Poster No:
1800
Submission Type:
Abstract Submission
Authors:
Rasheed Abid1, Md Tahmid Yasar1, Abdur Raquib Ridwan2, Yingjuan Wu2, Mohammad Niaz2, David Bennett2, Konstantinos Arfanakis2
Institutions:
1Illinois Institute of Technology, Chicago, IL, 2Rush University Medical Center, Chicago, IL
First Author:
Co-Author(s):
Introduction:
Quantitative Susceptibility Mapping (QSM) offers insights into brain iron homeostasis, vital for understanding age-related neuropathologies [1]. However, there is no study that compares in-vivo magnetic susceptibility of aging brains in their cortical regions with actual autopsy-studied iron concentration levels. The aim of this study is two-folds - (1) To analyze the relationship between iron-concentration levels with average magnetic susceptibility in the recently introduced MIITRA-QSM template. (2) Correlation between log-scaled iron-concentration level with magnetic susceptibility in the subject's native space, adjusted for age and antemortem interval.
Methods:
Data:
In this study, 3D T1-weighted MPRAGE and multi-echo 3D GRE data from a community-based aging study [2], recently developed high-resolution MIITRA-QSM template [3] in MIITRA atlas space [4], gray matter labels in the template space [5] was used for analysis.
Process:
Step 1: Using the MIITRA-QSM template, inferior-temporal, anterior-cingulate, and middle-frontal cortex, average magnetic susceptibility values were calculated in each hemisphere. For 308 non-demented older adults (aged 67.8-97.2 years) from the study [2], average iron concentration levels were plotted against the normalized median susceptibility values from the template space. Linear regression was performed to analyze the correlation.
Step 2: For 20 subjects (between 71 and 101 years of age, 16 female and antemortem interval between 0.4 to 2.4 years), from the aging study [2], we examined post-mortem iron concentration and magnetic susceptibility in their native brain space, for the same set of cortical regions. This approach involved short antemortem intervals and direct MRI-to-autopsy comparisons. Individual susceptibility values were correlated with iron concentrations through linear regression, adjusting for age and antemortem interval. Pairwise correlations were determined for the following parameters: magnetic susceptibility, iron level, sex, age and antemortem interval.
Results:
Regression analysis showed a significant correlation (R² = 0.892, p-value = 0.00453) between iron concentrations and MIITRA-QSM derived susceptibility values (fig 1). Adjusted for age and antemortem interval, linear regression shows strong positive relationship between in-vivo magnetic susceptibility and iron levels (R = 0.83, p-value < 0.05) (fig 2a). Pairwise correlation also shows a positive relationship between iron levels and magnetic susceptibility (fig 2b).
Conclusions:
Our results demonstrate that based on iron-concentration levels, MIITRA-QSM is highly representative of the older-adult brain for cortical regions. Moreover, considering age, sex and short-antemortem interval, individual-specific QSM can effectively reflect iron concentrations in the cortical regions of the older-adult brain.
Lifespan Development:
Aging 2
Neuroinformatics and Data Sharing:
Brain Atlases 1
Keywords:
Aging
Atlasing
MRI
1|2Indicates the priority used for review
By submitting your proposal, you grant permission for the Organization for Human Brain Mapping (OHBM) to distribute your work in any format, including video, audio print and electronic text through OHBM OnDemand, social media channels, the OHBM website, or other electronic publications and media.
I accept
The Open Science Special Interest Group (OSSIG) is introducing a reproducibility challenge for OHBM 2025. This new initiative aims to enhance the reproducibility of scientific results and foster collaborations between labs. Teams will consist of a “source” party and a “reproducing” party, and will be evaluated on the success of their replication, the openness of the source work, and additional deliverables. Click here for more information.
Propose your OHBM abstract(s) as source work for future OHBM meetings by selecting one of the following options:
I do not want to participate in the reproducibility challenge.
Please indicate below if your study was a "resting state" or "task-activation” study.
Other
Healthy subjects only or patients (note that patient studies may also involve healthy subjects):
Healthy subjects
Was this research conducted in the United States?
Yes
Are you Internal Review Board (IRB) certified?
Please note: Failure to have IRB, if applicable will lead to automatic rejection of abstract.
Yes, I have IRB or AUCC approval
Were any human subjects research approved by the relevant Institutional Review Board or ethics panel?
NOTE: Any human subjects studies without IRB approval will be automatically rejected.
Yes
Were any animal research approved by the relevant IACUC or other animal research panel?
NOTE: Any animal studies without IACUC approval will be automatically rejected.
Not applicable
Please indicate which methods were used in your research:
Structural MRI
For human MRI, what field strength scanner do you use?
3.0T
Which processing packages did you use for your study?
FSL
Free Surfer
Provide references using APA citation style.
[1] Madden, David J., and Jenna L. Merenstein. "Quantitative susceptibility mapping of brain iron in healthy aging and cognition. " NeuroImage 282 (2023): 120401.
[2] Bennett DA, Buchman AS, Boyle PA, et al. Religious Orders Study and Rush Memory and Aging Project. J Alzheimers Dis. 2018;64(s1):S161-S189.
[3] Abid R., Ridwan A.R., Wu Y., Niaz M.R., Zhang S., Evia A., Bennett D.A., Arfanakis K., Development of a high-resolution magnetic susceptibility template of the older adult brain in MIITRA space. Proc. Int. Soc. for Magn. Reson. in Med. (ISMRM) 2023.
[4] Ridwan, Abdur Raquib, et al. "Development and evaluation of a high performance T1‐weighted brain template for use in studies on older adults." Human Brain Mapping 42.6 (2021): 1758-1776.
[5] Niaz, M.R., Ridwan, A.R., Wu, Y., Zhang, S., Bennett, D.A.A. and Arfanakis, K. (2023), Interoperability of the MIITRA atlas with complementary atlases: development of a comprehensive array of gray matter labels. Alzheimer's Dement., 19: e081601. https://doi.org/10.1002/alz.081601
No