Mohammad-Reza Nazem-Zadeh1, Hossein Rahimzadeh 2, Hadi Kamkar 3, Narges Hoseini-Tabatabaei 4, Sohrab Hashemi-Fesharaki 5, and Jafar Mehvari Habibabadi 6
1Research Center for Molecular and Cellular Imaging, Tehran University of Medical Sciences, Tehran, Iran (Islamic Republic of), 2Biomedical Engineering and Medical Physics, Shahid Beheshti University of Medical Sciences, Tehran, Iran (Islamic Republic of), 3Bioinformatics and Biophysics, Tarbiat Modares University, Tehran, Iran (Islamic Republic of), 4Medical School, Tehran University of Medical Sciences, Tehran, Iran (Islamic Republic of), 5Pars Advanced and Minimally Invasive Medical Manners Research Center, Pars Hospital, Iran University of Medical Sciences, Tehran, Iran (Islamic Republic of), 6Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran (Islamic Republic of)
Synopsis
Keywords: Epilepsy, Perfusion, ASL Perfusion MRI, Lateralization of TLE, Blood Teritorry
Motivation: To enhance lateralization of drug-resistant mesial temporal lobe epilepsy (mTLE) for improved surgery decisions. Using arterial spin labeling (ASL) MRI, this study explores vascular territories to differentiate left and right mTLE.
Goal(s): To assess ASL MRI's potential in distinguishing between mTLE types by studying cerebral blood flow changes.
Approach: It involves comparing mTLE groups to controls using ASL MRI and vascular territory analysis, identifying specific brain regions affecting lateralization.
Results: They highlight vascular territory changes crucial in distinguishing mTLE types, emphasizing the clinical significance of ASL MRI.
Impact: This
research may significantly impact treatment decisions, benefitting individuals
with challenging mTLE and guiding future epilepsy research.
Introduction:
Epilepsy is a prevalent neurological disorder affecting millions
globally, with mesial temporal lobe epilepsy (mTLE) being one of the most
common forms. For individuals with drug-resistant mTLE, epilepsy surgery
becomes necessary, with a key consideration being the localization of the
seizure focus in the left or right temporal lobe [1].
Recent advancements in neuroimaging, particularly arterial spin labeling (ASL)
MRI, a noninvasive method for perfusion analysis, provide an opportunity to
improve this critical aspect of epilepsy treatment [2-4]. ASL MRI, which measures blood flow, can be enhanced by utilizing
a vascular territory atlas to aid in determining the lateralization of mTLE.
This study seeks to explore the potential of vascular territory analysis with
ASL MRI in distinguishing between left and right mTLE and its relevance in
clinical practice.Methods:
In this research, Pulsed ASL MRI data from 15 healthy volunteers
and 23 left mTLE, 22 right mTLE were collected using a 3 T Siemens Prisma MRI
scanner. The analysis was conducted using the Bayesian Inference for Arterial
Spin Labeling MRI (BASIL) toolbox, providing pre-processing and post-processing
procedures for CBF mapping. The vascular territory brain template is employed
to compute CBF (cerebral blood flow) in each vascular territory, encompassing
the entire gray matter nourished by the ACA, MCA, and PCA, with subdivisions
into proximal, intermediate, and distal areas, resulting in a total of 18
regions of interest (ROIs) [5].
Result:
Intra-cohort comparison using paired
T-test between left and right brain hemispheres showed significant differences
for control cohort in left and right distal ACA, distal MCA, proximal ACA,
proximal MCA, and proximal PCA. There was a significant difference between
bilateral regions of right mTLE in distal ACA, intermediate PCA, proximal ACA,
proximal MCA, and proximal PCA. In patients with left mTLE, the comparison of
bilateral regions did not reveal any significant difference in any of the ROIs.
Inter-cohort comparison of ROIs was
performed using SPSS’s independent T-Test. left mTLE vs. control data
comparison resulted in a significant difference in left intermediate PCA. Right
mTLE cohort was different in left intermediate ACA, regions compared to control
cohort. Statistical comparison of right mTLE vs. left mTLE showed a significant
difference in right distal MCA.
Discussion:
The use of vascular territories has
proven valuable in studying various cerebrovascular and neurological diseases,
including Moyamoya disease and Alzheimer's disease [6, 7]. While certain regions of interest (ROIs) were
effective in distinguishing right and left mTLE from control cohorts,
differentiation between left and right mTLE was challenging. Notably, the right
distal anterior cerebral artery (ACA) vascular territory's significance in
separating the two mTLE subcohorts suggests that hypoperfusion in this region
could serve as a potential imaging biomarker for lateralization in temporal
lobe epilepsy.
Comparing left mTLE with the control
group revealed significant differences in the left intermediate posterior
cerebral artery (PCA) territory. This region is considered highly susceptible
to minor vessel disease or autoregulation issues [8]. The observed drop in cerebral blood flow (CBF) can be
attributed to its supply to the left parahippocampus and the left occipital
lobe. This aligns with findings of hypoperfusion in the left inferior occipital
and left parahippocampus regions in both voxel-wise and ROI analyses.
In the comparison between right mTLE
and control cohorts, significant differences were observed in the left
intermediate anterior cerebral artery (ACA) territory, which supplies various
brain regions including the superior frontal gyrus and frontal pole. These
findings support previous research [9, 10] indicating cortical thinning in the superior frontal lobe in right mTLE and
disruptions in cerebrocerebellar functional networks, emphasizing the relevance
of CBF changes in the left intermediate ACA to existing studies.
Conclusion:
The results of this study underscore
the importance of considering vascular territory analysis in the assessment of
mTLE lateralization. While previous research often focused on structural
changes in the gray matter, the significance of vascular territory changes cannot
be underestimated. By considering vascular territory changes, clinicians may be
better equipped to make informed decisions regarding surgical interventions,
especially when faced with challenging cases of mTLE.Acknowledgements
No acknowledgement found.References
1. Sheikh SR, Nair D,
Gross RE, GonzalezâMartinez J. Tracking a changing paradigm and the modern face
of epilepsy surgery: a comprehensive and critical review on the hunt for the
optimal extent of resection in mesial temporal lobe epilepsy. Epilepsia.
2019;60(9):1768-93.
2. Rahimzadeh H,
Kamkar H, Hoseini-Tabatabaei N, Mobarakeh NM, Habibabadi JM, Hashemi-Fesharaki
S-S, et al. Alteration of intracranial blood perfusion in temporal lobe
epilepsy, an arterial spin labeling study. Heliyon. 2023;9(4).
3. Yoganathan K,
Malek N, Torzillo E, Paranathala M, Greene J. Neurological update: structural
and functional imaging in epilepsy surgery. Journal of Neurology.
2023;270(5):2798-808.
4. Fallahi A, Pooyan
M, Habibabadi JM, Nazem-Zadeh M-R. Comparison of multimodal findings on
epileptogenic side in temporal lobe epilepsy using self-organizing maps.
Magnetic Resonance Materials in Physics, Biology and Medicine.
2022;35(2):249-66.
5. Mutsaerts H, Van
Dalen J, Heijtel D, Groot P, Majoie C, Petersen E, et al. Cerebral perfusion
measurements in elderly with hypertension using arterial spin labeling. PloS
one. 2015;10(8):e0133717.
6. Huang C-W, Hsu
S-W, Chang Y-T, Huang S-H, Huang Y-C, Lee C-C, et al. Cerebral perfusion
insufficiency and relationships with cognitive deficits in Alzheimer’s disease:
a multiparametric neuroimaging study. Scientific reports. 2018;8(1):1-14.
7. Dounavi M-E, Low
A, McKiernan EF, Mak E, Muniz-Terrera G, Ritchie K, et al. Evidence of cerebral
hemodynamic dysregulation in middle-aged APOE ε4 carriers: The PREVENT-Dementia
study. Journal of Cerebral Blood Flow & Metabolism. 2021;41(11):2844-55.
8. Huang C-W, Hsu
S-W, Chang Y-T, Huang S-H, Huang Y-C, Lee C-C, et al. Cerebral perfusion
insufficiency and relationships with cognitive deficits in Alzheimer’s disease:
a multiparametric neuroimaging study. Scientific reports. 2018;8(1):1541.
9. Zhou X, Zhang Z,
Liu J, Qin L, Pang X, Zheng J. Disruption and lateralization of
cerebellar–cerebral functional networks in right temporal lobe epilepsy: a
resting-state fMRI study. Epilepsy & Behavior. 2019;96:80-6.
10. Jber M, Habibabadi JM, Sharifpour R, Marzbani H, Hassanpour
M, Seyfi M, et al. Temporal and extratemporal atrophic manifestation of
temporal lobe epilepsy using voxel-based morphometry and corticometry: clinical
application in lateralization of epileptogenic zone. Neurological Sciences.
2021;42(8):3305-25.