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Published on: December 6, 2016
Phenogroup-based stratification of cardiovascular risk in obstructive sleep apnea
Anastasya Maria Kosasih1, Yihui Ou2, Chieh-Yang Koo1
1Department of Cardiology, National University Heart Centre, Singapore, Singapore.
Insights
Obstructive sleep apnea (OSA) increases cardiovascular risk in patients with coronary artery disease (CAD) after revascularization. Risk varies by patient phenogroup, suggesting tailored risk assessment for better outcomes.
Area of Science:
- Cardiology
- Sleep Medicine
- Clinical Research
Background:
- Obstructive sleep apnea (OSA) presents diverse patient phenotypes.
- The prognostic impact of OSA in coronary artery disease (CAD) patients undergoing revascularization is not fully understood.
Purpose of the Study:
- To investigate the association between OSA and major adverse cardiac and cerebrovascular events (MACCE) in revascularized CAD patients.
- To explore whether this association differs across distinct patient phenogroups.
Main Methods:
- Pooled data from 2318 CAD patients undergoing percutaneous coronary intervention or coronary artery bypass grafting.
- Latent class analysis identified three patient phenogroups.
- Cox regression evaluated the association between OSA (apnea-hypopnea index ≥15) and MACCE over a mean follow-up of 1.9 years.
Main Results:
- Three phenogroups were identified: Younger-Sleepy-Hypoxia, Cardiorenal-Metabolic, and Old-Lean-Chinese.
- OSA prevalence was high and similar across groups (45.5-50.7%).
- OSA was linked to increased MACCE risk overall (adjusted HR 1.55) and specifically within the Younger-Sleepy-Hypoxia and Cardiorenal-Metabolic phenogroups.
Conclusions:
- OSA is associated with heightened cardiovascular risk in revascularized CAD patients.
- The prognostic significance of OSA varies across identified patient phenogroups.
- Phenogroup-based risk stratification may enhance patient management, pending further validation.
Background:
Obstructive sleep apnea (OSA) exhibits substantial phenotypic heterogeneity, but its prognostic relevance in patients with coronary artery disease (CAD) undergoing revascularization remains uncertain.
Methods:
We pooled data from two prospective cohorts of CAD patients undergoing percutaneous coronary intervention or coronary artery bypass grafting (n = 2318). Major adverse cardiac and cerebrovascular events (MACCE; cardiovascular death, non-fatal myocardial infarction, non-fatal stroke, and unplanned revascularization) were assessed over a mean follow-up of 1.9 ± 1.1 years. Latent class analysis using nine clinical variables identified phenogroups. Associations between OSA (apnea-hypopnea index ≥15) and MACCE were evaluated using Cox regression.
Results:
Three phenogroups were identified: (1) Younger-Sleepy-Hypoxia (42.2%), (2) Cardiorenal-Metabolic (30.9%), and (3) Old-Lean-Chinese (26.9%). OSA prevalence was similar across groups (45.5%, 50.7%, and 47.8%). The overall incidence of MACCE was 11.4% and did not differ significantly across phenogroups (p = 0.127). OSA was associated with increased MACCE risk in the overall cohort (adjusted HR 1.55, 95% CI 1.20-2.00; p < 0.001). In phenogroup analyses, this association was significant in phenogroup 1 (adjusted HR 1.57, 95% CI 1.04-2.36; p = 0.030), borderline in phenogroup 2 (adjusted HR 1.55, 95% CI 0.98-2.43; p = 0.059), and not significant in phenogroup 3 (adjusted HR 1.32, 95% CI 0.81-2.16; p = 0.263).
Conclusions:
In revascularized CAD patients, OSA was associated with increased cardiovascular risk in the overall cohort, with heterogeneity across phenogroups. These findings support phenogroup-based risk stratification, pending external validation.
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