Measurement of transverse relaxation times of J-coupled metabolites in the human visual cortex at 4 T

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Accurate quantification of 1H NMR spectra often requires knowledge of the relaxation times to correct for signal losses due to relaxation and saturation. In human brain, T2 values for singlets such as N-acetylaspartate, creatine, and choline have been reported, but few T 2 values are available for J-coupled spin systems. The purpose of this study was to measure the T2 relaxation times of J-coupled metabolites in the human occipital lobe using the LASER sequence. Spectra were acquired at multiple echo times and were analyzed with an LCModel using basis sets simulated at each echo time. Separate basis spectra were used for resonances of protons belonging to the same molecule but having very different T2 values (e.g., two separate basis spectra were used for the singlet and multiplet signal in N-acetylaspartate). The T2 values for the N-acetylaspartate multiplet (149 ± 12 ms), glutamate (125 ± 10 ms), myo-inositol (139 ± 20 ms), and taurine (196 ± 28 ms) were successfully measured in the human visual cortex at 4 T. These measured T 2 relaxation times have enabled the accurate and absolute quantification of cerebral metabolites at longer echo times.

Original languageEnglish (US)
Pages (from-to)891-897
Number of pages7
JournalMagnetic resonance in medicine
Volume67
Issue number4
DOIs
StatePublished - Apr 2012

Keywords

  • LASER
  • LCModel
  • glutamate
  • myo-inositol
  • separated basis set
  • taurine

Fingerprint

Dive into the research topics of 'Measurement of transverse relaxation times of J-coupled metabolites in the human visual cortex at 4 T'. Together they form a unique fingerprint.

Cite this