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. 2025 Apr 17;15(1):13245.
doi: 10.1038/s41598-025-93402-w.

Sex and other predictors of mortality in long-term follow-up of patients with cardiovascular disease and COVID-19: a single-center retrospective study

Collaborators, Affiliations

Sex and other predictors of mortality in long-term follow-up of patients with cardiovascular disease and COVID-19: a single-center retrospective study

Maryla Kocowska-Trytko et al. Sci Rep. .

Abstract

Male sex is a well-known predictor of short-term prognosis in patients with coronavirus disease (COVID-19). Data, however, on long-term outcomes are scarce. We aimed to assess the differences in mortality between sexes and find other important predictors of survival from a long-term perspective. Data from all patients retrieved from a database of COVID-19 patients hospitalized at University Hospital in Krakow, Poland, between February 13, 2020, and May 10, 2021, were analyzed for clinical in-hospital data and after a 42 months follow-up period. Of the 4071 COVID-19 patients hospitalized, 2183 were men (53.6%). Males were on average younger and more likely to have concomitant chronic obstructive pulmonary disease, heart failure, coronary artery disease (including acute and chronic coronary syndrome) compared to women. In terms of laboratory findings, more advanced inflammatory markers and troponin I were predominantly observed in male patients than in female patients. Males were found to have a greater predisposition for relevant cardiovascular comorbidities and were more likely to have died during the 42 months follow-up. Additionally, higher levels of troponin I, N-terminal pro B-type natriuretic peptide and D-dimer were associated with a greater risk of death. Kaplan-Meier survival analyses revealed a worse 42 months survival for men up to the age of 65 years. Cardiovascular comorbidities, male sex and older age, as well as higher concentrations of markers indicating a thrombotic state and myocardial injury, were associated with poorer long-term prognosis in patients with COVID-19.

Keywords: COVID-19; Cardiovascular comorbidities; Outcome; Sex.

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Conflict of interest statement

Declarations. Competing interests: The authors declare no competing interests. Ethics approval: The study was a retrospective analysis of the medical records of discharged patients and did not affect patient safety or the occurrence of possible complications, therefore obtaining consent from the study participants was not necessary. The study was conducted in accordance with the guidelines of the Declaration of Helsinki and with the aforementioned methodology was approved by the Bioethics Committee of Jagiellonian University in Krakow (Poland) (decision number 1072.6120.278.2020). The authors confirm that the obtaining of informed consent from the study participants was waived by the Bioethics Committee of the Jagiellonian University in Krakow (Poland). Consent for publication: Not applicable.

Figures

Fig. 1
Fig. 1
Flowchart of the study.
Fig. 2
Fig. 2
Multiple Cox regressions demonstrating the hazard ratios for the 42 months mortality in model including comorbidities and demographic data. Abbreviations: HR, hazard ratio.
Fig. 3
Fig. 3
Kaplan‒Meier curves depicting proportional survival rates at the 42 months follow-up stratified by sex in the whole group (a) and in the age subgroups (b, c).
Fig. 4
Fig. 4
ROC curves to establish cutoff points for troponin I, N-terminal pro-B-type natriuretic peptide, D-dimer, C-reactive protein and interleukin-6 as predictors of 42 months mortality.
Fig. 5
Fig. 5
Multiple Cox regressions demonstrating the hazard ratios for 42 months mortality in the model with laboratory tests. Abbreviations: CRP, C-reactive protein; HR, hazard ratio; NT-proBNP, N-terminal pro-B-type natriuretic peptide.
Fig. 6
Fig. 6
Kaplan‒Meier curves displaying proportional survival rate at the 42 months follow-up stratified by the levels of troponin I (a), NT-proBNP (b), D-dimer (c), CRP (d), and interleukin-6 (e). Abbreviations: CRP, C-reactive protein; NT-proBNP, N-terminal pro B-type natriuretic peptide; IL-6, interleukin-6; TnI, troponin I.

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