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High-Sensitivity Cardiac Troponin I for Risk Stratification in Older Adults
Olive Tang1, Kunihiro Matsushita1, Josef Coresh1
1Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, USA.
Insights
High-sensitivity cardiac troponin I (hs-cTnI) improves cardiovascular risk prediction in older adults. Elevated hs-cTnI identifies high-risk individuals, even without prior cardiovascular disease (CVD), offering better discrimination than hs-troponin T (hs-cTnT).
Area of Science:
- Cardiology
- Biomarkers
- Geriatric Medicine
Background:
- Traditional cardiovascular risk factors are less predictive in older adults.
- High-sensitivity cardiac troponin I (hs-cTnI) indicates subclinical cardiomyocyte damage and is linked to cardiovascular risk in middle-aged populations.
- The predictive value of hs-cTnI in older adults requires further investigation, particularly in comparison to hs-troponin T (hs-cTnT).
Purpose of the Study:
- To evaluate if hs-cTnI predicts mortality and cardiovascular risk in older adults beyond traditional factors.
- To compare the discriminatory power of hs-cTnI versus hs-cTnT in this population.
- To identify high-risk individuals using hs-cTnI levels, irrespective of existing cardiovascular disease (CVD).
Main Methods:
- Prospective cohort study of 5,876 participants (ages 66-90) from the Atherosclerosis Risk in Communities (ARIC) Study.
- Cox regression analysis assessed the association of hs-cTnI categories with mortality and incident CVD (atherosclerotic CVD, heart failure).
- Analyses were adjusted for traditional cardiovascular risk factors and compared hs-cTnI's performance against hs-cTnT.
Main Results:
- Elevated hs-cTnI was independently associated with increased mortality (HR=2.38) and incident CVD (HR=3.41), ASCVD (HR=2.02), and heart failure (HR=6.16).
- Participants with elevated hs-cTnI but no prior CVD had mortality risks comparable to those with established CVD.
- hs-cTnI significantly improved risk prediction models and demonstrated greater discrimination than hs-cTnT for cardiovascular mortality and heart failure.
Conclusions:
- hs-cTnI enhances mortality and CVD risk stratification in older adults, surpassing traditional risk factors.
- Elevated hs-cTnI identifies a high-risk group, even in the absence of diagnosed CVD.
- hs-cTnI offers superior risk discrimination for specific cardiovascular outcomes compared to hs-cTnT in older populations.
Background/Objectives:
Traditional cardiovascular risk factors are less predictive in older age. High-sensitivity cardiac troponin I (hs-cTnI) is a marker of subclinical cardiomyocyte damage associated with cardiovascular risk in middle-aged adults. We hypothesized hs-cTnI would be indicative of mortality and cardiovascular risk beyond traditional cardiovascular risk factors in older adults and may be more discriminatory compared to hs-troponin T (hs-cTnT).
Design:
Prospective cohort study.
Setting:
Population-based Atherosclerosis Risk in Communities (ARIC) Study.
Participants:
We included 5,876 ARIC participants at Visit 5 (2011-2013).
Outcomes And Measures:
We used Cox regression for the association of hs-cTnI categories (women: <4, 4-<10, ≥10 ng/ml; men: <6, 6-<12, ≥12 ng/ml, prevalent cardiovascular disease (CVD)) with mortality and incident CVD (atherosclerotic CVD [ASCVD]: coronary heart disease or stroke, or heart failure).
Results:
Participants were ages 66 to 90, 23% black, 42% male, and 24% had prevalent CVD. There were 1,053 (321 CVD) deaths (median follow-up 6.3 years). Participants with elevated hs-cTnI and no CVD (7% of participants) had mortality risk similar to those with a history of CVD (55.6 vs 55.7 deaths/1,000 person-years, P = .99). After adjustment, elevated hs-cTnI and no CVD (hazard ratio (HR) = 2.38, 95% confidence interval (CI) = 1.85-3.06) and prevalent CVD (HR = 2.21, 95% CI = 1.90-2.57) remained associated with mortality, compared to low hs-cTnI and no CVD. Elevated hs-cTnI was independently associated with incident CVD (HR = 3.41, 95% CI = 2.58-4.51), ASCVD (HR = 2.02, 95% CI = 1.36-2.98), and heart failure (HR = 6.16, 95% CI = 4.24-8.95). The addition of hs-cTnI significantly improved C-statistics for all outcomes and added greater discrimination than hs-cTnT for cardiovascular mortality and incident heart failure.
Conclusions:
Hs-cTnI improves mortality and CVD risk stratification in older adults beyond traditional risk factors and improved model discrimination more than hs-cTnT for certain outcomes. Elevated hs-cTnI without CVD identifies a high-risk group with comparable mortality risk as those with a history of clinical CVD.
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