Association of Interleukin-32 and Interleukin-34 with Cardiovascular Disease and Short-Term Mortality in COVID-19

Author:

Kaufmann Christoph C.1,Ahmed Amro1,Muthspiel Marie1,Rostocki Isabella2,Pogran Edita1ORCID,Zweiker David13ORCID,Burger Achim Leo1,Jäger Bernhard1,Aicher Gabriele4,Spiel Alexander O.5ORCID,Vafai-Tabrizi Florian6,Gschwantler Michael78,Fasching Peter2,Wojta Johann91011,Huber Kurt1811

Affiliation:

1. 3rd Medical Department with Cardiology and Intensive Care Medicine, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

2. Department of Endocrinology and Rheumatology, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

3. Division of Cardiology, Medical University of Graz, 8036 Graz, Austria

4. Department of Laboratory Medicine, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

5. Department of Emergency Medicine, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

6. 2nd Medical Department with Pneumology and Karl-Landsteiner-Institute for Lung Research and Pulmonary Oncology, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

7. Department of Gastroenterology and Hepatology, Klinik Ottakring (Wilhelminenhospital), 1160 Vienna, Austria

8. Medical School, Sigmund Freud University, 1020 Vienna, Austria

9. Department of Internal Medicine 2, Division of Cardiology, Medical University of Vienna, 1090 Vienna, Austria

10. Core Facilities, Medical University of Vienna, 1090 Vienna, Austria

11. Ludwig Boltzmann Institute for CV Research, 1090 Vienna, Austria

Abstract

Background: Excess cardiovascular (CV) morbidity and mortality has been observed in patients with COVID-19. Both interleukin-32 (IL-32) and interleukin-34 (IL-34) have been hypothesized to contribute to CV involvement in COVID-19. Methods: This prospective, observational study of patients with laboratory-confirmed COVID-19 infection was conducted from 6 June to 22 December 2020 in a tertiary care hospital in Vienna, Austria. IL-32 and IL-34 levels on admission were collected and tested for their association with CV disease and short-term mortality in patients with COVID-19. CV disease was defined by the presence of coronary artery disease, heart failure, stroke or atrial fibrillation and patients were stratified by CV disease burden. Results: A total of 245 eligible patients with COVID-19 were included, of whom 37 (15.1%) reached the primary endpoint of 28-day mortality. Of the total sample, 161 had no CV disease (65.7%), 69 had one or two CV diseases (28.2%) and 15 patients had ≥three CV diseases (6.1%). Median levels of IL-32 and IL-34 at admission were comparable across the three groups of CV disease burden. IL-32 and IL-34 failed to predict mortality upon both univariable and multivariable Cox regression analysis. The two CV disease groups, however, had a significantly higher risk of mortality within 28 days (one or two CV diseases: crude HR 4.085 (95% CI, 1.913–8.725), p < 0.001 and ≥three CV diseases: crude HR 13.173 (95% CI, 5.425–31.985), p < 0.001). This association persisted for those with ≥three CV diseases after adjustment for age, gender and CV risk factors (adjusted HR 3.942 (95% CI, 1.288–12.068), p = 0.016). Conclusion: In our study population of hospitalized patients with COVID-19, IL-32 and IL-34 did not show any associations with CV disease or 28-day mortality in the context of COVID-19. Patients with multiple CV diseases, however, had a significantly increased risk of short-term mortality.

Funder

Bürgermeisterfond der Stadt Wien

Association for the Promotion of Research on Arteriosclerosis, Thrombosis, and Vascular Biology

Ludwig Boltzmann Cluster for CV Research

Publisher

MDPI AG

Subject

General Medicine

Reference44 articles.

1. Covid-19—Navigating the Uncharted;Fauci;N. Engl. J. Med.,2020

2. Unexpected Detection of SARS-CoV-2 Antibodies in the Prepandemic Period in Italy;Apolone;Tumori,2021

3. The Socio-Economic Implications of the Coronavirus Pandemic (COVID-19): A Review;Nicola;Int. J. Surg.,2020

4. (2023, January 20). WHO Coronavirus (COVID-19) Dashboard. Available online: https://covid19.who.int.

5. Cardiac Involvement of COVID-19: A Comprehensive Review;Chang;Am. J. Med. Sci.,2021

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