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Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study

BACKGROUND: Tumour necrosis factor (TNF) inhibitors are used in the treatment of certain autoimmune diseases but given the role of TNF in tumour biology and atherosclerosis, such therapies may influence the risk of cancer and cardiovascular disease. We conducted a Mendelian randomization study to ex...

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Autores principales: Yuan, Shuai, Carter, Paul, Bruzelius, Maria, Vithayathil, Mathew, Kar, Siddhartha, Mason, Amy M., Lin, Ang, Burgess, Stephen, Larsson, Susanna C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452586/
https://www.ncbi.nlm.nih.gov/pubmed/32805626
http://dx.doi.org/10.1016/j.ebiom.2020.102956
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author Yuan, Shuai
Carter, Paul
Bruzelius, Maria
Vithayathil, Mathew
Kar, Siddhartha
Mason, Amy M.
Lin, Ang
Burgess, Stephen
Larsson, Susanna C.
author_facet Yuan, Shuai
Carter, Paul
Bruzelius, Maria
Vithayathil, Mathew
Kar, Siddhartha
Mason, Amy M.
Lin, Ang
Burgess, Stephen
Larsson, Susanna C.
author_sort Yuan, Shuai
collection PubMed
description BACKGROUND: Tumour necrosis factor (TNF) inhibitors are used in the treatment of certain autoimmune diseases but given the role of TNF in tumour biology and atherosclerosis, such therapies may influence the risk of cancer and cardiovascular disease. We conducted a Mendelian randomization study to explore whether TNF levels are causally related to cardiovascular disease and cancer. METHODS: Single-nucleotide polymorphisms associated with TNF levels at genome-wide significance were identified from a genome-wide association study of 30 912 European-ancestry individuals. Three TNF-associated single-nucleotide polymorphisms associated with higher risk of autoimmune diseases were used as instrumental variables. Summary-level data for 14 cardiovascular diseases, overall cancer and 14 site-specific cancers were obtained from UK Biobank and consortia. FINDINGS: Genetically-predicted TNF levels were positively associated with coronary artery disease (odds ratio (OR) 2.25; 95% confidence interval (CI) 1.50, 3.37) and ischaemic stroke (OR 2.27; 95% CI 1.50, 3.43), and inversely associated with overall cancer (OR 0.54; 95% CI 0.42, 0.69), breast cancer (OR 0.51; 95% CI 0.39, 0.67), and colorectal cancer (OR 0.20; 95% CI 0.09, 0.45). There were suggestive associations of TNF with venous thromboembolism (OR 2.18; 95% CI 1.32, 3.59), endometrial cancer (OR 0.25; 95% CI 0.07, 0.94), and lung cancer (OR 0.45; 95% CI 0.21, 0.94). INTERPRETATION: This study found evidence of causal associations of increased TNF levels with higher risk of common cardiovascular diseases and lower risk of overall and certain cancers.
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spelling pubmed-74525862020-09-03 Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study Yuan, Shuai Carter, Paul Bruzelius, Maria Vithayathil, Mathew Kar, Siddhartha Mason, Amy M. Lin, Ang Burgess, Stephen Larsson, Susanna C. EBioMedicine Research paper BACKGROUND: Tumour necrosis factor (TNF) inhibitors are used in the treatment of certain autoimmune diseases but given the role of TNF in tumour biology and atherosclerosis, such therapies may influence the risk of cancer and cardiovascular disease. We conducted a Mendelian randomization study to explore whether TNF levels are causally related to cardiovascular disease and cancer. METHODS: Single-nucleotide polymorphisms associated with TNF levels at genome-wide significance were identified from a genome-wide association study of 30 912 European-ancestry individuals. Three TNF-associated single-nucleotide polymorphisms associated with higher risk of autoimmune diseases were used as instrumental variables. Summary-level data for 14 cardiovascular diseases, overall cancer and 14 site-specific cancers were obtained from UK Biobank and consortia. FINDINGS: Genetically-predicted TNF levels were positively associated with coronary artery disease (odds ratio (OR) 2.25; 95% confidence interval (CI) 1.50, 3.37) and ischaemic stroke (OR 2.27; 95% CI 1.50, 3.43), and inversely associated with overall cancer (OR 0.54; 95% CI 0.42, 0.69), breast cancer (OR 0.51; 95% CI 0.39, 0.67), and colorectal cancer (OR 0.20; 95% CI 0.09, 0.45). There were suggestive associations of TNF with venous thromboembolism (OR 2.18; 95% CI 1.32, 3.59), endometrial cancer (OR 0.25; 95% CI 0.07, 0.94), and lung cancer (OR 0.45; 95% CI 0.21, 0.94). INTERPRETATION: This study found evidence of causal associations of increased TNF levels with higher risk of common cardiovascular diseases and lower risk of overall and certain cancers. Elsevier 2020-08-14 /pmc/articles/PMC7452586/ /pubmed/32805626 http://dx.doi.org/10.1016/j.ebiom.2020.102956 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research paper
Yuan, Shuai
Carter, Paul
Bruzelius, Maria
Vithayathil, Mathew
Kar, Siddhartha
Mason, Amy M.
Lin, Ang
Burgess, Stephen
Larsson, Susanna C.
Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title_full Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title_fullStr Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title_full_unstemmed Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title_short Effects of tumour necrosis factor on cardiovascular disease and cancer: A two-sample Mendelian randomization study
title_sort effects of tumour necrosis factor on cardiovascular disease and cancer: a two-sample mendelian randomization study
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7452586/
https://www.ncbi.nlm.nih.gov/pubmed/32805626
http://dx.doi.org/10.1016/j.ebiom.2020.102956
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