# PAPP-A Protein Diagnostic and Prognostic Significance in Acute Coronary Syndromes Without Persistent ST-T-Segment Elevation

**Authors:** Monika Różycka-Kosmalska, Rafał Frankowski, Mikołaj Grabarczyk, Kasper Sipowicz, Anna Pękala-Wojciechowska, Tadeusz Pietras, Grzegorz Opielak, Marcin Kosmalski

PMC · DOI: 10.3390/jcm15041455 · Journal of Clinical Medicine · 2026-02-12

## TL;DR

This study examines the usefulness of the PAPP-A protein as a diagnostic and prognostic marker for non-ST-elevation acute coronary syndromes.

## Contribution

The study evaluates PAPP-A's potential as a prognostic tool in NSTE-ACS patients, despite limited diagnostic value.

## Key findings

- PAPP-A levels were not significantly different between NSTEMI and UA patients.
- Higher PAPP-A levels correlated with increased risk of adverse outcomes after 12 months.
- PAPP-A shows limited diagnostic utility but potential for risk estimation in NSTE-ACS patients.

## Abstract

Background: There are ongoing attempts to find a reliable, highly sensitive and specific early indicator of myocardial ischemia. Recently, a potential new function for the “non-pregnancy”-related pregnancy-associated plasma protein-A (PAPP-A) protein has been reported in many papers, including that the protein could be used in diagnosing heart conditions. Hence, our study aimed to determine the diagnostic and prognostic significance of PAPP-A protein in individuals diagnosed with non-ST-elevation acute coronary syndromes (NSTE-ACSs). Methods: The study comprised 100 consecutive patients (68 males and 32 females), aged from 42 to 83 years (mean age: 64.2 years). We assessed PAPP-A protein levels, anthropometric measurements, basic laboratory tests, ECG recordings, and coronary angiography for each patient. The participants were subsequently divided into two groups: non-ST-elevation myocardial infarction (NSTEMI, n = 74) or unstable angina (UA, n = 25). Results: The levels of PAPP-A protein in patients with NSTEMI were slightly higher than those in patients with UA, but the difference was not statistically significant (7.93 ± 6.35 mIU/L vs. 6.52 ± 5.45 mIU/L, p = 0.253). Higher PAPP-A protein levels (≥5.83 mIU/L) were associated with a numerically higher, but not statistically significant, risk of NSTEMI (OR = 1.37; 95% CI: 0.56–3.36). After 12 months, there was a significant correlation between the amount of labelled PAPP-A protein and the likelihood of experiencing acute myocardial infarction, cardiovascular death, and the necessity for unplanned coronary angiography. Conclusions: The diagnostic utility of PAPP-A protein in NSTE-ACS is limited, both in the NSTEMI and UA patient groups. However, its measurement can be used to estimate the annual risk for these groups of patients.

## Linked entities

- **Proteins:** PAPPA (pappalysin 1)
- **Diseases:** myocardial ischemia (MONDO:0024644), unstable angina (MONDO:0006805), acute myocardial infarction (MONDO:0004781)

## Full-text entities

- **Genes:** ACE (angiotensin I converting enzyme) [NCBI Gene 1636] {aka ACE1, CD143, DCP, DCP1}, ACCS (1-aminocyclopropane-1-carboxylate synthase homolog (inactive)) [NCBI Gene 84680] {aka ACS, PHACS}, PAPPA (pappalysin 1) [NCBI Gene 5069] {aka ASBABP2, DIPLA1, IGFBP-4ase, PAPA, PAPP-A, PAPPA1}, IGF1 (insulin like growth factor 1) [NCBI Gene 3479] {aka IGF, IGF-I, IGFI, MGF}, PRG2 (proteoglycan 2, pro eosinophil major basic protein) [NCBI Gene 5553] {aka BMPG, MBP, MBP1, proMBP}, FGB (fibrinogen beta chain) [NCBI Gene 2244] {aka HEL-S-78p}, CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TNNT2 (troponin T2, cardiac type) [NCBI Gene 7139] {aka CMD1D, CMH2, CMPD2, LVNC6, RCM3, TnTC}
- **Diseases:** atherosclerotic plaque (MESH:D058226), stenoses (MESH:D003251), ischemia (MESH:D007511), CE (MESH:D058617), UCA (MESH:D003323), myocardial necrosis (MESH:D009336), exertional angina (MESH:C564288), UA (MESH:D000789), coronary stenosis (MESH:D023921), infectious diseases (MESH:D003141), embolic obstruction (MESH:D004617), type 2 diabetes mellitus (MESH:D003924), NSTE-ASC (MESH:D065309), HF (MESH:D006333), STEMI (MESH:D000072657), depression (MESH:D003866), Obesity (MESH:D009765), myocardial injury (MESH:D009202), chest pain (MESH:D002637), muscle injury (MESH:D009135), stroke (MESH:D020521), coronary artery disease (MESH:D003324), Overweight (MESH:D050177), heart conditions (MESH:D006331), AMI (MESH:D009203), renal failure (MESH:D051437), CD (MESH:D002318), ischemic (MESH:D002545), Down syndrome (MESH:D004314), IHD (MESH:D017202), rupture (MESH:D012421), diabetes (MESH:D003920), cardiac arrest (MESH:D006323), NSTE-ACS (MESH:D000168), heart rhythm (HR) abnormalities (MESH:D006330), NSTE-ACS (MESH:D000072658), injury to (MESH:D014947), UA:15.5 (MESH:C566611), inflammatory (MESH:D007249), Restenosis (MESH:D023903), one-, two-, or three-vessel disease (MESH:D058529), thrombosis (MESH:D013927), carotid (MESH:D016893), pain (MESH:D010146), hypertension (MESH:D006973), cardiomyocyte death (MESH:D003643), ACSs (MESH:D054058), atherosclerotic (MESH:D050197)
- **Chemicals:** metoprolol succinate (MESH:D008790), simvastatin (MESH:D019821), heparin (MESH:D006493), hs (MESH:D006859), creatinine (MESH:D003404), cholesterol (MESH:D002784), glycemia (MESH:D001786), acetylsalicylic acid (MESH:D001241), lipid (MESH:D008055), uric acid (MESH:D014527), triglycerides (MESH:D014280), ramipril (MESH:D017257), clopidogrel (MESH:D000077144), -molecular-weight heparin (-), trimetazidine (MESH:D014292), TG (MESH:D013866), TC (MESH:D013667), zinc (MESH:D015032)
- **Species:** Homo sapiens (human, species) [taxon 9606]

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## References

106 references — full list in the complete paper: https://tomesphere.com/paper/PMC12942605/full.md

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Source: https://tomesphere.com/paper/PMC12942605