Evidence map›Paper›PMID 34255304›Full record

ReviewJournal of racial and ethnic health disparities2022

SARS-CoV-2 Infection and Racial Disparities in Children: Protective Mechanisms and Severe Complications Related to MIS-C.

Sanjana Kurup, Regan Burgess, Fatou Tine, Ann Chahroudi, Dexter L Lee

Open access · hybridAbstract readReview
In one paragraph

Review in Journal of racial and ethnic health disparities, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.4field-weighted citation impact, top 5% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

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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

5 authors at 2 institutions in 1 country.

Sanjana Kurup *Department of Physiology and Biophysics, Howard University College of Medicine, 520 W Street, NW, Washington, DC, 20059, USA.
Regan Burgess *Department of Physiology and Biophysics, Howard University College of Medicine, 520 W Street, NW, Washington, DC, 20059, USA.
Fatou Tine *Department of Physiology and Biophysics, Howard University College of Medicine, 520 W Street, NW, Washington, DC, 20059, USA.
Ann ChahroudiDepartment of Pediatrics, Emory University School of Medicine, Atlanta, GA, 30322, USA.
Dexter L LeeDepartment of Physiology and Biophysics, Howard University College of Medicine, 520 W Street, NW, Washington, DC, 20059, USA. dllee@Howard.edu.ORCID 0000-0001-6282-7079
Howard University · USEmory University · US

Funding

Sleep Disorders in Adults with Sickle Cell Disease: Frequency, Associations with Cardiovascular and Pain Indicators, and Responses to TreatmentU54MD007597 · NIMHD · HOWARD UNIVERSITY · PI William M. Southerland · 2019 to 2026
$37.7M
The Role of PPAR-alpha during Angiotensin II HypertensionK01HL092593 · NHLBI · HOWARD UNIVERSITY · PI LEE, DEXTER L · 2008 to 2012
$576k
NHLBI NIH HHS K01 HL092593NIMHD NIH HHS U54 MD007597
6 · The paper itself

Abstract

A novel coronavirus has resulted in a pandemic with over 176 million confirmed cases and over 3.8 million recorded deaths. In the USA, SARS-CoV-2 infection has a significant burden on minority communities, especially Hispanic and Black communities, which are overrepresented in cases compared to their percentage in the population. SARS-CoV-2 infection can manifest differently in children and adults, with children tending to have less severe disease. A review of current literature was performed to identify the hypothesized protective immune mechanisms in children, and to describe the rare complication of multisystem inflammatory syndrome in children (MIS-C) that has been documented in children post-SARS-CoV-2 infection. Epidemiologic data and case studies have indicated that children are less susceptible to more severe clinical features of SARS-CoV-2 infection, a finding that may be due to differences in the cytokine response generated by the innate immune system, high amounts of ACE-2 which maintain homeostatic functions by preventing inflammation, and trained immunity acquired from regular vaccinations. Despite these protective mechanisms, children are still susceptible to severe complications, such as MIS-C. The racial disparities seen in MIS-C are extremely apparent, and certain populations are more affected. Most specifically, 33% of MIS-C patients are Hispanic/Latino, and 30% Black. Current studies published on MIS-C do not detail whether certain symptoms are more present in certain racial/ethnic groups. Knowledge of these disparities could assist health care professionals with devising appropriate strategies for post-acute SARS-CoV-2 infection follow-up in children as well as vaccine distribution in specific communities to help slow the spread of SARS-CoV-2 infection, and ultimately reduce the potential for complications such as MIS-C.

Indexed as

COVID-19ChildHumansPandemicsSARS-CoV-2Systemic Inflammatory Response SyndromeHealth disparitiesKawasaki DiseaseMIS-CPediatricsSARS-CoV-2

Identifiers

PMID34255304
PMCPMC8276539
OpenAlexW3181503570

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.