Key result
HF and kidney dysfunction phenotype linked to ~174% higher CV risk in T2DM with ASCVD.
Observational (n=14,671)
Hazard Ratio: 2.74 (95% CI 2.29–3.29)
Absolute Event Rate: 16.8% vs 8.6%
Randomized trial identifies diverse cardiovascular phenotypes in patients with type 2 diabetes, suggesting tailored treatment approaches.
OBJECTIVE: Phenotypic heterogeneity among patients with type 2 diabetes mellitus (T2DM) and atherosclerotic cardiovascular disease (ASCVD) is ill defined. We used cluster analysis machine-learning algorithms to identify phenotypes among trial participants with T2DM and ASCVD. RESEARCH DESIGN AND METHODS: We used data from the Trial Evaluating Cardiovascular Outcomes with Sitagliptin (TECOS) study (n = 14,671), a cardiovascular outcome safety trial comparing sitagliptin with placebo in patients with T2DM and ASCVD (median follow-up 3.0 years). Cluster analysis using 40 baseline variables was conducted, with associations between clusters and the primary composite outcome (cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for unstable angina) assessed by Cox proportional hazards models. We replicated the results using the Exenatide Study of Cardiovascular Event Lowering (EXSCEL) trial. RESULTS: Four distinct phenotypes were identified: cluster I included Caucasian men with a high prevalence of coronary artery disease; cluster II included Asian patients with a low BMI; cluster III included women with noncoronary ASCVD disease; and cluster IV included patients with heart failure and kidney dysfunction. The primary outcome occurred, respectively, in 11.6%, 8.6%, 10.3%, and 16.8% of patients in clusters I to IV. The crude difference in cardiovascular risk for the highest versus lowest risk cluster (cluster IV vs. II) was statistically significant (hazard ratio 2.74 [95% CI 2.29-3.29]). Similar phenotypes and outcomes were identified in EXSCEL. CONCLUSIONS: In patients with T2DM and ASCVD, cluster analysis identified four clinically distinct groups. Further cardiovascular phenotyping is warranted to inform patient care and optimize clinical trial designs.
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Sharma et al. (2021) conducted an observational in Type 2 diabetes mellitus and atherosclerotic cardiovascular disease (n=14,671). Cluster IV phenotype (heart failure and kidney dysfunction) vs. Cluster II phenotype (Asian patients with low BMI) was evaluated on Cardiovascular death, nonfatal myocardial infarction, nonfatal stroke, or hospitalization for unstable angina (HR 2.74, 95% CI 2.29-3.29). Among patients with T2DM and ASCVD, a phenotype with heart failure and kidney dysfunction had higher cardiovascular risk than the lowest-risk cluster (HR 2.74; 95% CI 2.29-3.29).
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