Key result
High myeloperoxidase and uric acid are linked to impaired diastolic function and decreased left atrial strain.
Why the study?
Bioactive myeloperoxidase contributes to oxidative stress, inflammation, and vascular dysfunction associated with HFpEF, prompting investigation of the association of plasma MPO and serum uric acid with echocardiographic variables in a populational setting.
Are high plasma MPO and SUA levels associated with echocardiographic markers of impaired diastolic function in healthy individuals?
Cross-Sectional (n=1,677)
Are high plasma MPO and SUA levels associated with echocardiographic markers of impaired diastolic function in healthy individuals?
p-value: p=<0.001
High plasma MPO and SUA levels are associated with early echocardiographic markers of diastolic dysfunction in healthy individuals, suggesting a potential role in early HFpEF development.
May flag early diastolic impairment in healthy adults; hypothesis-generating for MPO/SUA in HFpEF development.
BACKGROUND: Myeloperoxidase (MPO), a neutrophil-derived enzyme, is associated with oxidative stress and inflammation, which contribute to the pathophysiology of heart failure with preserved ejection fraction (HFpEF). Bioactive MPO causes vascular dysfunction and accumulation of serum uric acid (SUA). We investigated the association of plasma MPO and SUA with echocardiographic variables in a populational setting. METHODS: This was a cross-sectional analysis of the fourth visit of the STANISLAS cohort (N=1677 participants, age 49±14 years, 48% male), a population of initially healthy individuals. Participants were divided into four groups according to median plasma MPO and SUA levels. Adjusted linear regression models were used to assess the relationship of plasma MPO and SUA with echocardiographic markers. RESULTS: Participants with high MPO and high SUA were older, had more diabetes, a higher body mass index, lower estimated glomerular filtration rate and higher systolic blood pressure. In multivariable regression analyses, compared with patients with low MPO and low SUA, they had decreased left atrial reservoir strain (mean±SE=-1.43±0.62, p=0.022), decreased mitral annular e' velocity (mean±SE=-0.60±0.16, p<0.001) and more impaired left ventricular systolic global longitudinal strain (mean±SE=0.50±0.23, p=0.029). In contrast, high MPO with low SUA was not associated with impaired diastolic function. CONCLUSIONS: In a population setting, high MPO and SUA, indicative of high bioactive MPO, were associated with early markers of diastolic dysfunction, suggesting a potential role of the MPO pathway in the early development of HFpEF.
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Wang et al. (2025) conducted a cross-sectional in Healthy individuals (n=1,677). High plasma myeloperoxidase (MPO) and high serum uric acid (SUA) vs. Low MPO and low SUA was evaluated on Echocardiographic markers of impaired diastolic function (p=<0.001). High plasma myeloperoxidase and serum uric acid were associated with decreased mitral annular e' velocity (mean diff -0.60, p<0.001) and left atrial reservoir strain (p=0.022).
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