About this trial
Calcific aortic stenosis (CAS) can cause severe adverse cardiac events, but there are currently no effective drugs that can prevent or delay the progression of the disease. Our trial aims to investigate the effect of PCSK9 inhibitors on preventing or delaying the progression of CAS.
Eligibility criteria
Qualifiers
Aged 18-85 years old, clinically diagnosed with mild or moderate CAVS (echocardiography shows ejection fraction > 50%; valve orifice area > 1.0 cm²; left ventricular stroke volume index > 35 ml/m²; flow velocity ≥ 2 m/s and < 4 m/s, or mean transvalvular pressure gradient < 40 mmHg) and currently not requiring valve replacement therapy;
LDL-C ≥ 2.6 and < 4.9 mmol/L, or Lp(a) ≥ 30 mg/dL, or receiving statin therapy due to a clinical diagnosis of hypercholesterolemia/hyperlipidemia;
Patients who can understand the purpose of the trial, voluntarily participate, sign the informed consent form, and are willing to undergo clinical follow-up in accordance with the trial requirements.
The position and method of measurement have been further clarified in ultrasonic measurement to ensure comparability among all enrolled patients, as follows: Aortic valve peak flow velocity, aortic valve mean pressure gradient, and valve orifice area (select images of at least 3 consecutive cardiac cycles with stable heart rate; for atrial fibrillation, select images of more than 5 consecutive cardiac cycles; obtain the peak blood flow velocity of the aortic valve orifice using continuous wave Doppler in the apical 5-chamber view; calculate the instantaneous aortic valve pressure gradient using the simplified Bernoulli equation, and calculate the standardized aortic valve orifice area using the continuity equation; all participating sonographers will receive unified training, perform measurements in fixed views and retain images, which will then be reviewed by two experienced sonographers who are blinded to the trial in the core laboratory).
Disqualifiers
Any previous treatment with PCSK9 inhibitors;
Patients must be treated with PCSK9 inhibitors by physician's judgment;
Patients who cannot maintain PCSK9 inhibitor use for 24 months;
Contraindications or hypersensitivity to PCSK9 inhibitors;
Trial design
Treatments tested in this trial
- Treatment with PCSK9 inhibitors
- Treatment without PCSK9 inhibitors
Treatment groups
Sponsors and collaborators
Beijing Anzhen Hospital
Lead sponsor
Beijing Jishuitan Hospital
Collaborator
Chinese Academy of Medical Sciences, Fuwai Hospital
Collaborator
Beijing Hospital
Collaborator
Nanchong Central Hospital
Collaborator
Peking University First Hospital
Collaborator
Beijing Luhe Hospital
Collaborator