Evidence map›Paper›PMID 41686719›Full record

Trial reportNeuroimmunomodulation2026

The Effect of Low-Dose Acetylsalicylic Acid on Cellular Immune Responses to Experimental Sleep Restriction in Healthy Humans.

Larissa C Engert, Rammy Dang, Bryan Chatterton, Surya Daniel, Janet M Mullington, Monika Haack

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Neuroimmunomodulation, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Larissa C EngertDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA, lcengert@bidmc.harvard.edu.
Rammy DangDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Bryan ChattertonDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Surya DanielDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Janet M MullingtonDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA.
Monika HaackDepartment of Neurology, Beth Israel Deaconess Medical Center, Boston, Massachusetts, USA, mhaack@bidmc.harvard.edu.

Funding

The Harvard Clinical and Translational Science CenterUL1TR002541 · NCATS · HARVARD MEDICAL SCHOOL · PI NADLER, LEE MARSHALL · 2018 to 2022
$93.0M
Harvard Clinical and Translational Science CenterUM1TR004408 · NCATS · HARVARD MEDICAL SCHOOL · PI Lindsey Robert Baden, Lee Marshall Nadler · 2023 to 2026
$43.3M
ZINC STATUS AND T CELL DISORDER IN MILD HUMAN ZINC DEFICIENCYM01RR001032 · NCRR · BETH ISRAEL DEACONESS MEDICAL CENTER · PI MANTZOROS, CHRISTOS S · 1985 to 2008
$32.3M
Patterns of Sleep Restriction and Recovery: The Inflammatory Resolution PathwaysR01HL136310 · NHLBI · BETH ISRAEL DEACONESS MEDICAL CENTER · PI HAACK, MONIKA · 2018 to 2022
$4.1M
NCATS NIH HHS UL1 TR002541NCATS NIH HHS UM1 TR004408NCRR NIH HHS M01 RR001032NHLBI NIH HHS R01 HL136310
6 · The paper itself

Abstract

introductionSleep deficiency is known to increase the risk for multiple disease conditions involving immunopathology, in which inflammation is thought to be a mechanism for disease development. Thus, one potential way to mitigate negative health consequences of deficient sleep is to target inflammation. We investigated whether low-dose acetylsalicylic acid (ASA, aspirin) administration prior to and during exposure to an experimental sleep restriction challenge affects cellular immune responses to sleep restriction.

methodsWe studied 46 healthy humans (19F/27M, age range 19-63 years) in a randomized trial with 3 protocols each consisting of a 14-day at-home phase followed by an 11-day (10-night) in-laboratory stay (sleep restriction/ASA, sleep restriction/placebo, control sleep/placebo) with daily ASA (81 mg/day) or placebo intake across the entire study period (at-home and in-laboratory). During in-laboratory stays, sleep opportunity under both sleep restriction conditions was 8 h during 2 pre-challenge nights, 4 h during 5 nights of restricted sleep, and 8 h during 3 nights of recovery sleep. Under the control sleep condition, participants had a sleep opportunity of 8 h/night throughout the protocol. Blood samples were analyzed prior to and following 5 nights of sleep restriction/control sleep, and after 2 nights of recovery sleep. Data were analyzed using generalized linear mixed models.

resultsExperimental sleep restriction increased WBC, lymphocyte, monocyte, eosinophil, basophil, CD4 T-cell counts, and the CD4/CD8 T-cell ratio compared to control sleep under placebo (p < 0.01). Low-dose ASA had no effect at pre-challenge for most cell types. However, low-dose ASA attenuated the eosinophil and basophil responses to sleep restriction and reduced elevation of the CD4/CD8 T-cell ratio (p < 0.01). Monocyte counts stayed elevated after 2 nights of recovery sleep in the sleep restriction/ASA condition compared to control sleep, whereas monocyte counts recovered under placebo intake (p < 0.01).

conclusionThe present study shows that low-dose ASA can counteract certain cellular immune responses to sleep restriction, in particular elevations in eosinophil and basophil counts as well as the CD4/CD8 T-cell ratio, while not affecting most immune cell counts prior to the sleep restriction challenge.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalAspirinImmunity, CellularSleep DeprivationAdultDouble-Blind MethodFemaleHumansMaleMiddle AgedYoung AdultAnti-Inflammatory Agents, Non-SteroidalAspirinBasophilsCD4/CD8 T-cell ratioEosinophilsLow-dose aspirinMonocytesRecovery sleepSleep restriction

Identifiers

PMID41686719
PMCPMC13014424

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.