4.5 Article

Human brain-structure resolved T-2 relaxation times of proton metabolites at 3 Tesla

Journal

MAGNETIC RESONANCE IN MEDICINE
Volume 57, Issue 6, Pages 983-989

Publisher

WILEY
DOI: 10.1002/mrm.21250

Keywords

H-1 MR spectroscopy; T-2 relaxation; human brain metabolites; 3T; gray and white matter

Funding

  1. NATIONAL INSTITUTE OF BIOMEDICAL IMAGING AND BIOENGINEERING [R01EB001015] Funding Source: NIH RePORTER
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R56NS050520, R01NS050520] Funding Source: NIH RePORTER
  3. NIBIB NIH HHS [EB01015] Funding Source: Medline
  4. NINDS NIH HHS [NS050520] Funding Source: Medline

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The transverse relaxation times, T-2, of N-acetylaspartate (NAA), total choline (Cho), and creatine (Cr) obtained at 3T in several human brain regions of eight healthy volunteers are reported. They were obtained simultaneously in 320 voxels with three-dimensional (3D) proton MR spectroscopy (H-1-MRS) at 1 cm(3) spatial resolution. A two-point protocol, optimized for the least error per given time by adjusting both the echo delay (TEi) and number of averages, Ni, at each point, was used. Eight healthy subjects (four males and four females, age = 26 +/- 2 years) underwent the hour-long procedure of four 15-min, 3D acquisitions (TE1 = 35 ms, N-1 = 1; and TE2 = 285 ms, N-2 = 3). The results reveal that across all subjects the NAA and Cr T(2)s in gray matter (GM) structures (226 +/- 17 and 137 +/- 12 ms, respectively) were 13-17% shorter than the corresponding T(2)s in white matter (WM; 264 +/- 10 and 155 +/- 7 ms, respectively). The T(2)s of Cho did not differ between GM and WM (207 +/- 17 and 202 +/- 8, respectively). For the purpose of metabolic quantification, these values justify to within +/- 10% the previous use of one T2 per metabolite for 1) the entire brain and 2) all subjects. These T-2 values (which to our knowledge were obtained for the first time at this field, spatial resolution, coverage, and precision) are essential for reliable absolute metabolic quantification.

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