ReviewExperimental physiology2026
Musculoskeletal decay and bone-muscle crosstalk during physical disuse: Mechanisms and integrated countermeasures.
Review 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.
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.
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.
Who cites it
1 citing paper in PubMed.
- Musculoskeletal decay and bone-muscle crosstalk during physical disuse: Mechanisms and integrated countermeasures.Experimental physiology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
6 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Older adults experience a markedly increased risk of falls and fractures following hospital discharge, largely due to the rapid musculoskeletal deterioration associated with bed rest. Although age-related muscle and bone loss typically develops gradually, acute physical inactivity accelerates key biological processes underlying sarcopenia and osteoporosis, including muscle atrophy, anabolic resistance, increased bone resorption and reduced mechanical loading. Emerging evidence indicates that muscle, bone and adipose tissue communicate through interconnected biochemical pathways; however, the shared biological mechanisms underlying this crosstalk during acute unloading remain poorly understood. To review the effects of disuse on the muscle-bone-adipose axis, emphasizing disruption of inter-tissue signalling pathways and evaluating integrated countermeasures, a narrative review was conducted using PubMed, Scopus and Web of Science, focusing on human bed rest and disuse studies, musculoskeletal crosstalk and multimodal interventions involving exercise and nutrition in older adults. Disuse rapidly disrupts musculoskeletal homeostasis by uncoupling bone turnover and inducing muscle anabolic resistance. These changes are accompanied by alterations in myokine and osteokine signalling, including increased myostatin, reduced irisin, elevated RANKL, bone and muscle steatosis, and sclerostin upregulation, further compromising muscle-bone interactions. Evidence supports multimodal interventions combining resistance exercise with optimized protein intake (1.2-1.5 g/kg/day) and nutritional supplements, including β-hydroxy-β-methylbutyrate, vitamin D and creatine, to attenuate muscle and bone loss. Preventing disuse-related musculoskeletal decline requires recognizing muscle and bone as an integrated functional unit. Tailored multimodal strategies may preserve musculoskeletal health and functional independence in hospitalized older adults, although implementation must consider frailty, comorbidities, safety and feasibility.
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Registered trials
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.