Evidence map›Paper›PMID 37369825›Full record

ArticleScientific reports2023

Metabolomic and gut microbiome profiles across the spectrum of community-based COVID and non-COVID disease.

Marc F Österdahl, Ronan Whiston, Carole H Sudre, Francesco Asnicar, Nathan J Cheetham, Aitor Blanco Miguez, Vicky Bowyer, Michela Antonelli, Olivia Snell, Liane Dos Santos Canas and 12 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.4field-weighted citation impact, top 17% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 7 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Review
  6. Review
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

22 authors at 3 institutions in 2 countries.

Marc F Österdahl *King's College London, London, UK. marc.osterdahl@kcl.ac.uk.
Ronan Whiston *King's College London, London, UK.
Carole H SudreKing's College London, London, UK.
Francesco AsnicarUniversity of Trento, Trento, Italy.
Nathan J CheethamKing's College London, London, UK.
Aitor Blanco MiguezUniversity of Trento, Trento, Italy.
Vicky BowyerKing's College London, London, UK.
Michela AntonelliKing's College London, London, UK.
Olivia SnellKing's College London, London, UK.
Liane Dos Santos CanasKing's College London, London, UK.
Christina HuZOE Global Ltd, London, UK.
Jonathan WolfZOE Global Ltd, London, UK.
Cristina MenniKing's College London, London, UK.
Michael MalimKing's College London, London, UK.
Deborah HartKing's College London, London, UK.
Tim SpectorKing's College London, London, UK.
Sarah BerryKing's College London, London, UK.
Nicola SegataUniversity of Trento, Trento, Italy.
Katie DooresKing's College London, London, UK.
Sebastien OurselinKing's College London, London, UK.
Emma L DuncanKing's College London, London, UK.
Claire J StevesKing's College London, London, UK.
King's College London · GBUniversity of Trento · ITZOE (United Kingdom) · GB

Funding

British Heart FoundationDepartment of HealthMedical Research Council MC_PC_20051Medical Research Council MC_PC_20059Medical Research Council MR/M004422/1Medical Research Council MR/S023747/1Medical Research Council MR/T005351/1Medical Research Council MR/W005611/1Wellcome TrustWellcome Trust 203148/Z/16/ZWellcome Trust 215010/Z/18/Z
6 · The paper itself

Abstract

Whilst most individuals with SARS-CoV-2 infection have relatively mild disease, managed in the community, it was noted early in the pandemic that individuals with cardiovascular risk factors were more likely to experience severe acute disease, requiring hospitalisation. As the pandemic has progressed, increasing concern has also developed over long symptom duration in many individuals after SARS-CoV-2 infection, including among the majority who are managed acutely in the community. Risk factors for long symptom duration, including biological variables, are still poorly defined. Here, we examine post-illness metabolomic profiles, using nuclear magnetic resonance (Nightingale Health Oyj), and gut-microbiome profiles, using shotgun metagenomic sequencing (Illumina Inc), in 2561 community-dwelling participants with SARS-CoV-2. Illness duration ranged from asymptomatic (n = 307) to Post-COVID Syndrome (n = 180), and included participants with prolonged non-COVID-19 illnesses (n = 287). We also assess a pre-established metabolomic biomarker score, previously associated with hospitalisation for both acute pneumonia and severe acute COVID-19 illness, for its association with illness duration. We found an atherogenic-dyslipidaemic metabolic profile, including biomarkers such as fatty acids and cholesterol, was associated with longer duration of illness, both in individuals with and without SARS-CoV-2 infection. Greater values of a pre-existing metabolomic biomarker score also associated with longer duration of illness, regardless of SARS-CoV-2 infection. We found no association between illness duration and gut microbiome profiles in convalescence. This highlights the potential role of cardiometabolic dysfunction in relation to the experience of long duration symptoms after symptoms of acute infection, both COVID-19 as well as other illnesses.

Indexed as

COVID-19Gastrointestinal MicrobiomePneumoniaHospitalizationHumansSARS-CoV-2

Identifiers

PMID37369825
PMCPMC10300098
OpenAlexW4382245237

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.