Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data.

Soltani, F.; Jenkins, DA.; Kaura, A.; Bradley, J.; Black, N.; Farrant, JP.; Williams, SG.; Mulla, A.; Glampson, B.; Davies, J.; Papadimitriou, D.; Woods, K.; Shah, AD.; Thursz, MR.; Williams, B.; Asselbergs, FW.; Mayer, EK.; Herbert, C.; Grant, S.; Curzen, N.; Squire, I.; Johnson, T.; O'Gallagher, K.; Shah, AM.; Perera, D.; Kharbanda, R.; Patel, RS.; Channon, KM.; Lee, R.; Peek, N.; Mayet, J.; Miller, CA.

Phenogrouping heart failure with preserved or mildly reduced ejection fraction using electronic health record data.

All Authors

Soltani, F.

Jenkins, DA.

Kaura, A.

Bradley, J.

Black, N.

Farrant, JP.

Williams, SG.

Mulla, A.

Glampson, B.

Davies, J.

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LTHT Author

Herbert, Christopher

LTHT Department

NIHR Leeds Biomedical Research Centre

Publication Date

2024

Item Type

Journal Article
Multicenter Study
Comparative Study
Research Support, Non-U.S. Gov't

Abstract

BACKGROUND: Heart failure (HF) with preserved or mildly reduced ejection fraction includes a heterogenous group of patients. Reclassification into distinct phenogroups to enable targeted interventions is a priority. This study aimed to identify distinct phenogroups, and compare phenogroup characteristics and outcomes, from electronic health record data. METHODS: 2,187 patients admitted to five UK hospitals with a diagnosis of HF and a left ventricular ejection fraction >= 40% were identified from the NIHR Health Informatics Collaborative database. Partition-based, model-based, and density-based machine learning clustering techniques were applied. Cox Proportional Hazards and Fine-Gray competing risks models were used to compare outcomes (all-cause mortality and hospitalisation for HF) across phenogroups. RESULTS: Three phenogroups were identified: (1) Younger, predominantly female patients with high prevalence of cardiometabolic and coronary disease; (2) More frail patients, with higher rates of lung disease and atrial fibrillation; (3) Patients characterised by systemic inflammation and high rates of diabetes and renal dysfunction. Survival profiles were distinct, with an increasing risk of all-cause mortality from phenogroups 1 to 3 (p < 0.001). Phenogroup membership significantly improved survival prediction compared to conventional factors. Phenogroups were not predictive of hospitalisation for HF. CONCLUSIONS: Applying unsupervised machine learning to routinely collected electronic health record data identified phenogroups with distinct clinical characteristics and unique survival profiles.