Shortened activated partial thromboplastin time, a hemostatic marker for hypercoagulable state during acute coronary event
Received 13 September 2009; received in revised form 7 February 2010; accepted 9 February 2010. published online 08 March 2010.
Various factors may contribute to a hypercoagulable state and acute vascular thrombosis. A prospective study was conducted involving 165 coronary heart disease (CHD) patients from the Cardiology Unit, Hospital Universiti Sains Malaysia. The purpose of this study was to investigate the relationship among factor VIII (FVIII), prothrombin time (PT), activated partial thromboplastin time (APTT), and activated protein C resistance (APC-R) state among CHD patients and to look for potential clinical applications from these laboratory findings. There were 110 cases diagnosed as acute coronary syndrome (ACS), whereas another 55 were stable coronary artery disease (SCAD) patients. PT, APTT, FVIII, and APC-R assays were performed on all subjects. There was a significant difference between the FVIII level and the APTT results (P value < 0.0001). A negative relationship was found between the FVIII level and the APTT from linear regression analysis (R2 = 10%, P value < 0.0001). For each 1% increase in the FVIII level, the APTT was reduced by 0.013 s (95% confidence interval (CI) between –0.019 and –0.007). Interestingly, none of the SCAD patients had abnormally short APTT. Approximately 68.4% of cases with a positive APC-R assay were found to have a high FVIII level. In conclusion, the APTT test is a potential hemostatic marker for hypercoagulable state including in arterial thrombosis.
aHaematology Department, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia
bCardiology Unit, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia
cDepartment of Community Medicine, School of Medical Sciences, Universiti Sains Malaysia, Health Campus, Kelantan, Malaysia
Reprint requests: Dr. Wan Zaidah Abdullah, Haematology Department, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kelantan, Malaysia
Supported by Grant 1001/PPSP/812004 from the Universiti Sains Malaysia (USM)