Key result
Elevated brain natriuretic peptide was associated with increased all-cause mortality in univariable analysis (HR 2.61), but lost significance after adjusting for age, inflammation, and handgrip strength.
Why the study?
Fluid overload and overhydration are risk factors for mortality in CKD, prompting an evaluation of the relationships between BNP, overhydration, and all-cause mortality in haemodialysis patients.
Observational (n=64)
No
Hazard Ratio: 2.61 (95% CI 1.34–5.11)
Absolute Event Rate: 71% vs 40%
p-value: p=0.005
While elevated BNP is correlated with all-cause mortality in hemodialysis patients, it is not an independent predictor when adjusting for age, inflammation (CRP), and frailty (handgrip strength).
BACKGROUND: Brain natriuretic peptide (BNP) is a hormone secreted from the heart in response to fluid overload. In patients with chronic kidney disease (CKD), inadequate fluid management during haemodialysis may cause fluid overload and overhydration (OH), risk factors for mortality. The aim of this exploratory pilot study was to analyse the relationships between BNP, OH and all-cause mortality in patients with CKD and haemodialysis. METHODS: In this prospective observational study, five-year survival was analysed in 64 patients with CKD and haemodialysis. Bivariate correlations were performed to analyse the relationships between BNP, OH, and all-cause mortality. Cox regression analysis was performed to adjust the relationship between BNP and all-cause mortality for selected clinical and biochemical characteristics, collected at baseline. RESULTS: By the end of the study, 33 patients (52%) had died. In bivariate correlation analysis age (r = 0.38), BNP (r = 0.48), handgrip strength (r=-0.34), lean tissue index (r=-0.41) and CRP level (r=-0.34, p = 0.007) were significantly associated with all-cause mortality. In a linear regression model, BNP was found to be a significant predictor of all-cause mortality (HR 2.61). However, after adjusting for age, handgrip strength, and CRP, BNP was no longer a statistically significant predictor of all-cause mortality. Instead, age, handgrip strength and CRP were significant predictors of all-cause mortality (HR 1.04; HR 0.95 and HR 2.61, respectively). CONCLUSIONS: In this study, BNP was correlated with all-cause mortality in patients with CKD and haemodialysis, but OH was not. When adjusting for other clinical and biochemical factors, age, inflammation, and handgrip strength were found to be independent and more important predictors of all-cause mortality than BNP.
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Svensson et al. (2025) conducted an observational in Chronic kidney disease on haemodialysis (n=64). Brain natriuretic peptide (BNP) vs. Low BNP (≤ 500 pg/ml) was evaluated on All-cause mortality (HR 2.61, 95% CI 1.34-5.11, p=0.005). Elevated brain natriuretic peptide was associated with increased all-cause mortality in univariable analysis (HR 2.61), but lost significance after adjusting for age, inflammation, and handgrip strength.
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