Presurgical fMRI is increasingly performed in large medical centers across the US and in the world, including here at Johns Hopkins. It is commonly used in brain tumor and epilepsy patients to noninvasively locate essential cortical sensorimotor and language areas and to determine the language dominant hemisphere prior to surgery, thus helping to reduce the need for invasive diagnostic procedures such as intraoperative cortical stimulation mapping. However, a significant subpopulation of patients undergoing presurgical fMRI are affected by the well-known problems of geometric distortion and signal dropout (thus compromised sensitivity) in regions with large magnetic susceptibility effects when using the current standard BOLD fMRI method: gradient echo (GRE) echo-planar-imaging (EPI). These include several frontal and temporal regions particularly relevant for language mapping in presurgical fMRI. Furthermore, such susceptibility artifacts can also arise from cavities related to previous surgery, calcified structures, hemorrhage, and metal implants. For instance, about 25% of our presurgical fMRI referrals have undergone prior resection and are being considered for a second resection, who will suffer from susceptibility artifacts related to resection cavities and surgical metallic craniotomy hardware. Although many methods have been developed to mitigate these problems, most are region dependent or require extra data acquisition. We have recently developed a T2-prepared (T2prep) BOLD fMRI method, which showed minimal distortion and dropout and sufficient BOLD sensitivity in the entire brain even in the presence of metallic head implants, and superior BOLD sensitivity than GRE EPI in regions affected by large susceptibility artifacts. The method was initially developed at ultra-high magnetic field (7 Tesla, 7T). The goal of this R21 is to optimize and validate T2prep BOLD for presurgical fMRI in tumor patients on 3T clinical MRI scanners.
Aim 1 : To optimize whole-brain T2prep BOLD fMRI for typical presurgical fMRI paradigms in healthy volunteers on 3T clinical MRI scanners. The multiband techniques will be implemented for T2prep BOLD. Image quality, functional sensitivity and specificity (in regions with small or large susceptibility effects) will be compared with GRE EPI BOLD fMRI (current standard).
Aim 2 : To determine whether T2prep BOLD fMRI can be used as a complementary method for presurgical planning in brain tumor patients with large susceptibility artifacts at 3T. Functional results from patients using typical presurgical fMRI paradigms will be compared between T2prep BOLD and GRE EPI BOLD fMRI, and will be validated by intraoperative cortical stimulation mapping data. If the proposed research is successful, it is expected to benefit a significant subset of patients undergoing presurgical fMRI. As presurgical fMRI protocols often consist of several functional scans, T2prep BOLD fMRI can be feasibly incorporated into existing clinical protocols. Besides, we also expect the T2prep BOLD approach to be useful for other functional studies in neuroscience and clinical research as an alternative fMRI tool that can assess brain functions in previously less explored brain territories due to susceptibility related signal losses in EPI BOLD fMRI.

Public Health Relevance

This project is intended to optimize and validate a novel functional MRI (fMRI) pulse sequence as an alternative approach for presurgical functional mapping in brain tumor patients. The new method allows the detection of neural activities in brain regions with large magnetic susceptibility effects (air-tissue interfaces) and in the presence of metal head implants, which is normally extremely difficult and sometimes impossible with the current standard BOLD fMRI method (GRE EPI BOLD fMRI) due to severe signal dropouts and image distortion. If the proposed research is successful, it is expected to benefit a significant subset of patients undergoing presurgical fMRI, who suffer from large magnetic susceptibility artifacts that often arise from previous resections and metal implants.

Agency
National Institute of Health (NIH)
Institute
National Institute of Biomedical Imaging and Bioengineering (NIBIB)
Type
Exploratory/Developmental Grants (R21)
Project #
5R21EB023538-02
Application #
9337439
Study Section
Neuroscience and Ophthalmic Imaging Technologies Study Section (NOIT)
Program Officer
Wang, Shumin
Project Start
2016-09-01
Project End
2019-06-30
Budget Start
2017-07-01
Budget End
2019-06-30
Support Year
2
Fiscal Year
2017
Total Cost
Indirect Cost
Name
Hugo W. Moser Research Institute Kennedy Krieger
Department
Type
DUNS #
155342439
City
Baltimore
State
MD
Country
United States
Zip Code
21205
Hua, Jun; Liu, Peiying; Kim, Tae et al. (2018) MRI techniques to measure arterial and venous cerebral blood volume. Neuroimage :
Agarwal, Shruti; Hua, Jun; Sair, Haris I et al. (2018) Repeatability of language fMRI lateralization and localization metrics in brain tumor patients. Hum Brain Mapp 39:4733-4742
Hua, Jun; Miao, Xinyuan; Agarwal, Shruti et al. (2017) Language Mapping Using T2-Prepared BOLD Functional MRI in the Presence of Large Susceptibility Artifacts-Initial Results in Patients With Brain Tumor and Epilepsy. Tomography 3:105-113