Increased vulnerability to COVID‐19 in chronic kidney disease

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Increased vulnerability to COVID‐19 in chronic kidney disease. / Carlson, N.; Nelveg‐kristensen, K.‐e.; Freese Ballegaard, E.; Feldt‐rasmussen, B.; Hornum, M.; Kamper, A.‐lise; Gislason, G.; Torp‐pedersen, C.

In: Journal of Internal Medicine, Vol. 290, No. 1, 01.07.2021, p. 166-178.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Carlson, N, Nelveg‐kristensen, K, Freese Ballegaard, E, Feldt‐rasmussen, B, Hornum, M, Kamper, A, Gislason, G & Torp‐pedersen, C 2021, 'Increased vulnerability to COVID‐19 in chronic kidney disease', Journal of Internal Medicine, vol. 290, no. 1, pp. 166-178. https://doi.org/10.1111/joim.13239

APA

Carlson, N., Nelveg‐kristensen, K. ., Freese Ballegaard, E., Feldt‐rasmussen, B., Hornum, M., Kamper, A. ., Gislason, G., & Torp‐pedersen, C. (2021). Increased vulnerability to COVID‐19 in chronic kidney disease. Journal of Internal Medicine, 290(1), 166-178. https://doi.org/10.1111/joim.13239

Vancouver

Carlson N, Nelveg‐kristensen K, Freese Ballegaard E, Feldt‐rasmussen B, Hornum M, Kamper A et al. Increased vulnerability to COVID‐19 in chronic kidney disease. Journal of Internal Medicine. 2021 Jul 1;290(1):166-178. https://doi.org/10.1111/joim.13239

Author

Carlson, N. ; Nelveg‐kristensen, K.‐e. ; Freese Ballegaard, E. ; Feldt‐rasmussen, B. ; Hornum, M. ; Kamper, A.‐lise ; Gislason, G. ; Torp‐pedersen, C. / Increased vulnerability to COVID‐19 in chronic kidney disease. In: Journal of Internal Medicine. 2021 ; Vol. 290, No. 1. pp. 166-178.

Bibtex

@article{ba4501b970d744b8873cc6bb69516475,
title = "Increased vulnerability to COVID‐19 in chronic kidney disease",
abstract = "BackgroundThe significance of chronic kidney disease on susceptibility to COVID-19 and subsequent outcomes remains unaddressed.ObjectiveTo investigate the association of estimated glomerular filtration rate (eGFR) on risk of contracting COVID-19 and subsequent adverse outcomes.MethodsRates 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.ResultsEstimated glomerular filtration rate was inversely associated with rate of hospital-diagnosed COVID-19: eGFR 61–90 mL/min/1.73m2 HR 1.13 (95% CI 1.03–1.25), P = 0.011; eGFR 46–60 mL/min/1.73m2 HR 1.26 (95% CI 1.06–1.50), P = 0.008; eGFR 31–45 mL/min/1.73m2 HR 1.68 (95% CI 1.34–2.11), P < 0.001; and eGFR ≤ 30 mL/min/1.73m2 3.33 (95% CI 2.50–4.42), P < 0.001 (eGFR > 90 mL/min/1.73m2 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/1.73m2 13.9% (95% CI 9.7–15.0); eGFR 90–61 mL/min/1.73m2 16.1% (95% CI 14.5–17.7); eGFR 46–60 mL/min/1.73m2 17.8% (95% CI 14.7–21.2); eGFR 31–45 mL/min/1.73m2 22.6% (95% CI 18.2–26.2); and eGFR ≤ 30 mL/min/1.73m2 23.6% (95% CI 18.1–29.1).ConclusionsRenal 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.",
author = "N. Carlson and K.‐e. Nelveg‐kristensen and {Freese Ballegaard}, E. and B. Feldt‐rasmussen and M. Hornum and A.‐lise Kamper and G. Gislason and C. Torp‐pedersen",
year = "2021",
month = jul,
day = "1",
doi = "10.1111/joim.13239",
language = "English",
volume = "290",
pages = "166--178",
journal = "Journal of Internal Medicine",
issn = "0955-7873",
publisher = "Wiley-Blackwell",
number = "1",

}

RIS

TY - JOUR

T1 - Increased vulnerability to COVID‐19 in chronic kidney disease

AU - Carlson, N.

AU - Nelveg‐kristensen, K.‐e.

AU - Freese Ballegaard, E.

AU - Feldt‐rasmussen, B.

AU - Hornum, M.

AU - Kamper, A.‐lise

AU - Gislason, G.

AU - Torp‐pedersen, C.

PY - 2021/7/1

Y1 - 2021/7/1

N2 - BackgroundThe significance of chronic kidney disease on susceptibility to COVID-19 and subsequent outcomes remains unaddressed.ObjectiveTo investigate the association of estimated glomerular filtration rate (eGFR) on risk of contracting COVID-19 and subsequent adverse outcomes.MethodsRates 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.ResultsEstimated glomerular filtration rate was inversely associated with rate of hospital-diagnosed COVID-19: eGFR 61–90 mL/min/1.73m2 HR 1.13 (95% CI 1.03–1.25), P = 0.011; eGFR 46–60 mL/min/1.73m2 HR 1.26 (95% CI 1.06–1.50), P = 0.008; eGFR 31–45 mL/min/1.73m2 HR 1.68 (95% CI 1.34–2.11), P < 0.001; and eGFR ≤ 30 mL/min/1.73m2 3.33 (95% CI 2.50–4.42), P < 0.001 (eGFR > 90 mL/min/1.73m2 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/1.73m2 13.9% (95% CI 9.7–15.0); eGFR 90–61 mL/min/1.73m2 16.1% (95% CI 14.5–17.7); eGFR 46–60 mL/min/1.73m2 17.8% (95% CI 14.7–21.2); eGFR 31–45 mL/min/1.73m2 22.6% (95% CI 18.2–26.2); and eGFR ≤ 30 mL/min/1.73m2 23.6% (95% CI 18.1–29.1).ConclusionsRenal 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.

AB - BackgroundThe significance of chronic kidney disease on susceptibility to COVID-19 and subsequent outcomes remains unaddressed.ObjectiveTo investigate the association of estimated glomerular filtration rate (eGFR) on risk of contracting COVID-19 and subsequent adverse outcomes.MethodsRates 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.ResultsEstimated glomerular filtration rate was inversely associated with rate of hospital-diagnosed COVID-19: eGFR 61–90 mL/min/1.73m2 HR 1.13 (95% CI 1.03–1.25), P = 0.011; eGFR 46–60 mL/min/1.73m2 HR 1.26 (95% CI 1.06–1.50), P = 0.008; eGFR 31–45 mL/min/1.73m2 HR 1.68 (95% CI 1.34–2.11), P < 0.001; and eGFR ≤ 30 mL/min/1.73m2 3.33 (95% CI 2.50–4.42), P < 0.001 (eGFR > 90 mL/min/1.73m2 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/1.73m2 13.9% (95% CI 9.7–15.0); eGFR 90–61 mL/min/1.73m2 16.1% (95% CI 14.5–17.7); eGFR 46–60 mL/min/1.73m2 17.8% (95% CI 14.7–21.2); eGFR 31–45 mL/min/1.73m2 22.6% (95% CI 18.2–26.2); and eGFR ≤ 30 mL/min/1.73m2 23.6% (95% CI 18.1–29.1).ConclusionsRenal 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.

U2 - 10.1111/joim.13239

DO - 10.1111/joim.13239

M3 - Journal article

C2 - 33452733

VL - 290

SP - 166

EP - 178

JO - Journal of Internal Medicine

JF - Journal of Internal Medicine

SN - 0955-7873

IS - 1

ER -

ID: 280613861