Key result
Diet modification to a normal-salt diet reversed HFpEF phenotypes and prolonged survival in rats, despite systolic blood pressure remaining high (~200 mmHg).
Why the study?
Hypertension-induced inflammation and subsequent ventricular fibrosis are believed to underlie HFpEF, but the role of diet modification in its progression required investigation.
Does switching from a high-salt to a normal-salt diet improve diastolic function and HFpEF phenotypes in a rat model?
RCT
randomly assigned
Does switching from a high-salt to a normal-salt diet improve diastolic function and HFpEF phenotypes in a rat model?
In a rat model of HFpEF, reducing dietary salt intake reversed diastolic dysfunction and improved survival despite persistent hypertension and hypertrophy.
Dahl Salt-Sensitive (DSS) rats develop heart failure with preserved ejection fraction (HFpEF) when fed a high-salt (8 % NaCl) diet. Hypertension-induced inflammation and subsequent ventricular fibrosis are believed to underlie the development of HFpEF. We investigated the role of diet modification in the progression of HFpEF using male DSS rats, fed either a high-salt diet from7 weeks of age to induce HFpEF, ora normal-salt (0.3% NaCl) diet as controls. After echocardiographic confirmation of diastolic dysfunction at 14-15 weeks of age along with HF manifestations, the HFpEF rats were randomly assigned to either continue a high-salt diet or switch to a normal-salt diet for an additional 4 weeks. HFpEF rats with diet modification showed improved diastolic function (reduced E/E' ratio in echocardiogram), increased functional capacity (increased treadmill exercise distance), and reduced pulmonary congestions (lung/body weight ratio), compared to high-salt-fed HFpEF rats. Systolic blood pressure remained high (~200 mmHg), and ventricular hypertrophy remained unchanged. Ventricular arrhythmia inducibility (100 % inducible) and corrected QT interval (on ECG) did not change in HFpEF rats after diet modification. HFpEF rats with diet modification showed prolonged survival and reduced ventricular fibrosis (Masson's trichrome staining) compared to high-salt-fed HFpEF rats. Hence, the modification of diet (from high-salt to normal-salt diet) reversed HFpEF phenotypes without affecting blood pressure or ventricular hypertrophy.
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Kim et al. (2023) conducted an RCT in Heart failure with preserved ejection fraction (HFpEF). Normal-salt diet vs. High-salt (8% NaCl) diet was evaluated on Diastolic function, functional capacity, pulmonary congestion, and survival. Diet modification to a normal-salt diet reversed HFpEF phenotypes and prolonged survival in rats, despite systolic blood pressure remaining high (~200 mmHg).
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