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May 20, 2014Clinical Chemistry67 citationsOpen Access

Revision of the Troponin T Release Mechanism from Damaged Human Myocardium

KSKarin StarnbergAJAnders JeppssonBLBertil Lindahl

Key Result

Over 80% of cardiac troponin T can be extracted from human cardiac tissue in 90 minutes using large volumes of human serum at 37 °C, suggesting the diffusible fraction is larger than previously reported.

Structured PICO

P
Population
Human cardiac tissue (in vitro model)
I
Intervention
In vitro extraction in human serum at 37 °C
C
Comparator
Extraction in low-salt extraction buffer at 0 °C or equal volume of serum and heart tissue
O
Outcome
Percentage of cTnT extractedsurrogate

The diffusible fraction of cTnT from damaged myocardium is likely much larger than previously thought and dependent on local plasma flow, revising the understanding of troponin release kinetics post-MI.

Abstract

BACKGROUND: Cardiac troponin T (cTnT) is released from damaged heart tissue in patients with acute myocardial infarction. It is presumed that most cTnT is tightly bound and released following the degradation of myofibrils in necrotic cardiomyocytes, resulting in sustained increases in circulating cTnT. Evidence of a large irreversibly bound fraction is based on the inability to extract most cTnT from cardiac tissue in cold low-salt extraction buffers. METHODS: Here we examined in vitro extraction of cTnT from human cardiac tissue in serum at 37 °C. RESULTS: We found that over 80% of the cTnT can be extracted from human cardiac tissue in 90 min using large volumes of human serum at 37 °C. The release ratio was highly dependent on the extraction volume and was only 3% if an equal volume of serum and heart tissue was used. In contrast, extraction of the cytoplasmic cardiac damage markers myoglobin and creatinine kinase was much less affected by changing these conditions. Purified cTnT was poorly soluble in a low-salt extraction buffer at 0 °C, previously used to define the free cTnT fraction. CONCLUSIONS: Our data indicate that the diffusible fraction of cTnT is likely substantially larger in vivo than previously reported and likely is not fixed but dependent on local plasma flow. It is therefore possible that the sustained increase in circulating cTnT after myocardial infarction is at least in part due to a slow washout of cTnT that interacts reversibly with tropomyosin in myofibrils.

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Cite This Study

Starnberg et al. (2014) studied Acute myocardial infarction. In vitro extraction in human serum at 37 °C vs. Extraction in cold low-salt extraction buffers at 0 °C was evaluated on Extraction of cTnT from human cardiac tissue. Over 80% of cardiac troponin T can be extracted from human cardiac tissue in 90 minutes using large volumes of human serum at 37 °C, suggesting the diffusible fraction is larger than previously reported.

synapsesocial.com/papers/6a5e12882170d496c6709dc2https://doi.org/10.1373/clinchem.2013.217943
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Different intracellular compartmentations of cardiac troponins and myosin heavy chains: a causal connection to their different early release after myocardial damage1998 · 149 citations
  2. 2A Possible Mechanism behind Faster Clearance and Higher Peak Concentrations of Cardiac Troponin I Compared with Troponin T in Acute Myocardial Infarction2020 · 51 citations
  3. 3Cardiac troponins: Mechanisms of release and role in healthy and diseased subjects2022 · 12 citations
  4. 4Pathophysiological Analysis of Serum Troponin T Release Kinetics in Evolving Ischemic Myocardial Injury1996 · 24 citations
  5. 5Multi‐Site Coronary Vein Sampling Study on Cardiac Troponin T Degradation in Non–ST‐Segment–Elevation Myocardial Infarction: Toward a More Specific Cardiac Troponin T Assay2019 · 22 citations