Jie Kong, Yijing Su, Xinyun Zhu, Jingjing Zhao, Haojie Chen, Xiaoxiang Chen, Yingying Gao
Severe thrombocytopenia was associated with arterial thrombotic manifestations in APS, particularly cerebral infarction. PLT <50×109/L may provide additional clinical risk information but may also reflect cumulative disease burden and overall APS severity.
OBJECTIVE: Thrombocytopenia in APS is often regarded primarily as a bleeding-related manifestation, but the relationship between platelet-count severity and thrombotic manifestations remains uncertain. We evaluated the association between severe thrombocytopenia and arterial thrombotic manifestations in patients with antiphospholipid syndrome (APS).
METHODS: In a two-center baseline cohort of 313 patients with APS, baseline platelet count (PLT) was categorized as PLT <50×109/L, PLT 50-<100×109/L, or PLT ≥100×109/L. Associations with prevalent baseline thrombotic manifestations were assessed using multivariable logistic regression in 300 patients with primary APS or systemic lupus erythematosus-associated APS. In the Renji follow-up cohort (n=254), 48-month thrombotic events were evaluated using Kaplan-Meier curves and Cox models.
RESULTS: PLT <50×109/L was associated with a higher frequency of arterial thrombosis (66.7%), particularly cerebral infarction (62.7%), whereas venous thrombosis was most frequent in the PLT 50-<100×109/L group (68.4%). After multivariable adjustment, PLT <50×109/L remained associated with a higher prevalence of arterial thrombosis (aOR 2.16, 95% CI 1.07-4.35, P = 0.032) and cerebral infarction (aOR 2.37, 95% CI 1.18-4.73, P = 0.015). During 48-month follow-up, PLT <50×109/L was associated with increased risks of any thrombotic event (HR 3.28, 95% CI 1.54-6.97, P = 0.002), arterial thrombotic event (HR 3.95, 95% CI 1.39-11.21, P = 0.010), and cerebral infarction (HR 4.11, 95% CI 1.44-11.73, P = 0.008), but not venous-related events.
CONCLUSION: Severe thrombocytopenia was associated with arterial thrombotic manifestations in APS, particularly cerebral infarction. PLT <50×109/L may provide additional clinical risk information but may also reflect cumulative disease burden and overall APS severity.