Evidence map›Paper›PMID 38871359›Full record

ArticleThe Journal of infectious diseases2024

Interleukin-1 Receptor Antagonist Gene (IL1RN) Variants Modulate the Cytokine Release Syndrome and Mortality of COVID-19.

Mukundan Attur, Christopher Petrilli, Samrachana Adhikari, Eduardo Iturrate, Xiyue Li, Stephanie Tuminello, Nan Hu, Aravinda Chakravarti, David Beck, Steven B Abramson

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
  3. SARS-CoV-2 and Environmental Changes: The Perfect Storm.Current issues in molecular biology · 2024
    Review
  4. Article
  5. Article
  6. Article
  7. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Mukundan AtturDivision of Rheumatology, Department of Medicine, New York University Langone Orthopedic Hospital, New York University Langone Health, New York, New York, USA.ORCID 0000-0001-7080-8118
Christopher PetrilliDepartment of Medicine, New York University Grossman School of Medicine, New York University Langone Health, New York, New York, USA.
Samrachana AdhikariDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Eduardo IturrateDepartment of Medicine, New York University Grossman School of Medicine, New York University Langone Health, New York, New York, USA.
Xiyue LiDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Stephanie TuminelloDivision of Biostatistics, Department of Population Health, New York University Grossman School of Medicine, New York, New York, USA.
Nan HuCenter for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, New York, USA.
Aravinda ChakravartiDepartment of Medicine, New York University Grossman School of Medicine, New York University Langone Health, New York, New York, USA.
David BeckDepartment of Medicine, New York University Grossman School of Medicine, New York University Langone Health, New York, New York, USA.
Steven B AbramsonDepartment of Medicine, New York University Grossman School of Medicine, New York University Langone Health, New York, New York, USA.ORCID 0000-0002-0668-6344

Funding

Vaccine FacilityP30CA016087 · NCI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ADRIANA HEGUY · 1985 to 2026
$83.1M
Regulation of Inflammation by IL1RN polymorphismsR21AR078466 · NIAMS · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI ABRAMSON, STEVEN B · 2021 to 2022
$408k
NCI NIH HHS P30 CA016087NIAMS NIH HHS R21 AR078466NIH HHS R21-AR078466-01
6 · The paper itself

Abstract

backgroundWe examined effects of single-nucleotide variants (SNVs) of IL1RN, the gene encoding the anti-inflammatory interleukin 1 receptor antagonist (IL-1Ra), on the cytokine release syndrome (CRS) and mortality in patients with acute severe respiratory syndrome coronavirus 2 (SARS-CoV-2) infection.

methodsIL1RN CTA haplotypes formed from 3 SNVs (rs419598, rs315952, rs9005) and the individual SNVs were assessed for association with laboratory markers of inflammation and mortality. We studied 2589 patients hospitalized with SARS-CoV-2 between March 2020 and March 2021.

resultsMortality was 15.3% and lower in women than men (13.1% vs 17.3%, P = .0003). Carriers of the CTA-1/2 IL1RN haplotypes exhibited decreased inflammatory markers and increased plasma IL-1Ra. Evaluation of the individual SNVs of the IL1RN, carriers of the rs419598 C/C SNV exhibited significantly reduced inflammatory biomarker levels and numerically lower mortality compared to the C/T-T/T genotype (10.0% vs 17.8%, P = .052) in men, with the most pronounced association observed in male patients ≤74 years old, whose mortality was reduced by 80% (3.1% vs 14.0%, P = .030).

conclusionsThe IL1RN haplotype CTA and C/C variant of rs419598 are associated with attenuation of the CRS and decreased mortality in men with acute SARS-CoV-2 infection. The data suggest that the IL1RN pathway modulates the severity of coronavirus disease 2019 (COVID-19) via endogenous anti-inflammatory mechanisms.

Indexed as

COVID-19Cytokine Release SyndromeHaplotypesInterleukin 1 Receptor Antagonist ProteinPolymorphism, Single NucleotideSARS-CoV-2AdultAgedBiomarkersFemaleGenotypeHumansMaleMiddle AgedBiomarkersIL1RN protein, humanInterleukin 1 Receptor Antagonist Proteingenetic variation and mortalityIL1RNinflammationSARS-CoV-2

Identifiers

PMID38871359
PMCPMC11175666

What OpenQuestion holds

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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.