PulseExploreJournal ClubDebatesTrendingResearchersJournals
Instagram
HomeExploreJournal ClubTrending
Synapse
⌘+K
Synapse
January 10, 2026Nature Communications8 citationsOpen Access

Calcium channel blockers increase the risk of aortic aneurysm and dissection

TMTianfeng MaZCZeyu CaiXXXinming Xu

Key Result

Calcium channel blockers increased the risk of aortic aneurysm and dissection by 31% compared to untreated hypertensive patients (HR = 1.31) in a large cohort study.

Key Points

  • Investigate the relationship between calcium channel blockers and the risk of aortic aneurysm and dissection.
  • Analyzed data from 501,878 AAD-free participants in the UK Biobank.
  • Followed participants for a median of 13.5 years.
  • Conducted mouse models to assess effects of CCBs on aortic stiffness and AAD development.
  • Evaluated post-stent surgery outcomes in type B aortic dissection patients.
  • CCB users had a 31% higher risk of AAD compared to untreated hypertensive patients.
  • In mouse models, CCBs worsened aortic stiffness and AAD progression.
  • CCBs limited AAD regression in patients post-endovascular repair.

Structured PICO

Does calcium channel blocker use increase the risk of aortic aneurysm and dissection in hypertensive patients?

P
Population
501,878 initially AAD-free participants in the UK Biobank (28.3% with hypertension), 95 patients with type B aortic dissection who underwent thoracic endovascular aortic repair (TEVAR) from the GUEST study, and multiple mouse models of AAD (AngII-infused, BAPN-induced, and elastase-induced).
I
Intervention
Calcium channel blockers (CCBs), including dihydropyridines (amlodipine, nifedipine), benzothiazepines (diltiazem), and phenylalkylamines (verapamil).
C
Comparator
Hypertensive patients not receiving antihypertensive treatment, or users of other antihypertensive medications (e.g., ARBs like losartan).
O
Outcome
Incidence of aortic aneurysm and dissection (AAD) over a median follow-up of 13.5 years.hard clinical

Calcium channel blockers significantly increase the risk of aortic aneurysm and dissection in hypertensive patients and limit aortic regression after endovascular repair, suggesting caution when prescribing CCBs to patients at risk for AAD.

Abstract

Aortic aneurysm and dissection (AAD) are life-threatening conditions without effective medications. Impaired contractility of vascular smooth muscle cells (VSMCs) is strongly linked to AAD, but the role of calcium channel blockers (CCBs), which directly inhibits VSMC contractility, in AAD remains unclear. Here we showed data from 501,878 initially AAD-free participants in UK Biobank. Over a median follow-up of 13.5 years, CCB users had higher AAD risk (HR = 1.31) than hypertensive patients not receiving antihypertensive treatment. In mouse models of AAD, CCBs significantly aggravated aortic stiffness and AAD development. For patients with type B aortic dissection who underwent endovascular repair, CCBs limited AAD regression compared with other antihypertensives. Moreover, silencing of protein kinase cGMP-dependent 1 (PRKG1) significantly mitigated CCB-aggravated AAD progression. These findings suggest that CCBs may increase AAD risk and post-stent surgery prognosis, highlighting the need for caution when prescribing CCBs to hypertensive patients at risk for AAD.

Ask AI
Helpful
Bookmark
Share
View Full Paper

Cite This Study

Ma et al. (2025) studied this question. Calcium channel blockers increased the risk of aortic aneurysm and dissection by 31% compared to untreated hypertensive patients (HR = 1.31) in a large cohort study.

synapsesocial.com/papers/6963222391e05aa366cb8a5ehttps://doi.org/10.1038/s41467-025-68086-5
Ask AI
Helpful
Bookmark
Share
View Full Paper