Evidence map›Paper›PMID 41853886›Full record

ArticleExperimental physiology2026

The effects of bed rest on cardiometabolic health: A systematic review and meta-analysis.

Konstantinos Prokopidis, Tyler Daubrah-Scott, Alyssa Varanoske, Jordi Morwani-Mangnani, David D Church, Colleen S Deane, Bethan E Phillips, Emily J Arentson-Lantz

Abstract read
In one paragraph

Article in Experimental physiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

8 authors.

Konstantinos ProkopidisDepartment of Musculoskeletal Biology, Institute of Life Course and Medical Sciences, University of Liverpool, Liverpool, UK.ORCID https://orcid.org/0000-0002-6264-9388
Tyler Daubrah-ScottCentre of Metabolism, Ageing & Physiology, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.ORCID https://orcid.org/0009-0004-8865-6705
Alyssa VaranoskeKBR Inc., Houston, Texas, USA.
Jordi Morwani-MangnaniLeiden University Medical Centre, Leiden, The Netherlands.
David D ChurchDepartment of Geriatrics, Donald W. Reynolds Institute on Aging, Center for Translational Research in Aging and Longevity, University of Arkansas for Medical Sciences, Little Rock, Arkansas, USA.
Colleen S DeaneHuman Development & Health, Faculty of Medicine, University of Southampton, Southampton General Hospital, Southampton, UK.ORCID https://orcid.org/0000-0002-2281-6479
Bethan E PhillipsCentre of Metabolism, Ageing & Physiology, MRC Versus Arthritis Centre for Musculoskeletal Ageing Research, Nottingham NIHR Biomedical Research Centre, University of Nottingham, Nottingham, UK.ORCID https://orcid.org/0000-0002-1430-1870
Emily J Arentson-LantzDepartment of Nutrition Sciences and Health Behavior, University of Texas Medical Branch, Galveston, Texas, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Horizontal bed rest (HBR) and head-down tilt (HDT) are models of physical inactivity. In this systematic review and meta-analysis, we aimed to quantify changes in cardiometabolic outcomes during HBR and HDT in healthy adults. Following the PRISMA guidelines, we searched PubMed, Scopus, Web of Science and Cochrane Library until 1 October 2025. Included studies recruited healthy adults (≥18 years of age) undergoing ≥2 days of HBR or HDT. A meta-analysis with mean differences (MD) and 95% confidence intervals (CI), using random-effects modelling was conducted. Forty-four studies were included. HBR (≤14 days) reduced fasting glucose (MD, -0.15 mmol/L, P = 0.00033). HBR (≤14 days) and HDT (≤60 days) increased insulin (HBR: MD, 7.07 pmol/L; HDT: MD, 9.65 pmol/L; P < 0.0001). The homeostatic model assessment for insulin resistance was increased under both models (HBR ≤30 days: MD, 0.10, P = 0.0004; HDT ≤60 days: MD, 0.24, P < 0.0001). HDT lowered total cholesterol (MD: -13.89 mg/dL, P = 0.000467); HBR raised triglycerides (MD, 18.96 mg/dL, P < 0.0001), and high-density lipoprotein cholesterol was decreased in both models (HBR ≤14 days: MD, -4.53 mg/dL, P = 0.000608; HDT ≤60 days: MD, -6.89; P < 0.0001). C-Reactive protein was elevated in HBR (MD, 1.57; P < 0.0001), and tumour necrosis factor alpha was elevated in both (HBR ≤14 days: MD, 1.33, P < 0.0001; HDT ≤21 days: MD, 0.40; P = 0.00643). In conclusion, HBR and HDT induce model- and duration-specific changes in glucose metabolism and lipid profiles. Interventions that could mitigate these effects may be warranted.

Indexed as

bed restcardiometabolic healthinsulin resistancelipid profilemuscle disuse

Identifiers

PMID41853886
PMCPMC13394784

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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.