Key result
Baseline marinobufagenin excretion was positively associated with percentage change in left ventricular mass index in obese adults (Std. β = 0.336; p=0.003), but not in normal weight adults.
Why the study?
The adverse effects of marinobufagenin on cardiac remodeling may be exacerbated in obesity, prompting evaluation of whether it relates to changes in left ventricular mass index over time in obese versus non-obese adults.
Is baseline marinobufagenin (MBG) excretion associated with increased left ventricular mass index (LVMi) over time in obese compared to non-obese adults?
Cohort (n=275)
Is baseline marinobufagenin (MBG) excretion associated with increased left ventricular mass index (LVMi) over time in obese compared to non-obese adults?
Effect estimate: Std. β = 0.336
p-value: p=0.003
Baseline marinobufagenin excretion predicts increased left ventricular mass over 4.5 years in obese but not normal-weight young adults, suggesting a mechanism for salt-induced cardiac remodeling in obesity.
MBG excretion may flag remodeling risk in obese adults; leaves open causal role and need for prospective trials.
The endogenous Na+/K+-ATPase inhibitor, marinobufagenin (MBG), strongly associates with salt intake and a greater left ventricular mass index (LVMi) in humans and was shown to promote cardiac fibrosis and hypertrophy in animals. The adverse effects of MBG on cardiac remodeling may be exacerbated with obesity, due to an increased sensitivity of Na+/K+-ATPase to MBG. This study determined whether MBG is related to the change in LVMi over time in adults with a body mass index (BMI) ≥30 kg/m2 (obese) and <30 kg/m2 (non-obese). The study followed 275 healthy participants (aged 20–30 years) from the African-Prospective study on the Early Detection and Identification of Cardiovascular disease and Hypertension (African-PREDICT) study over 4.5 years. At baseline, we measured 24 h urine MBG excretion. MBG levels were positively associated with salt intake. LVMi was determined by two-dimensional echocardiography at baseline and after >4.5 years. With multivariate adjusted analyses in obese adults (N = 56), we found a positive association of follow-up LVMi (Adjusted (Adj.) R2 = 0.35; Std. β = 0.311; p = 0.007) and percentage change in LVMi (Adj. R2 = 0.40; Std. β = 0.336; p = 0.003) with baseline MBG excretion. No association of LVMi (Adj. R2 = 0.37; p = 0.85) or percentage change in LVMi (Adj. R2 = 0.19; p = 0.68) with MBG excretion was evident in normal weight adults (N = 123). These findings suggest that obese adults may be more sensitive to the adverse cardiac effects of MBG and provide new insight into the potential role of dietary salt, by way of MBG, in the pathogenesis of cardiac remodeling in obese individuals.
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Strauss‐Kruger et al. (2020) conducted a cohort in Healthy participants (obese and non-obese) (n=275). Marinobufagenin (MBG) excretion vs. Normal weight adults was evaluated on Percentage change in left ventricular mass index (LVMi) (Std. β = 0.336, p=0.003). Baseline marinobufagenin excretion was positively associated with percentage change in left ventricular mass index in obese adults (Std. β = 0.336; p=0.003), but not in normal weight adults.
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