Evidence map›Paper›PMID 29041989›Full record

ArticleMicrobiome2017

Links of gut microbiota composition with alcohol dependence syndrome and alcoholic liver disease.

Veronika B Dubinkina, Alexander V Tyakht, Vera Y Odintsova, Konstantin S Yarygin, Boris A Kovarsky, Alexander V Pavlenko, Dmitry S Ischenko, Anna S Popenko, Dmitry G Alexeev, Anastasiya Y Taraskina and 15 more

Registry-linked trialOpen access · goldAbstract read
In one paragraph

Article in Microbiome, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04544020 (Changes in gUt micRobiota After Enteral Feeding), which is not on this map. Cited by 266 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
266citing papers in PubMed, 3 pooled it
11.0field-weighted citation impact, top 1% 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.

NCT04544020 completednot on this mapstarted 2019, after this paper: background citation

Changes in gUt micRobiota After Enteral Feeding (in Alcoholic Hepatitis)

TypeobservationalSponsorUniversity of AberdeenRan2019 to 2023Enrolled6ConditionsAlcoholic HepatitisArmsNG feeding
3 · Its place in the literature

Who cites it

266 citing papers in PubMed, 3 syntheses or guidelines pooled it, 461 citations in OpenAlex.

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206 more citing papers are in PubMed but not listed here.

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

25 authors at 7 institutions in 2 countries.

Veronika B DubinkinaMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Alexander V TyakhtFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia. a.tyakht@gmail.com.
Vera Y OdintsovaFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Konstantin S YaryginMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Boris A KovarskyFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Alexander V PavlenkoMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Dmitry S IschenkoMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Anna S PopenkoFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Dmitry G AlexeevMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Anastasiya Y TaraskinaSaint-Petersburg Bekhterev Psychoneurological Research Institute, Bekhtereva 3, Saint-Petersburg, 192019, Russia.
Regina F NasyrovaSaint-Petersburg Bekhterev Psychoneurological Research Institute, Bekhtereva 3, Saint-Petersburg, 192019, Russia.
Evgeny M KrupitskySaint-Petersburg Bekhterev Psychoneurological Research Institute, Bekhtereva 3, Saint-Petersburg, 192019, Russia.
Nino V ShalikianiMoscow Clinical Scientific Center, Shosse Entuziastov 86, Moscow, 111123, Russia.
Igor G BakulinMoscow Clinical Scientific Center, Shosse Entuziastov 86, Moscow, 111123, Russia.
Petr L ShcherbakovMoscow Clinical Scientific Center, Shosse Entuziastov 86, Moscow, 111123, Russia.
Lyubov O SkorodumovaFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Andrei K LarinFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Elena S KostryukovaMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Rustam A AbdulkhakovKazan State Medical University, Butlerova 49, Kazan, 420012, Russia.
Sayar R AbdulkhakovKazan State Medical University, Butlerova 49, Kazan, 420012, Russia.
Sergey Y MalaninKazan Federal University, Kremlyovskaya 18, Kazan, 420008, Russia.
Ruzilya K IsmagilovaKazan Federal University, Kremlyovskaya 18, Kazan, 420008, Russia.
Tatiana V GrigoryevaKazan Federal University, Kremlyovskaya 18, Kazan, 420008, Russia.
Elena N IlinaFederal Research and Clinical Center of Physical-Chemical Medicine, Malaya Pirogovskaya 1a, Moscow, 119435, Russia.
Vadim M GovorunMoscow Institute of Physics and Technology, Institutskiy per. 9, Dolgoprudny, Moscow Region, 141700, Russia.
Research Institute of Physical Chemical Medicine · RUKazan Federal University · RUMoscow Clinical Scientific Center · RUMoscow Institute of Physics and Technology · RUSt.Petersburg V.M.Bekhterev Psychoneurological Research Institute · RUKazan State Medical University · RUUrbana University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAlcohol abuse has deleterious effects on human health by disrupting the functions of many organs and systems. Gut microbiota has been implicated in the pathogenesis of alcohol-related liver diseases, with its composition manifesting expressed dysbiosis in patients suffering from alcoholic dependence. Due to its inherent plasticity, gut microbiota is an important target for prevention and treatment of these diseases. Identification of the impact of alcohol abuse with associated psychiatric symptoms on the gut community structure is confounded by the liver dysfunction. In order to differentiate the effects of these two factors, we conducted a comparative "shotgun" metagenomic survey of 99 patients with the alcohol dependence syndrome represented by two cohorts-with and without liver cirrhosis. The taxonomic and functional composition of the gut microbiota was subjected to a multifactor analysis including comparison with the external control group.

resultsAlcoholic dependence and liver cirrhosis were associated with profound shifts in gut community structures and metabolic potential across the patients. The specific effects on species-level community composition were remarkably different between cohorts with and without liver cirrhosis. In both cases, the commensal microbiota was found to be depleted. Alcoholic dependence was inversely associated with the levels of butyrate-producing species from the Clostridiales order, while the cirrhosis-with multiple members of the Bacteroidales order. The opportunist pathogens linked to alcoholic dependence included pro-inflammatory Enterobacteriaceae, while the hallmarks of cirrhosis included an increase of oral microbes in the gut and more frequent occurrence of abnormal community structures. Interestingly, each of the two factors was associated with the expressed enrichment in many Bifidobacterium and Lactobacillus-but the exact set of the species was different between alcoholic dependence and liver cirrhosis. At the level of functional potential, the patients showed different patterns of increase in functions related to alcohol metabolism and virulence factors, as well as pathways related to inflammation.

conclusionsMultiple shifts in the community structure and metabolic potential suggest strong negative influence of alcohol dependence and associated liver dysfunction on gut microbiota. The identified differences in patterns of impact between these two factors are important for planning of personalized treatment and prevention of these pathologies via microbiota modulation. Particularly, the expansion of Bifidobacterium and Lactobacillus suggests that probiotic interventions for patients with alcohol-related disorders using representatives of the same taxa should be considered with caution. Taxonomic and functional analysis shows an increased propensity of the gut microbiota to synthesis of the toxic acetaldehyde, suggesting higher risk of colorectal cancer and other pathologies in alcoholics.

Indexed as

AdultAlcoholismBifidobacteriumDysbiosisEnterobacteriaceaeEthanolFecesFemaleGastrointestinal MicrobiomeHumansInflammationLactobacillusLiverLiver CirrhosisLiver Diseases, AlcoholicMaleEthanolVirulence FactorsAcetaldehydeAlcoholic dependence syndromeAlcoholic liver cirrhosisBifidobacteriumGut-brain axisHuman gut microbiotaLactobacillusMetagenomeVirulence factors

Identifiers

PMID29041989
PMCPMC5645934
OpenAlexW2765961991

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Registered trials

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.