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Reduced total number of enlarged perivascular spaces in post-traumatic epilepsy patients with unilateral lesions - a feasibility study.
Hlauschek, Gernot; Lossius, Morten I; Schwartz, Daniel L; Silbert, Lisa C; Hicks, Amelia J; Ponsford, Jennie L; Vivash, Lucy; Sinclair, Benjamin; Kwan, Patrick; O'Brien, Terrence J; Shultz, Sandy R; Law, Meng; Spitz, Gershon.
Afiliação
  • Hlauschek G; Division of Clinical Neuroscience, National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway; The University of Oslo, Oslo, Norway; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia. Electronic address: gernot.hlauschek@monash.edu.
  • Lossius MI; Division of Clinical Neuroscience, National Centre for Epilepsy, Oslo University Hospital, Oslo, Norway; The University of Oslo, Oslo, Norway. Electronic address: mortenl@ous-hf.no.
  • Schwartz DL; Oregon Health & Science University, Oregon Alzheimer's Disease Research Center, Neurology, Advanced Imaging Research Center, USA. Electronic address: schwartd@ohsu.edu.
  • Silbert LC; Oregon Health & Science University, Oregon Alzheimer's Disease Research Center, Neurology, Advanced Imaging Research Center, USA. Electronic address: silbertl@ohsu.edu.
  • Hicks AJ; Monash-Epworth Rehabilitation Research Centre, Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia. Electronic address: amelia.hicks@monash.edu.
  • Ponsford JL; Monash-Epworth Rehabilitation Research Centre, Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia. Electronic address: jennie.ponsford@monash.edu.
  • Vivash L; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Neurology, The Alfred, Melbourne, Australia,; Departments of Medicine and Neurology, The University of Melbourne, Royal Melbourne Hospital, Parkville, Australia. Electronic address: lucy.viva
  • Sinclair B; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Neurology, The Alfred, Melbourne, Australia,. Electronic address: ben.sinclair@monash.edu.
  • Kwan P; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Neurology, The Alfred, Melbourne, Australia,; Departments of Medicine and Neurology, The University of Melbourne, Royal Melbourne Hospital, Parkville, Australia. Electronic address: patrick.k
  • O'Brien TJ; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Neurology, The Alfred, Melbourne, Australia,; Departments of Medicine and Neurology, The University of Melbourne, Royal Melbourne Hospital, Parkville, Australia. Electronic address: te.obrien
  • Shultz SR; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Neurology, The Alfred, Melbourne, Australia,; Department of Medicine, Royal Melbourne Hospital, The University of Melbourne, Parkville, Australia; Health Sciences, Vancouver Island University
  • Law M; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Department of Radiology, The Alfred, Melbourne, Australia. Electronic address: meng.law@monash.edu.
  • Spitz G; Department of Neurosciences, Central Clinical School, Monash University, Melbourne, Australia; Monash-Epworth Rehabilitation Research Centre, Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Clayton, Australia. Electronic address: gershon.spitz@monas
Seizure ; 113: 1-5, 2023 Dec.
Article em En | MEDLINE | ID: mdl-37847935
ABSTRACT

BACKGROUND:

We investigated the value of automated enlarged perivascular spaces (ePVS) quantification to distinguish chronic traumatic brain injury (TBI) patients with post-traumatic epilepsy (PTE+) from chronic TBI patients without PTE (PTE-) in a feasibility study.

METHODS:

Patients with and without PTE were recruited and underwent an MRI post-TBI. Multimodal auto identification of ePVS algorithm was applied to T1-weighted MRIs to segment ePVS. The total number of ePVS was calculated and corrected for white matter volume, and an asymmetry index (AI) derived.

RESULTS:

PTE was diagnosed in 7 out of the 99 participants (male=69) after a median time of less than one year since injury (range 10-22). Brain lesions were observed in all 7 PTE+ cases (unilateral=4, 57%; bilateral=3, 43%) as compared to 40 PTE- cases (total 44%; unilateral=17, 42%; bilateral=23, 58%). There was a significant difference between PTE+ (M=1.21e-4, IQR [8.89e-5]) and PTE- cases (M=2.79e-4, IQR [6.25e-5]) in total corrected numbers of ePVS in patients with unilateral lesions (p=0.024). No differences in AI, trauma severity and lesion volume were seen between groups.

CONCLUSION:

This study has shown that automated quantification of ePVS is feasible and provided initial evidence that individuals with PTE with unilateral lesions may have fewer ePVS compared to TBI patients without epilepsy. Further studies with larger sample sizes should be conducted to determine the value of ePVS quantification as a PTE-biomarker.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia Pós-Traumática / Substância Branca / Lesões Encefálicas Traumáticas / Malformações do Sistema Nervoso Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia Pós-Traumática / Substância Branca / Lesões Encefálicas Traumáticas / Malformações do Sistema Nervoso Limite: Humans / Male Idioma: En Ano de publicação: 2023 Tipo de documento: Article