Table 2

Some randomised controlled trials (RCTs) of lipid-lowering therapy patients who had a stroke

RCTEUREKASTARSASSORTSPARCLTSTINSPIRES
PopulationIschaemic strokeIschaemic strokeIschaemic strokeStroke or TIAIschaemic stroke/TIAIschaemic stroke/TIA
Age, years>20≥18≥20≥18≥1835–80
NIHSS4–220–200–5
premorbid mRS0–30–10–20–30–30–2
Blood lipidLDL-C ≤190 mg/dL
TG ≤500 mg/dL
Dyslipidaemia or LDL-C ≥100 mg/dLLDL-C 100–190 mg/dLLDL-C ≥100 mg/dL with or without statin usage
Start≤48 hours≤12 hours≤24 hours1–6 monthsIschaemic stroke ≤3 months
TIA ≤15 days
≤72 hours
InterventionRosuvastatinSimvastatinAtorvastatin, pitavastatin, or rosuvastatin for days 1–84.AtorvastatinAny type of statin with or without other lipid-lowering drugs, with target LDL-C ≤70 mg/dLAtorvastatin (80 mg/day) for the first 21 days followed by 40 mg daily for days 22–90
ControlPlaceboPlaceboAtorvastatin, pitavastatin, or rosuvastatin for days 7–84.PlaceboAny type of statin with or without other lipid-lowering drugs, with target LDL-C 90–110 mg/dLPlacebo for days 1–3, followed by atorvastatin(40 mg/day) for days 4–90.
DoseRosuvastatin 20 mg/daySimvastatin 40 mg/dayAtorvastatin 20 mg/day, pitavastatin 4 mg/day or rosuvastatin 5 mg/day, with LDL-C maintained <1.8 mmol/LAtorvastatin 80 mg/dayAny dose
Primary outcomeNew
ischaemic lesions on DWI at five or 14 days
Proportion of independent patients (mRS ≤2) at 90 daysPatient disability at 90 daysA first non-fatal or fatal strokeMajor cardiovascular eventsStroke at 90 days
Follow-up14 days90 days90 days4.9 years (median)3.5 years (median)90 days
N316104257473128606100
ResultNo significanceNo significanceNo significanceAtorvastatin decreased the incidence of strokes.The target LDL-C ≤70 mg/dL reduced the incidence of cardiovascular events.
  • DWI, diffusion-weighted imaging; LDL-C, low-density lipoprotein cholesterol; mRS, modified Rankin Scale; NIHSS, National Institutes of Health Stroke Scale; TST, treat Stroke to target.