# The prognostic value of secreted frizzled-related protein 2 in elderly patients with heart failure: a single-center retrospective study

**Authors:** Peng Yu, Kailing Lin, Liman Wang, Chaochao Deng, Wenfei Zeng, Huizhen Yu

PMC · DOI: 10.1038/s41598-025-11765-6 · Scientific Reports · 2025-08-04

## TL;DR

This study shows that high levels of SFRP2 in the blood predict worse outcomes for elderly patients with worsening heart failure.

## Contribution

SFRP2 is identified as an independent predictor of mortality and readmission in elderly heart failure patients.

## Key findings

- Elevated SFRP2 levels were significantly associated with mortality and readmission in elderly heart failure patients.
- SFRP2 levels predicted outcomes independently of NT-proBNP levels.
- Higher SFRP2 levels indicate poorer clinical outcomes beyond traditional biomarkers.

## Abstract

This study was conducted to assess the prognostic value of secreted frizzled-related protein 2 (SFRP2) for mortality and readmission in elderly patients with acute exacerbation of chronic heart failure (HF). Elderly patients hospitalized for worsening chronic HF were enrolled in the present study. We detected the concentration of serum SFRP2 in these patients. The primary endpoint of this study was defined as all-cause mortality and the secondary endpoint was a composite of all-cause mortality and readmission due to HF, acute myocardial infarction, and malignant arrhythmia during a median follow-up period of 450 (interquartile range 224–942) days. Multivariable Cox proportional hazard models were performed to evaluate the prognostic value of SFRP2. Of 161 patients at baseline, we observed 72 events (25 deaths and 47 readmissions). Serum SFRP2 levels were significantly elevated in elderly HF patients with events relative to those without and control subjects (all P < 0.001). The Kaplan-Meier analysis showed a significantly increased risk of all-cause mortality and cardiovascular readmissions stratified by the optimal cut-off value of serum SFRP2 level (log-rank P < 0.005). An elevated SFRP2 level and N-terminal pro-B-type natriuretic peptide (NT-proBNP) level was independently and significantly associated with the primary endpoint and secondary endpoint (adjusted hazard ratio [HR] 2.334, 95% confidence interval [CI] 1.059–5.147;P = 0.036 and HR 2.326, 95% CI 1.426–3.794;P = 0.001, respectively) in multivariable Cox regression analysis. A higher level of serum SFRP2 can be considered as an independent predictor of poorer clinical outcomes for elderly patients with acute exacerbation of chronic heart failure, indicating that evaluation of SFRP2 could provide more useful information for the long-term prognosis in these patients beyond NT-proBNP.

## Linked entities

- **Genes:** SFRP2 (secreted frizzled related protein 2) [NCBI Gene 6423]
- **Proteins:** SFRP2 (secreted frizzled related protein 2)
- **Diseases:** heart failure (MONDO:0005252), acute myocardial infarction (MONDO:0004781)

## Full-text entities

- **Genes:** COG2 (component of oligomeric golgi complex 2) [NCBI Gene 22796] {aka CDG2Q, LDLC}, SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}, Sfrp2 (secreted frizzled-related protein 2) [NCBI Gene 20319] {aka Sdf5}, ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, Ctnnb1 (catenin beta 1) [NCBI Gene 12387] {aka Bfc, Catnb, Mesc}, CTNNB1 (catenin beta 1) [NCBI Gene 1499] {aka CTNNB, EVR7, MRD19, NEDSDV, armadillo}, SFRP2 (secreted frizzled related protein 2) [NCBI Gene 6423] {aka FRP-2, SARP1, SDF-5}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}
- **Diseases:** based (MESH:D019292), dilated cardiomyopathy (MESH:D002311), cardiac diseases (MESH:D006331), Diabetes mellitus (MESH:D003920), acute stroke (MESH:D020521), acute coronary syndrome (MESH:D054058), Renal Disease (MESH:D007674), arrhythmia (MESH:D001145), hypertrophic cardiomyopathy (MESH:D002312), abnormalities of cardiac function (MESH:D000014), RVD (MESH:D018497), Myocardial fibrosis (MESH:D005355), infarcted heart (MESH:D007238), HF (MESH:D006333), infections (MESH:D007239), renal failure (MESH:D051437), inflammation (MESH:D007249), malignancy (MESH:D009369), acute myocardial infarction (MESH:D009203), obesity (MESH:D009765), cardiac death (MESH:D003643), DM (MESH:D009223), hepatic or renal dysfunction (MESH:D008107), hepatic disease (MESH:D056486), hypertension (MESH:D006973), cardiovascular death (MESH:D002318), ischemic heart disease (MESH:D017202), HCM (MESH:D000092183), ischemic (MESH:D002545)
- **Chemicals:** cholesterol (MESH:D002784), K+ (MESH:D011188), creatinine (MESH:D003404), TC (-), TG (MESH:D014280), Na+ (MESH:D012964), bilirubin (MESH:D001663), glycemia (MESH:D001786)
- **Species:** Cricetus cricetus (black-bellied hamster, species) [taxon 10034], Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12322027/full.md

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Source: https://tomesphere.com/paper/PMC12322027