Evidence map›Paper›PMID 39604802›Full record

ArticleEndocrinology and metabolism (Seoul, Korea)2025

Carnitine Metabolite as a Potential Circulating Biomarker for Sarcopenia in Men.

Je Hyun Seo, Jung-Min Koh, Han Jin Cho, Hanjun Kim, Young-Sun Lee, Su Jung Kim, Pil Whan Yoon, Won Kim, Sung Jin Bae, Hong-Kyu Kim and 2 more

Abstract read
In one paragraph

Article in Endocrinology and metabolism (Seoul, Korea), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Trial
  2. Review
  3. Review
  4. 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

12 authors.

Je Hyun SeoVeterans Medical Research Institute, Veterans Health Service Medical Center, Seoul, Korea.
Jung-Min KohDivision of Endocrinology and Metabolism, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Han Jin ChoBiomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Hanjun KimBiomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Young-Sun LeeBiomedical Research Center, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Su Jung KimDepartment of Convergence Medicine, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Pil Whan YoonDepartment of Orthopedic Surgery, Seoul Now Hospital, Anyang, Korea.
Won KimDepartment of Rehabilitation Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Sung Jin BaeHealth Screening and Promotion Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Hong-Kyu KimHealth Screening and Promotion Center, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.
Hyun Ju YooDepartment of Convergence Medicine, Asan Institute for Life Sciences, Asan Medical Center, Seoul, Korea.
Seung Hun LeeDivision of Endocrinology and Metabolism, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Korea.

Funding

Asan Institute for Life Sciences, Asan Medical Center 2023IP0041Ministry of Health and Welfare RS-2021-DD120859Ministry of Science and ICTMinistry of Trade, Industry and EnergyNational Research Foundation of Korea 2022R1A2C1003661National Research Foundation of Korea 2022R1A2C1007901National Research Foundation of Korea 2022R1C1C1002929
6 · The paper itself

Abstract

backgruoundSarcopenia, a multifactorial disorder involving metabolic disturbance, suggests potential for metabolite biomarkers. Carnitine (CN), essential for skeletal muscle energy metabolism, may be a candidate biomarker. We investigated whether CN metabolites are biomarkers for sarcopenia.

methodsAssociations between the CN metabolites identified from an animal model of sarcopenia and muscle cells and sarcopenia status were evaluated in men from an age-matched discovery (72 cases, 72 controls) and a validation (21 cases, 47 controls) cohort.

resultsAn association between CN metabolites and sarcopenia showed in mouse and cell studies. In the discovery cohort, plasma C5-CN levels were lower in sarcopenic men (P=0.005). C5-CN levels in men tended to be associated with handgrip strength (HGS) (P=0.098) and were significantly associated with skeletal muscle mass (P=0.003). Each standard deviation increase in C5-CN levels reduced the odds of low muscle mass (odd ratio, 0.61; 95% confidence interval [CI], 0.42 to 0.89). The area under the receiver operating characteristic curve (AUROC) of CN score using a regression equation of C5-CN levels, for sarcopenia was 0.635 (95% CI, 0.544 to 0.726). In the discovery cohort, addition of CN score to HGS significantly improved AUROC from 0.646 (95% CI, 0.575 to 0.717; HGS only) to 0.727 (95% CI, 0.643 to 0.810; P=0.006; HGS+CN score). The improvement was confirmed in the validation cohort (AUROC=0.563; 95% CI, 0.470 to 0.656 for HGS; and AUROC=0.712; 95% CI, 0.569 to 0.855 for HGS+CN score; P=0.027).

conclusionC5-CN, indicative of low muscle mass, is a potential circulating biomarker for sarcopenia in men. Further studies are required to confirm these results and explore sarcopenia-related metabolomic changes.

Indexed as

BiomarkersCarnitineSarcopeniaAgedAged, 80 and overAnimalsCase-Control StudiesCohort StudiesHand StrengthHumansMaleMiceMiddle AgedMuscle, SkeletalBiomarkersCarnitineAgingBiomarkersCarnitineMetabolomicsSarcopenia

Identifiers

PMID39604802
PMCPMC11898317

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.