Unsupervised Cluster Analysis of Patients With Aortic Stenosis Reveals Distinct Population With Different Phenotypes and Outcomes

Author:

Kwak Soongu1,Lee Yunhwan2,Ko Taehoon3,Yang Seokhun1,Hwang In-Chang4,Park Jun-Bean1,Yoon Yeonyee E.4,Kim Hack-Lyoung5,Kim Hyung-Kwan1,Kim Yong-Jin1,Cho Goo-Yeong4,Sohn Dae-Won1,Won Sungho2ORCID,Lee Seung-Pyo1ORCID

Affiliation:

1. Department of Internal Medicine (S.K., S.Y., J.-B.P., H.-K.K., Y.-J.K., D.-W.S., S.-P.L.), Seoul National University Hospital

2. Department of Public Health Sciences, Seoul National University (Y.L., S.W.)

3. Office of Hospital Information (T.K.), Seoul National University Hospital

4. Department of Internal Medicine, Seoul National University Bundang Hospital, Gyeonggi-do (I.-C.H., Y.E.Y., G.-Y.C.)

5. Department of Internal Medicine, Seoul Metropolitan Government-Seoul National University Boramae Medical Center, South Korea (H.-L.K.).

Abstract

Background: There is a lack of studies investigating the heterogeneity of patients with aortic stenosis (AS). We explored whether cluster analysis identifies distinct subgroups with different prognostic significances in AS. Methods: Newly diagnosed patients with moderate or severe AS were prospectively enrolled between 2013 and 2016 (n=398, mean 71 years, 55% male). Among demographics, laboratory, and echocardiography parameters (n=32), 11 variables were selected through dimension reduction and used for unsupervised clustering. Phenotypes and causes of mortality were compared between the clusters. Results: Three clusters with markedly different features were identified. Cluster 1 (n=60) was predominantly associated with cardiac dysfunction, cluster 2 (n=86) consisted of elderly with comorbidities, especially end-stage renal disease, whereas cluster 3 (n=252) demonstrated neither cardiac dysfunction nor comorbidities. Although AS severity did not differ, there was a significant difference in adverse outcomes between the clusters during a median 2.4 years follow-up (mortality rate, 13.3% versus 19.8% versus 6.0% for cluster 1, 2, and 3, P <0.001). Particularly, compared with cluster 3, cluster 1 was associated with only cardiac mortality (adjusted hazard ratio, 7.37 [95% CI, 2.00–27.13]; P =0.003), whereas cluster 2 was associated with higher noncardiac mortality (adjusted hazard ratio, 3.35 [95% CI, 1.26–8.90]; P =0.015). Phenotypes and association of clusters with specific outcomes were reproduced in an independent validation cohort (n=262). Conclusions: Unsupervised cluster analysis of patients with AS revealed 3 distinct groups with different causes of death. This provides a new perspective in the categorization of patients with AS that takes into account comorbidities and extravalvular cardiac dysfunction.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging

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