Evidence map›Paper›PMID 39374077›Full record

SynthesisAmerican journal of physiology. Cell physiology2024

Effects of age on human skeletal muscle: a systematic review and meta-analysis of myosin heavy chain isoform protein expression, fiber size, and distribution.

Christopher Lee, Philip C Woods, Amanda E Paluch, Mark S Miller

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in American journal of physiology. Cell physiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
–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

18 citing papers in PubMed, 1 synthesis or guideline pooled it.

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  8. HR-pQCT skeletal phenotype clustering associated with muscle function in older men and women: The Study of Muscle, Mobility and Aging (SOMMA).Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2026
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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

4 authors.

Christopher LeeDepartment of Kinesiology, University of Massachusetts, Amherst, Massachusetts, United States.ORCID 0000-0002-1317-5622
Philip C WoodsDepartment of Kinesiology, University of Massachusetts, Amherst, Massachusetts, United States.ORCID 0000-0001-5768-9708
Amanda E PaluchDepartment of Kinesiology, University of Massachusetts, Amherst, Massachusetts, United States.ORCID 0000-0003-4244-9511
Mark S MillerDepartment of Kinesiology, University of Massachusetts, Amherst, Massachusetts, United States.ORCID 0000-0001-8309-8258

Funding

Sex-specific adaptation to different resistance exercise programs in older adultsR01AG047245 · NIA · UNIVERSITY OF MASSACHUSETTS AMHERST · PI MILLER, MARK STUART · 2017 to 2021
$2.4M
HHS | NIH | National Institute on Aging (NIA) AG-047245NIA NIH HHS R01 AG047245
6 · The paper itself

Abstract

Human studies examining the cellular mechanisms behind sarcopenia, or age-related loss of skeletal muscle mass and function, have produced inconsistent results. A systematic review and meta-analysis were performed to determine the aging effects on protein expression, size, and distribution of fibers with various myosin heavy chain (MyHC) isoforms. Study eligibility included MyHC comparisons between young (18-49 yr) and older (≥60 yr) adults, with 27 studies identified. Relative protein expression was higher with age for the slow-contracting MyHC I fibers, with correspondingly lower fast-contracting MyHC II and IIA values. Fiber sizes were similar with age for MyHC I, but smaller for MyHC II and IIA. Fiber distributions were similar with age. When separated by sex, the few studies that examined females showed atrophy of MyHC II and IIA fibers with age, but no change in MyHC protein expression. Additional analyses by measurement technique, physical activity, and muscle biopsies provided important insights. In summary, age-related atrophy in fast-contracting fibers lead to more of the slow-contracting, lower force-producing isoform in older male muscles, which helps explain their age-related loss in whole muscle force, velocity, and power. Exercise or pharmacological interventions that shift MyHC expression toward faster isoforms and/or increase fast-contracting fiber size should decrease the prevalence of sarcopenia. Our findings also indicate that future studies need to include or focus solely on females, measure MyHC IIA and IIX isoforms separately, examine fiber type distribution, sample additional muscles to the vastus lateralis (VL), and incorporate an objective measurement of physical activity.

Indexed as

AgingMuscle Fibers, SkeletalMyosin Heavy ChainsProtein IsoformsAdolescentAdultAge FactorsFemaleHumansMaleMiddle AgedMuscle ContractionMuscle, SkeletalMuscular AtrophySarcopeniaYoung AdultMyosin Heavy ChainsProtein IsoformsagingMHCMyHCsarcopeniasex

Identifiers

PMID39374077
PMCPMC11684863

What OpenQuestion holds

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Read underepoch 390

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.