Evidence map›Paper›PMID 39507451›Full record

ArticleAnnals of translational medicine2024

Association between sore throat and early immune responses against COVID-19 before and after the emergence of the Omicron variant.

Yusuke Takegoshi, Kentaro Nagaoka, Toshiki Kido, Hitoshi Kawasuji, Yushi Murai, Makito Kaneda, Kou Kimoto, Hideki Tani, Hideki Niimi, Yoshitomo Morinaga and 1 more

Abstract read
In one paragraph

Article in Annals of translational medicine, 2024. 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
–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

2 citing papers in PubMed.

  1. Article
  2. Article
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

11 authors.

Yusuke TakegoshiDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Kentaro NagaokaDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.ORCID https://orcid.org/0000-0003-3484-4554
Toshiki KidoFirst Department of Internal Medicine, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Hitoshi KawasujiDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Yushi MuraiDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Makito KanedaDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Kou KimotoDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.
Hideki TaniDepartment of Virology, Toyama Institute of Health, Toyama, Japan.
Hideki NiimiClinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan.
Yoshitomo MorinagaClinical and Research Center for Infectious Diseases, Toyama University Hospital, Toyama, Japan.
Yoshihiro YamamotoDepartment of Clinical Infectious Diseases, Graduate School of Medicine and Pharmaceutical Sciences, Toyama University, Toyama, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Sore throat is a prevalent symptom of coronavirus disease 2019 (COVID-19), particularly when caused by the Omicron variants. However, the association between sore throat and immune responses to different severe acute respiratory syndrome coronavirus 2 variants remains unclear. This study aimed to elucidate the characteristics of immune responses associated with sore throat in patients with COVID-19 before and after the emergence of Omicron. Methods: In this prospective observational study, we enrolled patients with COVID-19 hospitalized between December 2020 and April 2022, which covered the pre-Omicron and Omicron (BA.1 variant) endemic periods. Sore throat was assessed using a daily questionnaire, including an analog scale for sore throat grade (0 to 3) from admission until discharge. Serum levels of immune indicators were assessed using enzyme-linked immunosorbent assay. Results: A total of 47 patients infected with Omicron and 136 patients infected with preceding variants were included in the analyses. The frequency of sore throat was significantly higher in participants infected with Omicron than that in those infected with preceding variants (66% Conclusions: Infection with the Omicron variant is characterized by increased sore throat frequency and altered associations between sore throat and several immune indicators, including IFN-α, IL-6, and IFN-λ1.

Indexed as

Coronavirus disease 2019 (COVID-19)immune responsesevere acute respiratory syndrome coronavirus 2 (SARS-CoV-2)sore throat

Identifiers

PMID39507451
PMCPMC11534754

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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.