MASLD and HFpEF share significant pathophysiological overlap, and the severity of liver fibrosis correlates with HFpEF prognosis, underscoring the need for multidisciplinary management.
Metabolic dysfunction-associated steatotic liver disease (MASLD) has rapidly become the leading cause of chronic liver disease and cirrhosis worldwide, driven by the global surge in metabolic disorders such as obesity, diabetes, hypertension, and dyslipidemia. In parallel, heart failure with preserved ejection fraction (HFpEF) has surpassed heart failure with reduced ejection fraction (HFrEF) as the predominant form of heart failure, particularly in individuals with metabolic comorbidities. Mounting evidence points to a significant overlap in the pathophysiological underpinnings of MASLD and HFpEF, with metabolic dysfunction serving as a common foundation. This review synthesizes current knowledge on the mechanistic links between MASLD and HFpEF, examining metabolic, inflammatory, and fibrotic pathways. We also explore the clinical implications of this association, including diagnostic considerations and therapeutic targets. Shared risk factors and inflammatory pathways have highlighted a strong bidirectional association between MASLD and cardiovascular diseases, particularly HFpEF. Significantly, the degree of hepatic fibrosis in MASLD correlates with HFpEF prognosis and severity, emphasizing the systemic nature of these conditions. Emerging pharmacological and lifestyle-based interventions aimed at managing both conditions underscore the importance of integrated, multidisciplinary care in improving long-term outcomes.
Brar et al. (Thu,) studied this question.
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