Decreased Endogenous Nitric Oxide Production in Patients with Acute Decompensated Heart Failure with Preserved Ejection Fraction

<b>Background:</b> Heart failure with a preserved ejection fraction (HFpEF) accounts for approximately 50% of patients with heart failure. Endothelial dysfunction has been documented in HFpEF, and impaired nitric oxide (NO) production may be a contributing factor in patients decompensating from chronic to acute HFpEF. Plasma nitrite (NO<sub>2</sub><sup>-</sup>), but not plasma nitrate (NO<sub>3</sub><sup>-</sup>), is highly reflective of local nitric oxide production. However, plasma NO<sub>2</sub><sup>-</sup> levels in relation to chronic and acute HFpEF patients have not been studied. <b>Methods:</b> Plasma NO<sub>2</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup> concentrations were quantified with gas-phase chemiluminescence. Plasma asymmetric dimethylarginine (ADMA), an endogenous inhibitor of NO production, and arterial stiffness were also quantified. Samples were collected from 19 participants with chronic HFpEF and 16 participants with acute HFpEF. <b>Results:</b> Plasma NO<sub>2</sub><sup>-</sup> concentrations were lower in participants with acute HFpEF when compared to the chronic HFpEF group (<i>p</i> = 0.022). NO<sub>3</sub><sup>-</sup>, ADMA and indices of arterial stiffness did not display any significant between-group differences. <b>Conclusions:</b> We present novel NO<sub>2</sub><sup>-</sup> data, which has not been previously quantified in patients with acute HFpEF. Our results indicate that plasma concentrations of NO<sub>2</sub><sup>-</sup> may be decreased in patients with acute HFpEF compared to patients with chronic HFpEF, suggesting a dysregulated NO pathway. Further studies are required to confirm these findings in this patient population.

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Journal
Journal of Clinical Medicine
Published
2025-08-22
DOI
https://doi.org/10.3390/jcm14175928
Primary Topic
Cardiovascular Function and Risk Factors
Type
article
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0.00

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article

Decreased Endogenous Nitric Oxide Production in Patients with Acute Decompensated Heart Failure with Preserved Ejection Fraction

Sara Vogrin, Roman Falls, Bing H. Wang, Christopher Neil
Journal of Clinical Medicine
Cardiovascular Function and Risk Factors
article

Decreased Endogenous Nitric Oxide Production in Patients with Acute Decompensated Heart Failure with Preserved Ejection Fraction

Sara Vogrin, Roman Falls, Bing H. Wang, Christopher Neil
article en

Abstract

<b>Background:</b> Heart failure with a preserved ejection fraction (HFpEF) accounts for approximately 50% of patients with heart failure. Endothelial dysfunction has been documented in HFpEF, and impaired nitric oxide (NO) production may be a contributing factor in patients decompensating from chronic to acute HFpEF. Plasma nitrite (NO<sub>2</sub><sup>-</sup>), but not plasma nitrate (NO<sub>3</sub><sup>-</sup>), is highly reflective of local nitric oxide production. However, plasma NO<sub>2</sub><sup>-</sup> levels in relation to chronic and acute HFpEF patients have not been studied. <b>Methods:</b> Plasma NO<sub>2</sub><sup>-</sup> and NO<sub>3</sub><sup>-</sup> concentrations were quantified with gas-phase chemiluminescence. Plasma asymmetric dimethylarginine (ADMA), an endogenous inhibitor of NO production, and arterial stiffness were also quantified. Samples were collected from 19 participants with chronic HFpEF and 16 participants with acute HFpEF. <b>Results:</b> Plasma NO<sub>2</sub><sup>-</sup> concentrations were lower in participants with acute HFpEF when compared to the chronic HFpEF group (<i>p</i> = 0.022). NO<sub>3</sub><sup>-</sup>, ADMA and indices of arterial stiffness did not display any significant between-group differences. <b>Conclusions:</b> We present novel NO<sub>2</sub><sup>-</sup> data, which has not been previously quantified in patients with acute HFpEF. Our results indicate that plasma concentrations of NO<sub>2</sub><sup>-</sup> may be decreased in patients with acute HFpEF compared to patients with chronic HFpEF, suggesting a dysregulated NO pathway. Further studies are required to confirm these findings in this patient population.

Journal of Clinical MedicineVol. 14(17)
Baker Heart and Diabetes Institute (AU), Western Health (AU), RMIT University (AU)
Medical Research Council, National Health and Medical Research Council
Openalex Percentile: Top 66%
Cardiovascular Function and Risk Factors
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