Unsupervised Cluster Analysis in Patients with Cardiorenal Syndromes: Identifying Vascular Aspects

Author:

de Freminville Jean-Baptiste12ORCID,Halimi Jean-Michel345,Maisons Valentin36ORCID,Goudot Guillaume27ORCID,Bisson Arnaud48ORCID,Angoulvant Denis48,Fauchier Laurent48ORCID

Affiliation:

1. Service de Cardiologie-Médecine Vasculaire, Hôpital Trousseau, Centre Hospitalier Regional Universitaire de Tours, 37044 Tours Cedex 9, France

2. Service de Medecine Vasculaire, Hopital Europeen Georges Pompidou, Assistance Publique Hôpitaux de Paris, Université Paris Cité, 75015 Paris, France

3. Néphrologie-Immunologie Clinique, Hôpital Bretonneau, Centre Hospitalier Regional Universitaire de Tours, 37000 Tours, France

4. Faculté de Medecine, UMR Inserm University of Tours 1327 ISCHEMIA “Membrane Signalling and Inflammation in Reperfusion Injuries”, 37044 Tours, France

5. F-CRIN INI-CRCT, 10, Boulevard Tonnellé, 37032 Tours, France

6. INSERM U1246 SPHERE, Universities of Nantes and Tours, 37044 Tours, France

7. INSERM U970 PARCC, Université Paris Cité, 75015 Paris, France

8. Service de Cardiologie, Centre Hospitalier Universitaire Trousseau et Faculté de Médecine, 37044 Tours, France

Abstract

Background/Objectives: Cardiorenal syndrome (CRS) is a disorder of the heart and kidneys, with one type of organ dysfunction affecting the other. The pathophysiology is complex, and its actual description has been questioned. We used clustering analysis to identify clinically relevant phenogroups among patients with CRS. Methods: Data for patients admitted from 1 January 2012 to 31 December 2012 were collected from the French national medico-administrative database. Patients with a diagnosis of heart failure and chronic kidney disease and at least 5 years of follow-up were included. Results: In total, 13,665 patients were included and four clusters were identified. Cluster 1 could be described as the vascular–diabetes cluster. It comprised 1930 patients (14.1%), among which 60% had diabetes, 94% had coronary artery disease (CAD), and 80% had peripheral artery disease (PAD). Cluster 2 could be described as the vascular cluster. It comprised 2487 patients (18.2%), among which 33% had diabetes, 85% had CAD, and 78% had PAD. Cluster 3 could be described as the metabolic cluster. It comprised 2163 patients (15.8%), among which 87% had diabetes, 67% dyslipidemia, and 62% obesity. Cluster 4 comprised 7085 patients (51.8%) and could be described as the low-vascular cluster. The vascular cluster was the only one associated with a higher risk of cardiovascular death (HR: 1.48 [1.32–1.66]). The metabolic cluster was associated with a higher risk of kidney replacement therapy (HR: 1.33 [1.17–1.51]). Conclusions: Our study supports a new classification of CRS based on the vascular aspect of pathophysiology differentiating microvascular or macrovascular lesions. These results could have an impact on patients’ medical treatment.

Publisher

MDPI AG

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