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- Ensayo clínico NCT07933757
AIM2-NLRP3 Inflammasome Dual Inhibitor on hsCRP
The Effect of AIM2-NLRP3 Inflammasome Dual Inhibitor on hsCRP in Patients After Coronary Intervention Therapy
Residual inflammatory risk remains a major contributor to adverse cardiovascular outcomes despite guideline-directed therapy. Although colchicine reduces cardiovascular events, its anti-inflammatory effects may extend beyond NLRP3 inhibition to involve AIM2 inflammasome suppression. We hypothesized that dual NLRP3/AIM2 inhibition may provide an effective strategy for targeting residual inflammatory risk. Using molecular docking and a THP-1 cell-based dual-inflammasome model, we screened approved drugs and identified leflunomide, eplerenone, and artesunate as candidate agents with greater IL-1β inhibitory activity than colchicine at clinically relevant concentrations. These findings highlight dual inflammasome inhibition as a potential therapeutic strategy for coronary heart disease.
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
Despite advances in contemporary preventive and therapeutic strategies, coronary heart disease (CHD) remains a leading cause of morbidity and mortality worldwide. Residual inflammatory risk (RIR) persists in a substantial proportion of patients despite guideline-directed medical therapy and contributes to recurrent cardiovascular events, including myocardial infarction, stroke, and cardiovascular death. Accumulating evidence has established inflammation as a key driver of atherosclerotic cardiovascular disease, highlighting the need for targeted anti-inflammatory therapies to address this unmet clinical need. Notably, two large-scale randomized controlled trials, COLCOT and LoDoCo2, demonstrated that low-dose colchicine reduces cardiovascular events in patients with coronary artery disease, providing compelling clinical evidence for the therapeutic potential of targeting inflammation. These findings subsequently led to the approval of colchicine by the US Food and Drug Administration (FDA) for the reduction of cardiovascular risk in adults with established atherosclerotic cardiovascular disease.
The anti-inflammatory effects of colchicine are thought to involve the disruption of microtubule dynamics and the suppression of NLRP3 inflammasome activation, thereby attenuating downstream interleukin (IL)-1β and IL-6 signaling and reducing high-sensitivity C-reactive protein (hsCRP) levels. Among the inflammasomes implicated in cardiovascular diseases, NLRP3 and AIM2 have emerged as important contributors to inflammatory signaling in atherosclerotic disease. However, whether effective attenuation of residual inflammatory risk requires simultaneous targeting of multiple inflammasome pathways remains unclear. In our previous studies, we evaluated three pharmacological inhibitors of the NLRP3 inflammasome in patients with CHD. Notably, only colchicine, a nonselective inhibitor of NLRP3 inflammasome activation, significantly reduced hsCRP levels, whereas the more selective NLRP3 inhibitors tranilast and oridonin did not produce a comparable effect. Given that colchicine can also suppress AIM2 inflammasome activation, these findings raise the possibility that its clinical anti-inflammatory efficacy may extend beyond NLRP3 inhibition. We therefore hypothesized that concomitant inhibition of the NLRP3 and AIM2 inflammasomes may represent a more effective therapeutic strategy for mitigating residual inflammatory risk in patients with CHD.
To explore this hypothesis and identify clinically available therapeutic alternatives, we performed an integrated drug-repurposing strategy combining molecular docking-based virtual screening with functional validation in a THP-1 cell-based model of dual NLRP3 and AIM2 inflammasome activation. By integrating inhibitory efficacy against both inflammasome pathways with clinically achievable plasma drug concentrations, we identified the candidate drugs with IL-1β inhibitory activity exceeding that of colchicine: leflunomide, eplerenone, and artesunate. These findings provide a rationale for further investigating dual inflammasome inhibition as a potential therapeutic approach to targeting residual inflammatory risk in CHD.
Tipo de estudio
Inscripción (Estimado)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Hubei
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Wuhan, Hubei, Porcelana, 430022
- Department of Cardiology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Volunteer to participate, understand and sign an informed consent form.
- Age ≥ 18 years old, regardless of gender.
- Patient diagnosed with coronary heart disease requiring percutaneous coronary intervention.
- Complete all planned percutaneous coronary intervention during hospitalization.
- Patient must be treated according to national guidelines for standard treatment of coronary heart disease.
Exclusion Criteria:
- Known hypersensitivity or allergy to colchicine, eplerenone, leflunomide, or artesunate.
- Use of colchicine, eplerenone, leflunomide, or artesunate within 30 days before screening.
- Hepatic dysfunction, defined as alanine aminotransferase (ALT) levels greater than 3 times the upper limit of normal (ULN).
- Renal dysfunction, defined as an estimated glomerular filtration rate (eGFR) of less than 60 mL/min/1.73 m².
- Hyperkalemia, defined as a serum potassium level greater than 5.0 mmol/L.
- Thrombocytopenia, defined as a platelet count of less than 100 × 10⁹/L.
- Leukopenia, defined as a white blood cell count of less than 3.0 × 10⁹/L.
- Anemia, defined as a hemoglobin level of less than 90 g/L.
- Requirement for potassium supplementation or potassium-sparing diuretics, including amiloride, spironolactone, triamterene, etc.
- Current treatment with potent CYP3A4 inhibitors, including ketoconazole, itraconazole, clarithromycin, etc.
- Uncontrolled infectious diseases.
- Known immune diseases or immune-related diseases such as systemic lupus erythematosus, asthma, inflammatory bowel disease, gout, malignant tumor, etc.
- Current or planned use of medications outside the study protocol that may affect immune or inflammatory responses, including nonsteroidal anti-inflammatory drugs (NSAIDs), systemic corticosteroids, immunomodulatory agents, chemotherapeutic agents, etc.
- Pregnant women, lactating women or women of childbearing age who do not use effective contraceptives.
- Any other circumstances in which the investigator judges that the patient is not suitable to participate in the study.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Sin intervención: Control group
Standard treatment for coronary heart disease |
|
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Experimental: Colchicine group
Colchicine+standard treatment for coronary heart disease |
Colchicine 0.5mg PO Qd |
|
Experimental: Eplerenone group
Eplerenone+standard treatment for coronary heart disease |
Eplerenone 50mg PO Qd |
|
Experimental: Leflunomide group
Leflunomide+standard treatment for coronary heart disease |
Leflunomide 10mg PO Qd |
|
Experimental: Artesunate group
Artesunate+standard treatment for coronary heart disease |
Artesunate 50mg PO Bid |
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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The change in hsCRP
Periodo de tiempo: 4 weeks
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The change in hsCRP compared to baseline |
4 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Major adverse cardiac and cerebrovascular event (MACCE)
Periodo de tiempo: 4 weeks
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Composite endpoint of all cause death, non fatal myocardial infarction, non fatal stroke, and revascularization due to ischemia |
4 weeks
|
|
Plasma OLINK proteomics detection
Periodo de tiempo: 4 weeks
|
The change in plasma OLINK proteomics |
4 weeks
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|
Peripheral blood mononuclear cell mass spectrometry proteomics detection
Periodo de tiempo: 4 weeks
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The change in peripheral blood mononuclear cell mass spectrometry proteomics |
4 weeks
|
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Blood drug concentration
Periodo de tiempo: 4 weeks
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Blood drug concentration in different interventions |
4 weeks
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Colaboradores e Investigadores
Publicaciones y enlaces útiles
Publicaciones Generales
- Yu M, Sun MY, Yang F, Yuan YF, Zhang YM, Ruan CC, Ji Y, Libby P, Cheng X. Taming inflammation in coronary artery disease: lessons learned, translational breakthroughs, and future directions. Sci Bull (Beijing). 2026 Sep 30:S2095-9273(26)01206-5. doi: 10.1016/j.scib.2026.09.081. Online ahead of print.
- Yu M, Zhu ZF, Yang F, Yuan YF, Liao SD, Liu ML, Cheng X. Different Anti-inflammatory Drugs on High-Sensitivity C-Reactive Protein in Patients After Percutaneous Coronary Intervention: A Pilot Randomized Clinical Trial. J Cardiovasc Pharmacol. 2024 Mar 1;83(3):234-242. doi: 10.1097/FJC.0000000000001509.
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio (Estimado)
Finalización primaria (Estimado)
Finalización del estudio (Estimado)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Actual)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades Vasculares
- Enfermedades cardiovasculares
- Procesos Patológicos
- Enfermedades cardíacas
- Isquemia miocardica
- Condiciones Patológicas, Signos y Síntomas
- Inflamación
- Enfermedad coronaria
- Químicos orgánicos
- Compuestos heterocíclicos, 1 anillo
- Compuestos heterocíclicos
- Azoles
- Hidrocarburos
- Terpenos
- Alcaloides
- Compuestos policíclicos
- Químicos inorgánicos
- Embarazos
- Esteroides
- Compuestos de anillo fusionado
- Lactonas
- Embarazo
- Especies reactivas de oxígeno
- Radicales libres
- Artemisininas
- Sesquiterpenos
- Isoxazoles
- Leflunomida
- Artesunato
- Eplerenona
- Colchicina
Otros números de identificación del estudio
- ANDI
Plan de datos de participantes individuales (IPD)
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Información sobre medicamentos y dispositivos, documentos del estudio
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Estudia un producto de dispositivo regulado por la FDA de EE. UU.
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