ISMRM & ISMRT Annual Meeting & Exhibition • 10-15 May 2025 • Honolulu, Hawai'i

ISMRM & ISMRT 2025 Annual Meeting & Exhibition

Digital Poster

AD: Neurofluids & Vasculature

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AD: Neurofluids & Vasculature
Digital Poster
Neuro
Thursday, 15 May 2025
Exhibition Hall
13:15 -  14:15
Session Number: D-180
No CME/CE Credit

 
Computer Number: 145
4570. Association between the cerebral blood transit times, amyloid-β pathology and cognitive decline in non-dementia adults
Y. Zhang, X. Luo, J. Sun, P. Huang
The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Impact: This study highlights the role of prolonged blood transit times in AD progression, linking cerebrovascular dysfunction with Aβ pathology and cognitive decline.
 
Computer Number: 146
4571. Enlargement of perivascular spaces is associated with accelerated Aβ accumulation
L. Liu, Q. Zeng, H. Hong, M. Lin, R. Zhang, P. Huang
Department of Radiology, The Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, China
Impact: We found that  higher PVS burden is associated with faster rates of Aβ accumulation. This insight enhances our understanding of mechanisms and trajectory of Aβ accumulation, which could aid in developing therapeutic strategies to delay the progression of Alzheimer’s disease.
 
Computer Number: 147
4572. Choroid plexus and perivascular space enlargement in Alzheimer's disease: a 7T MRI study
W. Zhang, H. Liu, L. Qian, D. Wang, L. Shen, W. Liao
Department of Radiology, Xiangya Hospital of Central South University, Changsha, China
Impact: This study suggests that CPV and enlarged PVS may serve as new non-invasive MRI marker for glymphatic dysfunction in AD.
 
Computer Number: 148
4573. Longitudinal cerebral blood flow reduction associated with fast cognitive decline in elderly adults at an individual level
T. Zhao, S. Cen, J. Tang, S. H. Chung, E. Joe, V. Marmarelis, H. Chui, L. Yan
Northwestern University, Chicago, United States
Impact: This study fills the gap of research in the association between longitudinal changes of CBF and cognitive functions at an individual level.  
 
Computer Number: 149
4574. Linking Brain Reserve to Glymphatic system Function in Mild Cognitive Impairment: Evidenced by Choroid Plexus Volume and DTI-ALPS
z. liang, L. yang, Y. WenXia, Z. YanHu, Z. Yu, G. Xing, A. Kai, L. GuangYao, Z. Jing
The Second Hospital & Clinical Medical School, Lanzhou university, lanzhou, China
Impact: Our findings highlight that MCI patients exhibited decreased glymphatic activity compared to NCs, and glymphatic activity could be used to evaluate brain reserve in MCI, which is further related to cognitive impairment
 
Computer Number: 150
4575. Cerebral Blood Flow Associations with Apolipoprotein E4 and Cerebral Amyloid Burden in Cognitively Intact Individuals
S. Nikolova, G. Dumkrieger, L. Baxter, B. Woodruff, R. Caselli, O. Dumitrascu
Mayo Clinic, Phoenix, United States
Impact: Our results will impact researchers and clinicians, enhancing early Alzheimer’s diagnosis and intervention. Future research may explore lifestyle and other vascular-targeting modifications for APOE4 carriers, allowing for personalized treatment strategies, and improving patient outcomes.
 
Computer Number: 151
4576. Imaging Indicators of the Glymphatic System in T2DM: Correlation with Cognition, and Choroid Plexus Volume-Mediated Impact on WMH-Cognition
s. yu, W. Wang, H. Jiang
The First Affiliated Hospital of Dalian Medical University, Dalian City, China
Impact: In T2DM, limited literature evaluates the glymphatic system multidimensionally. Our study pioneers mediation analysis of the glymphatic system's role in CSVD-cognition link.
 
Computer Number: 152
4577. Evaluation of Surgery for Improving Brain Glymphatic Circulation in Slowing Advanced Alzheimer’s Disease Progression by Glymphatic MRI
H. Ma, S. Ai, P-Y Wu, Y. Zhang
Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
Impact:  A decrease in ALPS indicates a lower cerebrospinal fluid clearance rate in AD patients, while increased FW-WM suggests fluid accumulation in the brain’s interstitial space. Postoperative changes imply improved cerebrospinal fluid clearance and a reduction in prior accumulation.
 
Computer Number: 153
4578. Test-retest reliability of Cerebral Blood Flow and Cerebrovascular Reactivity using novel M2-PCASL sequence in healthy adults.
J. Todd, M-J Mateos, I. Budeir, D. Qiu
Emory University, Georgia Institue of Technology, Atlanta, United States
Impact: Reliable estimation of cerebrovascular parameters is essential for scientists and clinicians to study these parameters in neurodegenerative diseases such as Alzheimer's Disease and will enable the discovery of disease biomarkers and potential drug targets for therapeutics.
 
Computer Number: 154
4579. A preliminary study of MRI-Derived Glymphatic System indices in early normal elderly people
M. Huang, X. Lyu, Y. Yin, P. Wu, B. Gao
Affiliated Hospital of Guizhou Medical University, Guiyang, China
Impact: These findings may provide new evidence for the influence of GS function on aging and many other neurodegenerative disease in clinical practice.
 
Computer Number: 155
4580. Impact of Sleep on Extracellular Space in Human Brains: A Simultaneous Study with Sodium MRI and EEG
K. Watson, X. Chen, Y-C Lin, N-M Kumbella, J. Quimbo, S. Henin, Z. Rockowitz, A. Liu, A. Masurkar, J. Babb, Y. Ge, Y. Lui, Y. Qian
New York University Grossman School of Medicine, New York, United States
Impact: Our findings confirmed the impact of sleep on extracellular volume fraction in the human brain, which may influence cerebrospinal fluid clearance and has potential implications for Alzheimer's Disease progression.
 
Computer Number: 156
4581. Integrated DTI-ALPS and Radiomics for Alzheimer's Disease Diagnosis and Cognitive Function Evaluation
X. Mao, L. Han, Z. Jia
Affiliated Hospital and Medical School of Nantong University, Nantong, China
Impact: DTI-ALPS shows promise as a valuable tool for accessing GS alterations in AD. Integrated ALPS index and radiomics can improve diagnostic capabilities and assess cognitive function in patients with AD.
 
Computer Number: 157
4582. Perfusion Imaging via Pseudo Continuous Arterial Spin Labeling in Transgenic Rat Model of Alzheimer’s Disease on High Carbohydrate High Fat Diet
D. Almanza, M. Koletar, G. Stanisz, J. McLaurin, B. Stefanovic
University of Toronto, Toronto, Canada
Impact: We established an assay of hippocampal neurovascular function for studying the sequelae of AD and its vascular comorbidities that is of high translational potential given limited aging/neurodegeneration dependent effects on somatosensation and ease of delivering somatosensory stimuli.
 
Computer Number: 158
4583. The age-related trend in the diffusion tensor image analysis along the perivascular space (DTI-ALPS)
X. Lyu, Y. Yin, Y. Sun, X. Lei, K. Ai, B. Gao
The Affiliated Hospital of Guizhou Medical University, Guiyang, China
Impact: This study contributes to understanding the relationship between ALPS and age and the differences in ALPS between the two hemispheres of the brain.
 
Computer Number: 159
4584. The coupling of global brain activity and cerebrospinal fluid flow as a potential predictive marker of amyloid-β accumulation
Y. Tanaka, K. Kamagata, Y. Saito, K. Takabayashi, R. Iseki, W. Uchida, C. Andica, A. Hagiwara, A. Wada, T. Akashi, O. Abe, S. Aoki
Juntendo University Graduate School of Medicine, Tokyo, Japan
Impact: This study clarifies that reduced CSF clearance causes brain Aβ accumulation and demonstrates that gBOLD-CSF coupling could serve as a non-invasive biomarker for predicting future brain Aβ accumulation, potentially enabling pre-preclinical Alzheimer's disease interventions that target clearance dysfunction.
 
 
Computer Number: 160
4585. Progressive cerebrovascular impairment in transgenic Alzheimer’s disease mouse models: a 12-month longitudinal study
H. Lee, S. Mirrione, N. Ruiz Uribe, S. Huang, R. Bennett, Y-F Yen
Massachusetts General Hospital, Charlestown, United States
Impact: This study delineates the timeline of cerebrovascular change in AD models, enhancing our ability to interpret in vivo vascular imaging in humans. Future cross-sectional ex vivo microscopy will help validate in vivo MRI measures relevant to AD pathology.
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