Relationships between renal function variations and relative changes in cardiac troponin T concentrations based on
Denis Monneret1, Matteo Fasiolo2, Dominique Bonnefont-Rousselot3,4
1Service de Biochimie et Biologie Moléculaire, Laboratoire de Biologie Médicale Multisite (LBMMS), Hospices Civils de Lyon (HCL), Lyon, France.
Relative changes in high-sensitive cardiac troponin T (hs-cTnT) are primarily linked to creatinine variations, with minor impacts on myocardial injury diagnosis when accounting for renal function. This study models these associations using a quantile generalized additive model.
Area of Science:
- Cardiology
- Nephrology
- Biostatistics
Background:
- High-sensitive cardiac troponin T (hs-cTnT) is a key biomarker for myocardial injury.
- The interplay between hs-cTnT and renal function markers like creatinine (cre) and estimated glomerular filtration rate (eGFR) is recognized, but the precise nature of their variations requires further investigation.
- Understanding these relationships is crucial for accurate clinical interpretation.
Purpose of the Study:
- To model the relationship between relative changes in hs-cTnT (Δhs-cTnT) and variations in creatinine (Δcre) or estimated glomerular filtration rate (ΔeGFR).
- To quantify the impact of renal function variations on the interpretation of Δhs-cTnT.
- To utilize a quantile generalized additive model (qgam) for robust statistical analysis.
Main Methods:
- Analysis of concomitant plasma Δhs-cTnT and Δcre data from a large cohort (n=106567) of patients aged 18-100 years.
- Data collected over a 5.8-year period with time variation (Δtime) between 3 hours and 7 days.
- Quantile generalized additive models (qgam) were employed to fit relationships between Δhs-cTnT and covariates including Δcre, ΔeGFR, age, Δtime, and hour of blood sampling (HSB).
Main Results:
- Δhs-cTnT showed a significant positive, nonlinear association with Δcre (e.g., +55% for +100% Δcre).
- Δhs-cTnT exhibited a negative association with ΔeGFR (e.g., -20% for +100% ΔeGFR).
- Adjusting Δhs-cTnT interpretations for renal function resulted in statistically significant but minor diagnostic discrepancies (<2%) for myocardial injury compared to unadjusted interpretations.
Conclusions:
- Considering renal function variations when interpreting relative changes in cardiac troponin T has a minimal impact on the diagnosis rate of myocardial injury.
- The primary driver for Δhs-cTnT variations is Δcre, with secondary influences from age, Δtime, and HSB.
- Statistical modeling confirms the need to acknowledge renal status but highlights its limited effect on diagnostic outcomes in this context.
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