Antihypertensive Drugs for the Prevention of Atrial Fibrillation: A Drug Target Mendelian Randomization Study.

IF 6.9 1区 医学 Q1 PERIPHERAL VASCULAR DISEASE Hypertension Pub Date : 2024-08-01 Epub Date: 2024-06-19 DOI:10.1161/HYPERTENSIONAHA.123.21858
Sven Geurts, Martijn J Tilly, Zuolin Lu, Bruno H C Stricker, Jaap W Deckers, Natasja M S de Groot, Clint L Miller, M Arfan Ikram, Maryam Kavousi
{"title":"Antihypertensive Drugs for the Prevention of Atrial Fibrillation: A Drug Target Mendelian Randomization Study.","authors":"Sven Geurts, Martijn J Tilly, Zuolin Lu, Bruno H C Stricker, Jaap W Deckers, Natasja M S de Groot, Clint L Miller, M Arfan Ikram, Maryam Kavousi","doi":"10.1161/HYPERTENSIONAHA.123.21858","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>We investigated the potential impact of antihypertensive drugs for atrial fibrillation (AF) prevention through a drug target Mendelian randomization study to avoid the potential limitations of clinical studies.</p><p><strong>Methods: </strong>Validated published single-nucleotide polymorphisms (SNPs) that mimic the action of 12 antihypertensive drug classes, including alpha-adrenoceptor blockers, adrenergic neuron blockers, angiotensin-converting enzyme inhibitors, angiotensin-II receptor blockers, beta-adrenoceptor blockers, centrally acting antihypertensive drugs, calcium channel blockers, loop diuretics, potassium-sparing diuretics and mineralocorticoid receptor antagonists, renin inhibitors, thiazides and related diuretic agents, and vasodilators were used. We estimated, via their corresponding gene and protein targets, the downstream effect of these drug classes to prevent AF via systolic blood pressure using 2-sample Mendelian randomization analyses. The SNPs were extracted from 2 European genome-wide association studies for the drug classes (n=317 754; n=757 601) and 1 European genome-wide association study for AF (n=1 030 836).</p><p><strong>Results: </strong>Drug target Mendelian randomization analyses supported the significant preventive causal effects of lowering systolic blood pressure per 10 mm Hg via alpha-adrenoceptor blockers (n=11 SNPs; odds ratio [OR], 0.34 [95% CI, 0.21-0.56]; <i>P</i>=2.74×10<sup>-05</sup>), beta-adrenoceptor blockers (n=17 SNPs; OR, 0.52 [95% CI, 0.35-0.78]; <i>P</i>=1.62×10<sup>-03</sup>), calcium channel blockers (n=49 SNPs; OR, 0.50 [95% CI, 0.36-0.70]; <i>P</i>=4.51×10<sup>-05</sup>), vasodilators (n=19 SNPs; OR, 0.53 [95% CI, 0.34-0.84]; <i>P</i>=7.03×10<sup>-03</sup>), and all 12 antihypertensive drug classes combined (n=158 SNPs; OR, 0.64 [95% CI, 0.54-0.77]; <i>P</i>=8.50×10<sup>-07</sup>) on AF risk.</p><p><strong>Conclusions: </strong>Our results indicated that lowering systolic blood pressure via protein targets of various antihypertensive drugs seems promising for AF prevention. Our findings inform future clinical trials and have implications for repurposing antihypertensive drugs for AF prevention.</p>","PeriodicalId":13042,"journal":{"name":"Hypertension","volume":null,"pages":null},"PeriodicalIF":6.9000,"publicationDate":"2024-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11251507/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Hypertension","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1161/HYPERTENSIONAHA.123.21858","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/6/19 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
引用次数: 0

Abstract

Background: We investigated the potential impact of antihypertensive drugs for atrial fibrillation (AF) prevention through a drug target Mendelian randomization study to avoid the potential limitations of clinical studies.

Methods: Validated published single-nucleotide polymorphisms (SNPs) that mimic the action of 12 antihypertensive drug classes, including alpha-adrenoceptor blockers, adrenergic neuron blockers, angiotensin-converting enzyme inhibitors, angiotensin-II receptor blockers, beta-adrenoceptor blockers, centrally acting antihypertensive drugs, calcium channel blockers, loop diuretics, potassium-sparing diuretics and mineralocorticoid receptor antagonists, renin inhibitors, thiazides and related diuretic agents, and vasodilators were used. We estimated, via their corresponding gene and protein targets, the downstream effect of these drug classes to prevent AF via systolic blood pressure using 2-sample Mendelian randomization analyses. The SNPs were extracted from 2 European genome-wide association studies for the drug classes (n=317 754; n=757 601) and 1 European genome-wide association study for AF (n=1 030 836).

Results: Drug target Mendelian randomization analyses supported the significant preventive causal effects of lowering systolic blood pressure per 10 mm Hg via alpha-adrenoceptor blockers (n=11 SNPs; odds ratio [OR], 0.34 [95% CI, 0.21-0.56]; P=2.74×10-05), beta-adrenoceptor blockers (n=17 SNPs; OR, 0.52 [95% CI, 0.35-0.78]; P=1.62×10-03), calcium channel blockers (n=49 SNPs; OR, 0.50 [95% CI, 0.36-0.70]; P=4.51×10-05), vasodilators (n=19 SNPs; OR, 0.53 [95% CI, 0.34-0.84]; P=7.03×10-03), and all 12 antihypertensive drug classes combined (n=158 SNPs; OR, 0.64 [95% CI, 0.54-0.77]; P=8.50×10-07) on AF risk.

Conclusions: Our results indicated that lowering systolic blood pressure via protein targets of various antihypertensive drugs seems promising for AF prevention. Our findings inform future clinical trials and have implications for repurposing antihypertensive drugs for AF prevention.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
预防心房颤动的抗高血压药物:药物靶点孟德尔随机化研究》。
背景:我们通过药物靶点孟德尔随机化研究调查了降压药对房颤预防的潜在影响,以避免临床研究的潜在局限性:验证已发表的单核苷酸多态性(SNPs),模拟 12 类抗高血压药物的作用,包括α-肾上腺素受体阻滞剂、肾上腺素能神经元阻滞剂、血管紧张素转换酶抑制剂、血管紧张素-Ⅱ受体阻滞剂、β-肾上腺素受体阻滞剂、血管紧张素-Ⅲ受体阻滞剂、血管紧张素-Ⅳ受体阻滞剂、血管紧张素-Ⅴ受体阻滞剂和血管紧张素-Ⅵ受体阻滞剂、我们使用了β肾上腺素受体阻滞剂、中枢作用的降压药、钙通道阻滞剂、襻利尿剂、保钾利尿剂和矿物质皮质激素受体拮抗剂、肾素抑制剂、噻嗪类和相关利尿剂以及血管扩张剂。我们通过相应的基因和蛋白靶点,使用双样本孟德尔随机分析法估算了这些药物类别通过收缩压预防房颤的下游效应。SNPs提取自2项欧洲药物类别全基因组关联研究(n=317 754;n=757 601)和1项欧洲房颤全基因组关联研究(n=1 030 836):结果:药物目标孟德尔随机分析支持通过α-肾上腺素受体阻滞剂(n=11 SNPs; odds ratio [OR], 0.34 [95% CI, 0.21-0.56]; P=2.74×10-05)、β-肾上腺素受体阻滞剂(n=17 SNPs; OR, 0.52 [95% CI, 0.35-0.78];P=1.62×10-03)、钙通道阻滞剂(n=49 SNPs;OR,0.50 [95% CI,0.36-0.70];P=4.51×10-05)、血管扩张剂(n=19 SNPs;OR,0.53 [95% CI,0.34-0.84];P=7.03×10-03),以及所有12类降压药合计(n=158个SNPs;OR,0.64 [95% CI,0.54-0.77];P=8.50×10-07)对房颤风险的影响:我们的研究结果表明,通过各种降压药的蛋白靶点降低收缩压似乎有望预防房颤。我们的研究结果为未来的临床试验提供了参考,并对将降压药重新用于房颤预防具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
Hypertension
Hypertension 医学-外周血管病
CiteScore
15.90
自引率
4.80%
发文量
1006
审稿时长
1 months
期刊介绍: Hypertension presents top-tier articles on high blood pressure in each monthly release. These articles delve into basic science, clinical treatment, and prevention of hypertension and associated cardiovascular, metabolic, and renal conditions. Renowned for their lasting significance, these papers contribute to advancing our understanding and management of hypertension-related issues.
期刊最新文献
Evolutionary Characteristics in Primary Aldosteronism Patients. Rhythmic Contractions of Lymph Vessels and Lymph Flow Are Disrupted in Hypertensive Rats. Hyperadrenergic Postural Tachycardia Syndrome: Clinical Biomarkers and Response to Guanfacine. Predictive and Diagnostic Value of the Angiogenic Proteins in Patients With Chronic Kidney Disease. GPER Stimulation Attenuates Cardiac Dysfunction in a Rat Model of Preeclampsia.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1