TY - JOUR
T1 - Multi-parametric neuroimaging reproducibility
T2 - A 3-T resource study
AU - Landman, Bennett A.
AU - Huang, Alan J.
AU - Gifford, Aliya
AU - Vikram, Deepti S.
AU - Lim, Issel Anne L.
AU - Farrell, Jonathan A.D.
AU - Bogovic, John A.
AU - Hua, Jun
AU - Chen, Min
AU - Jarso, Samson
AU - Smith, Seth A.
AU - Joel, Suresh
AU - Mori, Susumu
AU - Pekar, James J.
AU - Barker, Peter B.
AU - Prince, Jerry L.
AU - van Zijl, Peter C.M.
N1 - Funding Information:
This research was supported by NIH grants NCRR P41RR015241 (Peter C.M. Zijl), 1R01NS056307 (Jerry Prince), 1R21NS064534-01A109 (Bennett A. Landman/Jerry L. Prince), 1R03EB012461-01 (Bennett A. Landman). Dr. Peter C.M. van Zijl is a paid lecturer for Philips Healthcare and has technology licensed to them. This arrangement has been approved by Johns Hopkins University in accordance with its conflict of interest policies.
PY - 2011/2/14
Y1 - 2011/2/14
N2 - Modern MRI image processing methods have yielded quantitative, morphometric, functional, and structural assessments of the human brain. These analyses typically exploit carefully optimized protocols for specific imaging targets. Algorithm investigators have several excellent public data resources to use to test, develop, and optimize their methods. Recently, there has been an increasing focus on combining MRI protocols in multi-parametric studies. Notably, these have included innovative approaches for fusing connectivity inferences with functional and/or anatomical characterizations. Yet, validation of the reproducibility of these interesting and novel methods has been severely hampered by the limited availability of appropriate multi-parametric data. We present an imaging protocol optimized to include state-of-the-art assessment of brain function, structure, micro-architecture, and quantitative parameters within a clinically feasible 60-min protocol on a 3-T MRI scanner. We present scan-rescan reproducibility of these imaging contrasts based on 21 healthy volunteers (11 M/10 F, 22-61 years old). The cortical gray matter, cortical white matter, ventricular cerebrospinal fluid, thalamus, putamen, caudate, cerebellar gray matter, cerebellar white matter, and brainstem were identified with mean volume-wise reproducibility of 3.5%. We tabulate the mean intensity, variability, and reproducibility of each contrast in a region of interest approach, which is essential for prospective study planning and retrospective power analysis considerations. Anatomy was highly consistent on structural acquisition (~1-5% variability), while variation on diffusion and several other quantitative scans was higher (~ < 10%). Some sequences are particularly variable in specific structures (ASL exhibited variation of 28% in the cerebral white matter) or in thin structures (quantitative T2 varied by up to 73% in the caudate) due, in large part, to variability in automated ROI placement. The richness of the joint distribution of intensities across imaging methods can be best assessed within the context of a particular analysis approach as opposed to a summary table. As such, all imaging data and analysis routines have been made publicly and freely available. This effort provides the neuroimaging community with a resource for optimization of algorithms that exploit the diversity of modern MRI modalities. Additionally, it establishes a baseline for continuing development and optimization of multi-parametric imaging protocols.
AB - Modern MRI image processing methods have yielded quantitative, morphometric, functional, and structural assessments of the human brain. These analyses typically exploit carefully optimized protocols for specific imaging targets. Algorithm investigators have several excellent public data resources to use to test, develop, and optimize their methods. Recently, there has been an increasing focus on combining MRI protocols in multi-parametric studies. Notably, these have included innovative approaches for fusing connectivity inferences with functional and/or anatomical characterizations. Yet, validation of the reproducibility of these interesting and novel methods has been severely hampered by the limited availability of appropriate multi-parametric data. We present an imaging protocol optimized to include state-of-the-art assessment of brain function, structure, micro-architecture, and quantitative parameters within a clinically feasible 60-min protocol on a 3-T MRI scanner. We present scan-rescan reproducibility of these imaging contrasts based on 21 healthy volunteers (11 M/10 F, 22-61 years old). The cortical gray matter, cortical white matter, ventricular cerebrospinal fluid, thalamus, putamen, caudate, cerebellar gray matter, cerebellar white matter, and brainstem were identified with mean volume-wise reproducibility of 3.5%. We tabulate the mean intensity, variability, and reproducibility of each contrast in a region of interest approach, which is essential for prospective study planning and retrospective power analysis considerations. Anatomy was highly consistent on structural acquisition (~1-5% variability), while variation on diffusion and several other quantitative scans was higher (~ < 10%). Some sequences are particularly variable in specific structures (ASL exhibited variation of 28% in the cerebral white matter) or in thin structures (quantitative T2 varied by up to 73% in the caudate) due, in large part, to variability in automated ROI placement. The richness of the joint distribution of intensities across imaging methods can be best assessed within the context of a particular analysis approach as opposed to a summary table. As such, all imaging data and analysis routines have been made publicly and freely available. This effort provides the neuroimaging community with a resource for optimization of algorithms that exploit the diversity of modern MRI modalities. Additionally, it establishes a baseline for continuing development and optimization of multi-parametric imaging protocols.
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UR - http://www.scopus.com/inward/citedby.url?scp=78650936662&partnerID=8YFLogxK
U2 - 10.1016/j.neuroimage.2010.11.047
DO - 10.1016/j.neuroimage.2010.11.047
M3 - Article
C2 - 21094686
AN - SCOPUS:78650936662
SN - 1053-8119
VL - 54
SP - 2854
EP - 2866
JO - NeuroImage
JF - NeuroImage
IS - 4
ER -