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Chasing shadows: What determines DTI metrics in gray matter regions? An in vitro and in vivo study
Author(s) -
Rulseh Aaron M.,
Keller Jiří,
Tintěra Jaroslav,
Kožíšek Milan,
Vymazal Josef
Publication year - 2013
Publication title -
journal of magnetic resonance imaging
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.563
H-Index - 160
eISSN - 1522-2586
pISSN - 1053-1807
DOI - 10.1002/jmri.24065
Subject(s) - fractional anisotropy , diffusion mri , ferritin , in vivo , nuclear magnetic resonance , putamen , in vitro , chemistry , white matter , nuclear medicine , pathology , magnetic resonance imaging , biology , physics , medicine , neuroscience , biochemistry , genetics , radiology
Purpose To characterize the relationship between superparamagnetic ferritin‐bound iron and diffusion tensor scalars in vitro, and validate the results in vivo. Materials and Methods The in vitro model consisted of a series of 40‐mL 1.1% agarose gels doped with ferritin covering and exceeding those concentrations normally found within healthy human gray matter. Additionally, regions of interest were placed in the caudate, putamen, and globus pallidus of 29 healthy volunteer subjects 19–80 years of age. Carr‐Purcell‐Meiboom‐Gill sequence (CPMG) and diffusion tensor imaging (DTI) data were collected at 1.5 Tesla (T) and 3T in vitro, and at 1.5T in vivo. Results In vitro, linear relationships were observed between ferritin‐bound iron concentration, R 2 (1/T 2 ) and 1/SNR. Eigenvalue repulsion with increasing R 2 (decreasing SNR) was reflected in an artifactual increase of fractional anisotropy. In vivo, similar relationships were observed, with mean diffusivity also decreasing linearly with increasing R 2 . Lambda 3 showed the strongest correlation with R 2 both in vitro and in vivo. Conclusion The observation that DTI metrics correlate with ferritin‐bound iron is an important consideration in the design and interpretation of studies exploring the diffusion characteristics of gray matter regions, especially in studies focused on adolescence as well as diseases associated with altered brain‐iron load such as pantothenate kinase‐associated neurodegeneration, Huntington disease and multiple system atrophy. J. Magn. Reson. Imaging 2013;38:1103–1110. © 2013 Wiley Periodicals, Inc.