Literature DB >> 28958033

An Objective Short Sleep Insomnia Disorder Subtype Is Associated With Reduced Brain Metabolite Concentrations In Vivo: A Preliminary Magnetic Resonance Spectroscopy Assessment.

Christopher B Miller1,2, Caroline D Rae3,4, Michael A Green3, Brendon J Yee1,2,5, Christopher J Gordon1,6, Angela L D'Rozario1,7, Simon D Kyle8, Colin A Espie8, Ronald R Grunstein1,2,5, Delwyn J Bartlett1,2.   

Abstract

Objectives: To evaluate brain metabolites in objective insomnia subtypes defined from polysomnography (PSG): insomnia with short sleep duration (I-SSD) and insomnia with normal sleep duration (I-NSD), relative to good sleeping controls (GSCs).
Methods: PSG empirically grouped insomnia patients into I-SSD (n = 12: mean [SD] total sleep time [TST] = 294.7 minutes [30.5]) or I-NSD (n = 19: TST = 394.4 minutes [34.9]). 1H magnetic resonance spectroscopy (MRS) acquired in the left occipital cortex (LOCC), left prefrontal cortex, and anterior cingulate cortex was used to determine levels of creatine, aspartate, glutamate, and glutamine (referenced to water). Glutathione, glycerophosphocholine, lactate, myoinositol, and N-acetylaspartate measurements were also obtained. Sixteen GSCs were included for comparison. Multivariate analysis of variance was used to evaluate differences in creatine, aspartate, glutamate, and glutamine.
Results: Aspartate and glutamine concentrations were reduced in the LOCC in I-SSD compared with I-NSD (both p < .05, d = .80-.99). Creatine displayed a nonsignificant mean reduction in I-SSD compared with I-NSD (p = .05, d = .58). Glutamine was reduced in I-SSD compared with controls (p < .05, d = .93). There were no differences in metabolites between all (I-SSD and I-NSD) insomnia patients and controls. In patients with insomnia, LOCC glutamine concentrations were found to be positively correlated with TST (r = .43, p < .05) and negatively correlated with wake-time after sleep onset (r = -.40, p < .05). Conclusions: Results indicate that I-SSD is associated with reduced brain metabolites in the LOCC compared with I-NSD and control concentrations of aspartate, glutamine, and creatine. Clinical Trial Registration: Insomnia MRS imaging sleep study: Australia New Zealand Clinical Trials Registry (ANZCTR): https://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?ACTRN=12612000050853. Trial Identification Number: 12612000050853. © Sleep Research Society 2017. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.

Entities:  

Keywords:  brain imaging and phenotyping; insomnia; magnetic resonance spectroscopy; sleep and the brain

Mesh:

Substances:

Year:  2017        PMID: 28958033     DOI: 10.1093/sleep/zsx148

Source DB:  PubMed          Journal:  Sleep        ISSN: 0161-8105            Impact factor:   5.849


  3 in total

1.  Insomnia with objective short sleep duration and risk of incident cardiovascular disease and all-cause mortality: Sleep Heart Health Study.

Authors:  Suzanne M Bertisch; Benjamin D Pollock; Murray A Mittleman; Daniel J Buysse; Lydia A Bazzano; Daniel J Gottlieb; Susan Redline
Journal:  Sleep       Date:  2018-06-01       Impact factor: 5.849

2.  Insomnia with objective short sleep duration in women with temporomandibular joint disorder: quantitative sensory testing, inflammation and clinical pain profiles.

Authors:  Sheera F Lerman; Chung Jung Mun; Carly A Hunt; Shriya Kunatharaju; Luis F Buenaver; Patrick H Finan; Claudia M Campbell; Jane Phillips; Julio Fernandez-Mendoza; Jennifer A Haythornthwaite; Michael T Smith
Journal:  Sleep Med       Date:  2022-01-08       Impact factor: 3.492

3.  Effect of acute total sleep deprivation on plasma melatonin, cortisol and metabolite rhythms in females.

Authors:  Aya Honma; Victoria L Revell; Pippa J Gunn; Sarah K Davies; Benita Middleton; Florence I Raynaud; Debra J Skene
Journal:  Eur J Neurosci       Date:  2019-05-02       Impact factor: 3.386

  3 in total

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