Evidence map›Paper›PMID 41377334›Full record

ArticleAnnals of medicine and surgery (2012)2025

Epicardial adipose tissue: a potential biomarker and therapeutic target in patients with paradoxical low-gradient aortic stenosis and preserved ejection fraction.

Qamar Abbas, Muhammad Ali Johar, Maliha Khalid, Muhammad Talha, Aminath Waafira

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Article in Annals of medicine and surgery (2012), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Qamar AbbasDepartment of Medicine, King Edward Medical University, Lahore, Pakistan.
Muhammad Ali JoharDepartment of Medicine, King Edward Medical University, Lahore, Pakistan.
Maliha KhalidDepartment of Medicine, Jinnah Sindh Medical University, Karachi, Pakistan.ORCID https://orcid.org/0009-0001-3413-2752
Muhammad TalhaDepartment of Medicine, King Edward Medical University, Lahore, Pakistan.
Aminath WaafiraSchool of Medicine, The Maldives National University, Malé, Maldives.ORCID https://orcid.org/0009-0000-3283-1982

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Paradoxical low-flow, low-gradient (LFLG) aortic stenosis (AS) with preserved ejection fraction (ASpEF) is a severe AS subtype associated with worse prognosis and increased mortality compared with high-gradient AS. Epicardial adipose tissue (EAT), a metabolically active visceral fat depot surrounding the myocardium, has emerged as a potential biomarker and therapeutic target in this population. EAT influences myocardial and valvular pathology through mechanical compression, metabolic alterations, and secretion of inflammatory mediators such as IL-6, MCP-1, and TNF-α, contributing to left ventricular remodeling and aortic valve degeneration. Recent metabolomic studies demonstrate significant associations between EAT thickness and both positively and negatively correlated metabolites, underscoring its complex role in disease progression. Despite its promise, challenges remain due to limited understanding of EAT-myocardium interactions, variable patient presentation, and confounding factors such as insulin resistance and obesity. Further research is warranted to clarify EAT's pathophysiological role, prognostic value, and therapeutic potential in managing paradoxical LFLG ASpEF.

Indexed as

aortic stenosiscardiac remodelingepicardial adipose tissuelow-gradient AS

Identifiers

PMID41377334
PMCPMC12688993

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