ANGPTL3 and Cardiovascular Outcomes in Patients With Acute Coronary Syndrome and Obstructive Sleep Apnea
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Updated: Aug 29, 2025

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Published on: October 18, 2024
Qianwen Lv1,2, Xiaolu Jiao1,2, Huahui Yu1,2
1Key Laboratory of Upper Airway Dysfunction-Related Cardiovascular Diseases Beijing An Zhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung, and Blood Vessel Diseases Beijing China.
Insights
Elevated angiopoietin-like protein 3 (ANGPTL3) significantly increases cardiovascular event risk in acute coronary syndrome (ACS) patients, particularly those with obstructive sleep apnea (OSA). ANGPTL3 levels aid in refining risk stratification for ACS patients with OSA.
Area of Science:
- Cardiovascular Medicine
- Endocrinology
- Sleep Medicine
Background:
- Acute coronary syndrome (ACS) poses a significant cardiovascular risk.
- Obstructive sleep apnea (OSA) is increasingly recognized as a cardiovascular risk factor.
- The role of angiopoietin-like protein 3 (ANGPTL3) in cardiovascular events (CVEs) post-ACS, especially in conjunction with OSA, requires further elucidation.
Purpose of the Study:
- To investigate the impact of elevated ANGPTL3 levels on the incidence of CVEs in patients with ACS.
- To determine if this impact differs between patients with and without OSA.
- To assess the predictive value of ANGPTL3 in cardiovascular risk stratification for ACS patients, considering OSA status.
Main Methods:
- Prospective cohort study including 1174 patients with ACS who underwent percutaneous coronary intervention.
- Patients were categorized based on OSA status (apnea-hypopnea index ≥15 events/h) and ANGPTL3 plasma levels.
- Cardiovascular events (CVEs) were tracked over a median follow-up of 3.1 years using Cox proportional hazards models.
Main Results:
- Patients with ACS and OSA exhibited higher ANGPTL3 levels compared to those without OSA (P<0.001).
- Elevated ANGPTL3 levels (29≤ANGPTL3<42 mg/dL and ANGPTL3≥42 mg/dL) were associated with increased CVE risk in the overall ACS cohort.
- This association was significantly pronounced in patients with ACS and OSA (HRs 1.916 and 2.692, respectively), but not in those without OSA. ANGPTL3 addition improved risk model C-statistic in OSA and overall ACS groups.
Conclusions:
- Plasma ANGPTL3 levels possess a significant predictive impact on cardiovascular risk in ACS patients.
- This predictive value is particularly pronounced in ACS patients who also have OSA.
- ANGPTL3 may serve as a valuable biomarker for refining risk stratification and guiding treatment strategies in ACS patients with OSA.
Abstract:
Background The aim of this prospective study was to determine the impact of elevated ANGPTL3 (angiopoietin-like protein 3) on cardiovascular events (CVEs) following acute coronary syndrome (ACS) in patients with or without obstructive sleep apnea (OSA). Methods and Results A total of 1174 patients with ACS underwent successful percutaneous coronary intervention were included in this prospective cohort study (NCT03362385). Patients were categorized according to the apnea-hypopnea index (≥15 events/h, OSA) and further classified by ANGPTL3 levels. We analyzed the incidence of CVEs in patients with ACS according to the status of OSA and ANGPTL3. During a median of 3.1 years of follow-up, 217 (18.48%) CVEs occurred. The patients with ACS with OSA had higher ANGPTL3 levels than those without OSA (30.4 [20.9-43.2] versus 27.80 [19.1-41.5] ng/mL; P<0.001). In all patients with ACS, 29≤ANGPTL3<42 mg/dL and ANGPTL3≥42 mg/dL were associated with an increased risk of CVEs with hazard ratios (HRs) of 1.555 (95% CI, 1.010-2.498) and 2.489 (95% CI 1.613-3.840), respectively. When the status of OSA or not was incorporated in stratifying factors, 29≤ANGPTL3<42 mg/dL and ANGPTL3≥42 mg/dL were associated with a significantly higher risk of CVEs in patients with ACS with OSA (HR, 1.916 [95% CI, 1.019-3.601] and HR, 2.692 [95% CI, 1.379-4.503]) but not without OSA. Moreover, adding ANGPTL3 to the Cox model increased C-statistic values by 0.035 and 0.029 in the OSA group and all patients with ACS, respectively, but was not statistically improved in patients with ACS without OSA. Conclusions In conclusion, our study demonstrates a predictive impact of plasma ANGPTL3 on cardiovascular risk in patients with ACS, especially in patients with ACS with OSA. It might be of clinical value in refining risk stratification and tailoring treatment of patients with ACS and OSA. Registration URL: https://www.clinicaltrials.gov; Unique identifier: NCT03362385.
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