Evidence map›Paper›PMID 32123207›Full record

ArticleScientific reports2020

Identification of serum biomarkers for active pulmonary tuberculosis using a targeted metabolomics approach.

Yonggeun Cho, Youngmok Park, Bora Sim, Jungho Kim, Hyejon Lee, Sang-Nae Cho, Young Ae Kang, Sang-Guk Lee

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
1.2field-weighted citation impact, top 11% 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

44 citing papers in PubMed, 71 citations in OpenAlex.

  1. Review
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  3. Metabolomic signaling in sarcoidosis pathogenesis.Current opinion in immunology · 2026
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  19. Biomarker discovery for tuberculosis using metabolomics.Frontiers in molecular biosciences · 2023
    Review
  20. 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

8 authors at 2 institutions in 1 country.

Yonggeun Cho *Department of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Youngmok Park *Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.ORCID http://orcid.org/0000-0002-5669-1491
Bora SimInstitute of Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jungho KimDepartment of Clinical Vaccine Research, International Tuberculosis Research Center, Seoul, Republic of Korea.
Hyejon LeeInstitute of Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea.
Sang-Nae ChoInstitute of Immunology and Immunological Diseases, Yonsei University College of Medicine, Seoul, Republic of Korea.
Young Ae KangDivision of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea. mdkang@yuhs.ac.
Sang-Guk LeeDepartment of Laboratory Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea. comforter6@yuhs.ac.ORCID http://orcid.org/0000-0003-3862-3660
Yonsei University · KRCatholic University of Pusan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although tuberculosis (TB) is a severe health problem worldwide, the current diagnostic methods are far from optimal. Metabolomics is increasingly being used in the study of infectious diseases. We performed metabolome profiling to identify potential biomarkers in patients with active TB. Serum samples from 21 patients with active pulmonary TB, 20 subjects with latent TB infection (LTBI), and 28 healthy controls were analyzed using liquid chromatography-tandem mass spectrometry (LC-MS/MS) followed by multivariate and univariate analyses. Metabolic profiles indicated higher serum levels of glutamate, sulfoxy methionine, and aspartate and lower serum levels of glutamine, methionine, and asparagine in active TB patients than in LTBI subjects or healthy controls. The ratios between metabolically related partners (glutamate/glutamine, sulfoxy methionine/methionine, and aspartate/asparagine) were also elevated in the active TB group. There was no significant difference in the serum concentration of these metabolites according to the disease extent or risk of relapse in active TB patients. Novel serum biomarkers such as glutamate, sulfoxy methionine, aspartate, glutamine, methionine, and asparagine are potentially useful for adjunctive, rapid, and noninvasive pulmonary TB diagnosis.

Indexed as

MetabolomicsAdultAgedBiomarkersFemaleHumansMaleMiddle AgedMultivariate AnalysisTuberculosis, PulmonaryYoung AdultBiomarkers

Identifiers

PMID32123207
PMCPMC7052258
OpenAlexW3010197702

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.