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The Role of Epicardial Fat Thickness and B-type Natriuretic Peptide (BNP)/N-terminal Pro B-type Natriuretic Peptide
Areij Awad Osman Mohamed1, Sahla Shurahbeel Bashir Omer2, Musab Mukhtar3
1Cardiology, Sudan Heart Center, Khartoum, SDN.
Insights
Epicardial fat thickness (EFT) and natriuretic peptides (BNP/NT-proBNP) offer complementary insights for heart failure risk stratification. Their combined use aids personalized treatment by assessing inflammation, adiposity, and cardiac stress.
Area of Science:
- Cardiology and Cardiovascular Research
- Biomarkers and Diagnostic Tools
- Systematic Review and Meta-Analysis
Background:
- Heart failure (HF) presents a significant global health burden, demanding enhanced risk stratification methods.
- Epicardial adipose tissue (EAT), measured by epicardial fat thickness (EFT), and natriuretic peptides (BNP/NT-proBNP) are implicated in HF pathophysiology.
- Understanding the interplay between EFT and BNP/NT-proBNP is crucial for improving patient outcomes.
Purpose of the Study:
- To systematically review the combined role of EFT and BNP/NT-proBNP in stratifying risk for heart failure.
- To examine the pathophysiological mechanisms linking EFT and natriuretic peptides in diverse patient populations.
- To evaluate the clinical utility of combined EFT and BNP/NT-proBNP assessment for personalized HF management.
Main Methods:
- A systematic review adhering to PRISMA 2020 guidelines, screening 192 records from major databases (PubMed/MEDLINE, Embase, Scopus, Web of Science, Cochrane Library).
- Inclusion of 12 case-control studies assessing EFT and BNP/NT-proBNP in HF or at-risk populations.
- Methodological quality appraisal using the Newcastle-Ottawa Scale (NOS).
Main Results:
- Consistent correlation observed between EFT and elevated BNP/NT-proBNP levels, with variations across HF phenotypes.
- In HF with reduced ejection fraction (HFrEF), NT-proBNP linked more to muscle loss; in HF with preserved ejection fraction (HFpEF), EFT correlated with metabolic issues and inflammation.
- Lower EFT paradoxically predicted worse outcomes in nonischemic cardiomyopathy (NICMP), suggesting disease-related fat depletion.
Conclusions:
- Combined assessment of EFT and BNP/NT-proBNP provides complementary prognostic information, reflecting subclinical inflammation, adiposity, and myocyte stress.
- Findings support phenotype-specific interpretation of EFT and suggest personalized interventions based on combined biomarker profiles.
- Further research on standardized EFT measurement and EAT-modulating therapies is warranted.
Abstract:
Heart failure (HF) remains a global health challenge, necessitating improved risk stratification tools. This systematic review evaluates the combined role of epicardial fat thickness (EFT) and B-type natriuretic peptide (BNP)/N-terminal pro B-type natriuretic peptide (NT-proBNP) in HF risk stratification, examining their pathophysiological interplay and clinical utility across diverse populations, including a wide age range, various comorbidities (e.g., obesity, diabetes, and systemic sclerosis), and geographic regions. EFT, a measurable marker of epicardial adipose tissue (EAT) located between the myocardium and visceral pericardium, was evaluated alongside BNP/NT-proBNP, established biomarkers of cardiac stress. Following the Preferred Reporting Items for Systematic Reviews and Meta-Analyses 2020 guidelines, 12 case-control studies were included after screening 192 records from PubMed/MEDLINE, Embase, Scopus, Web of Science, and Cochrane Library. Studies assessed EFT and BNP/NT-proBNP in HF or at-risk populations. Methodological quality was appraised using the Newcastle-Ottawa Scale (NOS). EFT consistently correlated with elevated BNP/NT-proBNP, though patterns differed by HF phenotype. In HF with reduced ejection fraction (HFrEF), NT-proBNP associated more strongly with muscle loss than adiposity, while in HF with preserved ejection fraction (HFpEF), EFT was linked to metabolic comorbidities and inflammatory markers. Paradoxically, lower EFT predicted worse outcomes in nonischemic cardiomyopathy (NICMP), potentially reflecting disease-related fat depletion or cachexia; this finding underscores the need for phenotype-specific interpretation of EFT in risk stratification. Mechanistically, EAT contributed to myocardial remodeling via adipokine secretion and inflammatory signaling. Four studies had a low risk of bias (NOS ≥ 8), while one showed a high risk. The combined assessment of EFT and BNP/NT-proBNP offers complementary prognostic insights, EFT capturing subclinical inflammation and adiposity-related remodeling, while BNP/NT-proBNP reflects myocyte stress, potentially guiding personalized treatment decisions, including closer monitoring of HFpEF patients with elevated EFT and early nutritional or anti-inflammatory interventions in those with muscle loss and elevated NT-proBNP. Inclusion criteria encompassed adult populations with HF or related conditions, with exclusion of reviews, case reports, and non-English articles, supporting the methodological rigor of this synthesis. Standardized EFT measurement and targeted EAT-modulating therapies warrant further investigation.
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