Evidence map›Paper›PMID 35585256›Full record

ArticleEuropean journal of pediatrics2022

Intestinal microbiota composition of children with infection with severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and multisystem inflammatory syndrome (MIS-C).

Cansu Suskun, Omer Kilic, Dilek Yilmaz Ciftdogan, Sirin Guven, Adem Karbuz, Aslinur Ozkaya Parlakay, Yalcın Kara, Ebru Kacmaz, Aslihan Sahin, Aysun Boga and 13 more

Erratum issuedOpen access · bronzeAbstract readMulticenter Study
In one paragraph

Article in European journal of pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
4.4field-weighted citation impact, top 4% 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

34 citing papers in PubMed, 52 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 6 institutions in 2 countries.

Cansu SuskunDepartment of Pediatrics, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, TR-26040, Turkey.
Omer KilicDepartment of Pediatric Infectious Disease, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Dilek Yilmaz CiftdoganDepartment of Pediatric Infectious Disease, Izmir Katip Celebi University Faculty of Medicine, Izmir, Turkey.
Sirin GuvenDepartment of Pediatrics, Prof. Dr Ilhan Varank Training and Research Hospital, Istanbul, Turkey.
Adem KarbuzDepartment of Pediatric Infectious Disease, Dr. Cemil Tascioglu City Hospital, Istanbul, Turkey.
Aslinur Ozkaya ParlakayYildirim Beyazit University Faculty of Medicine Department of Pediatric Infectious Disease, Ankara City Hospital Department of Pediatric Infectious Disease, Ankara, Turkey.
Yalcın KaraDepartment of Pediatric Infectious Disease, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Ebru KacmazPediatric Intensive Care Unit, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Aslihan SahinDepartment of Pediatric Infectious Disease, Izmir Katip Celebi University Faculty of Medicine, Izmir, Turkey.
Aysun BogaDepartment of Pediatrics, Prof. Dr Ilhan Varank Training and Research Hospital, Istanbul, Turkey.
Didem Kizmaz IsancliDepartment of Pediatric Infectious Disease, Dr. Cemil Tascioglu City Hospital, Istanbul, Turkey.
Belgin GulhanDepartment of Pediatric Infectious Disease, Ankara City Hospital, Ankara, Turkey.
Saliha Kanik-YuksekDepartment of Pediatric Infectious Disease, Ankara City Hospital, Ankara, Turkey.
Eylem KiralPediatric Intensive Care Unit, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Gurkan BozanPediatric Intensive Care Unit, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Mehmet Ozgür ArslanogluPediatric Intensive Care Unit, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Mahmut Can KizilDepartment of Pediatric Infectious Disease, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Meltem DinleyiciDepartment of Social Pediatrics, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Tercan UsDepartment of Microbiology, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, Turkey.
Ahmet VarisDiagen Biotechnology, Ankara, Turkey.
Mucahit KayaDiagen Biotechnology, Ankara, Turkey.
Yvan VandenplasKidZ Health Castle, UZ Brussels, Vrije Universiteit Brussel, Brussels, Belgium.
Ener Cagri DinleyiciDepartment of Pediatrics, Eskisehir Osmangazi University Faculty of Medicine, Eskisehir, TR-26040, Turkey. timboothtr@yahoo.com.ORCID http://orcid.org/0000-0002-0339-0134
Eskişehir Osmangazi University · TRIstanbul Eye Hospital · TRIzmir Kâtip Çelebi University · TRMemorial Ankara Hospital · TRAnkara Yıldırım Beyazıt University · TRVrije Universiteit Brussel · BE

Funding

Eskisehir Osmangazi University Scientific Research Project TTU-2021-1750
6 · The paper itself

Abstract

Microbiota composition may play a role in the development, prognosis, or post-infection of COVID-19. There are studies evaluating the microbiota composition at the time of diagnosis and during the course of COVID-19, especially in adults, while studies in children are limited and no study available in children with multisystem inflammatory syndrome in children (MIS-C). This study was planned to compare intestinal microbiota composition in children diagnosed with MIS-C and acute COVID-19 infection with healthy children. In this prospective multicenter study, 25 children diagnosed with MIS-C, 20 with COVID-19 infection, and 19 healthy children were included. Intestinal microbiota composition was evaluated by 16 s rRNA gene sequencing. We observed changes of diversity, richness, and composition of intestinal microbiota in MIS-C cases compared to COVID-19 cases and in the healthy controls. The Shannon index was higher in the MIS-C group than the healthy controls (p < 0.01). At phylum level, in the MIS-C group, a significantly higher relative abundance of Bacteroidetes and lower abundance of Firmicutes was found compared to the control group. Intestinal microbiota composition changed in MIS-C cases compared to COVID-19 and healthy controls, and Faecalibacterium prausnitzii decreased; Bacteroides uniformis, Bacteroides plebeius, Clostridium ramosum, Eubacterium dolichum, Eggerthella lenta, Bacillus thermoamylovorans, Prevotella tannerae, and Bacteroides coprophilus were dominant in children with MIS-C. At species level, we observed decreased Faecalibacterium prausnitzii, and increased Eubacterium dolichum, Eggerthella lenta, and Bacillus thermoamylovorans in children with MIS-C and increased Bifidobacterium adolescentis and Dorea formicigenerasus in the COVID-19 group. Our study is the first to evaluate the microbiota composition in MIS-C cases. There is a substantial change in the composition of the gut microbiota: (1) reduction of F. prausnitzii in children with MIS-C and COVID-19; (2) an increase of Eggerthella lenta which is related with autoimmunity; and (3) the predominance of E. dolichum is associated with metabolic dysfunctions and obesity in children with MIS-C.

conclusionsAlterations of the intestinal microbiota might be part of pathogenesis of predisposing factor for MIS-C. It would be beneficial to conduct more extensive studies on the cause-effect relationship of these changes in microbiota composition and their effects on long-term prognosis. WHAT IS KNOWN: • Microbiota composition may play a role in the development, prognosis, or post-infection of COVID-19.  • However, the number of studies on children is limited, and no study on multisystem inflammatory syndrome in children is currently available (MIS-C). WHAT IS NEW: • In individuals with MIS-C, the composition of the gut microbiota changed dramatically. • Decreased Faecalibacterium prausnitzii have been observed, increased Eggerthella lenta, which was previously linked to autoimmunity, and predominance of Eubacterium dolichum which was linked to metabolic dysfunction and obesity.

Indexed as

COVID-19Gastrointestinal MicrobiomePediatric ObesityActinobacteriaAdultBacillotaBacillusChildFecesHumansProspective StudiesSARS-CoV-2Systemic Inflammatory Response SyndromeChildrenCOVID-19MicrobiomeMicrobiotaMIS-CMultisystem inflammatory syndrome in children

Identifiers

PMID35585256
PMCPMC9117086
OpenAlexW4280551466

What OpenQuestion 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 OpenQuestion graph.