# Mechanistic classification of isolated severe aortic regurgitation in a contemporary cohort of patients

**Authors:** Rudy R Unni, Munir Boodhwani, Ibrahim Jelaidan, David T Harnett, Samia Massalha, Calvin Liang, Graeme Prosperi-Porta, David Glineur, Ian G Burwash, Kwan-Leung Chan, Thais Coutinho, Angel Fu, Nadav Willner, David Messika-Zeitoun, Luc Beauchesne

PMC · DOI: 10.1093/ehjopen/oeaf042 · European Heart Journal Open · 2025-05-02

## TL;DR

This study classifies the mechanisms of severe aortic regurgitation in patients and finds that leaflet prolapse is the most common cause, especially in those with bicuspid aortic valves.

## Contribution

The study provides a contemporary classification of aortic regurgitation mechanisms and their surgical implications in a large patient cohort.

## Key findings

- Leaflet prolapse (Type II) was the most common AR mechanism, observed in 48.6% of patients.
- Bicuspid aortic valve patients had a higher frequency of multiple AR mechanisms compared to others.
- Aortic valve repair was performed in nearly half of surgical interventions, highlighting the importance of mechanism identification.

## Abstract

Aortic regurgitation (AR) arises from leaflet disease and/or dilatation of the functional aortic annulus complex. Understanding the mechanisms of AR informs surgical planning of valve and aorta repair. This study investigates the mechanisms, aetiologies, and outcomes of isolated native severe AR in a consecutive cohort of patients.

Patients with moderate-to-severe (3+)/severe (4+) native valve AR, identified from our institutional echocardiography database (2014–2018), were included. Exclusions were significant concomitant valve disease, endocarditis, or aortic dissection. AR was classified per the El-Khoury system: Type I (normal leaflet motion: Ia–ascending aorta/sinotubular junction dilatation, Ib–aortic root dilation, Ic–aortic annular dilation), Type II (leaflet prolapse), and Type III (leaflet restriction). Valve anatomy and clinical outcomes, including mortality and surgical intervention, were analyzed. Of 282 patients (77.3% male), 58.5% had multiple AR mechanisms. Type II (leaflet prolapse) was most common (48.6%), followed by Type III (36.2%). Bicuspid aortic valve (BAV) represented 35.5% of the population, with leaflet prolapse observed in 72%. Multiple mechanisms were more frequent in BAV (77% vs. 48%, P < 0.001). After a median follow-up of 4.7 years (available for 97.5% of patients), 158 (57.5%) underwent an intervention with 48.7% having an aortic valve repair or valve-sparing aortic root replacement.

Although leaflet prolapse (Type II) was the pre-dominant AR mechanism, multiple contributing mechanisms were often present, particularly in BAV patients. Aortic valve repair accounted for nearly half of surgical interventions, underscoring the importance of mechanism identification to optimize repair and avoid valve replacement.

Graphical Abstract

## Linked entities

- **Diseases:** endocarditis (MONDO:0005025)

## Full-text entities

- **Diseases:** rheumatic AV disease (MESH:D000082862), excessive leaflet motion/ (MESH:D009041), stenosis (MESH:D003251), rheumatic (MESH:D012216), Aortic valve (AV) prolapse (MESH:D001023), diastole (MESH:D006337), endocarditis (MESH:D004696), aorta (MESH:D000784), aortic root dilatation (MESH:D000094628), leaflet restriction (MESH:D002313), Leaflet prolapse (MESH:D011391), III (MESH:C537189), Ia (MESH:C535739), aortic or mitral stenosis (MESH:D008946), BAV (MESH:D000082882), AR (MESH:D001022), VHD (MESH:D006349), flail leaflet (MESH:D005409), aortic root and ascending aorta dilatation (MESH:D000094630), degenerative (MESH:D019636), leaflet disease (MESH:D004194), MR (MESH:D008944), Marfan syndrome (MESH:D008382), CVA (MESH:D020521), annular dilation (MESH:D002311), quadricuspid aortic valve (MESH:D000082902), AV endocarditis (MESH:D001024), died (MESH:D003643), UAV (MESH:C000655292), congenital valve abnormality (MESH:D000013), Congenital Heart Disease (MESH:D006330)
- **Chemicals:** P (MESH:D010758)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

6 references — full list in the complete paper: https://tomesphere.com/paper/PMC12076401/full.md

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Source: https://tomesphere.com/paper/PMC12076401