Evidence map›Paper›PMID 37106281›Full record

ArticleGeroScience2023

Sex-specific alteration in human muscle transcriptome with age.

Mohini Gharpure, Jie Chen, Resheek Nerella, Sagar Vyavahare, Sandeep Kumar, Carlos M Isales, Mark Hamrick, Satish Adusumilli, Sadanand Fulzele

Open access · greenAbstract read
In one paragraph

Article in GeroScience, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
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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

9 authors at 2 institutions in 1 country.

Mohini GharpureDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA.
Jie ChenDivision of Biostatistics and Data Science, Department of Population Health Sciences, Augusta University, Augusta, GA, USA.
Resheek NerellaDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA.
Sagar VyavahareDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA.
Sandeep KumarDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA.
Carlos M IsalesDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA.
Mark HamrickCenter for Healthy Aging, Augusta University, Augusta, GA, USA.
Satish AdusumilliUniversity of Notre Dame, Notre Dame, IN, USA.
Sadanand FulzeleDepartment of Medicine, Medical College of Georgia, Augusta University, GA, Augusta, USA. sfulzele@augusta.edu.ORCID 0000-0002-3510-6759
Augusta University · USUniversity of Notre Dame · US

Funding

THE LEPTIN-IGF1 AXIS IN MUSCULOSKELETAL AGINGP01AG036675 · NIA · AUGUSTA UNIVERSITY · PI CARLOS M. ISALES · 2011 to 2026
$31.5M
NIA NIH HHS P01 AG036675
6 · The paper itself

Abstract

Sarcopenia is a medical condition that progressively develops with age and results in reduced skeletal muscle mass, alteration in muscle composition, and decreased muscle strength. Several clinical studies suggested that sarcopenia disproportionally affects males and females with age. Despite this knowledge, the molecular mechanism governing the pathophysiology is not well understood in a sex-specific manner. In this study, we utilized human gastrocnemius muscles from males and females to identify differentially regulated genes with age. We found 269 genes with at least a twofold expression difference in the aged muscle transcriptome. Among the female muscle samples, there were 239 differentially regulated genes, and the novel protein-coding genes include KIF20A, PIMREG, MTRNR2L6, TRPV6, EFNA2, RNF24, and SFN. In aged male skeletal muscle, there were 166 differentially regulated genes, and the novel-protein coding genes are CENPK, CDKN2A, BHLHA15, and EPHA. Gene Ontology (GO) enrichment revealed glucose catabolism, NAD metabolic processes, and muscle fiber transition pathways that are involved in aged female skeletal muscle, whereas replicative senescence, cytochrome C release, and muscle composition pathways are disrupted in aged male skeletal muscle. Targeting these novels, differentially regulated genes, and signaling pathways could serve as sex-specific therapeutic targets to combat the age-related onset of sarcopenia and promote healthy aging.

Indexed as

Healthy AgingSarcopeniaAgedFemaleHumansMaleMuscle Fibers, SkeletalMuscle, SkeletalTranscriptomeAgingMuscleSarcopeniaSex

Identifiers

PMID37106281
PMCPMC10400750
OpenAlexW4367173654

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.