Evidence map›Paper›PMID 38111002›Full record

ArticleImmunity & ageing : I & A2023

Blood circulating bacterial DNA in hospitalized old COVID-19 patients.

Robertina Giacconi, Patrizia D'Aquila, Maurizio Cardelli, Francesco Piacenza, Elisa Pierpaoli, Giada Sena, Mirko Di Rosa, Anna Rita Bonfigli, Roberta Galeazzi, Antonio Cherubini and 9 more

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. 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

19 authors at 4 institutions in 1 country.

Robertina GiacconiAdvanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy.
Patrizia D'AquilaDepartment of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy.
Maurizio CardelliAdvanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy.
Francesco PiacenzaAdvanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy.
Elisa PierpaoliAdvanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy.
Giada SenaDepartment of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy.
Mirko Di RosaUnit of Geriatric Pharmacoepidemiology and Biostatistics, IRCCS INRCA, Ancona, Italy.
Anna Rita BonfigliScientific Direction, IRCCS INRCA, Ancona, Italy.
Roberta GaleazziClinical Laboratory and Molecular Diagnostic, Italian National Research Center On Aging, IRCCS INRCA, Ancona, Italy.
Antonio CherubiniGeriatria, Accettazione Geriatrica e Centro Di Ricerca Per L'invecchiamento, IRCCS INRCA, Ancona, Italy.
Massimiliano FedecostanteGeriatria, Accettazione Geriatrica e Centro Di Ricerca Per L'invecchiamento, IRCCS INRCA, Ancona, Italy.
Riccardo SarzaniDepartment of Clinical and Molecular Sciences, Università Politecnica Delle Marche, Ancona, Italy, Internal Medicine and Geriatrics, Italian National Research Centre On Aging, Hospital "U. Sestilli", IRCCS INRCA, Ancona, Italy.
Chiara Di PentimaDepartment of Clinical and Molecular Sciences, Università Politecnica Delle Marche, Ancona, Italy, Internal Medicine and Geriatrics, Italian National Research Centre On Aging, Hospital "U. Sestilli", IRCCS INRCA, Ancona, Italy.
Piero GiordanoDepartment of Clinical and Molecular Sciences, Università Politecnica Delle Marche, Ancona, Italy, Internal Medicine and Geriatrics, Italian National Research Centre On Aging, Hospital "U. Sestilli", IRCCS INRCA, Ancona, Italy.
Roberto AntonicelliCardiology Unit, IRCCS INRCA, Ancona, Italy.
Fabrizia LattanzioScientific Direction, IRCCS INRCA, Ancona, Italy.
Giuseppe PassarinoDepartment of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy.
Mauro Provinciali *Advanced Technology Center for Aging Research, IRCCS INRCA, Ancona, Italy.
Dina Bellizzi *Department of Biology, Ecology and Earth Sciences, University of Calabria, 87036, Rende, Italy. dina.bellizzi@unical.it.
Istituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Calabria · ITMarche Polytechnic University · ITIstituto Nazionale di Riposo e Cura per Anziani · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronavirus disease COVID-19 is a heterogeneous condition caused by SARS-CoV-2 infection. Generally, it is characterized by interstitial pneumonia that can lead to impaired gas-exchange, acute respiratory failure, and death, although a complex disorder of multi-organ dysfunction has also been described. The pathogenesis is complex, and a variable combination of factors has been described in critically ill patients. COVID-19 is a particular risk for older persons, particularly those with frailty and comorbidities. Blood bacterial DNA has been reported in both physiological and pathological conditions and has been associated with some haematological and laboratory parameters but, to date, no study has characterized it in hospitalized old COVID-19 patients The present study aimed to establish an association between blood bacterial DNA (BB-DNA) and clinical severity in old COVID-19 patients.

resultsBB-DNA levels were determined, by quantitative real-time PCRs targeting the 16S rRNA gene, in 149 hospitalized older patients (age range 65-99 years) with COVID-19. Clinical data, including symptoms and signs of infection, frailty status, and comorbidities, were assessed. BB-DNA was increased in deceased patients compared to discharged ones, and Cox regression analysis confirmed an association between BB-DNA and in-hospital mortality. Furthermore, BB-DNA was positively associated with the neutrophil count and negatively associated with plasma IFN-alpha. Additionally, BB-DNA was associated with diabetes.

conclusionsThe association of BB-DNA with mortality, immune-inflammatory parameters and diabetes in hospitalized COVID-19 patients suggests its potential role as a biomarker of unfavourable outcomes of the disease, thus it could be proposed as a novel prognostic marker in the assessment of acute COVID-19 disease.

Indexed as

AgingCirculating bacterial DNACOVID-19HospitalizationInflammationMortality

Identifiers

PMID38111002
PMCPMC10726536
OpenAlexW4389887687

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.