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Coronary Artery Disease Presentation and Its Association with Shortened Activated Partial Thromboplastin Time
Maryam Sotoudeh Anvari1, Mojgan Tavakoli1, Masoumeh Lotfi-Tokaldany1
1Tehran Heart Center, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Patients with ST-segment-elevation myocardial infarction (STEMI) showed lower activated partial thromboplastin time (APTT) levels. APTT may predict coronary stenosis severity in patients undergoing angiography.
Area of Science:
- Cardiology
- Clinical Laboratory Science
- Diagnostic Medicine
Background:
- Standard coagulation screening tests are crucial in clinical diagnostics.
- The relationship between clinical presentation and coagulation parameters in suspected coronary artery disease (CAD) lacks clear evidence.
- Investigating coagulation profiles can aid in understanding disease severity.
Purpose of the Study:
- To investigate the association between clinical presentations of coronary artery disease and standard coagulation parameters.
- To determine if coagulation tests can predict the extent and severity of coronary stenosis.
Main Methods:
- A cross-sectional study involving 539 patients undergoing coronary angiography.
- Patients were categorized by clinical presentation: STEMI, non-STEMI, unstable angina, and stable angina.
- Prothrombin time (PT), international normalized ratio (INR), and activated partial thromboplastin time (APTT) were measured pre-angiography.
Main Results:
- No significant differences in PT or INR were observed across clinical presentation groups.
- Activated partial thromboplastin time (APTT) was significantly lower in patients with ST-segment-elevation myocardial infarction (STEMI) and non-STEMI compared to angina groups.
- Adjusted analysis confirmed a significant association between clinical presentation and APTT, with lower APTT linked to more severe presentations (OR for 5s increase in APTT = 1.661, p=0.003).
Conclusions:
- Patients presenting with STEMI exhibited the lowest APTT values, while stable angina patients had the highest.
- Activated partial thromboplastin time (APTT) may serve as a predictive marker for the extent and severity of coronary stenosis in patients undergoing coronary angiography.
- Further research is warranted to validate APTT's role in predicting CAD severity.
Abstract:
Background: Standard coagulation screening tests are important constituents of basic examinations in clinical laboratories. There is no clear evidence of a relation between the type of clinical presentation and coagulation parameters in patients with suspected coronary artery disease. Methods: This cross-sectional study included 539 patients who underwent coronary angiography in Tehran Heart Center between November 2012 and January 2013. Patients presented with ST-segment-elevation myocardial infarction (STEMI), non-STEMI, unstable angina, or stable angina. Prothrombin time (PT), international normalized ratio (INR), and activated partial thromboplastin time (APTT) were measured before angiography and compared between the clinical presentation groups. Results: The mean age of the patients was 59.156 ± 11.05 years, and 47.7% were male. STEMI was reported in 41(7.6%) patients, non-STEMI in 42 (7.8%), unstable angina in 304 (56.4%), and stable angina in 152 (28.2%). No difference in the mean PT and INR was found between the groups. The mean APTT was significantly lower among the patients presenting with STEMI and non-STEMI (26.58 ± 2.32 s in the STEMI, 26.85 ± 2.41 s in the non-STEMI, 27.64 ± 2.54 s in the unstable, and 27.93 ± 2.53 s in the stable angina groups, respectively, p value = 0.005). After adjustment, the association between the patients' presentations and APTT was significant (OR for 5 s increase in APTT = 1.661, 95% CI = 1.184 to 2.332; p value = 0.003). Conclusion: We observed that the patients who presented with STEMI had the lowest value of APTT, whereas those who presented with stable angina had the highest. The value of APTT in patients undergoing coronary angiography may have a potential to predict the extent and severity of coronary stenosis.
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