Key result
Overweight and obesity affect ~80% of HFpEF patients, driving a distinct hemodynamic and neurohormonal phenotype.
Why the study?
Obesity is highly prevalent in patients with HFpEF and is associated with distinct pathophysiological mechanisms that require further understanding.
Supports addressing obesity in HFpEF; leaves open whether weight loss alters outcomes in this phenotype.
Obesity is a risk factor for heart failure and cardiovascular disease. Of particular note, over 80% of patients with heart failure with a preserved ejection fraction (HFpEF) are overweight or obese. In this study, we aimed to review the association between obesity and HFpEF. Obese patients with HFpEF exhibit a distinct phenotype. In addition to impaired left ventricular (LV) diastolic function and high filling pressures, obese patients with HFpEF possess other factors that cause elevated LV filling pressure, such as a greater dependence on plasma volume expansion, aggravated pericardial restraint, and increased ventricular interaction. Obesity can contribute to HFpEF through hemodynamic, neurohormonal, inflammatory, and mechanical mechanisms. An increased amount of body fat can induce plasma volume expansion, resulting in chamber remodeling, pericardial restraint, and ultimately elevations in LV filling pressure. Obesity can mediate the activation of sympathetic nervous system signaling and the renin-angiotensin-aldosterone system. These unique pathophysiological characteristics of individuals with both obesity and HFpEF suggest that obesity with HFpEF can be considered a specific phenotype. Future research is expected to clarify effective treatment modalities for obesity-related HFpEF.
No takes yet. Share an insight, caveat, or question.
Da Young Lee (2022) conducted a review in Heart failure with preserved ejection fraction (HFpEF) and obesity. Obesity was evaluated. Over 80% of patients with heart failure with a preserved ejection fraction are overweight or obese, presenting a distinct phenotype driven by hemodynamic and neurohormonal mechanisms.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: