# Evaluating the effect of renin-angiotension-aldosterone system inhibitors and beta blockers on the progression of bicuspid aortic valve aortopathy in adulthood: A retrospective cohort study

**Authors:** Nili Schamroth Pravda, Elchanan Samuel, Tamir Bental, Ofir Brem, Ilan Richter, Keren Skalsky, Miri Schamroth Pravda, Yaron Shapira, Ran Kornowski, Guy Witberg

PMC · DOI: 10.1016/j.ijcchd.2026.100653 · International Journal of Cardiology Congenital Heart Disease · 2026-01-12

## TL;DR

This study found that medications like RAASi and beta blockers did not significantly slow aortic enlargement in adults with bicuspid aortic valve.

## Contribution

The study provides new evidence on the lack of significant effect of RAASi and beta blockers in slowing BAV aortopathy progression.

## Key findings

- Chronic use of RAASi or beta blockers was not associated with reduced aortic dilation in BAV patients.
- The 10-year cumulative incidence of the primary endpoint was 14.6%, and 33.3% at 15 years.
- Multivariate analysis showed no significant risk reduction for the primary outcome with either medication.

## Abstract

Patients with a bicuspid aortic valve (BAV) often have an associated aortopathy and increased risk of aortic dissection. This study aimed to assess if the chronic use of renin-angiotensin-aldosterone system inhibitors (RAASi) or beta blockers (BB) may be associated with reducing the progression of aortic dilation in adult BAV patients.

A retrospective cohort study was performed including adult patients with BAV with serial echocardiography over ≥5 years. The cohort was subdivided according to chronic use of RAASi or BB. The primary outcome was a composite of progression of absolute ascending aortic diameter ≥4.5 cm or surgery for ascending aortic replacement.

Included were 262 patients with mean age of 54.3 ± 19.5 years and 75.1 % male. The average follow-up time was 10.8 ± 0.8 years. The cumulative incidence of the primary endpoint was 14.6 % at 10-year follow up and 33.3 % at 15-year follow up. While those with RAASi (n = 39) had the primary endpoint numerically less that those without RAASi chronic therapy (12.8 % vs 24.8 %, p = 0.147), on multivariate analysis there was no significant decreased risk for the primary outcome. (HR = 0.89, 95 % CI [0.34–2.86], p = 0.97). Similarly, there was no significant decreased risk of the primary outcome amongst those with chronic beta blocker use following multivariate analysis (HR = 0.96, 95 % CI [0.37–2.51], p = 0.95).

Our findings suggest that the chronic use of RAASi or BB was not associated with a blunted progression of BAV aortopathy in the adult population. These results highlight the need for larger, randomised studies to validate these observations and further explore potential preventative strategies in this population.

Fig. 1: Central Illustration.Image 1

One-sentence summary: This study investigates whether medications commonly used for heart conditions, specifically renin-angiotensin-aldosterone system inhibitors (RAASi) and beta blockers, may slow down the progression of aortic enlargement in adults with bicuspid aortic valve (BAV).

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** aortic dilatation (MESH:D002311), death (MESH:D003643), Hypertension (MESH:D006973), arterial hypertension (MESH:D000081029), aortic enlargement (MESH:D006529), BAV (MESH:D000082882), ascending aorta dilation (MESH:D000094630), aortic regurgitation (MESH:D001022), heart conditions (MESH:D006331), heart failure (MESH:D006333), aneurysm (MESH:D000783), valvular disease (MESH:D006349), aortic dissection (MESH:D000784), congenital cardiac abnormalities (MESH:D000013), aortic valve disease (MESH:D000082862), Marfan-associated aortopathy (MESH:D008382), aortic stenosis (MESH:D001024)
- **Chemicals:** RAAS (-), aldosterone (MESH:D000450)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Cell lines:** 955-20 — Mus musculus (Mouse), Embryonic stem cell (CVCL_PW37)

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12914844/full.md

## References

16 references — full list in the complete paper: https://tomesphere.com/paper/PMC12914844/full.md

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Source: https://tomesphere.com/paper/PMC12914844