<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Nie H</submitter><funding>Nanchang University Funding</funding><funding>National Natural Science Foundation of China</funding><funding>Jiangxi Provincial Health Commission</funding><pagination>116-135</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12063591</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(2)</volume><pubmed_abstract>&lt;h4>Objective&lt;/h4>To assess the impact of lipid-lowering drugs (LLDs) and antihypertensive drugs on the risk of aortic diseases.&lt;h4>Methods&lt;/h4>Mendelian randomization was utilized to analyse data from 500 000 participants in the UK Biobank to evaluate the effects of statins, PCSK9 inhibitors (PCSK9i), β-blockers, and calcium channel blockers on the risks of thoracic aortic aneurysm, abdominal aortic aneurysm, and aortic dissection (AD) using genetic variants as proxies. Real-world pharmacovigilance data from the FAERS (FDA Adverse Event Reporting System) database were used.&lt;h4>Results&lt;/h4>PCSK9i and statins significantly reduced the risks of aortic aneurysms and AD, respectively. Furthermore, the two LLDs reduced the risk of aortic diseases through certain metabolites. Meanwhile, real-wor</pubmed_abstract><journal>European heart journal. Cardiovascular pharmacotherapy</journal><pubmed_title>Lipid-lowering and antihypertensive drugs on aortic disease risk: insights from Mendelian randomization analysis and real-world pharmacovigilance data.</pubmed_title><pmcid>PMC12063591</pmcid><funding_grant_id>82460103</funding_grant_id><funding_grant_id>2024ZD005</funding_grant_id><funding_grant_id>82060095</funding_grant_id><funding_grant_id>2023efyA02</funding_grant_id><pubmed_authors>Wang Q</pubmed_authors><pubmed_authors>Zhao W</pubmed_authors><pubmed_authors>Zhou W</pubmed_authors><pubmed_authors>Nie H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Lipid-lowering and antihypertensive drugs on aortic disease risk: insights from Mendelian randomization analysis and real-world pharmacovigilance data.</name><description>&lt;h4>Objective&lt;/h4>To assess the impact of lipid-lowering drugs (LLDs) and antihypertensive drugs on the risk of aortic diseases.&lt;h4>Methods&lt;/h4>Mendelian randomization was utilized to analyse data from 500 000 participants in the UK Biobank to evaluate the effects of statins, PCSK9 inhibitors (PCSK9i), β-blockers, and calcium channel blockers on the risks of thoracic aortic aneurysm, abdominal aortic aneurysm, and aortic dissection (AD) using genetic variants as proxies. Real-world pharmacovigilance data from the FAERS (FDA Adverse Event Reporting System) database were used.&lt;h4>Results&lt;/h4>PCSK9i and statins significantly reduced the risks of aortic aneurysms and AD, respectively. Furthermore, the two LLDs reduced the risk of aortic diseases through certain metabolites. Meanwhile, real-wor</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2026-07-01T03:21:25.965Z</modification><creation>2026-07-01T03:12:08.355Z</creation></dates><accession>S-EPMC12063591</accession><cross_references><pubmed>39855644</pubmed><doi>10.1093/ehjcvp/pvaf001</doi></cross_references></HashMap>