Abstract P2135: Nicorandil improves health status outcomes in patients with angina pectoris: a prospective, multicenter, cohort study (GREAT)

Background: Coronary artery disease (CAD) is a major contributor to cardiovascular mortality, with angina pectoris affecting nearly half of CAD patients. The GREAT study aims to establish a large cohort of Chinese patients with angina pectoris, evaluating the effectiveness of anti-anginal treatments through the Seattle Angina Questionnaire (SAQ). Methods: This multicenter, prospective cohort study included 1556 adult CAD patients with angina pectoris receiving or eligible for oral anti-anginal therapy. Patients were observed over 12 months. All participants were registered on an ePRO system via a WeChat Mini program, allowing them to submit questionnaires and clinic visit data. The primary outcome was the 12-month change in the SAQ summary score (SAQ-SS) from baseline. Secondary outcomes included changes in SAQ-SS at 3, 6, and 9 months. Patients were categorized into two groups: those treated with nicorandil (nicorandil group) and those not receiving it (non-nicorandil group). Propensity score matching (PSM) was used to reduce bias and control for confounding factors. Results: A total of 1528 patients were analyzed (FAS), of which 529 (34.6%) were in the nicorandil group and 999 (65.4%) in the non-nicorandil group. Following PSM, 450 matched pairs were identified. Baseline characteristics were well-balanced. The median age was 60 years in the nicorandil group and 61 years in the non-nicorandil group, and most patients were male (74.2% and 73.3%, respectively). β-blockers were widely used (68.7% and 70.2%, respectively). Both groups showed improvements in mean SAQ-SS across all follow-up points, but the nicorandil group had significantly greater improvements (P<0.05). At 12 months, the nicorandil group had a mean SAQ-SS improvement of 17.6 points, compared to 15.1 points in the non-nicorandil group (P=0.003). Furthermore, nicorandil users had significantly greater improvements in the SAQ quality-of-life (18.9 vs 16.3; P=0.042) and physical limitation (11.7 vs 8.4; P=0.001) domains (Table 1). In terms of clinical benefit, a higher proportion of patients in the nicorandil group experienced large or very large improvements in SAQ-SS at 12 months (24.0% vs 20.7% for 20–29 points; 18.2% vs 12.0% for ≥30 points; P=0.005) (Table 2). Conclusion: This real-world evidence demonstrates that nicorandil-based regimens lead to superior health status improvements in patients with angina pectoris compared to non-nicorandil treatments.

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Journal
Circulation
Published
2025-03-11
DOI
https://doi.org/10.1161/cir.151.suppl_1.p2135
Primary Topic
Anesthesia and Neurotoxicity Research
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article
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article

Abstract P2135: Nicorandil improves health status outcomes in patients with angina pectoris: a prospective, multicenter, cohort study (GREAT)

Yaodong Ding, Xin Du, Yong Zeng, Xihai Zhao et al.
Circulation
Anesthesia and Neurotoxicity Research
article

Abstract P2135: Nicorandil improves health status outcomes in patients with angina pectoris: a prospective, multicenter, cohort study (GREAT)

Yaodong Ding, Xin Du, Yong Zeng, Xihai Zhao, Changsheng Ma
article en

Abstract

Background: Coronary artery disease (CAD) is a major contributor to cardiovascular mortality, with angina pectoris affecting nearly half of CAD patients. The GREAT study aims to establish a large cohort of Chinese patients with angina pectoris, evaluating the effectiveness of anti-anginal treatments through the Seattle Angina Questionnaire (SAQ). Methods: This multicenter, prospective cohort study included 1556 adult CAD patients with angina pectoris receiving or eligible for oral anti-anginal therapy. Patients were observed over 12 months. All participants were registered on an ePRO system via a WeChat Mini program, allowing them to submit questionnaires and clinic visit data. The primary outcome was the 12-month change in the SAQ summary score (SAQ-SS) from baseline. Secondary outcomes included changes in SAQ-SS at 3, 6, and 9 months. Patients were categorized into two groups: those treated with nicorandil (nicorandil group) and those not receiving it (non-nicorandil group). Propensity score matching (PSM) was used to reduce bias and control for confounding factors. Results: A total of 1528 patients were analyzed (FAS), of which 529 (34.6%) were in the nicorandil group and 999 (65.4%) in the non-nicorandil group. Following PSM, 450 matched pairs were identified. Baseline characteristics were well-balanced. The median age was 60 years in the nicorandil group and 61 years in the non-nicorandil group, and most patients were male (74.2% and 73.3%, respectively). β-blockers were widely used (68.7% and 70.2%, respectively). Both groups showed improvements in mean SAQ-SS across all follow-up points, but the nicorandil group had significantly greater improvements (P<0.05). At 12 months, the nicorandil group had a mean SAQ-SS improvement of 17.6 points, compared to 15.1 points in the non-nicorandil group (P=0.003). Furthermore, nicorandil users had significantly greater improvements in the SAQ quality-of-life (18.9 vs 16.3; P=0.042) and physical limitation (11.7 vs 8.4; P=0.001) domains (Table 1). In terms of clinical benefit, a higher proportion of patients in the nicorandil group experienced large or very large improvements in SAQ-SS at 12 months (24.0% vs 20.7% for 20–29 points; 18.2% vs 12.0% for ≥30 points; P=0.005) (Table 2). Conclusion: This real-world evidence demonstrates that nicorandil-based regimens lead to superior health status improvements in patients with angina pectoris compared to non-nicorandil treatments.

CirculationVol. 151(Suppl_1)
Beijing Anzhen Hospital (CN)
Openalex Percentile: Top 90%
Anesthesia and Neurotoxicity Research
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