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In vivo MRI signatures of hippocampal subfield pathology in intractable epilepsy
Human brain mapping, 2016-03, Vol.37 (3), p.1103-1119
Goubran, Maged
Bernhardt, Boris C.
Cantor-Rivera, Diego
Lau, Jonathan C.
Blinston, Charlotte
Hammond, Robert R.
de Ribaupierre, Sandrine
Burneo, Jorge G.
Mirsattari, Seyed M.
Steven, David A.
Parrent, Andrew G.
Bernasconi, Andrea
Bernasconi, Neda
Peters, Terry M.
Khan, Ali R.
2016
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Goubran, Maged
Bernhardt, Boris C.
Cantor-Rivera, Diego
Lau, Jonathan C.
Blinston, Charlotte
Hammond, Robert R.
de Ribaupierre, Sandrine
Burneo, Jorge G.
Mirsattari, Seyed M.
Steven, David A.
Parrent, Andrew G.
Bernasconi, Andrea
Bernasconi, Neda
Peters, Terry M.
Khan, Ali R.
Titel
In vivo MRI signatures of hippocampal subfield pathology in intractable epilepsy
Ist Teil von
Human brain mapping, 2016-03, Vol.37 (3), p.1103-1119
Ort / Verlag
United States: Blackwell Publishing Ltd
Erscheinungsjahr
2016
Quelle
Wiley Blackwell Single Titles
Beschreibungen/Notizen
Objectives Our aim is to assess the subfield‐specific histopathological correlates of hippocampal volume and intensity changes (T1, T2) as well as diff!usion MRI markers in TLE, and investigate the efficacy of quantitative MRI measures in predicting histopathology in vivo. Experimental Design We correlated in vivo volumetry, T2 signal, quantitative T1 mapping, as well as diffusion MRI parameters with histological features of hippocampal sclerosis in a subfield‐specific manner. We made use of on an advanced co‐registration pipeline that provided a seamless integration of preoperative 3 T MRI with postoperative histopathological data, on which metrics of cell loss and gliosis were quantitatively assessed in CA1, CA2/3, and CA4/DG. Principal Observations MRI volumes across all subfields were positively correlated with neuronal density and size. Higher T2 intensity related to increased GFAP fraction in CA1, while quantitative T1 and diffusion MRI parameters showed negative correlations with neuronal density in CA4 and DG. Multiple linear regression analysis revealed that in vivo multiparametric MRI can predict neuronal loss in all the analyzed subfields with up to 90% accuracy. Conclusion Our results, based on an accurate co‐registration pipeline and a subfield‐specific analysis of MRI and histology, demonstrate the potential of MRI volumetry, diffusion, and quantitative T1 as accurate in vivo biomarkers of hippocampal pathology. Hum Brain Mapp 37:1103–1119, 2016. © 2015 Wiley Periodicals, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 1065-9471
eISSN: 1097-0193
DOI: 10.1002/hbm.23090
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6867266
Format
–
Schlagworte
Adult
,
Cell Count
,
Cohort Studies
,
Diffusion Tensor Imaging
,
Drug Resistant Epilepsy - pathology
,
Drug Resistant Epilepsy - surgery
,
DTI
,
Female
,
hippocampal sclerosis
,
hippocampal subfields
,
Hippocampus - pathology
,
Hippocampus - surgery
,
histology
,
Humans
,
Image Processing, Computer-Assisted
,
Linear Models
,
Magnetic Resonance Imaging - methods
,
Male
,
Middle Aged
,
MRI
,
Neurons - pathology
,
Organ Size
,
Reproducibility of Results
,
Sclerosis
,
temporal lobe epilepsy
,
volumetry
,
Young Adult
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