Evidence map›Paper›PMID 37249281›Full record

ArticleImmunity, inflammation and disease2023

HIV and inflammatory markers are associated with persistent COVID-19 symptoms.

Patrick Kamanzi, Gina Mulundu, Keagan Mutale, Chibamba Mumba, Owen Ngalamika

Open access · goldAbstract read
In one paragraph

Article in Immunity, inflammation and disease, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 pooled it
2.5field-weighted citation impact, top 10% 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

8 citing papers in PubMed, 2 syntheses or guidelines pooled it, 12 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Observational
  6. Review
  7. Article
  8. 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

5 authors at 2 institutions in 1 country.

Patrick KamanziDermatology and Venereology Division, Department of Medicine, University of Teaching Hospital, University of Zambia School of Medicine, Lusaka, Zambia.
Gina MulunduDepartment of Pathology and Microbiology, University of Teaching Hospital, University of Zambia School of Medicine, Lusaka, Zambia.
Keagan MutaleHHV-8 Molecular Virology Laboratory, University Teaching Hospital, Lusaka, Zambia.
Chibamba MumbaDepartment of Pathology and Microbiology, University of Teaching Hospital, University of Zambia School of Medicine, Lusaka, Zambia.
Owen NgalamikaDermatology and Venereology Division, Department of Medicine, University of Teaching Hospital, University of Zambia School of Medicine, Lusaka, Zambia.ORCID 0000-0002-0648-4128
University of Zambia · ZMUniversity Teaching Hospital · ZM

Funding

Zambia AIDS Malignancies Diagnosis and Pathogenesis Program SupplementU54CA221204 · NCI · UNIVERSITY OF NEBRASKA LINCOLN · PI WOOD, CHARLES · 2017 to 2022
$3.8M
Biomarkers of Kaposi sarcoma recrudescence in ZambiaK43TW011095 · FIC · UNIVERSITY OF ZAMBIA · PI NGALAMIKA, OWEN · 2018 to 2023
$721k
FIC NIH HHS K43 TW011095NCI NIH HHS U54 CA221204
6 · The paper itself

Abstract

backgroundA proportion of COVID19 survivors may present with long-COVID, which is persistent symptoms lasting four or more weeks post SARS-CoV-2 infection. These symptoms may be mild to severe, and may affect different organ-systems of the body.

aimsThe main objective of this study was to determine the demographic, clinical and immunological factors associated with long COVID. MATERIALS &

methodsWe conducted a nested case control study, with a total of 94 study participants initially included, and 64 participants matched for age and sex for biomarker analyses.

results32/94 (34.1%) of all the participants had long COVID. Respiratory symptoms were the most common (59.5%) followed by the musculoskeletal symptoms (28.1%). HIV was an independent predictor of long COVID (adjusted odds ratio = 2.7; p = .037). In all the 64 matched cases and controls, IFN-β was significantly higher among controls than cases. After stratifying by HIV, IL6 was significantly higher among cases than controls in the HIV- group (2.06 vs. 0.81 pg/mL; p = .02). On the other hand, IFN-β was significantly higher among controls than cases in the HIV+ group (251 vs. 0 pg/mL; p = .01).

conclusionHIV infection is a risk factor for long COVID, and inflammatory markers associated with long COVID may be slightly different for HIV- and HIV+ individuals.

Indexed as

COVID-19HIV InfectionsCase-Control StudiesHumansPost-Acute COVID-19 SyndromeSARS-CoV-2biomarkerHIVimmunological factorslong COVID

Identifiers

PMID37249281
PMCPMC10165949
OpenAlexW4378744989

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.