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2026-07-13 PubMed

Higher Gastrin-17 and PRECISE-DAPT Scores Predict Upper GI Bleeding Risk After PCI with DAPT

Predictive Value of Serum Pepsinogen and Gastrin-17 in Patients With Acute Coronary Syndrome for Post-Percutaneous Coronary Intervention Oral Dual Antiplatelet Therapy-Associated Upper Gastrointestinal Bleeding.

Background

Patients with Acute Coronary Syndrome (ACS) often undergo percutaneous coronary intervention (PCI) and require dual antiplatelet therapy (DAPT) to prevent thrombotic events. However, DAPT significantly increases the risk of upper gastrointestinal bleeding (UGIB), a serious complication. Current risk stratification tools are imperfect, and there's a need for better predictive biomarkers. Serum Gastrin-17 (G-17) and pepsinogen (PG) are known indicators of gastric mucosal health, but their utility in predicting DAPT-associated UGIB in ACS patients post-PCI has been unclear.

Study Design

This retrospective, single-center study analyzed 334 patients with ACS who underwent PCI and received DAPT between 2021 and 2023. Patients were divided into a UGIB group (69 patients) and a non-UGIB group (265 patients). Clinical and laboratory data, including serum G-17 and PG levels, were collected. Researchers used multivariate logistic regression and ROC curve analysis to assess the predictive value of G-17, PRECISE-DAPT scores, ACS subtype, and the specific P2Y12 receptor antagonist used (e.g., ticagrelor) for UGIB risk.

Results

Compared to the non-UGIB group, patients in the UGIB group exhibited markedly higher Gastrin-17 levels and PRECISE-DAPT scores (p < 0.001). Additionally, ticagrelor was prescribed more commonly in the UGIB cohort (p < 0.001). The predictive power, assessed by the area under the curve (AUC), was 0.734 for G-17 alone and 0.794 for PRECISE-DAPT scores alone. When combined, their AUC increased to 0.844. > The AUC further improved to 0.878 after incorporating ticagrelor exposure, demonstrating superior exploratory value for identifying high-risk UGIB patients (p < 0.05). Furthermore, the concurrent use of proton pump inhibitors (PPIs) during DAPT significantly reduced the incidence of UGIB (34.78% vs. 65.22%, p < 0.05), highlighting PPIs as an important confounding factor for G-17 assessment.

Key Findings

  • UGIB group patients had significantly higher Gastrin-17 levels and PRECISE-DAPT scores (p < 0.001).
  • Ticagrelor use was more prevalent in patients experiencing UGIB (p < 0.001).
  • Combined G-17 and PRECISE-DAPT scores yielded an AUC of 0.844 for UGIB prediction.
  • Adding ticagrelor exposure to the combined assessment boosted the AUC to 0.878 (p < 0.05).
  • Concurrent PPI use reduced UGIB incidence from 65.22% to 34.78% (p < 0.05).

Why It Matters

This study suggests that integrating serum Gastrin-17 levels, PRECISE-DAPT scores, and ticagrelor exposure can significantly enhance the prediction of UGIB risk in ACS patients undergoing DAPT after PCI. This improved risk stratification could guide clinicians in identifying patients who would benefit most from prophylactic strategies, such as the co-prescription of PPIs, thereby reducing severe bleeding complications. While G-17 is a promising biomarker, its assessment requires careful consideration of concurrent PPI use, which can influence its levels. This finding moves towards a more personalized approach to DAPT management, potentially improving patient safety and outcomes.


gastrin-17 pepsinogen acute-coronary-syndrome upper-gi-bleeding dapt pci
Source: pubmed:42438996 · Ingested 2026-07-13 · Digest: gemini-2.5-flash