Evidence map›Paper›PMID 35568706›Full record

ArticleCell death & disease2022

Sex differences in global metabolomic profiles of COVID-19 patients.

Rocio Diaz Escarcega, Pedram Honarpisheh, Gabriela Delevati Colpo, Hilda W Ahnstedt, Lucy Couture, Shivanki Juneja, Glenda Torres, Guadalupe J Ortiz, James Sollome, Natalie Tabor and 5 more

Abstract read
In one paragraph

Article in Cell death & disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing 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

23 citing papers in PubMed.

  1. Article
  2. Host metabolic responses to SARS-CoV-2 and influenza viruses: parallels and contrasts.Metabolomics : Official journal of the Metabolomic Society · 2026
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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

15 authors.

Rocio Diaz Escarcega *Department of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Pedram Honarpisheh *Department of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Gabriela Delevati ColpoDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Hilda W AhnstedtDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Lucy CoutureDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.ORCID 0000-0002-1586-988X
Shivanki JunejaDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Glenda TorresDepartment of Neurosurgery, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Guadalupe J OrtizDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
James SollomeMetabolon, Inc., Morrisville, NC, USA.
Natalie TaborDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Bhanu P GaneshDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
H Alex ChoiDepartment of Neurosurgery, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Fudong LiuDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.
Louise D McCulloughDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA.ORCID 0000-0002-8050-1686
Andrey S TsvetkovDepartment of Neurology, the University of Texas McGovern Medical School at Houston, Houston, TX, USA. andrey.s.tsvetkov@uth.tmc.edu.ORCID 0000-0001-9749-9618

Funding

Sex specific immune response to SARS-CoV-2 leads to chronic neurologic symptomsR01MH127856 · NIMH · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI LIU, FUDONG, MCCULLOUGH, LOUISE D. · 2021 to 2025
$3.7M
G-quadruplex DNA in senescence of the neurovascular unitRF1AG068292 · NIA · UNIVERSITY OF TEXAS HLTH SCI CTR HOUSTON · PI MARRELLI, SEAN P, TSVETKOV, ANDREY · 2020 to 2020
$1.6M
NIA NIH HHS RF1 AG068292NIMH NIH HHS R01 MH127856
6 · The paper itself

Abstract

Coronavirus disease (COVID-19), caused by SARS-CoV-2, leads to symptoms ranging from asymptomatic disease to death. Although males are more susceptible to severe symptoms and higher mortality due to COVID-19, patient sex has rarely been examined. Sex-associated metabolic changes may implicate novel biomarkers and therapeutic targets to treat COVID-19. Here, using serum samples, we performed global metabolomic analyses of uninfected and SARS-CoV-2-positive male and female patients with severe COVID-19. Key metabolic pathways that demonstrated robust sex differences in COVID-19 groups, but not in controls, involved lipid metabolism, pentose pathway, bile acid metabolism, and microbiome-related metabolism of aromatic amino acids, including tryptophan and tyrosine. Unsupervised statistical analysis showed a profound sexual dimorphism in correlations between patient-specific clinical parameters and their global metabolic profiles. Identification of sex-specific metabolic changes in severe COVID-19 patients is an important knowledge source for researchers striving for development of potential sex-associated biomarkers and druggable targets for COVID-19 patients.

Indexed as

COVID-19SARS-CoV-2BiomarkersFemaleHumansMaleMetabolomicsSex CharacteristicsBiomarkers

Identifiers

PMID35568706
PMCPMC9106988

What Socratic 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 Socratic graph.