Tailored Risk Stratification in Severe Mitral Regurgitation and Heart Failure Using Supervised Learning Techniques.

HFmrEF HFpEF HFrEF heart failure machine learning secondary mitral regurgitation supervised learning

Journal

JACC. Advances
ISSN: 2772-963X
Titre abrégé: JACC Adv
Pays: United States
ID NLM: 9918419284106676

Informations de publication

Date de publication:
Aug 2022
Historique:
received: 09 05 2022
revised: 04 07 2022
accepted: 06 07 2022
medline: 26 8 2022
pubmed: 26 8 2022
entrez: 28 6 2024
Statut: epublish

Résumé

Secondary mitral regurgitation (sMR) in the setting of heart failure (HF) has considerable impact on quality of life, HF rehospitalizations, and mortality. Identification of high-risk cohorts is essential to understand disease trajectories and for risk stratification. This study aimed to provide a structured decision tree-like approach to risk stratification in patients with severe sMR and HF. This observational study included 1,317 patients with severe sMR from the entire HF spectrum. Clinical, echocardiographic, and laboratory data were extracted for all patients. The primary end point was all-cause mortality. Survival tree analysis, a supervised learning technique, was applied to identify patient subgroups at risk of mortality and further stratified by HF subtype (preserved, mildly reduced, and reduced ejection fraction). Using supervised learning (survival tree method), 8 distinct subgroups were identified that differed significantly in long-term survival. Subgroup 7, characterized by younger age (≤66 years), higher hemoglobin (>12.7 g/dL), and higher albumin levels (>40.6 g/L) had the best survival. In contrast, subgroup 5 displayed a 20-fold risk of mortality (hazard ratio: 20.38 [95% CI: 10.78-38.52]); Supervised machine learning reveals heterogeneity in the sMR risk spectrum, highlighting the clinical variability in the population. A decision tree-like model can help identify differences in outcomes among subgroups and can help provide tailored risk stratification.

Sections du résumé

Background UNASSIGNED
Secondary mitral regurgitation (sMR) in the setting of heart failure (HF) has considerable impact on quality of life, HF rehospitalizations, and mortality. Identification of high-risk cohorts is essential to understand disease trajectories and for risk stratification.
Objectives UNASSIGNED
This study aimed to provide a structured decision tree-like approach to risk stratification in patients with severe sMR and HF.
Methods UNASSIGNED
This observational study included 1,317 patients with severe sMR from the entire HF spectrum. Clinical, echocardiographic, and laboratory data were extracted for all patients. The primary end point was all-cause mortality. Survival tree analysis, a supervised learning technique, was applied to identify patient subgroups at risk of mortality and further stratified by HF subtype (preserved, mildly reduced, and reduced ejection fraction).
Results UNASSIGNED
Using supervised learning (survival tree method), 8 distinct subgroups were identified that differed significantly in long-term survival. Subgroup 7, characterized by younger age (≤66 years), higher hemoglobin (>12.7 g/dL), and higher albumin levels (>40.6 g/L) had the best survival. In contrast, subgroup 5 displayed a 20-fold risk of mortality (hazard ratio: 20.38 [95% CI: 10.78-38.52]);
Conclusions UNASSIGNED
Supervised machine learning reveals heterogeneity in the sMR risk spectrum, highlighting the clinical variability in the population. A decision tree-like model can help identify differences in outcomes among subgroups and can help provide tailored risk stratification.

Identifiants

pubmed: 38938405
doi: 10.1016/j.jacadv.2022.100063
pii: S2772-963X(22)00067-9
pmc: PMC11198388
doi:

Types de publication

Journal Article

Langues

eng

Pagination

100063

Informations de copyright

© 2022 The Authors.

Déclaration de conflit d'intérêts

This work was supported by a grant of the 10.13039/501100002428Austrian Science Fund (FWF – identification number: KLI-818B). The authors have reported that they have no relationships relevant to the contents of this paper to disclose.PERSPECTIVESCOMPETENCY IN PATIENT CARE AND PROCEDURAL SKILLS: In patients with severe sMR and HF, a heterogenous risk spectrum was identified by supervised learning techniques. Patients with younger age, better renal function, and higher hemoglobin values had the most favorable survival, whereas older patients with low serum albumin and higher NT-proBNP values experience a 20-fold risk increase in mortality. TRANSLATIONAL OUTLOOK: Further studies are needed to refine the therapeutic management for sMR in every HF subtype, taking into account the complex underlying heterogeneity in this population.

Auteurs

Gregor Heitzinger (G)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Georg Spinka (G)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Suriya Prausmüller (S)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Noemi Pavo (N)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Varius Dannenberg (V)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Carolina Donà (C)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Matthias Koschutnik (M)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Andreas Kammerlander (A)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Christian Nitsche (C)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Henrike Arfsten (H)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Stefan Kastl (S)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Guido Strunk (G)

Complexity Research, Vienna, Austria.

Martin Hülsmann (M)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Raphael Rosenhek (R)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Christian Hengstenberg (C)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Philipp E Bartko (PE)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.

Georg Goliasch (G)

Department of Internal Medicine II, Medical University of Vienna, Vienna, Austria.
Herzzentrum Währing, Vienna, Austria.

Classifications MeSH