Clinical and prognostic implications of high-sensitivity cardiac troponin T concentrations in type 2 non-ST elevation
K M Eggers1, T Baron1, A Gard1
1Department of Medical Sciences, Uppsala University, Uppsala, Sweden.
Insights
High-sensitivity cardiac troponin (hs-cTnT) levels independently predict adverse outcomes in type 2 myocardial infarction (MI). These findings in type 2 MI are similar to type 1 MI, highlighting diagnostic challenges.
Area of Science:
- Cardiology
- Biomarkers
- Clinical Medicine
Background:
- Limited evidence exists on cardiac troponin in type 2 myocardial infarction (MI).
- High-sensitivity cardiac troponin (hs-cTnT) is crucial in type 1 MI.
- This study investigates hs-cTnT in type 2 MI.
Purpose of the Study:
- To assess clinical and prognostic implications of hs-cTnT in type 2 MI.
- To compare hs-cTnT findings in type 2 MI with type 1 MI.
- To evaluate hs-cTnT's predictive value for mortality and adverse events.
Main Methods:
- Retrospective registry-based cohort study (SWEDEHEART).
- Included 4607 patients with type 2 MI and 43,405 with type 1 MI (excluding STEMI).
- Multivariable-adjusted regressions analyzed hs-cTnT associations with outcomes over 1.9 years.
Main Results:
- Hs-cTnT associated with risk factors/comorbidities in type 2 NSTEMI, similar to type 1 NSTEMI.
- Hs-cTnT independently predicted all-cause mortality and MACE in type 2 NSTEMI.
- Prognostic association of hs-cTnT was stronger in type 2 NSTEMI patients without prior cardiovascular disease.
Conclusions:
- Hs-cTnT concentrations independently predict adverse outcomes in type 2 NSTEMI.
- Similarities between type 1 and type 2 NSTEMI hs-cTnT findings are notable.
- These similarities underscore the diagnostic challenges in differentiating MI types.
Background:
While the clinical importance of cardiac troponin is well-known in type 1 myocardial infarction (MI), evidence on this topic in type 2 MI is limited. We assessed the clinical and prognostic implications of high-sensitivity cardiac troponin (hs-cTnT) concentrations in a large sample of patients with type 2 MI.
Methods:
Retrospective registry-based cohort study (SWEDEHEART) including 4607 patients with type 2 MI and 43,405 patients with type 1 MI, used for comparisons. Patients with ST-elevation MI were excluded. Multivariable-adjusted regressions were applied to investigate the associations of hs-cTnT concentrations (highest measured value during each hospitalization) with clinical variables and prognosis during a median follow-up of up to 1.9 years.
Results:
Hs-cTnT concentrations (median 264 [25th, 75th percentiles 112-654] ng/L) were significantly associated with various cardiovascular risk factors and comorbidities in type 2 non-ST elevation MI (NSTEMI) but only weakly with the underlying triggering condition. Most of these findings including the magnitude of hs-cTn release were similar to type 1 NSTEMI. Hs-cTnT (ln) independently predicted all-cause mortality (hazard ratio 1.13 [95% confidence interval 1.09-1.17]) and major adverse events (hazard ratio 1.13 [95% confidence interval 1.10-1.17]) in type 2 NSTEMI, similar as for type 1 NSTEMI according to interaction analysis. The associations of hs-cTnT (ln) with poor prognosis tended to be stronger in type 2 NSTEMI patients without known cardiovascular disease.
Conclusions:
Hs-cTnT concentrations independently predict adverse outcome in type 2 NSTEMI. The similarities to type 1 NSTEMI however, are striking and emphasize the difficulty to distinguish both MI types.
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