ReviewFrontiers in physiology2025
Pathophysiological mechanisms and emerging therapeutic strategies for muscle wasting: an integrative review.
Review in Frontiers in physiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled 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.
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
3 citing papers in PubMed, 1 synthesis or guideline pooled it.
- Systematic review and meta-analysis of biomarkers of sarcopenia and sarcopenic obesity.Medicine · 2026Pooled it
- Review
- Ribosome Biogenesis and Translational Control in Skeletal Muscle Atrophy and Hypertrophy: Mechanisms and Therapeutic Perspectives.Biomolecules · 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
8 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Muscle wasting is a continuum of diseases that entail incremental skeletal muscle mass, as well as functionality, loss and is an important cause of morbidity, mortality, as well as quality of life reduction. This pathophysiology, diagnosis, as well as emerging treatment of significant muscle wasting illnesses, that is, sarcopenia, cachexia, disuse muscle atrophy, as well as neuromuscular illnesses, entail intricate interactions of defective protein synthetic processes, upregulated proteolysis, inflammatory cytokine activation, defective mitochondria, as well as hormone disturbances. Diagnostic methodologies have progressed from crude body dimension measures to sophisticated imaging modalities, as well as molecular biomarkers, but standardization remains contentious. Treatments entail targeted nutrition, as well as exercise regimes, as well as emerging drugs, as well as regenerative medicine therapies. Preclinical-to-clinical translation gaps, even striking, still exist despite promising advances. Some of these include diagnosis-based inequalities, patients' heterogeneity, limited therapeutic advantages, as well as implementation difficulties within healthcare. Future directions have emphasis on personalized medicine strategies that entail multi-omics signatures, combinatorial therapy of several targets, electronic health platforms for dynamic surveillance, as well as prevention modalities. Integrated healthcare platforms, multinational collaborative platforms, as well as regulatory reforms favoring muscle health across the life continuum, are needed for accomplishing the emerging challenge of controlling emerging muscle wasting burdens of the old, as well as those beset by chronic illnesses.
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What Socratic holds
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.