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Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study
Elevated circulating copper levels have been associated with chronic kidney disease (CKD), kidney damage, and decline in kidney function. Using a two sample Mendelian randomization approach where copper-associated genetic variants were used as instrumental variables, genetically predicted higher cir...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840411/ https://www.ncbi.nlm.nih.gov/pubmed/35276868 http://dx.doi.org/10.3390/nu14030509 |
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author | Ahmad, Shafqat Ärnlöv, Johan Larsson, Susanna C. |
author_facet | Ahmad, Shafqat Ärnlöv, Johan Larsson, Susanna C. |
author_sort | Ahmad, Shafqat |
collection | PubMed |
description | Elevated circulating copper levels have been associated with chronic kidney disease (CKD), kidney damage, and decline in kidney function. Using a two sample Mendelian randomization approach where copper-associated genetic variants were used as instrumental variables, genetically predicted higher circulating copper levels were associated with higher CKD prevalence (odds ratio 1.17; 95% confidence interval 1.04, 1.32; p-value = 0.009). There was suggestive evidence that genetically predicted higher copper was associated with a lower estimated glomerular filtration rate and a more rapid kidney damage decline. In conclusion, we observed that elevated circulating copper levels may be a causal risk factor for CKD. |
format | Online Article Text |
id | pubmed-8840411 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-88404112022-02-13 Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study Ahmad, Shafqat Ärnlöv, Johan Larsson, Susanna C. Nutrients Communication Elevated circulating copper levels have been associated with chronic kidney disease (CKD), kidney damage, and decline in kidney function. Using a two sample Mendelian randomization approach where copper-associated genetic variants were used as instrumental variables, genetically predicted higher circulating copper levels were associated with higher CKD prevalence (odds ratio 1.17; 95% confidence interval 1.04, 1.32; p-value = 0.009). There was suggestive evidence that genetically predicted higher copper was associated with a lower estimated glomerular filtration rate and a more rapid kidney damage decline. In conclusion, we observed that elevated circulating copper levels may be a causal risk factor for CKD. MDPI 2022-01-25 /pmc/articles/PMC8840411/ /pubmed/35276868 http://dx.doi.org/10.3390/nu14030509 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Communication Ahmad, Shafqat Ärnlöv, Johan Larsson, Susanna C. Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title | Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title_full | Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title_fullStr | Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title_full_unstemmed | Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title_short | Genetically Predicted Circulating Copper and Risk of Chronic Kidney Disease: A Mendelian Randomization Study |
title_sort | genetically predicted circulating copper and risk of chronic kidney disease: a mendelian randomization study |
topic | Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8840411/ https://www.ncbi.nlm.nih.gov/pubmed/35276868 http://dx.doi.org/10.3390/nu14030509 |
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