Evidence map›Paper›PMID 41907243›Full record

ArticleFrontiers in medicine2026

Dysregulated metabolic homeostasis as a unifying death mechanism underlying the diverse clinical manifestations of COVID-19: insights from a retrospective analysis of sequential blood variables.

Zvia Agur, Yuri Kogan, Anat Ben Yaacov, Edward Itelman, Gad Segal

Abstract read
In one paragraph

Article in Frontiers in medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
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0citing papers in PubMed
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1 · What the graph read from it

What it found

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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Zvia AgurInstitute for Medical Biomathematics, Bene Ataroth, Israel.
Yuri KoganInstitute for Medical Biomathematics, Bene Ataroth, Israel.
Anat Ben YaacovInstitute for Medical Biomathematics, Bene Ataroth, Israel.
Edward ItelmanDepartment of Internal Medicine, Chaim Sheba Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Gad SegalDepartment of Internal Medicine, Chaim Sheba Medical Center, Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: COVID-19 presents diverse clinical manifestations associated with increased mortality, yet a unifying death mechanism remains elusive; here, we suggest such a mechanism that implies a simple way to lower deaths. This work differs from previous studies that use machine learning to identify mortality predictors. Methods: Viewing clinical deterioration to a severe stage as a distinct "junction" in disease progression, we collected 173 medical records of COVID-19 patients who deteriorated and divided them into two groups: those who died (nonsurvivors) and those who recovered after deterioration (survivors). We aligned patients' medical records by clinical deterioration time and statistically compared the two groups using standard blood variables. Results: Significant differences between the groups emerged only in the first week after clinical deterioration: nonsurvivors showed a rapid, simultaneous rise in lactate dehydrogenase ( Conclusion: Our findings highlight the importance of timing in COVID-19 treatment. Using an available machine learning algorithm to predict imminent deterioration enables prompt, short-term intervention with prophylactic mechanical ventilation and optimal antiglycolytic therapy. Implementing this approach requires further experimental and clinical validation. Identifying metabolism-related genetic or epigenetic anomalies in nonsurvivors will support our hypothesis and aid in classifying the high-risk patients.

Indexed as

ARDSglycolysishemostasishypercoagulabilitylactic acidosismetabolic homeostasismetabolic reprogrammingmitochondriopathy

Identifiers

PMID41907243
PMCPMC13017333

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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.