Contributions of Inflammation to Cardiometabolic Heart Failure with Preserved Ejection Fraction.


Journal

Annual review of pathology
ISSN: 1553-4014
Titre abrégé: Annu Rev Pathol
Pays: United States
ID NLM: 101275111

Informations de publication

Date de publication:
02 Oct 2024
Historique:
medline: 2 10 2024
pubmed: 2 10 2024
entrez: 2 10 2024
Statut: aheadofprint

Résumé

The most common form of heart failure is heart failure with preserved ejection fraction (HFpEF). While heterogeneous in origin, the most common form of HFpEF is the cardiometabolic manifestation. Obesity and aging promote systemic inflammation that appears integral to cardiometabolic HFpEF pathophysiology. Accumulation of immune cells within the heart, fueled by an altered metabolome, contribute to cardiac inflammation and fibrosis. In spite of this, broad anti-inflammatory therapy has not shown significant benefit in patient outcomes. Thus, understanding of the nuances to metabolic and age-related inflammation during HFpEF is paramount for more targeted interventions. Here, we review clinical evidence of inflammation in the context of HFpEF and summarize our mechanistic understanding of immunometabolic inflammation, highlighting pathways of therapeutic potential along the way.

Identifiants

pubmed: 39357068
doi: 10.1146/annurev-pathmechdis-111523-023405
doi:

Types de publication

Journal Article Review

Langues

eng

Sous-ensembles de citation

IM

Auteurs

Edward B Thorp (EB)

Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA; email: ebthorp@northwestern.edu, mallory.filipp@northwestern.edu.

Mallory Filipp (M)

Feinberg School of Medicine, Northwestern University, Chicago, Illinois, USA; email: ebthorp@northwestern.edu, mallory.filipp@northwestern.edu.

Classifications MeSH