Why the study?
Does an ASCVD risk score ≥ 20 calculated via the ACC/AHA Pooled Cohort risk equations predict residual-specific mortality in cardiovascular disease-free adults?
Cohort (n=11,171)
Yes
Does an ASCVD risk score ≥ 20 calculated via the ACC/AHA Pooled Cohort risk equations predict residual-specific mortality in cardiovascular disease-free adults?
The ACC/AHA Pooled Cohort risk equations demonstrate predictive validity for residual-specific mortality among US adults free of cardiovascular disease at baseline.
Answers are grounded in this paper and cite their sources.
May inform residual mortality stratification in primary prevention; hypothesis-generating for ASCVD equations, needs prospective validation.
OBJECTIVE: The predictive validity of the Pooled Cohort risk (PCR) equations for residual-specific mortality (deaths not resulting from the 9 leading causes of death) among a national sample of U.S. adults has not previously been evaluated, which was the purpose of this study. METHODS: Data from the 1999-2010 National Health and Nutrition Examination Survey were used, with participants followed up through 31 December 2011 to ascertain mortality status. The analyzed sample included 11,171 cardiovascular disease-free adults (40-79 years of age). The 10-year risk of a first atherosclerotic cardiovascular disease (ASCVD) event was determined from the PCR equations. RESULTS: For the entire sample, 849,202 person-months occurred with an incidence rate of 0.29 (95% CI: 0.25-0.33) residual-specific deaths per 1,000 person-months. The unweighted median follow-up duration was 72 months. For all analyses, ASCVD risk score (via the PCR equations) was significantly associated with residual-specific mortality. In a fully adjusted model including moderate-to-vigorous physical activity (MVPA), obesity, age (yrs; continuous measure), gender (male/female) and race-ethnicity (Mexican American, non-Hispanic white, non-Hispanic black and other) as covariates, those with an ASCVD ≥ 20 (vs. < 20) had a 91% increased hazard of residual-specific death during the follow-up period (HR = 1.91; 95% CI: 1.10-3.31). Expressed as probability, there was a 66% chance that those with ASCVD ≥ 20 (vs. < 20) would have a residual specific-death during the follow-up period. CONCLUSION: The 10-year predicted risk of a first ASCVD event via the PCR equations was directly associated with residual-specific mortality among those free of cardiovascular disease (CVD) at baseline, providing evidence of predictive validity of the PCR equations among this national sample of U.S. adults.
No takes yet. Share an insight, caveat, or question.
Edwards et al. (2016) conducted a cohort in Cardiovascular disease-free (n=11,171). ASCVD risk score ≥ 20 (via Pooled Cohort risk equations) vs. ASCVD risk score < 20 was evaluated on Residual-specific mortality (deaths not resulting from the 9 leading causes of death) (HR 1.91, 95% CI 1.10-3.31).
Synapse has enriched 10 related papers. Consider them for comparative context: