Evidence map›Paper›PMID 38978778›Full record

ArticleFrontiers in medicine2024

Bioinformatics and system biology approach to identify potential common pathogenesis for COVID-19 infection and sarcopenia.

Jun Zhong, Hui Yuan, Jinghong Yang, Yimin Du, Zheng Li, Xu Liu, Haibo Yang, Zhaojun Wang, Zi Wang, Lujun Jiang and 4 more

Abstract read
In one paragraph

Article in Frontiers in medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–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

5 citing papers in PubMed.

  1. Article
  2. Article
  3. Unravelling the Complexity of Sarcopenia Through a Systems Biology Approach.International journal of molecular sciences · 2025
    Review
  4. Identification of shared key genes and pathways in osteoarthritis and sarcopenia patients based on bioinformatics analysis.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2025
    Article
  5. Review
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

14 authors.

Jun Zhong *School of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Hui Yuan *School of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Jinghong YangSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Yimin DuSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Zheng LiDepartment of Orthopedics, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Xu LiuSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Haibo YangSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Zhaojun WangSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Zi WangSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Lujun JiangSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Zhiqiang RenSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Hongliang LiSchool of Clinical Medicine, Southwest Medical University, Luzhou, Sichuan, China.
Zhong LiDepartment of Orthopedics, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.
Yanshi LiuDepartment of Orthopedics, Affiliated Hospital of Southwest Medical University, Luzhou, Sichuan, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Sarcopenia is a condition characterized by age-related loss of muscle mass and strength. Increasing evidence suggests that patients with sarcopenia have higher rates of coronavirus 2019 (COVID-19) infection and poorer post-infection outcomes. However, the exact mechanism and connections between the two is unknown. In this study, we used high-throughput data from the GEO database for sarcopenia (GSE111016) and COVID-19 (GSE171110) to identify common differentially expressed genes (DEGs). We conducted GO and KEGG pathway analyses, as well as PPI network analysis on these DEGs. Using seven algorithms from the Cytoscape plug-in cytoHubba, we identified 15 common hub genes. Further analyses included enrichment, PPI interaction, TF-gene and miRNA-gene regulatory networks, gene-disease associations, and drug prediction. Additionally, we evaluated immune cell infiltration with CIBERSORT and assessed the diagnostic accuracy of hub genes for sarcopenia and COVID-19 using ROC curves. In total, we identified 66 DEGs (34 up-regulated and 32 down-regulated) and 15 hub genes associated with sarcopenia and COVID-19. GO and KEGG analyses revealed functions and pathways between the two diseases. TF-genes and TF-miRNA regulatory network suggest that FOXOC1 and hsa-mir-155-5p may be identified as key regulators, while gene-disease analysis showed strong correlations with hub genes in schizophrenia and bipolar disorder. Immune infiltration showed a correlation between the degree of immune infiltration and the level of infiltration of different immune cell subpopulations of hub genes in different datasets. The ROC curves for ALDH1L2 and KLF5 genes demonstrated their potential as diagnostic markers for both sarcopenia and COVID-19. This study suggests that sarcopenia and COVID-19 may share pathogenic pathways, and these pathways and hub genes offer new targets and strategies for early diagnosis, effective treatment, and tailored therapies for sarcopenia patients with COVID-19.

Indexed as

bioinformaticsbiomarkersCOVID-19pathogenesissarcopenia

Identifiers

PMID38978778
PMCPMC11228343

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.