Evidence map›Paper›PMID 9861016›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1998

Viral mediated expression of insulin-like growth factor I blocks the aging-related loss of skeletal muscle function.

E R Barton-Davis, D I Shoturma, A Musaro, N Rosenthal, H L Sweeney

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1998. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 203 papers.

0numbers the graph read from it
0cells of the map it votes in
203citing papers in PubMed
10.0field-weighted citation impact, top 1% of its field
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

203 citing papers in PubMed, 697 citations in OpenAlex.

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  10. Ablation of specific insulin-like growth factor I forms reveals the importance of cleavage for regenerative capacity and glycosylation for skeletal muscle storage.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2024
    Article
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  13. Mechanisms of Skeletal Muscle Atrophy and Molecular Circuitry of Stem Cell Fate in Skeletal Muscle Regeneration and Aging.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Review
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  19. Actions and interactions of IGF-I and MMPs during muscle regeneration.Seminars in cell & developmental biology · 2021
    Review
  20. Review

143 more citing papers are in PubMed but not listed here.

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

5 authors at 2 institutions in 1 country.

E R Barton-DavisDepartment of Physiology, A700 Richards Building, University of Pennsylvania School of Medicine, Philadelphia, PA 19104-6085, USA.
D I Shoturma
A Musaro
N Rosenthal
H L Sweeney
Massachusetts General Hospital · USUniversity of Pennsylvania · US

Funding

VIRAL DELIVERY INTO NEONATAL AND ADULT MAMMALSP01AR043648 · NIAMS · UNIVERSITY OF PENNSYLVANIA · PI WILSON, JAMES M · 1995 to 2000
$79k
TRANSGENIC MODULATION OF CONTRACTION INDUCED INJURYP01AG013329 · NIA · MASSACHUSETTS GENERAL HOSPITAL · PI ROSENTHAL, NADIA A · 1995 to 1999
–
NIAMS NIH HHS P01-AR/NS43648NIA NIH HHS P01-AG13329
6 · The paper itself

Abstract

During the aging process, mammals lose up to a third of their skeletal muscle mass and strength. Although the mechanisms underlying this loss are not entirely understood, we attempted to moderate the loss by increasing the regenerative capacity of muscle. This involved the injection of a recombinant adeno-associated virus directing overexpression of insulin-like growth factor I (IGF-I) in differentiated muscle fibers. We demonstrate that the IGF-I expression promotes an average increase of 15% in muscle mass and a 14% increase in strength in young adult mice, and remarkably, prevents aging-related muscle changes in old adult mice, resulting in a 27% increase in strength as compared with uninjected old muscles. Muscle mass and fiber type distributions were maintained at levels similar to those in young adults. We propose that these effects are primarily due to stimulation of muscle regeneration via the activation of satellite cells by IGF-I. This supports the hypothesis that the primary cause of aging-related impairment of muscle function is a cumulative failure to repair damage sustained during muscle utilization. Our results suggest that gene transfer of IGF-I into muscle could form the basis of a human gene therapy for preventing the loss of muscle function associated with aging and may be of benefit in diseases where the rate of damage to skeletal muscle is accelerated.

Indexed as

Gene Expression Regulation, DevelopmentalTranscription, GeneticAgingAnimalsDependovirusGenetic TherapyHumansInsulin-Like Growth Factor IIsometric ContractionMiceMice, Inbred C57BLMuscle DevelopmentMuscle, SkeletalRecombinant ProteinsRegenerationReverse Transcriptase Polymerase Chain ReactionInsulin-Like Growth Factor IRecombinant Proteins

Identifiers

PMID9861016
PMCPMC28090
OpenAlexW1966530677

What OpenQuestion holds

Textmetadata
Read underepoch 390

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 OpenQuestion graph.