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Clinical Articles
Evaluation of white matter microstructural impairment in temporal lobe epilepsy using peak width of skeletonized mean diffusivity
WEI Yuanyuan  LI Jinqin  SONG Dengyan  WANG Zhuo  YE Hao  YANG Wenrui  LI Jian  CHEN Bing 

Cite this article as WEI Y Y, LI J Q, SONG D Y, et al. Evaluation of white matter microstructural impairment in temporal lobe epilepsy using peak width of skeletonized mean diffusivity[J]. Chin J Magn Reson Imaging, 2026, 17(8): 57-63. DOI:10.12015/issn.1674-8034.2026.08.005.


[Abstract] Objective To explore the clinical value of the peak width of skeletonized mean diffusivity (PSMD) parameter in reflecting white matter damage and disease severity in patients with temporal lobe epilepsy (TLE).Materials and Methods A total of 32 patients with temporal lobe epilepsy with hippocampal sclerosis (TLE-HS), 31 patients with nonlesional temporal lobe epilepsy (TLE-NL), and 40 healthy controls (HC) were included. Diffusion tensor imaging (DTI) data of the brain were collected to calculate whole-brain white matter PSMD values. Differences among the three groups were compared, and the correlations between PSMD and disease duration, the National Hospital Seizure Severity Scale (NHS3), as well as the Montreal Cognitive Assessment (MoCA) were analyzed.Results The overall distribution of PSMD values differed significantly among the three groups (H = 17.950, P < 0.001). Post-hoc pairwise comparisons showed that the overall PSMD level in the TLE-HS group was higher than that in the HC group (P < 0.001). No statistically significant differences were observed between the TLE-NL group and the HC group, or between the TLE-HS group and the TLE-NL group. In the TLE-HS group, PSMD values were positively correlated with disease duration (r = 0.416, P = 0.018) and NHS3 scores (r = 0.542, P = 0.001), and negatively correlated with MoCA scores (r = -0.428, P = 0.015). In the TLE-NL group, PSMD values were positively correlated with disease duration (r = 0.423, P = 0.018) and NHS3 scores (r = 0.328, P = 0.072), but the latter correlation did not reach statistical significance. PSMD values in the TLE-NL group were negatively correlated with MoCA scores (r = -0.488, P = 0.005).Conclusions PSMD was higher in TLE-HS patients than in the HC group and was associated with disease duration, seizure severity, and cognitive impairment. In TLE-NL patients, PSMD was associated with disease duration and cognitive function, but its association with seizure severity did not reach statistical significance. PSMD may serve as a potential imaging biomarker for white matter damage and disease progression in TLE.
[Keywords] temporal lobe epilepsy;peak width of skeletonized mean diffusivity;white matter;diffusion tensor imaging;magnetic resonance imaging;cognitive

WEI Yuanyuan1   LI Jinqin1   SONG Dengyan1   WANG Zhuo1   YE Hao1   YANG Wenrui2   LI Jian2   CHEN Bing2*  

1 School of the First Clinical Medicine, Ningxia Medical University, Yinchuan 750004, China

2 Department of Radiology, General Hospital of Ningxia Medical University, Yinchuan 750004, China

Corresponding author: CHEN B, E-mail: chenbing135501@163.com

Conflicts of interest   None.

Received  2026-03-17
Accepted  2026-07-14
DOI: 10.12015/issn.1674-8034.2026.08.005
Cite this article as WEI Y Y, LI J Q, SONG D Y, et al. Evaluation of white matter microstructural impairment in temporal lobe epilepsy using peak width of skeletonized mean diffusivity[J]. Chin J Magn Reson Imaging, 2026, 17(8): 57-63. DOI:10.12015/issn.1674-8034.2026.08.005.

[1]
FERRARIO R, GIOVAGNOLI A R. Processing speed in temporal lobe epilepsy. A scoping review[J/OL]. Epilepsy Behav, 2023, 142: 109169 [2026-03-17]. https://www.sciencedirect.com/science/article/pii/S1525505023001516. DOI: 10.1016/j.yebeh.2023.109169.
[2]
SHAH P, BASSETT D S, WISSE L E M, et al. Structural and functional asymmetry of medial temporal subregions in unilateral temporal lobe epilepsy: A 7T MRI study[J]. Hum Brain Mapp, 2019, 40(8): 2390-2398. DOI: 10.1002/hbm.24530.
[3]
GLEICHGERRCHT E, KAESTNER E, HASSANZADEH R, et al. Redefining diagnostic lesional status in temporal lobe epilepsy with artificial intelligence[J]. Brain, 2025, 148(6): 2189-2200. DOI: 10.1093/brain/awaf020.
[4]
HOUSER C R, NOEBELS J L, AVOLI M, et al. Hippocampal sclerosis in temporal lobe epilepsy: New views and challenges[M/OL]//NOEBELS J L, AVOLI M, ROGAWSKI M A, et al. Jasper's basic mechanisms of the epilepsies. 5th ed. New York: Oxford University Press, 2024: 15-34. DOI: 10.1093/med/9780197549469.003.0002.
[5]
WANG Y T, YAN M N, LI J, et al. Application of Automatic Segmentation in the Volume of Subregions of Medial Temporal Lobe Epilepsy with Hippocampal Sclerosis[J]. Chinese Journal of Medical Imaging, 2025, 33(1): 18-24. DOI: 10.3969/j.issn.1005-5185.2025.01.004.
[6]
SHON Y, KIM Y, KOO B, et al. Group-specific regional white matter abnormality revealed in diffusion tensor imaging of medial temporal lobe epilepsy without hippocampal sclerosis[J]. Epilepsia, 2010, 51(4): 529-535. DOI: 10.1111/j.1528-1167.2009.02327.x.
[7]
LYRA K P, CHAIM K T, LEITE C C, et al. Corpus callosum diffusion abnormalities in refractory epilepsy associated with hippocampal sclerosis[J]. Epilepsy Res, 2017, 137: 112-118. DOI: 10.1016/j.eplepsyres.2017.09.008.
[8]
YANG W, NIU J, XIONG Y, et al. Gray matter microstructural abnormalities in temporal lobe epilepsy with hippocampal sclerosis and MRI negative[J/OL]. Eur J Radiol, 2025, 193: 112455 [2026-03-17]. https://www.sciencedirect.com/science/article/pii/S0720048X25004367. DOI: 10.1016/j.ejrad.2025.112455.
[9]
CHEN N, PENG J, XIONG F, et al. Peak width of skeletonized mean diffusivity: a novel biomarker for white matter damage in spinocerebellar ataxia type 2[J]. Neuroradiology, 2025, 67(1): 183-189. DOI: 10.1007/s00234-024-03499-5.
[10]
BALLERINI A, ARIENZO D, STASENKO A, et al. Spatial patterns of gray and white matter compromise relate to age of seizure onset in temporal lobe epilepsy[J/OL]. Neuroimage Clin, 2023, 39: 103473 [2026-03-17]. https://www.sciencedirect.com/science/article/pii/S2213158223001354. DOI: 10.1016/j.nicl.2023.103473.
[11]
MIRÓ J, GURTUBAY-ANTOLIN A, RIPOLLÉS P, et al. Interhemispheric microstructural connectivity in bitemporal lobe epilepsy with hippocampal sclerosis[J]. Cortex, 2015, 67: 106-121. DOI: 10.1016/j.cortex.2015.03.018.
[12]
RILEY J D, FRANKLIN D L, CHOI V, et al. Altered white matter integrity in temporal lobe epilepsy: Association with cognitive and clinical profiles[J]. Epilepsia, 2010, 51(4): 536-545. DOI: 10.1111/j.1528-1167.2009.02508.x.
[13]
AFZALI M, SOLTANIAN-ZADEH H, ELISEVICH K V. Tract based spatial statistical analysis and voxel based morphometry of diffusion indices in temporal lobe epilepsy[J]. Comput Biol Med, 2011, 41(12): 1082-1091. DOI: 10.1016/j.compbiomed.2011.05.006.
[14]
LI T, ZHANG Y, FU X, et al. Microstructural white matter alterations in Alzheimer's disease and amnestic mild cognitive impairment and its diagnostic value based on diffusion kurtosis imaging: a tract-based spatial statistics study[J]. Brain Imaging Behav, 2022, 16(1): 31-42. DOI: 10.1007/s11682-021-00474-z.
[15]
LIU Z, XU Y, AN J, et al. Altered brain white matter integrity in temporal lobe epilepsy: A TBSS study[J]. J Neuroimaging, 2015, 25(3): 460-464. DOI: 10.1111/jon.12154.
[16]
GROSS D W. Diffusion tensor imaging in temporal lobe epilepsy[J]. Epilepsia, 2011, 52(s4): 32-34. DOI: 10.1111/j.1528-1167.2011.03149.x.
[17]
SONE D, OTA M, MAIKUSA N, et al. White matter abnormalities in patients with temporal lobe epilepsy and amygdala enlargement: Comparison with hippocampal sclerosis and healthy subjects[J]. Epilepsy Res, 2016, 127: 221-228. DOI: 10.1016/j.eplepsyres.2016.09.011.
[18]
LUCKEY A M, GHOSH S, WANG C, et al. Biological validation of peak-width of skeletonized mean diffusivity as a VCID biomarker: The MarkVCID Consortium[J]. Alzheimers Dement, 2024, 20(12): 8814-8824. DOI: 10.1002/alz.14345.
[19]
RASING I, VLEGELS N, SCHIPPER M R, et al. Microstructural white matter damage on MRI is associated with disease severity in Dutch-type cerebral amyloid angiopathy[J]. J Cereb Blood Flow Metab, 2024, 44(11): 1253-1261. DOI: 10.1177/0271678X241261771.
[20]
ZANON ZOTIN M C, SCHOEMAKER D, RAPOSO N, et al. Peak width of skeletonized mean diffusivity in cerebral amyloid angiopathy: Spatial signature, cognitive, and neuroimaging associations[J/OL]. Front Neurosci, 2022, 16: 1051038 [2026-03-17]. https://www.frontiersin.org/articles/10.3389/fnins.2022.1051038. DOI: 10.3389/fnins.2022.1051038.
[21]
BAYKARA E, GESIERICH B, ADAM R, et al. A novel imaging marker for small vessel disease based on skeletonization of white matter tracts and diffusion histograms[J]. Ann Neurol, 2016, 80(4): 581-592. DOI: 10.1002/ana.24758.
[22]
ERTÜRK ÇETIN Ö, GÜNGÖR DOĞAN İ, ZANAPALıOĞLU Ü, et al. Seizures in inflammatory demyelinating disorders of the central nervous system[J/OL]. Mult Scler Relat Disord, 2024, 85: 105535 [2026-03-17]. https://www.sciencedirect.com/science/article/pii/S2211034824001246. DOI: 10.1016/j.msard.2024.105535.
[23]
DEARY I J, RITCHIE S J, MUÑOZ MANIEGA S, et al. Brain peak width of skeletonized mean diffusivity (PSMD) and cognitive function in later life[J/OL]. Front Psychiatry, 2019, 10: 524 [2026-03-17]. https://www.frontiersin.org/articles/10.3389/fpsyt.2019.00524. DOI: 10.3389/fpsyt.2019.00524.
[24]
XU M, XUE K, SONG X, et al. Peak width of skeletonized mean diffusivity as a neuroimaging biomarker in first-episode schizophrenia[J/OL]. Front Neurosci, 2024, 18: 1427947 [2026-03-17]. https://www.frontiersin.org/articles/10.3389/fnins.2024.1427947. DOI: 10.3389/fnins.2024.1427947.
[25]
LEE D A, LEE H, KIM S E, et al. Peak width of skeletonized mean diffusivity as a marker of small vessel disease in patients with temporal lobe epilepsy with hippocampal sclerosis[J]. Epilepsia, 2025, 66(2): 531-540. DOI: 10.1111/epi.18205.
[26]
LEE H J, LEE D A, PARK K M. White matter and glymphatic system alterations in patients with focal epilepsy: insights from PSMD and DTI-ALPS index[J]. Neuroradiology, 2025, 67(12): 3575-3585. DOI: 10.1007/s00234-025-03782-z.
[27]
SCHEFFER I E, BERKOVIC S, CAPOVILLA G, et al. ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology[J]. Epilepsia, 2017, 58(4): 512-521. DOI: 10.1111/epi.13709.
[28]
ZANON ZOTIN M C, YILMAZ P, SVEIKATA L, et al. Peak width of skeletonized mean diffusivity: A neuroimaging marker for white matter injury[J/OL]. Radiology, 2023, 306(3): e212780 [2026-03-17]. https://pubs.rsna.org/doi/10.1148/radiol.212780. DOI: 10.1148/radiol.212780.
[29]
LI J Q, BAI Y C, YAN M N, et al. Analysis of white matter volume of the temporal lobe in mesial temporal lobe epilepsy with hippocampal sclerosis based on automatic brain segmentation technique and its application value[J]. Radiologic Practice, 2024, 39(9): 1130-1137. DOI: 10.13609/j.cnki.1000-0313.2024.09.003.
[30]
SONG C, ZHANG X, ZHANG Y, et al. Comparison of spontaneous brain activity between hippocampal sclerosis and MRI-negative temporal lobe epilepsy[J/OL]. Epilepsy Behav, 2024, 157: 109751 [2026-03-17]. https://www.sciencedirect.com/science/article/pii/S1525505024002048. DOI: 10.1016/j.yebeh.2024.109751.
[31]
WANG K, XIE F, LIU C, et al. Shared functional network abnormality in patients with temporal lobe epilepsy and their siblings[J]. CNS Neurosci Ther, 2023, 29(4): 1109-1119. DOI: 10.1111/cns.14087.
[32]
WIRRELL E C, NABBOUT R, SCHEFFER I E, et al. Methodology for classification and definition of epilepsy syndromes with list of syndromes: Report of the ILAE Task Force on Nosology and Definitions[J]. Epilepsia, 2022, 63(6): 1333-1348. DOI: 10.1111/epi.17237.
[33]
CORRÊA D G, TIJMS B M, DICKS E, et al. Effects of seizure burden on structural global brain networks in patients with unilateral hippocampal sclerosis[J/OL]. Brain Behav, 2021, 11(8): e2237 [2026-03-17]. https://onlinelibrary.wiley.com/doi/10.1002/brb3.2237. DOI: 10.1002/brb3.2237.
[34]
YANG D, SUN Z, YU M, et al. Associations of MRI-derived glymphatic system impairment with global white matter damage and cognitive impairment in mild traumatic brain injury: A DTI-ALPS study[J]. J Magn Reson Imaging, 2024, 59(2): 639-647. DOI: 10.1002/jmri.28797.
[35]
ZANAO T A, SEITZ-HOLLAND J, O'DONNELL L J, et al. Exploring the impact of hippocampal sclerosis on white matter tracts and memory in individuals with mesial temporal lobe epilepsy[J]. Epilepsia Open, 2023, 8(3): 1111-1122. DOI: 10.1002/epi4.12793.
[36]
WHELAN C D, ALTMANN A, BOTÍA J A, et al. Structural brain abnormalities in the common epilepsies assessed in a worldwide ENIGMA study[J]. Brain, 2018, 141(2): 391-408. DOI: 10.1093/brain/awx341.
[37]
ZHANG Y, LIU Z, DOU W, et al. Study of the microstructure of brain white matter in medial temporal lobe epilepsy based on diffusion tensor imaging[J/OL]. Brain Behav, 2023, 13(4): e2919 [2026-03-17]. https://onlinelibrary.wiley.com/doi/10.1002/brb3.2919. DOI: 10.1002/brb3.2919.
[38]
KIM J, LEE D A, LEE H J, et al. Small-vessel-disease-induced white matter damage in occipital lobe epilepsy[J/OL]. Front Neurol, 2025, 16: 1538598 [2026-03-17]. https://www.frontiersin.org/articles/10.3389/fneur.2025.1538598. DOI: 10.3389/fneur.2025.1538598.

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