The association of tobacco smoking and metabolite levels in the anterior cingulate cortex of first-episode psychosis patients: A case-control and 6-month follow-up 1 H-MRS study

Merel Koster*, Marieke van der Pluijm, Elsmarieke van de Giessen, Anouk Schrantee, Carmen F. M. van Hooijdonk, Jean-Paul Selten, Jan Booij, Lieuwe de Haan, Tim Ziermans, Jentien Vermeulen

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Tobacco smoking is highly prevalent among patients with psychosis and associated with worse clinical outcomes. Neurometabolites, such as glutamate and choline, are both implicated in psychosis and tobacco smoking. However, the specific associations between smoking and neurometabolites have yet to be investigated in patients with psychosis. The current study examines associations of chronic smoking and neurometabolite levels in the anterior cingulate cortex (ACC) in first-episode psychosis (FEP) patients and controls. Proton magnetic resonance spectroscopy (1H MRS) data of 59 FEP patients and 35 controls were analysed. Associations between smoking status (i.e., smoker yes/no) or cigarettes per day and Glx (glutamate + glutamine, as proxy for glutamate) and total choline (tCh) levels were assessed at baseline in both groups separately. For patients, six months follow-up data were acquired for multi-cross-sectional analysis using linear mixed models. No significant differences in ACC Glx levels were found between smoking (n = 28) and non-smoking (n = 31) FEP patients. Smoking patients showed lower tCh levels compared to non-smoking patients at baseline, although not surving multiple comparisons correction, and in multi-cross-sectional analysis (pFDR = 0.08 and pFDR = 0.044, respectively). Negative associations were observed between cigarettes smoked per day, and ACC Glx (pFDR = 0.02) and tCh levels (pFDR = 0.02) in controls. Differences between patients and controls regarding Glx might be explained by pre-existing disease-related glutamate deficits or alterations at nicotine acetylcholine receptor level, resulting in differences in tobacco-related associations with neurometabolites. Additionally, observed alterations in tCh levels, suggesting reduced cellular proliferation processes, might result from exposure to the neurotoxic effects of smoking.
Original languageEnglish
Pages (from-to)144-152
Number of pages9
JournalSchizophrenia Research
Volume271
DOIs
Publication statusPublished - 1 Sept 2024

Keywords

  • Tobacco smoking
  • H-1-MRS
  • First episode psychosis
  • Glutamate
  • Choline
  • MAGNETIC-RESONANCE-SPECTROSCOPY
  • GLUTAMATE CONCENTRATIONS
  • NICOTINE DEPENDENCE
  • CIGARETTE-SMOKING
  • SCHIZOPHRENIA
  • GABA
  • RECEPTORS
  • DENSITY
  • DISORDERS
  • CANNABIS

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