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

ISMRM & ISMRT 2025 Annual Meeting & Exhibition

Digital Poster

Aging Health & Disease

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Aging Health & Disease
Digital Poster
Neuro
Monday, 12 May 2025
Exhibition Hall
08:15 -  09:15
Session Number: D-179
No CME/CE Credit

 
Computer Number: 129
1500. Genetic Influences on Brain Aging: Analyzing Sex Differences in the UK Biobank using Structural MRI
K. Ardila, A. Mohite, A. Addeh, A. Tyndall, C. Barha, Q. Long, M. E. MacDonald
University of Calgary, Calgary, Canada
Impact:

This study highlights the importance of sex-stratified analysis in understanding the genetic associations with brain aging. Findings pave the way for future work on personalized treatments and preventative measures for neurodegeneration based on individual genetic profiles and sex-specific risks.

 
Computer Number: 130
1501. Cerebral microbleeds in community-based older adults imaged both in-vivo and ex-vivo: A clinical, MRI and pathology study
M. T. Yasar, G. Nikseresht, A. R. Ridwan, S. Zhang, D. Bennett, J. Schneider, K. Arfanakis
Illinois Institute of Technology, Chicago, United States
Impact: We demonstrated that cerebral microbleeds (CMB) detected in-vivo were also detected ex-vivo. Also, cognitive impairment and cerebral amyloid angiopathy were associated with higher risk of CMB occurrence prior to death in older adults.  
 
Computer Number: 131
1502. Establishing Brain Reference Ranges in Indian Population: Comparison with Westerners and Validation for Parkinsonism Differential Diagnosis
P. B Venkategowda, T. Di Noto, K. Prabhu M, L. Bacha, B. Mehta, S. Kulkarni, G. Franco Piredda, V. Benegal, J. Saini, B. Holla, N. Sinha, R. Dawn Bharath, B. Maréchal
Magnetic Resonance, Siemens Healthcare Pvt. Ltd., Bengaluru, India
Impact: We release age-/sex-/ethnicity-specific reference ranges built from Indian and Western controls. We show notable variations highlighting the need for population-specific reference modeling. Additionally, our reference ranges enable the detection of specific atrophy patterns in patients with different Parkinsonian syndromes.
 
Computer Number: 132
1503. X Chromosome Genetic Overlap of Hormone, Lipid, and Brain Imaging Traits with Alzheimer’s Disease Reveals Novel Risk Genes
N. Cook, C. Yang, D. Reid, M. Belloy
Washington University, Saint Louis, United States
Impact: Integrating X chromosome genetic data for Alzheimer’s disease (AD) with related traits, we uncovered 20 AD risk loci, including several showing sex-specific effects. These findings provide new biological insights into AD and highlight potential sex-agnostic and sex-specific AD drug targets.
 
Computer Number: 133
1504. Maternal Diet Restriction During Pregnancy Leads to Divergent Hippocampal Enlargement Trajectories in Aging Baboon Offspring
B. Yang, W. Zhang, J. Li, H. Huber, C. Shively, L. Cox, P. Nathanielsz, G. Clarke
University of Texas Health Science Center at San Antonio, San Antonio, United States
Impact: These findings suggest early-life nutritional deficits can shape brain aging, offering a model to explore interventions that support healthy cognitive aging in individuals with prenatal and post-partum exposure to MUN.
 
Computer Number: 134
1505. Comparison of heart rate and heart rate variability metrics derived from laboratory ECG signals and BOLD fMRI
T. Kim, M. Scudder, A. Marsland, P. Gianaros
University of Pittsburgh, Pittsburgh, United States
Impact: Using MRI data alone to assess HR enables more comprehensive, integrated research on cardiac and brain interactions. It may contribute to enhancing multimodal data analysis and developing robust, non-invasive protocols for studying cardiac and brain interactions in various applications.
 
Computer Number: 135
1506. Measurement of tryptophan relaxation times in human brain using downfield 1H MRS at 7 T
R. P. R. Nanga, N. Wilson, M. Elliott, S. Swago, W. Witschey, R. Reddy
Perelman School of Medicine at The University of Pennsylvania, Philadelphia, United States
Impact: Reliable in vivo brain TRP relaxation measures in normal subjects could help establish reference values and also aid in utilizing it as a novel non-invasive in vivo biomarker for various aging-related and neuropsychiatric disorders.
 
Computer Number: 136
1507. Effects of Aging on Cerebral Morphology and Microstructure in Rhesus Macaques
A. Grigorian, C. Kroenke, H. Urbanski, S. Kohama, A. Weiss
Oregon Health & Science University, Portland, United States
Impact:        

Using a large age-diverse sample, we corroborate and extend previous findings of age-related brain changes in macaques, uncovering additional affected regions undetected with traditional imaging methods. This validates brain biomarkers in a translational animal model of normative human aging.

 
Computer Number: 137
1508. Brain tissue conductivity decreases with age
J. Cao, J. Philby, I. Ball, C. Rae
Neuroscience Research Australia, Randwick, Australia
Impact: Brain tissue conductivity is a potential biomarker for healthy aging, and the change over time is expected to be considered in many applications.
 
Computer Number: 138
1509. Automatic ventricle segmentation using quantitative MRI
M. Warntjes, A. Tisell, C. Georgiopoulos, R. Holmgren
Center for Medical Imaging Science and Visualization (CMIV), Linköping, Sweden
Impact: A fully automatic ventricle segmentation, using quantitative CSF maps as input, showed a high accuracy compared to manual segmentation. This allows a far more objective and accurate follow-up for Normal Pressure Hydrocephalus patients than the current method of visual inspection.
 
Computer Number: 139
1510. Impact of socioeconomic status on acuity of brain MRI findings
I. Raghuvanshi, B. Risk, G. Sadigh, J. Allen, C. Fleischer
Georgia Institute of Technology and Emory University, Atlanta, United States
Impact: We observed neighborhood socioeconomic status significantly correlates with acuity of brain MRI findings when adjusting for race, insurance coverage, encounter type, sex, age, and marital status, emphasizing the need for solutions to reduce socioeconomic barriers to receiving MRI scans.
 
Computer Number: 140
1511. Automated Estimation of White Matter Hyperintensity Burden from 2D T2w TSE as an Alternative to 3D FLAIR
J. Disselhorst, V. Dunet, G. Allali, H. Kitzler, N. Menjot de Champfleur, E. Le Bars, V. Ravano, T. Di Noto, T. Hilbert, B. Maréchal
Siemens Healthineers International AG, Lausanne, Switzerland
Impact: Using 2D T2w Turbo Spin Echo (TSE) sequences for white matter hyperintensity (WMH) volume estimation provides a dependable alternative to 3D FLAIR, particularly when quick scan protocols are necessary, but WMH estimation is still needed.
 
Computer Number: 141
1512. The effects of aerobic fitness and BMI on brain volumes and white matter hyperintensities in coronary artery disease
Z. Potvin-Jutras, S. Tremblay, S. Sanami, A. Rezaei, D. Sabra, B. Intzandt, L. Wright, C. Gagnon, A. Mainville-Berthiaume, O. Parent, M. Dadar, J. Iglesies-Grau, C. Steele, M. Gayda, A. Nigam, L. Bherer, C. Gauthier
Concordia University, Montreal, Canada
Impact: These findings support the importance of exercise and weight management in individuals with coronary artery disease to maintain brain health, especially in the middle cerebral arterial territory.
 
Computer Number: 142
1513. Mineral intake and changes in intracranial structure volume in community-dwelling adults
K. Akazawa, N. Kuriyama, E. Ozaki, D. Matsui, T. Koyama, Y. Otani, K. Watanabe, K. Sakai, Y. Marunaka, A. Takada, T. Mizuno, K. Yamada
Kyoto Prefectural University of Medicine, Kyoto, Japan
Impact: This result suggests a potential association between brain volume change and zinc. Furthermore, this study provides motivation to explore whether adequate zinc intake is necessary, even when sufficient levels of zinc are observed in blood data.
 
Computer Number: 143
1514. Deep and Periventricular White Matter Hyperintensity Segmentation and Their Relationship with Cognitive Decline and Vessel Hemodynamics
G. Li, S. H. Chung, J. Tang, E. Joe, H. Chui, L. Yan
northwestern university, chicago, United States
Impact: By clarifying PWMH's specific association with cognitive decline, our study emphasizes the importance of considering PWMH lesion counts in clinical assessments, potentially improving early diagnosis and management of cognitive impairment in the elderly.
 
Computer Number: 144
1515. Comparative Feasibility of Multimodal Imaging Indicators for Glymphatic Function in Hematological Diseases: Significant Age Effects
J. Liu, Y. Zhang, Y. Chen, W. Wang, H. Chen, Y. Cao, Y. Wang, Y. Huang, Y. Zhao, Z. Kang, D. Qin
The Second Hospital Of Dalian Medical University, Dalian, China
Impact: Imaging methods for evaluating glymphatic function should be selected carefully, with special consideration of age-related influences on DTI-ALPS index and CP volume, particularly when samples involve a wide age range.
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