Evidence map›Paper›PMID 34704369›Full record

ArticleJournal of cachexia, sarcopenia and muscle2021

Artificial-intelligence-driven discovery of prognostic biomarker for sarcopenia.

Heewon Chung, Yunju Jo, Dongryeol Ryu, Changwon Jeong, Seong-Kyu Choe, Jinseok Lee

Abstract read
In one paragraph

Article in Journal of cachexia, sarcopenia and muscle, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

  1. Review
  2. Article
  3. Machine Learning Applications and Sarcopenia.Advances in experimental medicine and biology · 2026
    Review
  4. Review
  5. Article
  6. Cancer therapy and cachexia.The Journal of clinical investigation · 2025
    Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Machine Learning Models to Predict Future Frailty in Community-Dwelling Middle-Aged and Older Adults: The ELSA Cohort Study.The journals of gerontology. Series A, Biological sciences and medical sciences · 2023
    Article
  14. Article
  15. Article
  16. Article
  17. Transcriptional Control ofInternational journal of molecular sciences · 2022
    Article
  18. Article
  19. Article
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

6 authors.

Heewon ChungDepartment of Biomedical Engineering, College of Electronics and Information, Kyung Hee University, Yongin-si, Gyeonggi-do, Republic of Korea.ORCID 0000-0002-4039-1419
Yunju JoDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.ORCID 0000-0002-6305-3324
Dongryeol RyuDepartment of Molecular Cell Biology, Sungkyunkwan University School of Medicine, Suwon, Republic of Korea.ORCID 0000-0001-5905-6760
Changwon JeongSarcopenia Total Solution Center, Wonkwang University School of Medicine, Iksan, Republic of Korea.ORCID 0000-0002-9305-4686
Seong-Kyu ChoeSarcopenia Total Solution Center, Wonkwang University School of Medicine, Iksan, Republic of Korea.ORCID 0000-0002-2102-973X
Jinseok LeeDepartment of Biomedical Engineering, College of Electronics and Information, Kyung Hee University, Yongin-si, Gyeonggi-do, Republic of Korea.ORCID 0000-0002-8580-490X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSarcopenia is defined as muscle wasting, characterized by a progressive loss of muscle mass and function due to ageing. Diagnosis of sarcopenia typically involves both muscle imaging and the physical performance of people exhibiting signs of muscle weakness. Despite its worldwide prevalence, a molecular method for accurately diagnosing sarcopenia has not been established.

methodsWe develop an artificial intelligence (AI) diagnosis model of sarcopenia using a published transcriptome dataset comprising patients from multiple ethnicities. For the AI model for sarcopenia diagnosis, we use a transcriptome database comprising 17 339 genes from 118 subjects. Among the 17 339 genes, we select 27 features as the model inputs. For feature selection, we use a random forest, extreme gradient boosting and adaptive boosting. Using the top 27 features, we propose a four-layer deep neural network, named DSnet-v1, for sarcopenia diagnosis.

resultsAmong isolated testing datasets, DSnet-v1 provides high sensitivity (100%), specificity (94.12%), accuracy (95.83%), balanced accuracy (97.06%) and area under receiver operating characteristics (0.99). To extend the number of patient data, we develop a web application (http://sarcopeniaAI.ml/), where the model can be accessed unrestrictedly to diagnose sarcopenia if the transcriptome is available. A focused analysis of the top 27 genes for their differential or co-expression with other genes implied the potential existence of race-specific factors for sarcopenia, suggesting the possibility of identifying causal factors of sarcopenia when a more extended dataset is provided.

conclusionsOur new AI model, DSnet-v1, accurately diagnoses sarcopenia and is currently available publicly to assist healthcare providers in diagnosing and treating sarcopenia.

Indexed as

Artificial IntelligenceSarcopeniaBiomarkersHumansIntelligencePrognosisBiomarkersArtificial intelligenceDiagnosisMuscle wastingSarcopeniaTranscriptome

Identifiers

PMID34704369
PMCPMC8718042

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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.