Association of renalase with clinical outcomes in hospitalized patients with COVID-19
Open Access
- 8 March 2022
- journal article
- research article
- Published by Public Library of Science (PLoS) in PLOS ONE
- Vol. 17 (3) , e0264178
Abstract
Renalase is a secreted flavoprotein with anti-inflammatory and pro-cell survival properties. COVID-19 is associated with disordered inflammation and apoptosis. We hypothesized that blood renalase levels would correspond to severe COVID-19 and survival. In this retrospective cohort study, clinicopathologic data and blood samples were collected from hospitalized COVID-19 subjects (March—June 2020) at a single institution tertiary hospital. Plasma renalase and cytokine levels were measured and clinical data abstracted from health records. Of 3,450 COVID-19 patients, 458 patients were enrolled. Patients were excluded if <18 years, or opted out of research. The primary composite outcome was intubation or death within 180 days. Secondary outcomes included mortality alone, intensive care unit admission, use of vasopressors, and CPR. Enrolled patients had mean age 64 years (SD±17), were 53% males, and 48% non-whites. Mean renalase levels was 14,108·4 ng/ml (SD±8,137 ng/ml). Compared to patients with high renalase, those with low renalase (< 8,922 ng/ml) were more likely to present with hypoxia, increased ICU admission (54% vs. 33%, p < 0.001), and cardiopulmonary resuscitation (10% vs. 4%, p = 0·023). In Cox proportional hazard model, every 1000 ng/ml increase in renalase decreased the risk of death or intubation by 5% (HR 0·95; 95% CI 0·91–0·98) and increased survival alone by 6% (HR 0·95; CI 0·90–0·98), after adjusting for socio-demographics, initial disease severity, comorbidities and inflammation. Patients with high renalase-low IL-6 levels had the best survival compared to other groups (p = 0·04). Renalase was independently associated with reduced intubation and mortality in hospitalized COVID-19 patients. Future studies should assess the pathophysiological relevance of renalase in COVID-19 disease.Keywords
Funding Information
- National Institutes of Health (DK098108)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK111251)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK007017)
- Office of Academic Affiliations, Department of Veterans Affairs (BX003250)
- U.S. Department of War (CA180514)
- National Institutes of Health (P30DK079310)
This publication has 45 references indexed in Scilit:
- Urinary renalase concentration in patients with preserved kidney function undergoing coronary angiographyNephrology, 2018
- Renalase Expression by Melanoma and Tumor-Associated Macrophages Promotes Tumor Growth through a STAT3-Mediated MechanismCancer Research, 2016
- Serum Renalase Levels Correlate with Disease Activity in Lupus NephritisPLOS ONE, 2015
- Valsartan Promoting Atherosclerotic Plaque Stabilization by Upregulating RenalaseJournal of Cardiovascular Pharmacology and Therapeutics, 2015
- Metabolic Function for Human Renalase: Oxidation of Isomeric Forms of β-NAD(P)H that Are Inhibitory to Primary MetabolismBiochemistry, 2015
- The Assessment of Renalase: Searching for the Best Predictor of Early Renal Dysfunction by Multivariate Modeling in Stable Renal Transplant RecipientsAnnals of Transplantation, 2015
- Low plasma renalase concentration in hypertensive patients after surgical repair of coarctation of aortaJournal of the American Society of Hypertension, 2014
- Renalase Prevents AKI Independent of Amine Oxidase ActivityJournal of the American Society of Nephrology, 2014
- Renalase regulates renal dopamine and phosphate metabolismAmerican Journal of Physiology-Renal Physiology, 2013
- Regulation of blood pressure and cardiovascular function by renalaseKidney International, 2009