Diagnostic Utility of Platelet Indices in Differentiating Clonal and Reactive Thrombocytosis: A Comparative Cross-Sectional Study
DOI:
https://doi.org/10.52206/jsmc.2026.16.2.1309Abstract
Background: Thrombocytosis, defined as an elevated platelet count, can be broadly categorized into clonal and reactive types. Clonal thrombocytosis is associated with myeloproliferative neoplasms, whereas reactive thrombocytosis occurs secondary to inflammatory, infectious, or neoplastic conditions. Differentiating between these entities is clinically important, as management strategies and prognostic implications differ significantly. Platelet indices have emerged as accessible and cost-effective markers that may aid in this distinction.
Objective: To compare platelet indices—platelet count, mean platelet volume (MPV), plateletcrit (PCT), and platelet distribution width (PDW)—between clonal and reactive thrombocytosis.
Methodology: This comparative cross-sectional study was conducted at Saidu Medical College, Swat, and included 70 patients diagnosed with thrombocytosis (35 clonal and 35 reactive). Platelet indices were measured using an automated hematology analyzer. Statistical analysis was performed using R software version 4.3.1, and group comparisons were made using independent samples t-test. A p-value of <0.05 was considered statistically significant.
Results: The mean age and gender distribution were comparable between the two groups (p > 0.05). Platelet count was significantly higher in the clonal thrombocytosis group (771.54 ± 217.90 ×10⁹/L) compared to the reactive group (665.23 ± 162.48 ×10⁹/L) (p = 0.024). MPV and PCT were also significantly elevated in clonal thrombocytosis (p < 0.001). In contrast, PDW was significantly higher in reactive thrombocytosis (p < 0.001). Stratified analysis by gender demonstrated consistent findings across both subgroups.
Conclusion: Platelet indices, particularly MPV, PCT, and PDW, demonstrate significant differences between clonal and reactive thrombocytosis and may serve as practical, cost-effective tools for preliminary differentiation. However, confirmation with molecular and histopathological investigations remains essential.
Keywords: Clonal thrombocytosis, MPV, Platelet indices, PCT, PDW, Platelet count, Reactive thrombocytosis.
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