Increased Vulnerability to COVID-19 in Chronic Kidney Disease
Overview
Authors
Affiliations
Background: The significance of chronic kidney disease on susceptibility to COVID-19 and subsequent outcomes remains unaddressed.
Objective: To investigate the association of estimated glomerular filtration rate (eGFR) on risk of contracting COVID-19 and subsequent adverse outcomes.
Methods: Rates of hospital-diagnosed COVID-19 were compared across strata of eGFR based on conditional logistic regression using a nested case-control framework with 1:4 matching of patients diagnosed with COVID-19 with controls from the Danish general population on age, gender, diabetes and hypertension. Risk of subsequent severe COVID-19 or death was assessed in a cohort study with comparisons across strata of eGFR based on adjusted Cox regression models with G-computation of results to determine 60-day risk standardized to the distribution of risk factors in the sample.
Results: Estimated glomerular filtration rate was inversely associated with rate of hospital-diagnosed COVID-19: eGFR 61-90 mL/min/1.73m HR 1.13 (95% CI 1.03-1.25), P = 0.011; eGFR 46-60 mL/min/1.73m HR 1.26 (95% CI 1.06-1.50), P = 0.008; eGFR 31-45 mL/min/1.73m HR 1.68 (95% CI 1.34-2.11), P < 0.001; and eGFR ≤ 30 mL/min/1.73m 3.33 (95% CI 2.50-4.42), P < 0.001 (eGFR > 90 mL/min/1.73m as reference), and renal impairment was associated with progressive increase in standardized 60-day risk of death or severe COVID-19; eGFR > 90 mL/min/1.73m 13.9% (95% CI 9.7-15.0); eGFR 90-61 mL/min/1.73m 16.1% (95% CI 14.5-17.7); eGFR 46-60 mL/min/1.73m 17.8% (95% CI 14.7-21.2); eGFR 31-45 mL/min/1.73m 22.6% (95% CI 18.2-26.2); and eGFR ≤ 30 mL/min/1.73m 23.6% (95% CI 18.1-29.1).
Conclusions: Renal insufficiency was associated with progressive increase in both rate of hospital-diagnosed COVID-19 and subsequent risk of adverse outcomes. Results underscore a possible vulnerability associated with impaired renal function in relation to COVID-19.
Type 2 diabetes and susceptibility to COVID-19: a machine learning analysis.
Shabestari M, Azizi R, Ghadiri-Anari A BMC Endocr Disord. 2024; 24(1):221.
PMID: 39434075 PMC: 11492751. DOI: 10.1186/s12902-024-01758-3.
Alishahi M, Mohajer S, Namazinia M, Mazloum S Int Urol Nephrol. 2024; 57(2):585-594.
PMID: 39259395 DOI: 10.1007/s11255-024-04201-7.
Stewart S, Kalra P, Blakeman T, Kontopantelis E, Cranmer-Gordon H, Sinha S BMC Med. 2024; 22(1):331.
PMID: 39148079 PMC: 11328380. DOI: 10.1186/s12916-024-03555-0.
New insights into the pathogenesis of SARS-CoV-2 during and after the COVID-19 pandemic.
Carvajal J, Garcia-Castillo V, Cuellar S, Campillay-Veliz C, Salazar-Ardiles C, Avellaneda A Front Immunol. 2024; 15:1363572.
PMID: 38911850 PMC: 11190347. DOI: 10.3389/fimmu.2024.1363572.
Mahapatra P, Sahoo K, Pati S Sci Rep. 2024; 14(1):12866.
PMID: 38834635 PMC: 11150371. DOI: 10.1038/s41598-024-60473-0.