The IDOze Study: The Link Between Sleep Disruption and Tryptophan-Kynurenine Pathway Activation in Women With Human Immunodeficiency Virus . (8th July 2022)
- Record Type:
- Journal Article
- Title:
- The IDOze Study: The Link Between Sleep Disruption and Tryptophan-Kynurenine Pathway Activation in Women With Human Immunodeficiency Virus . (8th July 2022)
- Main Title:
- The IDOze Study: The Link Between Sleep Disruption and Tryptophan-Kynurenine Pathway Activation in Women With Human Immunodeficiency Virus
- Authors:
- Rogando, Andrea C
Weber, Kathleen M
Xing, Jiaqian
Xue, Xiaonan
Yohannes, Tsion
Morack, Ralph
Qi, Qibin
Clish, Clary
Bullock, Kevin
Gustafson, Deborah
Anastos, Kathryn
Sharma, Anjali
Burgess, Helen J
French, Audrey L - Abstract:
- Abstract: Background: Poor sleep is associated with human immunodeficiency virus (HIV), particularly among women with HIV (WWH), although mechanisms are unclear. We explored cross-sectional associations between sleep disruption and tryptophan-kynurenine (T/K) pathway activation, measured by the kynurenine-to-tryptophan ratio (K:T). Methods: HIV-uninfected women (HIV – ) and WWH aged 35–70 years and on stable antiretroviral therapy were included. Sleep metrics were measured using wrist actigraphy. Plasma T/K pathway metabolites were measured using liquid chromatography–tandem mass spectrometry. Multivariate linear regression models examined relationships between K:T and actigraphy-based sleep metrics by HIV status. Results: WWH (n = 153) and HIV – women (n = 151) were demographically similar. Among WWH, median CD4 was 751 cells/µL; 92% had undetectable HIV RNA. Compared to HIV – women, WWH had higher K:T ( P < .001) and kynurenine ( P = .01) levels but similar tryptophan levels ( P = .25). Higher K:T was associated with more wake bouts ( P = .001), more time awake after sleep onset ( P = .01), and lower sleep efficiency ( P = .03) in WWH only. Conclusions: HIV infection was associated with T/K pathway activation; this activation was associated with poorer sleep efficiency and more fragmented sleep. While longitudinal studies are needed to elucidate the directionality of these associations, these findings may help identify treatments to reduce sleep disruption in WWH byAbstract: Background: Poor sleep is associated with human immunodeficiency virus (HIV), particularly among women with HIV (WWH), although mechanisms are unclear. We explored cross-sectional associations between sleep disruption and tryptophan-kynurenine (T/K) pathway activation, measured by the kynurenine-to-tryptophan ratio (K:T). Methods: HIV-uninfected women (HIV – ) and WWH aged 35–70 years and on stable antiretroviral therapy were included. Sleep metrics were measured using wrist actigraphy. Plasma T/K pathway metabolites were measured using liquid chromatography–tandem mass spectrometry. Multivariate linear regression models examined relationships between K:T and actigraphy-based sleep metrics by HIV status. Results: WWH (n = 153) and HIV – women (n = 151) were demographically similar. Among WWH, median CD4 was 751 cells/µL; 92% had undetectable HIV RNA. Compared to HIV – women, WWH had higher K:T ( P < .001) and kynurenine ( P = .01) levels but similar tryptophan levels ( P = .25). Higher K:T was associated with more wake bouts ( P = .001), more time awake after sleep onset ( P = .01), and lower sleep efficiency ( P = .03) in WWH only. Conclusions: HIV infection was associated with T/K pathway activation; this activation was associated with poorer sleep efficiency and more fragmented sleep. While longitudinal studies are needed to elucidate the directionality of these associations, these findings may help identify treatments to reduce sleep disruption in WWH by targeting residual inflammation and T/K pathway activation. Abstract : Elevated kynurenine-to-tryptophan ratio, a measure of indoleamine 2, 3-dioxygenase activation, was associated with significantly poorer sleep efficiency and a greater number of wake episodes after sleep onset in women with HIV compared with demographically similar uninfected women. … (more)
- Is Part Of:
- Journal of infectious diseases. Volume 226:Number 8(2022)
- Journal:
- Journal of infectious diseases
- Issue:
- Volume 226:Number 8(2022)
- Issue Display:
- Volume 226, Issue 8 (2022)
- Year:
- 2022
- Volume:
- 226
- Issue:
- 8
- Issue Sort Value:
- 2022-0226-0008-0000
- Page Start:
- 1451
- Page End:
- 1460
- Publication Date:
- 2022-07-08
- Subjects:
- HIV infection -- women -- sleep -- metabolomics -- kynurenine -- tryptophan -- IDO-1 -- indoleamine 2, 3-dioxygenase
Communicable diseases -- Periodicals
Diseases -- Causes and theories of causation -- Periodicals
Medicine -- Periodicals
Communicable Diseases -- Periodicals
Electronic journals
616.9 - Journal URLs:
- http://jid.oxfordjournals.org/content/by/year ↗
http://www.journals.uchicago.edu/JID/journal/ ↗
http://www.jstor.org/journals/00221899.html ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/infdis/jiac287 ↗
- Languages:
- English
- ISSNs:
- 0022-1899
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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