Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study
<br><strong>Background: <br></strong>Whether elevated blood pressure (BP) is a modifiable risk factor for atrial fibrillation (AF) is not established. We tested (1) whether the association between BP and risk of AF is causal, (2) whether it varies according to individual&...
| Main Authors: | , , , , , , , , |
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| Format: | Journal article |
| Language: | English |
| Published: |
BioMed Central
2021
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| _version_ | 1797084391042711552 |
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| author | Nazarzadeh Larzjan, M Pinho-Gomes, A-C Bidel, Z Canoy, D Dehghan, A Smith Byrne, K A Bennett, D Davey Smith, G Rahimi, K |
| author_facet | Nazarzadeh Larzjan, M Pinho-Gomes, A-C Bidel, Z Canoy, D Dehghan, A Smith Byrne, K A Bennett, D Davey Smith, G Rahimi, K |
| author_sort | Nazarzadeh Larzjan, M |
| collection | OXFORD |
| description | <br><strong>Background: <br></strong>Whether elevated blood pressure (BP) is a modifiable risk factor for atrial fibrillation (AF) is not established. We tested (1) whether the association between BP and risk of AF is causal, (2) whether it varies according to individual’s genetic susceptibility for AF, and (3) the extent to which specific BP-lowering drugs are expected to reduce this risk.
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Methods: <br></strong>First, causality of association was assessed through two-sample Mendelian randomization, using data from two independent genome-wide association studies that included a total of one million European population. Second, the UK Biobank data of 329,237 participants at baseline was used to study the effect of BP on AF according to genetic susceptibility of developing AF. Third, a possible treatment effect with major BP-lowering drug classes on AF risk was predicted through genetic variants in genes encode the therapeutic targets of each drug class. Estimated drug effects were compared with effects on incident coronary heart disease, for which direct trial evidence exists.
<br><strong>
Results: <br></strong> The two-sample Mendelian randomization analysis indicated that, on average, exposure to a higher systolic BP increased the risk of AF by 19% (odds ratio per each 10-mm Hg [OR]: 1.19 [1.12 to 1.27]). This association was replicated in the UK biobank using individual participant data. However, in a further genetic risk-stratified analysis, there was evidence for a linear gradient in the relative effects of systolic BP on AF; while there was no conclusive evidence of an effect in those with low genetic risk, a strong effect was observed among those with high genetic susceptibility for AF. The comparison of predicted treatment effects using genetic proxies for three main drug classes (angiotensin-converting enzyme inhibitors, beta-blockers and calcium channel blockers) suggested similar average effects for the prevention of atrial fibrillation and coronary heart disease.
<br><strong>
Conclusions: <br></strong>The effect of elevated BP on the risk of AF is likely to be causal, suggesting that BP-lowering treatment may be effective in AF prevention. However, average effects masked clinically important variations, with a more pronounced effect in individuals with high genetic susceptibility risk for AF. |
| first_indexed | 2024-03-07T01:54:46Z |
| format | Journal article |
| id | oxford-uuid:9b52a053-1dd5-49b6-b98e-8b59326149bb |
| institution | University of Oxford |
| language | English |
| last_indexed | 2024-03-07T01:54:46Z |
| publishDate | 2021 |
| publisher | BioMed Central |
| record_format | dspace |
| spelling | oxford-uuid:9b52a053-1dd5-49b6-b98e-8b59326149bb2022-03-27T00:28:16ZGenetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization studyJournal articlehttp://purl.org/coar/resource_type/c_dcae04bcuuid:9b52a053-1dd5-49b6-b98e-8b59326149bbEnglishSymplectic ElementsBioMed Central2021Nazarzadeh Larzjan, MPinho-Gomes, A-CBidel, ZCanoy, DDehghan, ASmith Byrne, KA Bennett, DDavey Smith, GRahimi, K<br><strong>Background: <br></strong>Whether elevated blood pressure (BP) is a modifiable risk factor for atrial fibrillation (AF) is not established. We tested (1) whether the association between BP and risk of AF is causal, (2) whether it varies according to individual’s genetic susceptibility for AF, and (3) the extent to which specific BP-lowering drugs are expected to reduce this risk. <br><strong> Methods: <br></strong>First, causality of association was assessed through two-sample Mendelian randomization, using data from two independent genome-wide association studies that included a total of one million European population. Second, the UK Biobank data of 329,237 participants at baseline was used to study the effect of BP on AF according to genetic susceptibility of developing AF. Third, a possible treatment effect with major BP-lowering drug classes on AF risk was predicted through genetic variants in genes encode the therapeutic targets of each drug class. Estimated drug effects were compared with effects on incident coronary heart disease, for which direct trial evidence exists. <br><strong> Results: <br></strong> The two-sample Mendelian randomization analysis indicated that, on average, exposure to a higher systolic BP increased the risk of AF by 19% (odds ratio per each 10-mm Hg [OR]: 1.19 [1.12 to 1.27]). This association was replicated in the UK biobank using individual participant data. However, in a further genetic risk-stratified analysis, there was evidence for a linear gradient in the relative effects of systolic BP on AF; while there was no conclusive evidence of an effect in those with low genetic risk, a strong effect was observed among those with high genetic susceptibility for AF. The comparison of predicted treatment effects using genetic proxies for three main drug classes (angiotensin-converting enzyme inhibitors, beta-blockers and calcium channel blockers) suggested similar average effects for the prevention of atrial fibrillation and coronary heart disease. <br><strong> Conclusions: <br></strong>The effect of elevated BP on the risk of AF is likely to be causal, suggesting that BP-lowering treatment may be effective in AF prevention. However, average effects masked clinically important variations, with a more pronounced effect in individuals with high genetic susceptibility risk for AF. |
| spellingShingle | Nazarzadeh Larzjan, M Pinho-Gomes, A-C Bidel, Z Canoy, D Dehghan, A Smith Byrne, K A Bennett, D Davey Smith, G Rahimi, K Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title | Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title_full | Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title_fullStr | Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title_full_unstemmed | Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title_short | Genetic susceptibility, elevated blood pressure and risk of atrial fibrillation: a Mendelian randomization study |
| title_sort | genetic susceptibility elevated blood pressure and risk of atrial fibrillation a mendelian randomization study |
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