Abstract:Objective To investigate the efficacy of Butylphthalide combined with dual antiplatelet therapy for acute progressive cerebral infarction (APCI) and its influence on peripheral blood 6-keto-prostaglandin F1α (6k-PGF1α), positive platelet α-granular membrane glycoprotein (CD62P), Thromboxane B2 (TXB2), homocysteine (Hcy), monocyte chemotactic protein 1 (MCP-1), and vascular endothelial cell cadherin (VE-cadherin).Methods From January 2018 to October 2019, 204 cases of APCI patients admitted to our hospital were randomly divided into two groups: the control group (n = 102) received standardized treatment and dual antiplatelet therapy, and the observation group (n = 102) received Butylphthalide treatment on the basis of control group. The National Institutes of Health Stroke Scale (NIHSS) score, Mini Mental State Examination Scale (MMSE) score, Montreal Cognitive Assessment Scale (MoCA) score, Barthel Index (BI) were evaluated before treatment, 2 weeks and 30 days after treatment. The levels of 6k-PGF1α, CD62P, TXB2, Hcy, MCP-1, and VE-cadherin in peripheral blood were measured before and after treatment.Results After treatment, the NIHSS scores of patients in the observation group were downtrend compared with before treatment and control group, and the BI, MMSE, MoCA scores showed climbed trend (all P < 0.05). Compared with control group, the differences after and before treatment of 6k-PGF1α, CD62P, TXB2, Hcy, MCP-1, VE-cadherin in observation group were higher (all P < 0.05). During the 90-day follow-up, the prognosis good rate (78.57% VS 63.54%) in the observation group was higher than the control group (P < 0.05).Conclusions Butylphthalide combined with dual antiplatelet therapy can down-regulate the peripheral blood 6k-PGF1α, CD62P, TXB2, Hcy, MCP-1, VE-cadherin of patients with APCI, improve the nerve function and protect cognitive function, and improve life activities and clinical prognosis.