Increasing evidence has demonstrated that sPRR [a truncated soluble form of (pro)renin receptor] levels may reflect the severity of several diseases, including kidney disease, hypertension, and heart failure (HF). Although previous studies using cohorts primarily consisting of HF patients with reduced ejection fraction revealed that increased plasma sPRR levels may be a promising evaluative indicator for HF, definitive information on the relationship between plasma sPRR levels and HF patients with preserved ejection fraction (HFpEF) is still insufficient and scarce. In the present study, we further clarified the status of plasma sPRR levels in HF patients by meta-analysis. We enrolled a cohort primarily consisting of HFpEF patients (87.8 %) to further determine the relationships between plasma sPRR levels and HFpEF. Meta-analysis showed a significant increase in plasma sPRR levels in HF patients, with substantial statistical heterogeneity. In our observational study, plasma sPRR levels were significantly higher in the HF group than in the non-HF group (17.4 ± 9.8 vs. 10.4 ± 3.4 ng/ml, p < 0.001) and positively correlated with age, B-type natriuretic peptide, creatine, urea nitrogen, plasma renin activity, angiotensin II, and left atrial diameter and negatively correlated with estimated glomerular filtration rate. Plasma sPRR levels (The average value ≥ 16.1 ± 7.2 ng/ml) and the diagnostic values (reflected by the area under the receiver operating characteristic curves ≥ 0.749) of sPRR were comparable for all subtypes of HF patients. Overall, plasma sPRR levels were significantly elevated in HF patients. Elevated plasma sPRR levels may be one of the underlying indicators for HF.

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http://dx.doi.org/10.1016/j.peptides.2024.171337DOI Listing

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Article Synopsis
  • Soluble prorenin receptor (sPRR) is a plasma biomarker linked to hypertension and cardiovascular diseases, but its specific role in kidney function and blood pressure regulation in humans is not well understood.
  • A study created a mouse model expressing human sPRR in the renal collecting duct to explore how it affects cardiorenal function, focusing on sex and daily circadian variations.
  • Results showed that female mice with increased levels of sPRR exhibited higher blood pressure, altered responses to blood pressure medications, and changes in kidney function only during their active phase, suggesting a complex interaction between sPRR and renal functions that may differ by sex.
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