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Severity of COVID-19 at elevated exposure to perfluorinated alkylates

BACKGROUND: The course of coronavirus disease 2019 (COVID-19) seems to be aggravated by air pollution, and some industrial chemicals, such as the perfluorinated alkylate substances (PFASs), are immunotoxic and may contribute as well. METHODS: From Danish biobanks, we obtained plasma samples from 323...

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Autores principales: Grandjean, P, Timmermann, C.A.G., Kruse, M., Nielsen, F., Vinholt, P. Just, Boding, L., Heilmann, C., Mølbak, K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605584/
https://www.ncbi.nlm.nih.gov/pubmed/33140071
http://dx.doi.org/10.1101/2020.10.22.20217562
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author Grandjean, P
Timmermann, C.A.G.
Kruse, M.
Nielsen, F.
Vinholt, P. Just
Boding, L.
Heilmann, C.
Mølbak, K.
author_facet Grandjean, P
Timmermann, C.A.G.
Kruse, M.
Nielsen, F.
Vinholt, P. Just
Boding, L.
Heilmann, C.
Mølbak, K.
author_sort Grandjean, P
collection PubMed
description BACKGROUND: The course of coronavirus disease 2019 (COVID-19) seems to be aggravated by air pollution, and some industrial chemicals, such as the perfluorinated alkylate substances (PFASs), are immunotoxic and may contribute as well. METHODS: From Danish biobanks, we obtained plasma samples from 323 subjects aged 30–70 years with known SARS-CoV-2 infection. The PFAS concentrations measured at the background exposures included five PFASs known to be immunotoxic. Register data was obtained to classify disease status, other health information, and demographic variables. We used ordinal and ordered logistic regression analyses to determine associations between PFAS concentrations and disease outcome. RESULTS: Plasma-PFAS concentrations were higher in males, in subjects with Western European background, and tended to increase with age, but were not associated with the presence of chronic disease. Of the study population, 108 (33%) had not been hospitalized, and of those hospitalized, 53 (16%) had been in intensive care or were deceased. Among the five PFASs considered, perfluorobutanoic acid (PFBA) showed an odds ratio (OR) of 2.19 (95% confidence interval, CI, 1.39–3.46) for increasing severities of the disease, although the OR decreased to 1.77 (95% CI, 1.09, 2.87) after adjustment for age, sex, sampling site and interval between blood sampling and diagnosis. CONCLUSIONS: Measures of individual exposures to immunotoxic PFASs included PFBA that accumulates in the lungs. Elevated plasma-PFBA concentrations were associated with an increased risk of more severe course of CIVID-19. Given the low background exposure levels in this study, the role of PFAS exposure in COVID-19 needs to be ascertained in populations with elevated exposures.
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spelling pubmed-76055842020-11-03 Severity of COVID-19 at elevated exposure to perfluorinated alkylates Grandjean, P Timmermann, C.A.G. Kruse, M. Nielsen, F. Vinholt, P. Just Boding, L. Heilmann, C. Mølbak, K. medRxiv Article BACKGROUND: The course of coronavirus disease 2019 (COVID-19) seems to be aggravated by air pollution, and some industrial chemicals, such as the perfluorinated alkylate substances (PFASs), are immunotoxic and may contribute as well. METHODS: From Danish biobanks, we obtained plasma samples from 323 subjects aged 30–70 years with known SARS-CoV-2 infection. The PFAS concentrations measured at the background exposures included five PFASs known to be immunotoxic. Register data was obtained to classify disease status, other health information, and demographic variables. We used ordinal and ordered logistic regression analyses to determine associations between PFAS concentrations and disease outcome. RESULTS: Plasma-PFAS concentrations were higher in males, in subjects with Western European background, and tended to increase with age, but were not associated with the presence of chronic disease. Of the study population, 108 (33%) had not been hospitalized, and of those hospitalized, 53 (16%) had been in intensive care or were deceased. Among the five PFASs considered, perfluorobutanoic acid (PFBA) showed an odds ratio (OR) of 2.19 (95% confidence interval, CI, 1.39–3.46) for increasing severities of the disease, although the OR decreased to 1.77 (95% CI, 1.09, 2.87) after adjustment for age, sex, sampling site and interval between blood sampling and diagnosis. CONCLUSIONS: Measures of individual exposures to immunotoxic PFASs included PFBA that accumulates in the lungs. Elevated plasma-PFBA concentrations were associated with an increased risk of more severe course of CIVID-19. Given the low background exposure levels in this study, the role of PFAS exposure in COVID-19 needs to be ascertained in populations with elevated exposures. Cold Spring Harbor Laboratory 2020-10-26 /pmc/articles/PMC7605584/ /pubmed/33140071 http://dx.doi.org/10.1101/2020.10.22.20217562 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Grandjean, P
Timmermann, C.A.G.
Kruse, M.
Nielsen, F.
Vinholt, P. Just
Boding, L.
Heilmann, C.
Mølbak, K.
Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title_full Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title_fullStr Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title_full_unstemmed Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title_short Severity of COVID-19 at elevated exposure to perfluorinated alkylates
title_sort severity of covid-19 at elevated exposure to perfluorinated alkylates
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7605584/
https://www.ncbi.nlm.nih.gov/pubmed/33140071
http://dx.doi.org/10.1101/2020.10.22.20217562
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