Normative quantitative relaxation atlases for characterization of cortical regions using magnetic resonance fingerprinting

Author:

Choi Joon Yul1,Hu Siyuan2,Su Ting-Yu12,Murakami Hiroatsu1,Tang Yingying13,Blümcke Ingmar14,Najm Imad1,Sakaie Ken5,Jones Stephen5ORCID,Griswold Mark6,Wang Zhong Irene1,Ma Dan2ORCID

Affiliation:

1. Charles Shor Epilepsy Center , Neurological Institute, Cleveland Clinic, 9500 Euclid Ave, Cleveland, OH 44106 , United States

2. Department of Biomedical Engineering , Case Western Reserve University, 10900 Euclid Ave, Cleveland, OH 44106 , United States

3. Department of Neurology , West China Hospital of Sichuan University, 37 Guoxue Ln, Wuhou District, Chengdu, Sichuan 610041 , China

4. Imaging Institute , Cleveland Clinic, 1950 E 89th St U Bldg, Cleveland, OH 44195 , United States

5. Department of Neuropathology , University of Erlangen, Schlobplatz 4, Erlangen 91054 , Germany

6. Department of Radiology , Case Western Reserve University, 11100 Euclid Ave, Cleveland, OH 44106 , United States

Abstract

Abstract Quantitative magnetic resonance (MR) has been used to study cyto- and myelo-architecture of the human brain non-invasively. However, analyzing brain cortex using high-resolution quantitative MR acquisition can be challenging to perform using 3T clinical scanners. MR fingerprinting (MRF) is a highly efficient and clinically feasible quantitative MR technique that simultaneously provides T1 and T2 relaxation maps. Using 3D MRF from 40 healthy subjects (mean age = 25.6 ± 4.3 years) scanned on 3T magnetic resonance imaging, we generated whole-brain gyral-based normative MR relaxation atlases and investigated cortical-region-based T1 and T2 variations. Gender and age dependency of T1 and T2 variations were additionally analyzed. The coefficient of variation of T1 and T2 for each cortical-region was 3.5% and 7.3%, respectively, supporting low variability of MRF measurements across subjects. Significant differences in T1 and T2 were identified among 34 brain regions (P < 0.001), lower in the precentral, postcentral, paracentral lobule, transverse temporal, lateral occipital, and cingulate areas, which contain sensorimotor, auditory, visual, and limbic functions. Significant correlations were identified between age and T1 and T2 values. This study established whole-brain MRF T1 and T2 atlases of healthy subjects using a clinical 3T scanner, which can provide a quantitative and region-specific baseline for future brain studies and pathology detection.

Funder

National Institutes of Health

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

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