소장자료
LDR | 05781nam 2200529 4500 | ||
001 | 0100799366▲ | ||
005 | 20240318104130▲ | ||
006 | m o d ▲ | ||
007 | cr#unu||||||||▲ | ||
008 | 240116s2023 us |||||||||||||||c||eng d▲ | ||
020 | ▼a9798380472562▲ | ||
035 | ▼a(MiAaPQ)AAI30530141▲ | ||
040 | ▼aMiAaPQ▼cMiAaPQ▲ | ||
082 | 0 | ▼a616▲ | |
100 | 1 | ▼aWu, Lin.▲ | |
245 | 1 | 0 | ▼aAdvanced Methodologies for Neuromodulation and Quantitative MRI With MB-SWIFT▼h[electronic resource]▲ |
260 | ▼a[S.l.]: ▼bUniversity of Minnesota. ▼c2023▲ | ||
260 | 1 | ▼aAnn Arbor : ▼bProQuest Dissertations & Theses, ▼c2023▲ | |
300 | ▼a1 online resource(153 p.)▲ | ||
500 | ▼aSource: Dissertations Abstracts International, Volume: 85-04, Section: B.▲ | ||
500 | ▼aAdvisor: Michaeli, Shalom;Mangia, Silvia.▲ | ||
502 | 1 | ▼aThesis (Ph.D.)--University of Minnesota, 2023.▲ | |
506 | ▼aThis item must not be sold to any third party vendors.▲ | ||
520 | ▼aIntroduction: Deep Brain Stimulation (DBS) treatment for Alzheimer's disease (AD) is becoming increasingly evident. In this study, we exploited a novel orientation-selective (OS) strategy recently introduced by our group for DBS, entitled orientation-selective DBS (OS-DBS). This strategy entails that, by using multiple contacts with independent current sources within a multi-electrode array, the electric field can be oriented along any desired orientation in space. Therefore, axons parallel to the electric field spatial gradients are preferentially activated. Moreover, we applied the OS methodology to epidural spinal cord stimulation. In order to detect pathological processes of AD non-invasively with magnetic resonance imaging (MRI) technology, an alternating Look-Locker (aLL) method was developed to study novel MRI biomarkers such as T1₩uD835₩uDF46 based on rotating frame MRI methods tailored to reveal neurodegeneration.Objectives and Methods: 1) For OS-ESCS, we introduced a similar OS approach for ESCS, and demonstrated orientation dependent brain activations as detected by brain fMRI. 2) To study OS-DBS of the subthalamic nucleus (STN), AD related targets including the entorhinal cortex (EC) and medial septal nucleus (MSN), to demonstrate the basic principle of OS and prove its feasibility and advantage in optimizing the stimulation of the target. Here, OS-DBS with a three-channel electrode was utilized to stimulate the rat STN, EC, and MSN to modulate the activation of brain networks connected to the stimulation sites. The induced brain activity was monitored with fMRI by Multi-Band Sweep Imaging with Fourier Transformation (MB-SWIFT) readout at 9.4 T. 3) The aLL method was proposed to perform simultaneous quantitative T1 and T1₩uD835₩uDF46, or T1 and B1 3D MRI mapping. Look-Locker scheme that alternates magnetization from the laboratory frame's +Z and -Z axes is combined with a 3D MB-SWIFT readout. The analytical solution describing the spin evolution during aLL and the correction required for segmented acquisition were derived. The simultaneous B1 and T1 mapping were demonstrated on a phantom. T1₩uD835₩uDF46 values in the rat brain in vivo and the Gd-DTPA phantom were compared to those obtained with a previously introduced steady-state (SS) method.Results: 1) For ESCS, orientation dependent activations were detected in brain areas that transmit the motor and sensory information. 2) OS-DBS of the STN reached maximal activation of related brain areas in correspondence with an in-plane 180°stimulation angle, which was consistent with the main mediolateral direction of the STN fibers confirmed with high resolution diffusion imaging and histology. Varying the in-plane OS-DBS stimulation angle in the EC resulted in the modulation of multiple downstream brain areas involved in memory and cognition. In contrast, no angle dependence of brain activation was observed when stimulating the MSN, consistent with predictions based on the electrode configuration and on the main axonal directions of the targets derived from diffusion MRI tractography and histology. 3) The aLL method allows for simultaneous T1 and B1 mapping, while the aLL method with the application of MP modules can provide simultaneous T1 and T1₩uD835₩uDF46 maps. T1₩uD835₩uDF46 values were similar with both aLL and SS techniques. However, aLL resulted in more robust quantitative mapping as compared with the SS method and provided the advantage of generating T1 maps in a single acquisition. Conclusions: 1) OS-ESCS allows the targeting of spinal fibers of different orientations, ultimately making stimulation less dependent on the precision of the electrode implantation. 2) OS-DBS stimulation angle modulates the activation of brain areas relevant to AD and Parkinson's disease (PD), thus holding great promise for DBS treatment of the diseases. 3) The proposed aLL method offers a new flexible tool for quantitative T1, T1₩uD835₩uDF46, and B1 mappings.▲ | ||
590 | ▼aSchool code: 0130.▲ | ||
650 | 4 | ▼aMedical imaging.▲ | |
650 | 4 | ▼aNeurosciences.▲ | |
650 | 4 | ▼aPathology.▲ | |
650 | 4 | ▼aBioinformatics.▲ | |
653 | ▼aAlternating Look-Locker▲ | ||
653 | ▼aAlzheimer's disease▲ | ||
653 | ▼aDeep Brain Stimulation▲ | ||
653 | ▼aMagnetic resonance imaging▲ | ||
653 | ▼aMulti-Band Sweep Imaging▲ | ||
690 | ▼a0574▲ | ||
690 | ▼a0317▲ | ||
690 | ▼a0715▲ | ||
690 | ▼a0571▲ | ||
710 | 2 | 0 | ▼aUniversity of Minnesota.▼bBiomedical Engineering.▲ |
773 | 0 | ▼tDissertations Abstracts International▼g85-04B.▲ | |
773 | ▼tDissertation Abstract International▲ | ||
790 | ▼a0130▲ | ||
791 | ▼aPh.D.▲ | ||
792 | ▼a2023▲ | ||
793 | ▼aEnglish▲ | ||
856 | 4 | 0 | ▼uhttp://www.riss.kr/pdu/ddodLink.do?id=T16933506▼nKERIS▼z이 자료의 원문은 한국교육학술정보원에서 제공합니다.▲ |
Advanced Methodologies for Neuromodulation and Quantitative MRI With MB-SWIFT[electronic resource]
자료유형
국외eBook
서명/책임사항
Advanced Methodologies for Neuromodulation and Quantitative MRI With MB-SWIFT [electronic resource]
개인저자
발행사항
[S.l.] : University of Minnesota. 2023 Ann Arbor : ProQuest Dissertations & Theses , 2023
형태사항
1 online resource(153 p.)
일반주기
Source: Dissertations Abstracts International, Volume: 85-04, Section: B.
Advisor: Michaeli, Shalom;Mangia, Silvia.
Advisor: Michaeli, Shalom;Mangia, Silvia.
학위논문주기
Thesis (Ph.D.)--University of Minnesota, 2023.
요약주기
Introduction: Deep Brain Stimulation (DBS) treatment for Alzheimer's disease (AD) is becoming increasingly evident. In this study, we exploited a novel orientation-selective (OS) strategy recently introduced by our group for DBS, entitled orientation-selective DBS (OS-DBS). This strategy entails that, by using multiple contacts with independent current sources within a multi-electrode array, the electric field can be oriented along any desired orientation in space. Therefore, axons parallel to the electric field spatial gradients are preferentially activated. Moreover, we applied the OS methodology to epidural spinal cord stimulation. In order to detect pathological processes of AD non-invasively with magnetic resonance imaging (MRI) technology, an alternating Look-Locker (aLL) method was developed to study novel MRI biomarkers such as T1\uD835\uDF46 based on rotating frame MRI methods tailored to reveal neurodegeneration.Objectives and Methods: 1) For OS-ESCS, we introduced a similar OS approach for ESCS, and demonstrated orientation dependent brain activations as detected by brain fMRI. 2) To study OS-DBS of the subthalamic nucleus (STN), AD related targets including the entorhinal cortex (EC) and medial septal nucleus (MSN), to demonstrate the basic principle of OS and prove its feasibility and advantage in optimizing the stimulation of the target. Here, OS-DBS with a three-channel electrode was utilized to stimulate the rat STN, EC, and MSN to modulate the activation of brain networks connected to the stimulation sites. The induced brain activity was monitored with fMRI by Multi-Band Sweep Imaging with Fourier Transformation (MB-SWIFT) readout at 9.4 T. 3) The aLL method was proposed to perform simultaneous quantitative T1 and T1\uD835\uDF46, or T1 and B1 3D MRI mapping. Look-Locker scheme that alternates magnetization from the laboratory frame's +Z and -Z axes is combined with a 3D MB-SWIFT readout. The analytical solution describing the spin evolution during aLL and the correction required for segmented acquisition were derived. The simultaneous B1 and T1 mapping were demonstrated on a phantom. T1\uD835\uDF46 values in the rat brain in vivo and the Gd-DTPA phantom were compared to those obtained with a previously introduced steady-state (SS) method.Results: 1) For ESCS, orientation dependent activations were detected in brain areas that transmit the motor and sensory information. 2) OS-DBS of the STN reached maximal activation of related brain areas in correspondence with an in-plane 180°stimulation angle, which was consistent with the main mediolateral direction of the STN fibers confirmed with high resolution diffusion imaging and histology. Varying the in-plane OS-DBS stimulation angle in the EC resulted in the modulation of multiple downstream brain areas involved in memory and cognition. In contrast, no angle dependence of brain activation was observed when stimulating the MSN, consistent with predictions based on the electrode configuration and on the main axonal directions of the targets derived from diffusion MRI tractography and histology. 3) The aLL method allows for simultaneous T1 and B1 mapping, while the aLL method with the application of MP modules can provide simultaneous T1 and T1\uD835\uDF46 maps. T1\uD835\uDF46 values were similar with both aLL and SS techniques. However, aLL resulted in more robust quantitative mapping as compared with the SS method and provided the advantage of generating T1 maps in a single acquisition. Conclusions: 1) OS-ESCS allows the targeting of spinal fibers of different orientations, ultimately making stimulation less dependent on the precision of the electrode implantation. 2) OS-DBS stimulation angle modulates the activation of brain areas relevant to AD and Parkinson's disease (PD), thus holding great promise for DBS treatment of the diseases. 3) The proposed aLL method offers a new flexible tool for quantitative T1, T1\uD835\uDF46, and B1 mappings.
주제
ISBN
9798380472562
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