Kapil Chaudhary1, Senthil Kumaran2, P Sarat Chandra3, Ashima Nehra4, and Manjari Tripathi1
1Neurology, AIIMS, New Delhi, India, 2NMR, AIIMS, New Delhi, India, 3Neurosurgery, AIIMS, New Delhi, India, 4Neuropsychology, AIIMS, New Delhi, India
Synopsis
Memory can be broadly
classified as sensory (process > 1 second), short term (>1 minute)
and long term encoding in which information is encoded, stored, and retrieved.
The surgical planning in drug refractory epilepsy (DRE) patients is usually
associated with memory deficits. We measured BOLD activation during semantic
verbal memory task using auditory stimulus and correlation with clinical
parameters in patients (pre and 6 month of post-surgery) and controls. Study
revealed anterior temporal
lobe resection (ATLR) including removal of medial structures surrounding
anterior temporal lobe may develop memory deficits in left TLE patients.
Introduction
The surgical planning in temporal lobe
epilepsy (TLE) and extra temporal lobe epilepsy (ETLE) patients is usually
associated with memory deficits. The
study was aimed to measure BOLD activation during semantic verbal memory task
using auditory stimulus and correlation with clinical parameters (age of
seizure onset, duration and PGI memory assessment) in cases (pre and 6 month of
post-surgery) and controls. Method
After obtaining
the institute ethics approval, 30 consecutive patients with temporal (n=20,
left mesial temporal sclerosis) and extra temporal lobe epilepsy (n=7 left
frontal lesion; n=2 left parieto-temporal and n=1 posterior occipito-temporal
lesion) and 24 healthy controls were recruited in this study (Table 1).
Standard diagnostic and exclusion criteria were followed. Auditory cue of a
standardized story in Hindi, using Super Lab presentation software was given to the subjects
using MR compatible auditory interface system (NordicNeuroLab, Norway). After
the story, patients were instructed to speak the answers in
this story based questions during fMRI scan.The fMRI
sessions were carried out using 1.5T MR scanner (Avanto, Siemens, Germany)
using 8 channel head coil. The stimuli were presented using a MR compatible
audio visual stimulus system with binocular goggles (Nordic Neuro Lab, Norway).
Single-shot echo planar imaging (EPI) sequence was used for the BOLD studies
(number of slices: 29, slice thickness 4.5 mm; TR: 2000 ms, TE: 24 ms, FOV: 230 mm,
resolution: 64x64 and total number of measurements: 72). Data analysis and group
comparisons were carried out using SPM8 (p≤0.001, cluster threshold 10).Results and discussion
The intra group
comparison analysis of BOLD activation in TLE subjects during the memory task,
elicited significant BOLD activation in left MTG during pre-surgery than
post-surgery. Right MTG along with hippocampal gyrus was hyper active during
post-surgery compared to pre-surgery. In
ETLE group significant BOLD
activation was observed in bilateral MTG along with hippocampal gyrus in
pre-surgical than post-surgical session. Clinical memory assessment was
abnormal in TLE compared to ETLE patients after 6 months of surgery (Figure 1).
Negative correlation was found in LMTG in patients with higher seizure
duration. Greater activation in hippocampus and LMTG correlated positively with
lower seizure duration (Table 2). The present study revealed changes in mesial
temporal lobe memory-encoding activation post-surgery in comparison to
pre-surgery in the TLE group. Similar recent studies have been revealed memory
dysfunction with longer seizure duration and resection of mesial temporal lobe [1-4]. ETLE group did not elicit
significant change in mesial temporal lobe during memory-encoding activation
and clinical assessment also revealed improvement post-surgery in comparison to
pre-surgery because of preserved memory function during surgery.Conclusion
Anterior temporal
lobe resection including removal of medial structures surrounding anterior
temporal lobe may cause changes in shape, size, configuration and neuronal
networks in temporal lobe region. Acknowledgements
Deparment of Neurology and NMR AIIMSReferences
1. Bonelli, S. et al.,
2010. Brain.133, 1186–1199.
2. Powell, H. et al.,
2008. JNNP.79, 686–693.
3. Sidhu,
M. et al., 2013. Brain.136, 1868-1888.
4. Sidhu MK, et al.,
2015. Epilepsy Research. 110, 1-9.