Evidence map›Paper›PMID 42851349›Full record

ArticleFrontiers in cellular and infection microbiology2026

Association between the glucose-to-lymphocyte ratio and prognosis in COVID-19 patients.

Cong Shi, Shengping Gong

Abstract read
In one paragraph

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

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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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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

Corrections and comments

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5 · Who and what money

Authors and funding

2 authors.

Cong ShiStem Cell Laboratory, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.
Shengping GongCancer Radiotherapy and Chemotherapy Center, The First Affiliated Hospital of Ningbo University, Ningbo, Zhejiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The coronavirus disease 2019 (COVID-19) pandemic has transitioned into an endemic stage and is no longer classified as a public health emergency of international concern. Nevertheless, the persistent emergence of novel variants with enhanced transmissibility and immune evasion potential suggests that the disease burden associated with COVID-19 remains substantial. This retrospective cohort enrolled 235 hospitalized COVID-19 patients infected during the Omicron BA.5 and BF.7 wave from December 29, 2022 to January 15, 2023. The prognostic value of biomarkers based on combined fasting glucose and lymphocyte counts in patients with COVID-19 has not been fully clarified. We measured inflammatory markers, the metabolic marker, and T-cell immune parameters to validate our Methods: We retrospectively analyzed a cohort of 235 individuals with COVID-19 to explore the prognostic value of GLR levels at diagnosis. All patients were followed up until the unified cutoff date of February 18, 2023, with all-cause mortality set as the primary endpoint. Two separate grouping methods were used: GLR stratification for evaluating its independent predictive ability, and severity grouping (mild-to-moderate vs severe) as clinical reference. The two groups only partially overlapped, so high GLR is not equivalent to severe illness. Patients were stratified into high GLR and low GLR groups. Overall survival (OS) was estimated via the Kaplan-Meier method and compared using the log-rank test. Results: Our findings revealed that GLR levels were significantly higher in severe patients than in mild-to-moderate patients. Meanwhile, beta2-microglobulin (β2-MG), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), and interleukin-10 (IL-10) were significantly elevated in the high GLR group, whereas apolipoprotein A1 (ApoA1), CD3 absolute value, CD4 absolute value, and CD8 absolute value were significantly lower. Furthermore, patients with high GLR levels exhibited significantly shorter OS ( Conclusions: Our data confirmed that GLR levels at initial diagnosis were significantly correlated with disease severity and prognosis in patients with COVID-19. As an easily calculated metabolic-immune indicator, GLR acts as a promising complementary candidate biomarker for mortality risk stratification in Omicron COVID-19 patients; further independent external validation is required before its routine clinical application.

Indexed as

Blood GlucoseCOVID-19LymphocytesAgedBiomarkersFemaleHumansLymphocyte CountMaleMiddle AgedPrognosisRetrospective StudiesSARS-CoV-2Severity of Illness IndexBiomarkersBlood GlucoseCOVID-19glucose-to-lymphocyte ratiohospitalizedmortalityprognosis

Identifiers

PMID42851349
PMCPMC13645524

What Socratic holds

Textmetadata
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Registered trials

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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 Socratic graph.