Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
2008-6-25
pubmed:abstractText
We assessed (1)H-MRS as a screening tool for detection of hippocampal sclerosis in patients with temporal lobe epilepsy (TLE). (1)H-MRS was carried out in the hippocampus of 23 patients with unilateral TLE. Metabolite alterations detected by (1)H-MRS correlated with degree of segmental neuronal cell loss and amount of astrogliosis. Positive correlation was found between total N-Acetylaspartate (tNAA) reduction and neuronal density in hippocampal CA1 (P < 0.001), CA3 (P = 0.015), and CA4 subfields (P = 0.031) and the dentate gyrus (P = 0.006). Neuronal cell loss in CA1 turned out to be the most predictive and only significant variable for tNAA reduction (P = 0.027). The association between myo-inositol (m-Ins) and astroglial glial fibrillary acidic protein (GFAP) expression revealed significantly increased m-Ins concentrations associated with diffuse astrogliosis (m-Ins = 6.4 +/- 1.1 institutional units) compared with gliosis restricted to isolated sectors of the hippocampus (i.e. hilus) (m-Ins = 5.2 +/- 1.2 institutional units) (P = 0.039). A negative correlation was found between m-Ins and neuronal loss in the CA4 subfield of the hippocampus (P = 0.028). Our results support (1)H-MRS as a suitable non-invasive method for preoperative identification of hippocampal sclerosis in patients with TLE. The extent of tNAA reduction correlates with hippocampal neuronal cell density. Furthermore, m-Ins is associated with the extent of hippocampal astrogliosis.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jul
pubmed:issn
0952-3480
pubmed:author
pubmed:issnType
Print
pubmed:volume
21
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
545-52
pubmed:meshHeading
pubmed-meshheading:18035849-Adolescent, pubmed-meshheading:18035849-Adult, pubmed-meshheading:18035849-Aspartic Acid, pubmed-meshheading:18035849-Biological Markers, pubmed-meshheading:18035849-Child, pubmed-meshheading:18035849-Child, Preschool, pubmed-meshheading:18035849-Epilepsy, Temporal Lobe, pubmed-meshheading:18035849-Female, pubmed-meshheading:18035849-Hippocampus, pubmed-meshheading:18035849-Humans, pubmed-meshheading:18035849-Infant, pubmed-meshheading:18035849-Magnetic Resonance Spectroscopy, pubmed-meshheading:18035849-Male, pubmed-meshheading:18035849-Middle Aged, pubmed-meshheading:18035849-Protons, pubmed-meshheading:18035849-Reproducibility of Results, pubmed-meshheading:18035849-Sclerosis, pubmed-meshheading:18035849-Sensitivity and Specificity, pubmed-meshheading:18035849-Statistics as Topic, pubmed-meshheading:18035849-Tissue Distribution
pubmed:year
2008
pubmed:articleTitle
Non-invasive detection of hippocampal sclerosis: correlation between metabolite alterations detected by (1)H-MRS and neuropathology.
pubmed:affiliation
Center Epilepsy Erlangen (ZEE), Department of Neurology, University of Erlangen-Nuremberg, Erlangen, Germany. thilo.hammen@uk-erlangen.de
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't