Evidence map›Paper›PMID 37598150›Full record

ArticleBMC public health2023

Health disparities in COVID-19: immune and vascular changes are linked to disease severity and persist in a high-risk population in Riverside County, California.

Kristina V Bergersen, Kathy Pham, Jiang Li, Michael T Ulrich, Patrick Merrill, Yuxin He, Sumaya Alaama, Xinru Qiu, Indira S Harahap-Carrillo, Keita Ichii and 5 more

Open access · goldAbstract read
In one paragraph

Article in BMC public health, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 11% 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, 12 citations in OpenAlex.

  1. Observational
  2. Article
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  4. Review
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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

15 authors at 3 institutions in 1 country.

Kristina V Bergersen *Division of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Kathy Pham *Division of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Jiang Li *Division of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Michael T Ulrich *Riverside University Health System Medical Center, Riverside, CA, U.S.
Patrick MerrillKaiser Permanente Riverside Medical Center, Riverside, CA, U.S.
Yuxin HeDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Sumaya AlaamaDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Xinru QiuDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Indira S Harahap-CarrilloDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Keita IchiiDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Shyleen FrostDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Marcus KaulDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Adam GodzikDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.
Erica C HeinrichDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.. erica.heinrich@medsch.ucr.edu.
Meera G NairDivision of Biomedical Sciences, School of Medicine, University of California Riverside, Riverside, CA, U.S.. meera.nair@medsch.ucr.edu.
University of California, Riverside · USKaiser Permanente Riverside Medical Center · USRiverside University Health System - Medical Center · US

Funding

Research Infrastructure CoreU54MD013368 · NIMHD · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI AYON, CECILIA · 2019 to 2023
$15.9M
Methamphetamine Effect on HIV PersistenceR01DA052209 · NIDA · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI KAUL, MARCUS · 2020 to 2024
$3.2M
Illumina NovaSeq 6000 Sequencing SystemS10OD026929 · OD · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI JEPSEN, KRISTEN LYNN · 2019 to 2019
$600k
NIDA NIH HHS R01 DA052209NIH HHS S10 OD026929NIMHD NIH HHS U54 MD013368
6 · The paper itself

Abstract

backgroundHealth disparities in underserved communities, such as inadequate healthcare access, impact COVID-19 disease outcomes. These disparities are evident in Hispanic populations nationwide, with disproportionately high infection and mortality rates. Furthermore, infected individuals can develop long COVID with sustained impacts on quality of life. The goal of this study was to identify immune and endothelial factors that are associated with COVID-19 outcomes in Riverside County, a high-risk and predominantly Hispanic community, and investigate the long-term impacts of COVID-19 infection.

methods112 participants in Riverside County, California, were recruited according to the following criteria: healthy control (n = 23), outpatients with moderate infection (outpatient, n = 33), ICU patients with severe infection (hospitalized, n = 33), and individuals recovered from moderate infection (n = 23). Differences in outcomes between Hispanic and non-Hispanic individuals and presence/absence of co-morbidities were evaluated. Circulating immune and vascular biomarkers were measured by ELISA, multiplex analyte assays, and flow cytometry. Follow-up assessments for long COVID, lung health, and immune and vascular changes were conducted after recovery (n = 23) including paired analyses of the same participants.

resultsCompared to uninfected controls, the severe infection group had a higher proportion of Hispanic individuals (n = 23, p = 0.012) than moderate infection (n = 8, p = 0.550). Disease severity was associated with changes in innate monocytes and neutrophils, lymphopenia, disrupted cytokine production (increased IL-8 and IP-10/CXCL10 but reduced IFNλ2/3 and IFNγ), and increased endothelial injury (myoglobin, VCAM-1). In the severe infection group, a machine learning model identified LCN2/NGAL, IL-6, and monocyte activation as parameters associated with fatality while anti-coagulant therapy was associated with survival. Recovery from moderate COVID infection resulted in long-term immune changes including increased monocytes/lymphocytes and decreased neutrophils and endothelial markers. This group had a lower proportion of co-morbidities (n = 8, p = 1.0) but still reported symptoms associated with long COVID despite recovered pulmonary function.

conclusionThis study indicates increased severity of COVID-19 infection in Hispanic individuals of Riverside County, California. Infection resulted in immunological and vascular changes and long COVID symptoms that were sustained for up to 11 months, however, lung volume and airflow resistance was recovered. Given the immune and behavioral impacts of long COVID, the potential for increased susceptibility to infections and decreased quality of life in high-risk populations warrants further investigation.

Indexed as

COVID-19CaliforniaHumansPatient AcuityPost-Acute COVID-19 SyndromeQuality of LifeCOVID-19Health disparitiesHispanicImmunologyLong COVIDSevere infection

Identifiers

PMID37598150
PMCPMC10439554
OpenAlexW4385999239

What Socratic 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 Socratic graph.