Evidence map›Paper›PMID 35942057›Full record

ArticleFrontiers in cellular and infection microbiology2022

Multiethnic Investigation of Risk and Immune Determinants of COVID-19 Outcomes.

Tomi Jun, Divij Mathew, Navya Sharma, Sharon Nirenberg, Hsin-Hui Huang, Patricia Kovatch, Edward John Wherry, Kuan-Lin Huang

Abstract read
In one paragraph

Article in Frontiers in cellular and infection microbiology, 2022. 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

5 · Who and what money

Authors and funding

8 authors.

Tomi JunDivision of Hematology and Medical Oncology, Tisch Cancer Institute, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Divij MathewInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.
Navya SharmaUniversity of California, Santa Barbara, Santa Barbara, CA, United States.
Sharon NirenbergScientific Computing, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Hsin-Hui HuangDepartment of Population Health Science and Policy, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Patricia KovatchScientific Computing, Icahn School of Medicine at Mount Sinai, New York, NY, United States.
Edward John WherryInstitute for Immunology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA, United States.
Kuan-Lin HuangDepartment of Genetics and Genomic Sciences, Center for Transformative Disease Modeling, Tisch Cancer Institute, Icahn Institute for Data Science and Genomic Technology, Icahn School of Medicine at Mount Sinai, New York, NY, United States.

Funding

Integrative Approaches for Identifying Causal Gene-Cell Type Pairs of Complex DiseaseR35GM138113 · NIGMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI Kuan-lin Huang · 2020 to 2026
$3.0M
NIGMS NIH HHS R35 GM138113
6 · The paper itself

Abstract

Background: Disparate COVID-19 outcomes have been observed between Hispanic, non-Hispanic Black, and White patients. The underlying causes for these disparities are not fully understood. Methods: This was a retrospective study utilizing electronic medical record data from five hospitals within a single academic health system based in New York City. Multivariable logistic regression models were used to identify demographic, clinical, and lab values associated with in-hospital mortality. Results: A total of 3,086 adult patients with self-reported race/ethnicity information presenting to the emergency department and hospitalized with COVID-19 up to April 13, 2020, were included in this study. While older age (multivariable odds ratio (OR) 1.06, 95% CI 1.05-1.07) and baseline hypoxia (multivariable OR 2.71, 95% CI 2.17-3.36) were associated with increased mortality overall and across all races/ethnicities, non-Hispanic Black (median age 67, interquartile range (IQR) 58-76) and Hispanic (median age 63, IQR 50-74) patients were younger and had different comorbidity profiles as compared to non-Hispanic White patients (median age 73, IQR 62-84; p < 0.05 for both comparisons). Among inflammatory markers associated with COVID-19 mortality, there was a significant interaction between the non-Hispanic Black population and interleukin-1-beta (interaction p-value 0.04). Conclusions: This analysis of a multiethnic cohort highlights the need for inclusion and consideration of diverse populations in ongoing COVID-19 trials targeting inflammatory cytokines.

Indexed as

COVID-19AdultAgedBlack or African AmericanHumansMiddle AgedRetrospective StudiesSARS-CoV-2White PeopleAfrican AmericanCOVID-19electronic medical recordinterleukin-1betarisk factors

Identifiers

PMID35942057
PMCPMC9355800

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Registered trials

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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.