Key result
High SBP with elevated hs-cTnT linked to ~139% higher cardiovascular mortality.
Why the study?
Whether cardiac biomarkers can provide insights into optimal blood pressure and related cardiovascular mortality risk in adults without cardiovascular disease was compelling to evaluate.
Do systolic and diastolic blood pressure levels, combined with cardiac biomarkers, predict cardiovascular mortality in adults without cardiovascular disease?
Cohort (n=11,242)
Do systolic and diastolic blood pressure levels, combined with cardiac biomarkers, predict cardiovascular mortality in adults without cardiovascular disease?
The combination of abnormal blood pressure (high SBP or low DBP) and elevated cardiac biomarkers (hs-cTnT) helps identify adults without known cardiovascular disease who are at highest risk for cardiovascular mortality.
May aid risk stratification in primary prevention without known CVD; hypothesis-generating and requires prospective validation before practice change.
Whether cardiac biomarkers can help provide insights into optimal blood pressure (BP) and BP-related cardiovascular mortality risk is compelling. The purpose of this study was to evaluate 1) the associations between systolic and diastolic blood pressure (SBP, DBP) and cardiac biomarkers; and 2) their association with cardiovascular mortality in adults without cardiovascular disease. Cross-sectional associations between SBP, DBP and cardiac biomarkers (high-sensitivity cardiac troponin T [hs-cTnT], N-terminal pro-brain natriuretic peptide [NT-proBNP], and high-sensitivity cardiac troponin I), and prospective associations with cardiovascular mortality were analyzed using the 1999 to 2004 U.S. National Health and Nutrition Examination Survey. Prevalence rate ratio (PRR)/incidence rate ratio was estimated using weighted Poisson regression models. SBP high was defined as ≥130 mm Hg, DBP low was defined as <70 mm Hg; and TNT high was defined as ≥14 ng/L. Among 11,242 adults, 2,355 deaths occurred during a median follow-up of 17.5 (IQR: 15.6-20.5) years. Compared with the reference group SBP 120 to 129 mm Hg, SBP ≥160 mm Hg had a nearly 2-fold higher adjusted PRR for hs-cTnT (1.76 [95% CI: 1.35-2.29]) and NT-proBNP (1.86 [95% CI: 1.59-2.17]). Compared with the reference group DBP 70 to 79 mm Hg, those with DBP <50 mm Hg had higher PRR for hs-cTnT (1.76 [1.39-2.23]) and NT-proBNP (1.41 [95% CI: 1.22-1.63]). Treating normal DBP, SBP, and low hs-cTnT as reference, incidence rate ratios (95% CIs) for cardiovascular mortality in SBP high TNT high was 2.39 (95% CI: 1.74-3.29) and for DBP low TNT high was 2.27 (95% CI: 1.62-3.18). Low DBP levels (<70 mm Hg) and high SBP (≥130 mm Hg) were independently associated with increased hs-cTnT or NT-proBNP. Their associations with cardiovascular mortality varied according to the presence of subclinical myocardial injury (hs-cTnT level). The combination of BP and cardiac biomarkers helps identify those at highest risk.
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Guo et al. (2025) conducted a cohort in Adults without cardiovascular disease (n=11,242). High systolic and low diastolic blood pressure with high cardiac biomarkers vs. Normal blood pressure and low cardiac biomarkers was evaluated on Cardiovascular mortality (IRR 2.39, 95% CI 1.74-3.29). High systolic blood pressure (≥130 mm Hg) with high hs-cTnT (≥14 ng/L) was associated with increased cardiovascular mortality compared to normal BP and low hs-cTnT (IRR 2.39; 95% CI 1.74-3.29).
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