Magnetic resonance spectroscopy and the menstrual cycle: A multi-centre assessment of menstrual cycle effects on GABA & GSH

  • Yulu Song
  • , James J. Prisciandaro
  • , Dace Apšvalka
  • , Mae Bernard
  • , Adam Berrington
  • , Miguel Castelo-Branco
  • , Mark K. Britton
  • , Marta M. Correia
  • , Koen Cuypers
  • , Aleksandra Domagalik
  • , Ulrike Dydak
  • , Niall W. Duncan
  • , Gerard E. Dwyer
  • , Tao Gong
  • , Ian Greenhouse
  • , Katarzyna Hat
  • , Melina Hehl
  • , Shiori Honda
  • , Chris Horton
  • , Steve C.N. Hui
  • Stephen R. Jackson, Daniella L. Jones, Maren S. Klan, In Kyoon Lyoo, Marius O. Mada, Bronte V. McNamara, Paul G. Mullins, Emlyn Muska, Shinichiro Nakajima, Hayami Nishio, Andreia C. Pereira, Eric C. Porges, Michelle Rowsell, Rubi Ruopp, Destin D. Shortell, Caitlin M. Smith, Stephan Swinnen, Antonia Šušnjar, Lin Yuan Tseng, Ines R. Violante, Sujung Yoon, Richard A.E. Edden, Katherine Dyke

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Background: Gamma-aminobutyric acid (GABA) and glutathione (GSH) play a significant role in the functioning of a healthy brain and can both be quantified using magnetic resonance spectroscopy (MRS). Several small-scale studies have suggested MRS measured GABA may fluctuate with the menstrual cycle, but the effects on GSH are unknown. Utilising recent developments in MRS acquisition, this multi-lab study explores this issue across 4 distinctive brain regions. New methods: Data were analysed from 12 independent sites from which a total of 30 women were scanned during three phases of their menstrual cycle corresponding to early follicular, ovulation and mid luteal phases. HERMES and HERCULES sequences were used to measure GABA and GSH in voxels located in the left motor cortex, left posterior insular, medial parietal and medial frontal. Linear mixed models were used to assess the variability contributed by site, participant and menstrual cycle phase. Results: Similar variance was attributed to site and menstrual cycle phase for both GABA and GSH data. No systematic changes in GABA or GSH were revealed for any voxel as a consequence of menstrual cycle phase. Comparison with existing methods: Despite our larger sample size and inclusion of more brain regions we fail to replicate previous findings of GABA change as a consequence of menstrual cycle phase. We also show for the first time that MRS measures of GSH so not significantly alter with cycle. Conclusions: Our findings suggest that the menstrual cycle has minimal impact on MRS measures of GABA and GSH. The presence of a menstrual cycle should not be used as justification for exclusion of women in MRS studies.

Original languageEnglish
Article number110430
JournalJournal of Neuroscience Methods
Volume418
DOIs
StatePublished - Jun 2025

Bibliographical note

Publisher Copyright:
© 2025 The Authors

Keywords

  • Gamma-aminobutyric acid (GABA)
  • Glutathione (GSH)
  • Hadamard Encoding and Reconstruction of MEGA-Edited
  • Magnetic resonance, spectroscopy (MRS)
  • Menstrual cycle
  • Oestrogen
  • Spectroscopy (HERMES)

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