𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Quantitative proton MR spectroscopic imaging of the mesial temporal lobe

✍ Scribed by Atilla Arslanoglu; David Bonekamp; Peter B. Barker; Alena Horská


Publisher
John Wiley and Sons
Year
2004
Tongue
English
Weight
235 KB
Volume
20
Category
Article
ISSN
1053-1807

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Purpose

To evaluate variations in regional metabolite concentrations in the anterior mesial temporal lobe (ATL), and compare metabolite concentrations between the allocortex and neocortex using quantitative proton MR spectroscopic imaging (MRSI).

Materials and Methods

Metabolite concentrations and ratios were measured in 20 healthy young subjects with the use of a multislice spin‐echo (SE) sequence (TR/TE = 2300/280 msec). Quantitation of MRSI data was performed by means of the phantom replacement methodology.

Results

The highest choline (Cho) concentration (4.1 ± 1.1 mM) was found in the ATL (P = 0.0015 compared to the middle mesial temporal lobe (MTL), and P = 0.0008 compared to the posterior mesial temporal lobe (PTL)). The ATL also had a higher Cho/creatine (Cr) ratio and a lower N‐acetyl aspartate (NAA)/Cho ratio compared to other examined regions (P < 0.0001 and P ≤ 0.052, respectively). In the allocortical regions, the average Cho concentration (3.5 ± 0.8 mM) was 68% higher, and the NAA concentration (9.5 ± 1.8 mM) was 13% lower than in the neocortex (P < 10^−6^ and P < 0.008, respectively). Cho/Cr was 64% higher, NAA/Cr 14% lower, and NAA/Cho 47% lower in the allocortex than in the neocortex (P < 10^−6^, P = 0.013, and P < 10^−6^, respectively).

Conclusion

The mesial temporal lobe shows high levels of Cho, which presumably reflect a difference in cellular composition between the allocortex and neocortex. Regional metabolite variations must be considered when pathological conditions involving the mesial temporal lobe are evaluated. J. Magn. Reson. Imaging 2004;20:772–778. © 2004 Wiley‐Liss, Inc.


📜 SIMILAR VOLUMES


Proton nuclear magnetic resonance spectr
✍ Hoby Hetherington; Dr Ruben Kuzniecky; Jullie Pan; Graeme Mason; Richard Morawet 📂 Article 📅 1995 🏛 John Wiley and Sons 🌐 English ⚖ 905 KB

We performed proton magnetic resonance spectroscopic imaging (MRSI) at high magnetic field (4.1 T) to study N-acetylaspartate, creatine, and choline levels in the brains of normal control subjects and patients with intractable temporal lobe epilepsy. We compared the results of MRSI to those of other

Quantitative proton MR spectroscopic ima
✍ Michael A. Jacobs; Alena Horská; Peter C.M. van Zijl; Peter B. Barker 📂 Article 📅 2001 🏛 John Wiley and Sons 🌐 English ⚖ 337 KB

## Abstract Quantitative, multislice proton MR spectroscopic imaging (MRSI) was used to investigate regional metabolite levels and ratios in the normal adult human posterior fossa. Six normal volunteers (36 ± 3 years, five male, one female) were scanned on a 1.5 T scanner using multislice MRSI at l

Rapid method for correction of CSF parti
✍ A. Horská; V.D. Calhoun; D.H. Bradshaw; P.B. Barker 📂 Article 📅 2002 🏛 John Wiley and Sons 🌐 English ⚖ 348 KB 👁 1 views

Partial volume effects with cerebrospinal fluid (CSF), if uncorrected, can lead to underestimation of metabolite concentrations in quantitative proton magnetic resonance spectroscopic imaging (MRSI) of the brain. A rapid method for the correction of CSF partial volume effects is described based on s

Proton MR spectroscopic imaging of the m
✍ Richard A.E. Edden; David Bonekamp; Mari A. Smith; Prachi Dubey; Peter B. Barker 📂 Article 📅 2007 🏛 John Wiley and Sons 🌐 English ⚖ 294 KB

## Abstract ## Purpose To demonstrate the feasibility of quantitative, one‐dimensional proton MR spectroscopic imaging (1D‐MRSI) of the upper cervical spine and medulla at 3.0 Tesla. ## Materials and Methods A method was developed for 1D‐point‐resolved spectroscopy sequence (PRESS)‐MRSI, excitin