Evidence map›Paper›PMID 35864532›Full record

ArticleCardiovascular diabetology2022

Proteomic analysis of cardiometabolic biomarkers and predictive modeling of severe outcomes in patients hospitalized with COVID-19.

Philip H Schroeder, Laura N Brenner, Varinderpal Kaur, Sara J Cromer, Katrina Armstrong, Regina C LaRocque, Edward T Ryan, James B Meigs, Jose C Florez, Richelle C Charles and 2 more

Abstract read
In one paragraph

Article in Cardiovascular diabetology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Philip H SchroederDiabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Laura N BrennerCenter for Genomic Medicine, Massachusetts General Hospital, Boston, MA, USA.
Varinderpal KaurDiabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Sara J CromerDiabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Katrina ArmstrongDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Regina C LaRocqueDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Edward T RyanDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
James B MeigsPrograms in Metabolism and Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA, USA.
Jose C FlorezDiabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Richelle C CharlesDepartment of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Josep M Mercader *Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA.
Aaron Leong *Diabetes Unit, Endocrine Division, Department of Medicine, Massachusetts General Hospital, Boston, MA, USA. asleong@mgh.harvard.edu.

Funding

TRAINING PROGRAM IN ENDOCRINOLOGY AND DIABETEST32DK007028 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI Karen K Miller · 1986 to 2026
$18.5M
TOPMed Omics of Type 2 Diabetes and Quantitative TraitsUM1DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MANNING, ALISA KNODLE · 2021 to 2025
$3.8M
TOPMed Omics of Cardiovascular Disease in DiabetesR01HL151855 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2020 to 2023
$3.3M
Genetics, glycemic control and the microbiome in cystic fibrosisK23DK125839 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI BRENNER, LAURA N · 2020 to 2024
$1.1M
The Effect of Socioeconomic Status on Outcomes in Type 2 Diabetes Clinical TrialsF32DK127545 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CROMER, SARA JANE · 2020 to 2020
$76k
NCEZID CDC HHS U01 CK000490NCEZID CDC HHS U01 CK000633NHLBI NIH HHS R01 HL151855NIDDK NIH HHS F32 DK127545NIDDK NIH HHS K23 DK125839NIDDK NIH HHS T32 DK007028NIDDK NIH HHS UM1 DK078616
6 · The paper itself

Abstract

backgroundThe high heterogeneity in the symptoms and severity of COVID-19 makes it challenging to identify high-risk patients early in the disease. Cardiometabolic comorbidities have shown strong associations with COVID-19 severity in epidemiologic studies. Cardiometabolic protein biomarkers, therefore, may provide predictive insight regarding which patients are most susceptible to severe illness from COVID-19.

methodsIn plasma samples collected from 343 patients hospitalized with COVID-19 during the first wave of the pandemic, we measured 92 circulating protein biomarkers previously implicated in cardiometabolic disease. We performed proteomic analysis and developed predictive models for severe outcomes. We then used these models to predict the outcomes of out-of-sample patients hospitalized with COVID-19 later in the surge (N = 194).

resultsWe identified a set of seven protein biomarkers predictive of admission to the intensive care unit and/or death (ICU/death) within 28 days of presentation to care. Two of the biomarkers, ADAMTS13 and VEGFD, were associated with a lower risk of ICU/death. The remaining biomarkers, ACE2, IL-1RA, IL6, KIM1, and CTSL1, were associated with higher risk. When used to predict the outcomes of the future, out-of-sample patients, the predictive models built with these protein biomarkers outperformed all models built from standard clinical data, including known COVID-19 risk factors.

conclusionsThese findings suggest that proteomic profiling can inform the early clinical impression of a patient's likelihood of developing severe COVID-19 outcomes and, ultimately, accelerate the recognition and treatment of high-risk patients.

Indexed as

Cardiovascular DiseasesCOVID-19BiomarkersHumansProteomicsSARS-CoV-2BiomarkersCardiometabolic biomarkersCOVID-19Predictive modelingProteomics

Identifiers

PMID35864532
PMCPMC9301894

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.