these parameters reflected variations in underlying tissue microstructure. A linear model was applied to the whole brain, including gray/white matter and deep brain structures, to determine the global model coefficients. Synthetic R-1 values were then calculated using these coefficients and compared with the measured R-1 maps. ResultsThe model's validity was demonstrated by correspondence between the synthetic and measured R-1 values and by high stability of the model coefficients across a large cohort. ConclusionA single set of global coefficients can be used to relate R-1, MT, and R-2* across the whole brain. Our population study demonstrates the robustness and stability of the model. Magn Reson Med, 2014.

  • 出版日期2015-3