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Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation

Whether renal function is causally associated with venous thromboembolism (VTE) is not yet fully elucidated. We conducted a two-sample Mendelian randomization (MR) study to determine the causal effect of renal function, measured as estimated glomerular filtration rate (eGFR), on VTE. Single-nucleoti...

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Autores principales: Yuan, Shuai, Bruzelius, Maria, Larsson, Susanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791872/
https://www.ncbi.nlm.nih.gov/pubmed/34043151
http://dx.doi.org/10.1007/s11239-021-02494-4
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author Yuan, Shuai
Bruzelius, Maria
Larsson, Susanna C.
author_facet Yuan, Shuai
Bruzelius, Maria
Larsson, Susanna C.
author_sort Yuan, Shuai
collection PubMed
description Whether renal function is causally associated with venous thromboembolism (VTE) is not yet fully elucidated. We conducted a two-sample Mendelian randomization (MR) study to determine the causal effect of renal function, measured as estimated glomerular filtration rate (eGFR), on VTE. Single-nucleotide polymorphisms associated with eGFR were selected as instrumental variables at the genome-wide significance level (p < 5 × 10(−8)) from a meta-analysis of 122 genome-wide association studies including up to 1,046,070 individuals. Summary-level data for VTE were obtained from the FinnGen consortium (6913 VTE cases and 169,986 non-cases) and UK Biobank study (4620 VTE cases and 356,574 non-cases). MR estimates were calculated using the random-effects inverse-variance weighted method and combined using fixed-effects meta-analysis. Genetically predicted decreased eGFR was significantly associated with an increased risk of VTE in both FinnGen and UK Biobank. For one-unit decrease in log-transformed eGFR, the odds ratios of VTE were 2.93 (95% confidence interval (CI) 1.25, 6.84) and 4.46 (95% CI 1.59, 12.5) when using data from FinnGen and UK Biobank, respectively. The combined odds ratio was 3.47 (95% CI 1.80, 6.68). Results were consistent in all sensitivity analyses and no horizontal pleiotropy was detected. This MR-study supported a casual role of impaired renal function in VTE. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11239-021-02494-4.
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spelling pubmed-87918722022-02-02 Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation Yuan, Shuai Bruzelius, Maria Larsson, Susanna C. J Thromb Thrombolysis Article Whether renal function is causally associated with venous thromboembolism (VTE) is not yet fully elucidated. We conducted a two-sample Mendelian randomization (MR) study to determine the causal effect of renal function, measured as estimated glomerular filtration rate (eGFR), on VTE. Single-nucleotide polymorphisms associated with eGFR were selected as instrumental variables at the genome-wide significance level (p < 5 × 10(−8)) from a meta-analysis of 122 genome-wide association studies including up to 1,046,070 individuals. Summary-level data for VTE were obtained from the FinnGen consortium (6913 VTE cases and 169,986 non-cases) and UK Biobank study (4620 VTE cases and 356,574 non-cases). MR estimates were calculated using the random-effects inverse-variance weighted method and combined using fixed-effects meta-analysis. Genetically predicted decreased eGFR was significantly associated with an increased risk of VTE in both FinnGen and UK Biobank. For one-unit decrease in log-transformed eGFR, the odds ratios of VTE were 2.93 (95% confidence interval (CI) 1.25, 6.84) and 4.46 (95% CI 1.59, 12.5) when using data from FinnGen and UK Biobank, respectively. The combined odds ratio was 3.47 (95% CI 1.80, 6.68). Results were consistent in all sensitivity analyses and no horizontal pleiotropy was detected. This MR-study supported a casual role of impaired renal function in VTE. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s11239-021-02494-4. Springer US 2021-05-27 2022 /pmc/articles/PMC8791872/ /pubmed/34043151 http://dx.doi.org/10.1007/s11239-021-02494-4 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Yuan, Shuai
Bruzelius, Maria
Larsson, Susanna C.
Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title_full Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title_fullStr Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title_full_unstemmed Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title_short Causal effect of renal function on venous thromboembolism: a two-sample Mendelian randomization investigation
title_sort causal effect of renal function on venous thromboembolism: a two-sample mendelian randomization investigation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8791872/
https://www.ncbi.nlm.nih.gov/pubmed/34043151
http://dx.doi.org/10.1007/s11239-021-02494-4
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