Evidence map›Paper›PMID 34989986›Full record

ArticleIndian journal of gastroenterology : official journal of the Indian Society of Gastroenterology2022

The role of gut microbiota in clinical complications, disease severity, and treatment response in severe alcoholic hepatitis.

Cyriac Abby Philips, Philip Augustine, Karthik Ganesan, Shatakshi Ranade, Varun Chopra, Kunal Patil, Sonie Shende, Rizwan Ahamed, Sandeep Kumbar, Sasidharan Rajesh and 7 more

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In one paragraph

Article in Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.1field-weighted citation impact, top 13% 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

15 citing papers in PubMed, 27 citations in OpenAlex.

  1. Article
  2. Review
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  4. Gut microbiota therapy in gastrointestinal diseases.Frontiers in cell and developmental biology · 2025
    Review
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  7. Article
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  12. Editorial commentary on the Indian Journal of Gastroenterology-January-February 2022.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2022
    Article
  13. Review
  14. Gut Barrier and Microbiota in Cirrhosis.Journal of clinical and experimental hepatology
    Review
  15. Gut Microbiome and Alcohol-associated Liver Disease.Journal of clinical and experimental hepatology
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 2 institutions in 1 country.

Cyriac Abby PhilipsThe Liver Unit and Monarch Liver Lab, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India. abbyphilips@gmail.com.ORCID 0000-0002-9587-336X
Philip AugustineGastroenterology and Advanced G.I. Endoscopy, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Karthik GanesanBiomedical Software and Instrumentation, Department of Bioinformatics, Helicalbio, Ann Arbor, MI, USA.
Shatakshi RanadeMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Varun ChopraMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Kunal PatilMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Sonie ShendeMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Rizwan AhamedGastroenterology and Advanced G.I. Endoscopy, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Sandeep KumbarGastroenterology and Advanced G.I. Endoscopy, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Sasidharan RajeshInterventional Radiology, The Liver Unit and Gastroenterology, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Tom GeorgeInterventional Radiology, The Liver Unit and Gastroenterology, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Meera MohananAnaesthesia and Critical Care, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Narain MohanThe Liver Unit and Monarch Liver Lab, Cochin Gastroenterology Group, Ernakulam Medical Center, Kochi, 682 028, India.
Nikhil PhadkeMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Mridula RaniMolecular, Cellular and Developmental Biology, Genepath-Dx, Pune, 411 004, India.
Arjun NarayananNational Urban Health Mission, Ernakulam District Hospital, Kochi, 682 011, India.
Suchetha M JaganNational Urban Health Mission, Ernakulam District Hospital, Kochi, 682 011, India.
General Hospital Ernakulam · INGenePath Dx (India) · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDysbiotic gut bacteria engage in the development and progression of severe alcoholic hepatitis (SAH). We aimed to characterize bacterial communities associated with clinical events (CE), identify significant bacteria linked to CE, and define bacterial relationships associated with specific CE and outcomes at baseline and after treatment in SAH.

methodsWe performed 16-s rRNA sequencing on stool samples (n=38) collected at admission and the last follow-up within 90 days in SAH patients (n=26; 12 corticosteroids; 14 granulocyte colony-stimulating factor, [G-CSF]). Validated pipelines were used to plot bacterial communities, profile functional metabolism, and identify significant taxa and functional metabolites. Conet/NetworkX® was utilized to identify significant non-random patterns of bacterial co-presence and mutual exclusion for clinical events.

resultsAll the patients were males with median discriminant function (DF) 64, Child-Turcotte-Pugh (CTP) 12, and model for end-stage liver disease (MELD) score 25.5. At admission, 27%, 42%, and 58% had acute kidney injury (AKI), hepatic encephalopathy (HE), and infections respectively; 38.5% died at end of follow-up. Specific bacterial families were associated with HE, sepsis, disease severity, and death. Lachnobacterium and Catenibacterium were associated with HE, and Pediococcus with death after steroid treatment. Change from Enterococcus (promotes AH) to Barnesiella (inhibits E. faecium) was significant after G-CSF. Phenylpropanoid-biosynthesis (innate-immunity) and glycerophospholipid-metabolism (cellular-integrity) pathways in those without infections and the death, respectively, were upregulated. Mutual interactions between Enterococcus cecorum, Acinetobacter schindleri, and Mitsuokella correlated with admission AKI.

conclusionsSpecific gut microbiota, their interactions, and metabolites are associated with complications of SAH and treatment outcomes. Microbiota-based precision medicine as adjuvant treatment may be a new therapeutic area.

Indexed as

Acute Kidney InjuryEnd Stage Liver DiseaseGastrointestinal MicrobiomeHepatitis, AlcoholicGranulocyte Colony-Stimulating FactorHumansMaleSeverity of Illness IndexGranulocyte Colony-Stimulating FactorAlcoholCirrhosisDysbiosisFecal transplantIntestinal bacteriaMetabolomicsMetagenomicsMicrobiomePortal hypertension

Identifiers

PMID34989986
OpenAlexW4206590997

What Socratic holds

Textmetadata
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.