Evidence map›Paper›PMID 35262096›Full record

ArticlemedRxiv : the preprint server for health sciences2022

Oropharyngeal Microbiome Profiled at Admission is Predictive of the Need for Respiratory Support Among COVID-19 Patients.

Evan S Bradley, Abigail L Zeamer, Vanni Bucci, Lindsey Cincotta, Marie-Claire Salive, Protiva Dutta, Shafik Mutaawe, Otuwe Anya, Christopher Tocci, Ann Moormann and 3 more

Open access · greenAbstract readPreprint
In one paragraph

Article in medRxiv : the preprint server for health sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 3 institutions in 1 country.

Evan S BradleyDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Abigail L ZeamerProgram in Microbiome Dynamics, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester MA, 01605.
Vanni BucciProgram in Microbiome Dynamics, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester MA, 01605.
Lindsey CincottaDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Marie-Claire SaliveDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Protiva DuttaDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Shafik MutaaweDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Otuwe AnyaDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
Christopher TocciBiology and Biotechnology, Worcester Polytechnique Institute, 100 Institute Road, Worcester, MA 01609.
Ann MoormannDepartment of Medicine, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester, MA 01655.
Doyle V WardProgram in Microbiome Dynamics, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester MA, 01605.
Beth A McCormickProgram in Microbiome Dynamics, University of Massachusetts Medical School, 55 Lake Avenue North, Worcester MA, 01605.
John P HaranDepartment of Emergency Medicine, UMass Memorial Medical Center 55 Lake Avenue North, Worcester MA, 01605.
UMass Memorial Health Care · USUniversity of Massachusetts Chan Medical School · USWorcester Polytechnic Institute · US

Funding

Understanding the Microbiome-gut-brain axisn Alzheimer disease and its Role in Cognitive DeclineRF1AG067483 · NIA · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI HARAN, JOHN PATRICK · 2020 to 2020
$3.3M
Enhancing racial and ethnic diversity inCOVID-19 research participation through storytelling (COVIDstory)U01CA261276 · NCI · UNIV OF MASSACHUSETTS MED SCH WORCESTER · PI MOORMANN, ANN M · 2020 to 2020
$2.0M
NCI NIH HHS U01 CA261276NIA NIH HHS RF1 AG067483
6 · The paper itself

Abstract

The clinical course of infection due to respiratory viruses such as Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV2), the causative agent of Coronavirus Disease 2019 (COVID-19) is thought to be influenced by the community of organisms that colonizes the upper respiratory tract, the oropharyngeal microbiome. In this study, we examined the oropharyngeal microbiome of suspected COVID-19 patients presenting to the Emergency Department and an inpatient COVID-19 unit with symptoms of acute COVID-19. Of 115 enrolled patients, 74 were confirmed COVID-19+ and 50 had symptom duration of 14 days or less; 38 acute COVID-19+ patients (76%) went on to require respiratory support. Although no microbiome features were found to be significantly different between COVID-19+ and COVID-19-patients, when we conducted random forest classification modeling (RFC) to predict the need of respiratory support for the COVID-19+ patients our analysis identified a subset of organisms and metabolic pathways whose relative abundance, when combined with clinical factors (such as age and Body Mass Index), was highly predictive of the need for respiratory support (F1 score 0.857). Microbiome Multivariable Association with Linear Models (MaAsLin2) analysis was then applied to the features identified as predicative of the need for respiratory support by the RFC. This analysis revealed reduced abundance of Importance: The microbial community that colonizes the upper airway, the oropharyngeal microbiome, has the potential to affect how patients respond to respiratory viruses such as SARS-CoV2, the causative agent of COVID-19. In this study, we investigated the oropharyngeal microbiome of COVID-19 patients using high throughput DNA sequencing performed on oral swabs. We combined patient characteristics available at intake such as medical comorbidities and age, with measured abundance of bacterial species and metabolic pathways and then trained a machine learning model to determine what features are predicative of patients needing respiratory support in the form of supplemental oxygen or mechanical ventilation. We found that decreased abundance of some bacterial species and increased abundance of pathways associated bacterial products biosynthesis was highly predictive of needing respiratory support. This suggests that the oropharyngeal microbiome affects disease course in COVID-19 and could be targeted for diagnostic purposes to determine who may need oxygen, or therapeutic purposes such as probiotics to prevent severe COVID-19 disease manifestations.

Identifiers

PMID35262096
PMCPMC8902889
OpenAlexW4214658745

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.