Acute ischemic stroke (AIS) is a cerebrovascular disease with high incidence, recurrence, and disability rates, posing a serious threat to human health. Symptomatic intracranial atherosclerotic stenosis (ICAS) is one of the most common causes of ischemic stroke globally. In Asian populations, ICAS is the predominant subtype, accounting for approximately 50% of all ischemic strokes. Despite aggressive and standardized medical therapy, patients with ICAS still face a high recurrence rate of stroke and incidence of early neurological deterioration (END). Over 50% of cases of END occur within 72 hours of AIS onset and are defined as an increase in the NIHSS score by ≥2 or 4 points from baseline, which is closely linked to clinical outcomes. Two previous randomized controlled trials (RCTs) found that combined clopidogrel and aspirin dual antiplatelet therapy can prevent END and improve neurological outcomes in AIS patients. However, the occurrence of END remains high, as drug resistance and swallowing difficulties may hinder timely administration.
Multiple RCTs have shown that statin therapy can reduce the risk of recurrent stroke and improve neurological outcomes, and it is consistently recommended by both domestic and international ischemic stroke guidelines. The SPARCL study, published in the New England Journal of Medicine, demonstrated that in patients with a history of recent stroke, lowering LDL-C from ≥2.6 mmol/L to \<1.8 mmol/L significantly reduces the risk of recurrent stroke and cardiovascular events. More recently, the INSPIRES study, published in JAMA Neurology, indicated that early statin therapy within 3 days of AIS onset significantly reduces adverse neurological outcomes, such as the proportion of patients with a 90-day mRS score of 2-6 (11.4% vs. 9.8%, P\<0.05), compared to delayed statin therapy, although no significant difference was observed in recurrent stroke events within 90 days. As stroke guidelines have evolved, the LDL-C target for secondary prevention has been lowered from 2.6 mmol/L to below 1.8 mmol/L. Statins and other lipid-lowering agents work through different mechanisms affecting cholesterol synthesis, absorption, and clearance, and their combined use can produce a synergistic effect. At the 2024 annual meeting of the Chinese Stroke Society, experts proposed a new concept for lipid management in AIS patients, focusing on residual lipid risk and early combination therapy to achieve more rapid, sustained, and stable lipid control.
Proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitors are a novel class of monoclonal antibody-based lipid-lowering drugs that reduce serum LDL-C levels by inhibiting the binding of PCSK9 to LDL receptors. PCSK9 inhibitors are highly effective in lowering lipid levels with minimal adverse effects and high safety. The main PCSK9 inhibitors approved for clinical use are alirocumab and evolocumab. Recent international guidelines have clearly stated that PCSK9 inhibitors can be used in combination with statins or other lipid-lowering agents or as monotherapy in patients who are statin-intolerant or for whom statins are contraindicated. Due to the complementary mechanisms of action between statins and PCSK9 inhibitors, their combined use has been shown to provide a greater-than-additive lipid-lowering effect. Post-hoc analyses of the FOURIER study, published in Stroke, and the ODYSSEY study, published in Circulation, confirmed that in patients with atherosclerotic cardiovascular disease, combination therapy with statins and PCSK9 inhibitors significantly reduced the risk of ischemic stroke (1.2% vs. 1.5%, P=0.005; 1.2% vs. 1.6%, P=0.01), with no significant difference in the risk of hemorrhagic stroke between the groups.
However, it remains unclear whether the combination of statins and PCSK9 inhibitors improves neurological outcomes in acute ischemic stroke, particularly in patients with ICAS, as high-quality evidence is lacking. A multicenter, prospective cohort study found that for AIS patients with ICAS, early combination therapy with statins and PCSK9 inhibitors within 7 days of onset significantly reduced the risk of early stroke recurrence within 30 days (5.59% vs. 2.16%, P=0.039). A single-center, retrospective cohort study demonstrated that early combination therapy with statins and PCSK9 inhibitors within 24 hours of stroke onset significantly reduced the incidence of early neurological deterioration (increase in NIHSS score ≥2 points) within 72 hours compared to statin monotherapy (31.9% vs. 12.5%, P=0.005). Another single-center, retrospective cohort study found that for AIS patients undergoing thrombectomy, early combination therapy with statins and PCSK9 inhibitors reduced the proportion of patients with an NIHSS score at discharge and an mRS score of ≤3 (35.6% vs. 52.4%, P=0.041) without increasing the risk of symptomatic intracranial hemorrhage (8.7% vs. 2.4%, P=0.16). Although the reduction in early neurological deterioration was not statistically significant (20.1% vs. 11.9%, P=0.21), these studies support the effectiveness and safety of statin and PCSK9 inhibitor combination therapy in improving neurological outcomes in AIS, providing a reliable foundation for further high-quality RCTs.
This multicenter, prospective, randomized controlled study aims to investigate and evaluate the effects of early combination therapy with PCSK9 inhibitors and statins on early neurological deterioration and other neurological outcome measures in patients with symptomatic intracranial atherosclerotic stenosis, which holds significant clinical value.
