Key result
Baseline elevation of cardiac troponin I differentiates between hemodialysis patients with and without severe CAD with a test accuracy of 0.72 (95% CI, 0.69-0.75, p < 0.001).
Why the study?
Elevated cTn-I is associated with CAD in asymptomatic hemodialysis patients, but the diagnostic value of chronically elevated baseline cTn-I in those presenting with acute cTn-I elevation needed investigation.
Does chronically elevated baseline cardiac troponin I predict the severity of coronary artery disease in hemodialysis patients presenting with an acute rise in cTn-I?
Observational (n=364)
Does chronically elevated baseline cardiac troponin I predict the severity of coronary artery disease in hemodialysis patients presenting with an acute rise in cTn-I?
Elevated baseline cTn-I accurately predicts the presence of severe angiographic coronary artery disease in hemodialysis patients presenting with acute symptomatic troponin elevation.
Baseline cTn-I may aid differentiation of severe CAD in hemodialysis patients with acute rises; leaves open prospective validation before practice change.
Elevation of cardiac troponin I (cTn-I) is associated with coronary artery disease (CAD) in asymptomatic patients with end-stage renal disease (ESRD) receiving hemodialysis. We aim to investigate the diagnostic value of chronically elevated cTn-I in ESRD patients presenting with an acute rise in serum cTn-I levels. We performed a retrospective analysis of 364 patients. Using coronary angiography, we correlated baseline elevation of cTn-I with the severity of CAD when hemodialysis patients present with acute symptomatic elevation in serum cTn-I. In hemodialysis patients presenting with a rise in serum cTn-I above baseline levels, 59% had severe CAD, and 17% had no angiographic evidence of CAD. Hemodialysis patients with severe CAD had significantly higher baseline cTn-I levels compared to patients with non-severe CAD or normal coronaries (p < 0.0001). Baseline elevation of cTn-I in the severe CAD group was correlated with the degree of CAD occlusion (r2 0.56, p < 0.0001), fitting a positive linear model. Furthermore, baseline cTn-I differentiates between patients with and without severe CAD with a test accuracy of 0.72 (95% CI, 0.69–0.75, p < 0.001). At a value of ≥0.2 ng/mL (cutoff for myocardial necrosis), the specificity of baseline cTn-I for underlying severe CAD was 0.95. Elevated baseline cTn-I has good accuracy for anticipating more advanced angiographic CAD when hemodialysis patients present with a symptomatic rise in serum cTn-I above baseline levels. Baseline elevation of cTn-I can be used for cardiac disease risk management in hemodialysis patients presenting with symptoms suggestive of CAD.
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Taha et al. (2021) conducted an observational in End-stage renal disease receiving hemodialysis with acute elevation in serum cTn-I (n=364). Baseline elevation of cardiac troponin I vs. Non-elevated baseline cardiac troponin I was evaluated on Presence of severe coronary artery disease (test accuracy 0.72, 95% CI 0.69-0.75, p=<0.001). Baseline elevation of cardiac troponin I differentiates between hemodialysis patients with and without severe CAD with a test accuracy of 0.72 (95% CI, 0.69-0.75, p < 0.001).
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