» Articles » PMID: 34803885

Prospective Quantitative Neuroimaging Analysis of Putative Temporal Lobe Epilepsy

Overview
Journal Front Neurol
Specialty Neurology
Date 2021 Nov 22
PMID 34803885
Citations 1
Authors
Affiliations
Soon will be listed here.
Abstract

A prospective study of individual and combined quantitative imaging applications for lateralizing epileptogenicity was performed in a cohort of consecutive patients with a putative diagnosis of mesial temporal lobe epilepsy (mTLE). Quantitative metrics were applied to MRI and nuclear medicine imaging studies as part of a comprehensive presurgical investigation. The neuroimaging analytics were conducted remotely to remove bias. All quantitative lateralizing tools were trained using a separate dataset. Outcomes were determined after 2 years. Of those treated, some underwent resection, and others were implanted with a responsive neurostimulation (RNS) device. Forty-eight consecutive cases underwent evaluation using nine attributes of individual or combinations of neuroimaging modalities: 1) hippocampal volume, 2) FLAIR signal, 3) PET profile, 4) multistructural analysis (MSA), 5) multimodal model analysis (MMM), 6) DTI uncertainty analysis, 7) DTI connectivity, and 9) fMRI connectivity. Of the 24 patients undergoing resection, MSA, MMM, and PET proved most effective in predicting an Engel class 1 outcome (>80% accuracy). Both hippocampal volume and FLAIR signal analysis showed 76% and 69% concordance with an Engel class 1 outcome, respectively. Quantitative multimodal neuroimaging in the context of a putative mTLE aids in declaring laterality. The degree to which there is disagreement among the various quantitative neuroimaging metrics will judge whether epileptogenicity can be confined sufficiently to a particular temporal lobe to warrant further study and choice of therapy. Prediction models will improve with continued exploration of combined optimal neuroimaging metrics.

Citing Articles

Nuclear imaging for localization and surgical outcome prediction in epilepsy: A review of latest discoveries and future perspectives.

Sukprakun C, Tepmongkol S Front Neurol. 2023; 13:1083775.

PMID: 36588897 PMC: 9800996. DOI: 10.3389/fneur.2022.1083775.

References
1.
Houston A, Kemp P, MacLeod M . A method for assessing the significance of abnormalities in HMPO brain SPECT images. J Nucl Med. 1994; 35(2):239-44. View

2.
Van Paesschen W, Dupont P, Van Driel G, Van Billoen H, Maes A . SPECT perfusion changes during complex partial seizures in patients with hippocampal sclerosis. Brain. 2003; 126(Pt 5):1103-11. DOI: 10.1093/brain/awg108. View

3.
Kobayashi E, DAgostino M, Lopes-Cendes I, Berkovic S, Li M, Andermann E . Hippocampal atrophy and T2-weighted signal changes in familial mesial temporal lobe epilepsy. Neurology. 2003; 60(3):405-9. DOI: 10.1212/wnl.60.3.405. View

4.
Bettus G, Guedj E, Joyeux F, Confort-Gouny S, Soulier E, Laguitton V . Decreased basal fMRI functional connectivity in epileptogenic networks and contralateral compensatory mechanisms. Hum Brain Mapp. 2008; 30(5):1580-91. PMC: 6870867. DOI: 10.1002/hbm.20625. View

5.
Jack Jr C . Hippocampal T2 relaxometry in epilepsy: past, present, and future. AJNR Am J Neuroradiol. 1996; 17(10):1811-4. PMC: 8337534. View