Evidence map›Paper›PMID 39048520›Full record

ArticleClinical and molecular hepatology2024

Gut microbiome and metabolome signatures in liver cirrhosis-related complications.

Satya Priya Sharma, Haripriya Gupta, Goo-Hyun Kwon, Sang Yoon Lee, Seol Hee Song, Jeoung Su Kim, Jeong Ha Park, Min Ju Kim, Dong-Hoon Yang, Hyunjoon Park and 10 more

Abstract read
In one paragraph

Article in Clinical and molecular hepatology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Review
  4. Article
  5. Review
  6. Gut microbiota in health and disease.Molecular biomedicine · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
  14. Review
  15. Article
  16. Gut microbes · 2025
    Article
  17. Article
  18. Article
  19. 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

20 authors.

Satya Priya SharmaInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Haripriya GuptaInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Goo-Hyun KwonInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Sang Yoon LeeInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Seol Hee SongInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Jeoung Su KimInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Jeong Ha ParkInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Min Ju KimInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Dong-Hoon YangInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Hyunjoon ParkInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Sung-Min WonInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Jin-Ju JeongInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Ki-Kwang OhInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Jung A EomInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Kyeong Jin LeeInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Sang Jun YoonInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Young Lim HamDepartment of Nursing Daewon University College Jecheon, Korea.
Gwang Ho BaikInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Dong Joon KimInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.
Ki Tae SukInstitute for Liver and Digestive Diseases, Hallym University, Chuncheon, Korea.

Funding

Hallym UniversityKorea Institute for Advancement of Technology P0020622Ministry of Education, Science and Technology 2020R1A6A1A03043026Ministry of Education, Science and Technology 2020R1I1A3073530National Research Foundation of Korea
6 · The paper itself

Abstract

BACKGROUND/

aimsShifts in the gut microbiota and metabolites are interrelated with liver cirrhosis progression and complications. However, causal relationships have not been evaluated comprehensively. Here, we identified complication-dependent gut microbiota and metabolic signatures in patients with liver cirrhosis.

methodsMicrobiome taxonomic profiling was performed on 194 stool samples (52 controls and 142 cirrhosis patients) via V3-V4 16S rRNA sequencing. Next, 51 samples (17 controls and 34 cirrhosis patients) were selected for fecal metabolite profiling via gas chromatography mass spectrometry and liquid chromatography coupled to time-of-flight mass spectrometry. Correlation analyses were performed targeting the gut-microbiota, metabolites, clinical parameters, and presence of complications (varices, ascites, peritonitis, encephalopathy, hepatorenal syndrome, hepatocellular carcinoma, and deceased).

resultsVeillonella bacteria, Ruminococcus gnavus, and Streptococcus pneumoniae are cirrhosis-related microbiotas compared with control group. Bacteroides ovatus, Clostridium symbiosum, Emergencia timonensis, Fusobacterium varium, and Hungatella_uc were associated with complications in the cirrhosis group. The areas under the receiver operating characteristic curve (AUROCs) for the diagnosis of cirrhosis, encephalopathy, hepatorenal syndrome, and deceased were 0.863, 0.733, 0.71, and 0.69, respectively. The AUROCs of mixed microbial species for the diagnosis of cirrhosis and complication were 0.808 and 0.847, respectively. According to the metabolic profile, 5 increased fecal metabolites in patients with cirrhosis were biomarkers (AUROC >0.880) for the diagnosis of cirrhosis and complications. Clinical markers were significantly correlated with the gut microbiota and metabolites.

conclusionCirrhosis-dependent gut microbiota and metabolites present unique signatures that can be used as noninvasive biomarkers for the diagnosis of cirrhosis and its complications.

Indexed as

FecesGastrointestinal MicrobiomeLiver CirrhosisMetabolomeRNA, Ribosomal, 16SAdultAgedCase-Control StudiesFemaleHumansMaleMiddle AgedROC CurveRNA, Ribosomal, 16SBiomarkerCirrhosisComplicationMetaboliteMicrobiota

Identifiers

PMID39048520
PMCPMC11540350

What OpenQuestion holds

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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.