STUDIES ON ACTIVATED PARTIAL THROMBOPLASTIN TIME, RED AND WHITE BLOOD CELL COUNTS IN CORONARY ARTERY DISEASE IN OWERRI, NIGERIA.

  • Chinedu-Madu Jane U Federal University Otueke, Bayelsa State, Nigeria.
  • Onyejiawa Favour C Imo State University, Owerri, Nigeria.
  • Aloy-Amadi Oluchi C Imo State University, Owerri, Nigeria.
Keywords: Activted Partial Thromboplastin Time, Red Blood Cell, White Blood Cell, Coronary Artery Disease

Abstract

Background: Coronary artery disease (CAD) is a multifactorial condition influenced by cardiovascular,  hematological and haemostatic factors. The knowledge of these parameters in CAD patients, including gender-based differences, is essential for personalized diagnosis and treatment.

Objective: To investigate red cell indices and aspartate aminotransferase in CAD patients  Federal Teaching Hospital, Owerri, Nigeria, and assess gender-based variations.

Methods: A cross-sectional study was conducted involving 30 CAD patients (19 males and 11 females) and 30 age-matched healthy controls. A total of 5 mL of venous blood was collected from each participant, with 3 mL placed in EDTA tubes for hematological analysis and 2 mls into sodium citrate containers for APTT determination..Haematological parameters were assessed using an automated hematology analyzer, while APTT was determined using a standard coagulometer and commercial reagents according to the manufacturer’s instructions.

. Statistical analysis was conducted using independent t-tests to compare group differences and Pearson correlation for association studies, with p < 0.05 considered statistically significant.

Results: CAD patients showed significantly higher mean activated partial thromboplastin time (APTT: 41.23 ± 4.09 )secsand white blood cell (WBC) count (15.23 ± 2.1) × 10⁹/L compared to controls (APTT: 28.30 ± 2.17)secs; WBC: (7.00 ± 1.68) × 10⁹/L with p-values of 0.002 and <0.001, respectively. Red blood cell (RBC) count was significantly lower in CAD patients (2.07 ± 0.35 )× 10¹²/L) compared to controls (4.01 ± 0.27 )× 10¹²/L. Among CAD patients, males had significantly higher APTT values (65.30 ± 14.48) secs than females (48.60 ± 8.95) secs(p = 0.035). No significant gender differences were observed in RBC and WBC counts. Correlation analysis revealed insignificant negative correlations of APTT with RBC (r = -0.025, p = 0.897), and WBC(r = -0.038, p = 0.843).

Conclusion: CAD patients in Owerri exhibit significant hematological abnormalities, including elevated APTT and WBC levels and reduced RBC counts. Although gender-related variations were observed in APTT, no significant correlations among APTT, RBC, and WBC suggest independent pathological mechanisms. Comprehensive hematological assessments should be incorporated into CAD management protocols. Further studies arewarranted to explore the underlying mechanisms of these hematological changes.

Author Biographies

Chinedu-Madu Jane U, Federal University Otueke, Bayelsa State, Nigeria.

Department of Haematology, 

Onyejiawa Favour C, Imo State University, Owerri, Nigeria.

Department of Medical Laboratory Science,

Aloy-Amadi Oluchi C, Imo State University, Owerri, Nigeria.

Department of Medical Laboratory Science, 

References

1. Roth GA, Mensah GA, Johnson CO, et al. Global burden of cardiovascular diseases and risk factors, 1990–2019: update from the GBD 2019 study. J Am CollCardiol. 2020;76(25):2982–3021.
2. Singh RB, Mengi SA, Xu YJ, Arneja AS, Dhalla NS. Pathogenesis of atherosclerosis: a multifactorial process. ExpClinCardiol. 2002;7(1):40–53.
3. SotoudehAnvari M, Tavakoli M, Lotfi-Tokaldany M, et al. Coronary artery disease presentation and its association with shortened activated partial thromboplastin time. J Tehran Heart Cent. 2018;13(1):1–5.
4. Cannon CP, McCabe CH, Wilcox RG, et al. Association of white blood cell count with increased mortality in acute myocardial infarction and unstable angina pectoris. Am J Cardiol. 2001;87(5):636–639.
5. Sabatine MS, Morrow DA, Giugliano RP, et al. Association of hemoglobin levels with clinical outcomes in acute coronary syndromes. Circulation. 2005;111(16):2042–2049.
6. Pradhan AD, Manson JE, Rifai N, Buring JE, Ridker PM. C-reactive protein, interleukin 6, and risk of developing type 2 diabetes mellitus. JAMA. 2001;286(3):327–334.
7. Sharma R, Goyal A, Sinha M, et al. Coagulation profile in patients of ischemic heart disease with reference to activated partial thromboplastin time. Int J Adv Med. 2018;5(3):612–615.
8. Cushman M, Glynn RJ, Goldhaber SZ, et al. Hormone replacement therapy and risk of venous thromboembolism in postmenopausal women. JAMA. 2004;292(13):1573–158,
9. Libby P. Inflammation in atherosclerosis.Nature. 2002;420(6917):868–874.
10. Madjid M, Awan I, Willerson JT, Casscells SW. Leukocyte count and coronary heart disease: implications for risk assessment. J Am CollCardiol. 2004;44(10):1945–1956.
11. Sharma R, Francis DP, Pitt B, Poole-Wilson PA, Coats AJ, Anker SD. Haemoglobin predicts survival in patients with chronic heart failure: a substudy of the ELITE II trial. EurHeart J. 2004;25(12):1021–1028.
12. Packard RR, Libby P. Inflammation in atherosclerosis: from vascular biology to biomarker discovery and risk prediction. Clin Chem. 2008;54(1):24–38.
Published
2025-04-30
How to Cite
Jane U, C.-M., Favour C, O., & Oluchi C, A.-A. (2025). STUDIES ON ACTIVATED PARTIAL THROMBOPLASTIN TIME, RED AND WHITE BLOOD CELL COUNTS IN CORONARY ARTERY DISEASE IN OWERRI, NIGERIA. IJO - International Journal of Health Sciences and Nursing ( ISSN: 2814-2098 ), 8(04), 01-09. Retrieved from https://ijojournals.com/index.php/hsn/article/view/1065