Evidence mapPaperPMID 39488926Full record

Trial reportSleep medicine2024

Impact of sleep restriction on biomarkers of thyroid function: Two pooled randomized trials.

Megan E Petrov, Faris M Zuraikat, Bin Cheng, Brooke Aggarwal, Sanja Jelic, Blandine Laferrère, Marie-Pierre St-Onge

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Sleep medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
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

7 authors.

Megan E PetrovEdson College of Nursing and Health Innovation, Arizona State University, Phoenix, AZ, USA. Electronic address: megan.petrov@asu.edu.
Faris M ZuraikatCenter of Excellence for Sleep & Circadian Research, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Division of General Medicine, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Institute of Human Nutrition, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: fmz2105@cumc.columbia.edu.
Bin ChengDepartment of Biostatistics, Mailman School of Public Health, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: bc2159@cumc.columbia.edu.
Brooke AggarwalCenter of Excellence for Sleep & Circadian Research, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Institute of Human Nutrition, Vagelos College of Physicians and Surgeons, Columbia University Irving Medical Center, New York, NY, USA; Division of Cardiology, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: baf2108@cumc.columbia.
Sanja JelicCenter of Excellence for Sleep & Circadian Research, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Columbia University Irving Medical Center, New York City, NY, USA. Electronic address: sj366@cumc.columbia.edu.
Blandine LaferrèreCenter of Excellence for Sleep & Circadian Research, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, Columbia University Irving Medical Center, New York City, NY, USA; Division of Endocrinology, Department of Medicine, Columbia University Irving Medical Center, New York City, NY, USA. Electronic address: bbl14@cumc.columbia.edu.
Marie-Pierre St-OngeCenter of Excellence for Sleep & Circadian Research, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA; Division of General Medicine, Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA. Electronic address: ms2554@cumc.columbia.edu.

Funding

Clinical and Translational Science AwardUL1TR001873 · NCATS · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI REILLY, MUREDACH P · 2016 to 2025
$99.0M
Vascular endothelial dysfunction in sleep apneaR01HL106041 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI JELIC, SANJA · 2011 to 2025
$6.6M
Mechanisms addressing the causal relationships of sleep, circadian rhythms, and cardiometabolic healthR35HL155670 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MARIE-PIERRE ST-ONGE · 2021 to 2026
$5.4M
Effect of long-term sleep restriction on energy balanceR01HL128226 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI ST-ONGE, MARIE-PIERRE · 2016 to 2019
$3.4M
Obstructive Sleep Apnea and Subclinical Lung Injury in Health and DiseaseR01HL137234 · NHLBI · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI GOTTLIEB, DANIEL J, JELIC, SANJA · 2018 to 2021
$3.2M
NCATS NIH HHS UL1 TR001873NHLBI NIH HHS R01 HL106041NHLBI NIH HHS R01 HL128226NHLBI NIH HHS R01 HL137234NHLBI NIH HHS R35 HL155670
6 · The paper itself

Abstract

backgroundChronic, mildly insufficient sleep is associated with increased cardiometabolic risk, but whether the regulation of thyroid hormones and related growth factors are mechanisms of this association is unclear. We investigated whether 6 wk of mild sleep restriction (SR) alters levels of free thyroxine (FT4), thyroid stimulating hormone (TSH), and fibroblast growth factor-21 (FGF-21), a modulator of FT4, in adults with adequate habitual sleep (AS; 7-9 h/night).

methodsHealthy adults participated in one of two randomized, crossover studies with identical 6-wk intervention phases: AS and SR (1.5 h/night < AS). Fasted blood samples were collected at baseline and endpoint of each phase. Outcomes were concentrations of FT4, TSH, and FGF-21 (women only). Linear mixed models tested the effects of SR vs AS on the outcomes, adjusting for baseline levels, week, sex, and sex-by-condition interaction.

resultsThirty participants (20 women; 73% racial/ethnic minority; age 21-64 y [M±SD = 36.2 ± 12.8 y]) were included. In the full sample, no effects of SR on FT4 (β±SE = 0.02 ± 0.04, p = 0.654) or TSH (β±SE = -0.02 ± 0.04, p = 0.650) were observed; however, there were sex-by-condition interactions for both FT4 (p-interaction = 0.056) and TSH (p-interaction = 0.049). In sex-stratified analyses, TSH was reduced in SR vs. AS in women (β±SE = -0.11 ± 0.04, p = 0.011, Cohen's f

conclusionProlonged mild SR reduces TSH in women, whereas FT4 and FGF-21 remain unaffected compared with AS. If sustained, disruptions to the thyrotropic axis in women may contribute to their more pronounced cardiometabolic risk in response to SR compared with men.

Indexed as

BiomarkersCross-Over StudiesFibroblast Growth FactorsSleep DeprivationThyrotropinThyroxineAdultFemaleHumansMaleMiddle AgedThyroid Function TestsThyroid GlandBiomarkersFibroblast Growth FactorsThyrotropinThyroxineGrowth factorsInsufficient sleepSexSubclinical hyperthyroidismThyrotropic axis

Identifiers

PMID39488926
PMCPMC11663093

What Socratic holds

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Registered trials

None linked

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 Socratic graph.