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Advances in MR for imaging glymphatic system and disease metabolism.

Topic:  Advances in MR for imaging glymphatic system and disease metabolism


Moderator: Hong Zhang, Post.doc



Speaker 1: Yiqi Ma, Ph.D. Candidate
Supervisor: Prof. Min Wu



Speaker 2: Wanting Li, M.M. Candidate
Supervisor: Prof. Su Lui



Date: 9/12/2024, 14:00

Location: The lab of HMRRC (10011, the 8th Teaching Building)


Speaker 1: Yiqi Ma, Ph.D. Candidate

Title: Hyperpolarized 13C MRI: State of the Art and Future Directions


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Keypoints:

  • Question: 1) How can hyperpolarized 13C MRI technology be used to detect and understand metabolic processes associated with human disease? 2) What is the current status and potential of hyperpolarized 13C MRI technology in clinical research and application? 3) What are the advantages of hyperpolarized 13C MRI compared to traditional imaging techniques such as PET?
Findings: 1) The hyperpolarized 13C MRI technique significantly enhances the MRI signal of 13C-labeled molecules, allowing real-time detection of enzyme-mediated metabolic processes associated with human disease. 2) Hyperpolarized 13C MRI technology has shown unique advantages and potential in monitoring early treatment effects in diseases such as prostate cancer, brain tumors and cardiometabolic diseases. 3) HP MRI with [1-13C]pyruvate provides information at a key branch point of metabolic pathways involved in downstream glucose metabolism—information that is not accessible to FDG PET. HP 13C probes can be imaged simultaneously to provide information on multiple metabolic processes while FDG PET can not.
Meaning: Hyperpolarized 13C MRI provides a new molecular imaging approach that can be used to better understand and detect metabolic changes in disease. This technique is expected to improve disease diagnosis, treatment monitoring and efficacy evaluation, especially in areas where traditional imaging techniques struggle to provide adequate information.

Speaker 2Wanting Li, M.M. Candidate

Title: Glymphatic system dysfunction predicts amyloid deposition, neurodegeneration, and clinical progression in Alzheimer's disease

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Keypoints:

  • Question: Can the dysfunction of the glymphatic system predict amyloid deposition, neurodegeneration, and clinical progression in Alzheimer's disease?

  • Findings: This study suggests that glymphatic impairment indicated by the ALPS index may occur before significant Aβ deposits, and predict amyloid deposition, neurodegeneration, and clinical progression in AD. The analysis along the perivascular space (ALPS) index is reduced in patients with Alzheimer's disease (AD) dementia, prodromal AD, and preclinical AD. Lower ALPS index predicted accelerated amyloid beta (Aβ) positron emission tomography (PET) burden and Aβ-positive transition. The decrease in the ALPS index occurs before cerebrospinal fluid Aβ42 reaches the positive threshold. ALPS index predicted brain atrophy, clinical progression, and cognitive decline. Aβ PET and brain atrophy mediated the link of ALPS index with cognitive decline.

  • Meaning: This study demonstrates for the first time the predictive effect of the ALPS index on amyloid deposition, brain atrophy, clinical progression, and cognitive decline in AD, and the mediating effect of amyloid and neurodegeneration on the glymphatic–cognitive decline association.