Glycerophosphocholine and Glycerophosphoethanolamine Are Not the Main Sources of the In Vivo (31)P MRS Phosphodiester Signals from Healthy Fibroglandular Breast Tissue at 7 T

Wybe J M van der Kemp, Bertine L Stehouwer, Jurgen H Runge, Jannie P Wijnen, Aart J Nederveen, Peter R Luijten, DWJ Klomp

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

PURPOSE: The identification of the phosphodiester (PDE) (31)P MR signals in the healthy human breast at ultra-high field.

METHODS: In vivo (31)P MRS measurements at 7 T of the PDE signals in the breast were performed investigating the chemical shifts, the transverse- and the longitudinal relaxation times. Chemical shifts and transverse relaxation times were compared with non-ambiguous PDE signals from the liver.

RESULTS: The chemical shifts of the PDE signals are shifted -0.5 ppm with respect to glycerophosphocholine (GPC) and glycerophosphoethanolamine (GPE), and the transverse and longitudinal relaxation times for these signals are a factor 3 to 4 shorter than expected for aqueous GPC and GPE.

CONCLUSION: The available experimental evidence suggests that GPC and GPE are not the main source of the PDE signals measured in fibroglandular breast tissue at 7 T. These signals may predominantly originate from mobile phospholipids.

Original languageEnglish
Article number29
JournalFrontiers in oncology
Volume6
DOIs
Publication statusPublished - 2016

Keywords

  • MRSI
  • 31P
  • relaxation time
  • 7 T
  • phosphodiester
  • breast
  • phospholipids

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