Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Age, host response, and mortality in COVID-19

1 Jul 2023

Abstract excerpt

Tweetable abstract Increased age is a strong risk factor for mortality in patients with COVID-19. Understanding the dynamic changes in plasma biomarkers associated with age is crucial for unravelling the intricate interplay between ageing, immune response and outcomes.https://bit.ly/3BWgSjP

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to COVID-19 Clinical Research Studies
Share to Long-Term Effects of COVID-19
Share to Respiratory Support and Mechanisms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 37419522
DOI: 10.1183/13993003.00796-2023

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Age, host response, and mortality in COVID-19PMID 37419522Read ↗

Identifying Age-Related Risk Factors in COVID-19 Independent of Disease SeveritySemantic proximity Read ↗

Longitudinal analyses reveal age-specific immune correlates of COVID-19 severitySemantic proximity Read ↗

Age-severity matched cytokine profiling reveals specific signatures in Covid-19 patientsSemantic proximity Read ↗

Host-Microbe Multiomic Profiling Reveals Age-Dependent COVID-19 ImmunopathologySemantic proximity Read ↗

Host-microbe multiomic profiling reveals age-dependent immune dysregulation associated with COVID-19 immunopathologySemantic proximity Read ↗

A time-resolved proteomic and diagnostic map characterizes COVID-19 disease progression and predicts outcomeSemantic proximity Read ↗

T-cell cellular stress and reticulocyte signatures, but not loss of naïve T lymphocytes, characterize severe COVID-19 in older adultsSemantic proximity Read ↗

A human circulating immune cell landscape in aging and COVID-19Semantic proximity Read ↗

Patients with moderate to severe COVID-19 have an impaired cytokine response with an exhausted and senescent immune phenotype.Semantic proximity Read ↗

Enhanced immune ageing associated with increasing COVID-19 disease severitySemantic proximity Read ↗

Aging-related cell type-specific pathophysiologic immune responses that exacerbate disease severity in aged COVID-19 patientsSemantic proximity Read ↗

Biological Aging, Immune Phenotypes, and Susceptibility to COVID-19 and Sepsis: A Mendelian Randomization Study.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.