Evidence map›Paper›PMID 37425266›Full record

ArticleFrontiers in pediatrics2023

Monocyte anisocytosis corresponds with increasing severity of COVID-19 in children.

Abigail S Kane, Brittany P Boribong, Maggie Loiselle, Anagha P Chitnis, Hector Chavez, Lyle L Moldawer, Shawn D Larson, Oluwakemi Badaki-Makun, Daniel Irimia, Lael M Yonker

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 26% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Monocyte Anisocytosis Changes in Patients After Major Burn Injuries.Journal of burn care & research : official publication of the American Burn Association · 2025
    Article
  3. Review
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

10 authors at 6 institutions in 1 country.

Abigail S KaneDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.
Brittany P BoribongDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.
Maggie LoiselleDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.
Anagha P ChitnisMucosal Immunology and Biology Research Center, Massachusetts General Hospital, Boston, MA, United States.
Hector ChavezDepartment of Pediatrics, Jackson Memorial Hospital, Miami, FL, United States.
Lyle L MoldawerDepartment of Surgery, University of Florida, Gainesville, FL, United States.
Shawn D LarsonDepartment of Surgery, University of Florida, Gainesville, FL, United States.
Oluwakemi Badaki-MakunDepartment of Pediatrics, Johns Hopkins School of Medicine, Baltimore, MD, United States.
Daniel IrimiaDepartment of Pediatrics, Harvard Medical School, Boston, MA, United States.
Lael M YonkerDepartment of Pediatrics, Massachusetts General Hospital, Boston, MA, United States.
Massachusetts General Hospital · USHarvard University · USUniversity of Florida · USBurn Institute · USJackson Memorial Hospital · USJohns Hopkins University · US

Funding

Defining neutrophil pathobiology in pediatric Long COVIDR01HL173059 · NHLBI · UT SOUTHWESTERN MEDICAL CENTER · PI Lael Yonker · 2024 to 2026
$2.4M
NHLBI NIH HHS R01 HL173059
6 · The paper itself

Abstract

Introduction: Although SARS-CoV-2 infection can lead to severe COVID-19 in children, the role of biomarkers for assessing the risk of progression to severe disease is not well established in the pediatric population. Given the differences in monocyte signatures associated with worsening COVID-19 in adults, we aimed to determine whether monocyte anisocytosis early in the infectious course would correspond with increasing severity of COVID-19 in children. Methods: We performed a multicenter retrospective study of 215 children with SARS-CoV-2 infection, Multisystem Inflammatory Syndrome in Children (MIS-C), convalescent COVID-19, and healthy age-matched controls to determine whether monocyte anisocytosis, quantified by monocyte distribution width (MDW) on complete blood count, was associated with increasing severity of COVID-19. We performed exploratory analyses to identify other hematologic parameters in the inflammatory signature of pediatric SARS-CoV-2 infection and determine the most effective combination of markers for assessing COVID-19 severity in children. Results: Monocyte anisocytosis increases with COVID-19 severity and need for hospitalization. Although other inflammatory markers such as lymphocyte count, neutrophil/lymphocyte ratio, C-reactive protein, and cytokines correlate with disease severity, these parameters were not as sensitive as MDW for identifying severe disease in children. An MDW threshold of 23 offers a sensitive marker for severe pediatric COVID-19, with improved accuracy when assessed in combination with other hematologic parameters. Conclusion: Monocyte anisocytosis corresponds with shifting hematologic profiles and inflammatory markers in children with COVID-19, and MDW serves as a clinically accessible biomarker for severe COVID-19 in children.

Indexed as

monocyte anisocytosismonocyte distribution widthmultisystem inflammatory syndromepediatric COVID-19SARS-COV-2 infection

Identifiers

PMID37425266
PMCPMC10326545
OpenAlexW4381929713

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.