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Ningún aumento de la presión arterial evaluado con el monitoreo de Holter de 24 horas en pacientes con migraña episódica durante el tratamiento inicial con anticuerpos monoclonales anti-CGRP: un estudio de observación prospectivo (SAFHYPER)

  • 0Digital and Predictive Medicine, Pharmacology and Clinical Metabolic Toxicology-Headache Center and Drug Abuse-Laboratory of Clinical Pharmacology and Pharmacogenomics, AOU Policlinico di Modena, Modena, Italy.

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Resumen

Este resumen es generado por máquina.

Los anticuerpos monoclonales relacionados con el gen de la calcitonina (CGRP) muestran seguridad cardiovascular a corto plazo en pacientes con migraña. El tratamiento temprano no aumentó significativamente la presión arterial ni mejoró los patrones de inmersión nocturna.

Área De La Ciencia

  • Ciencias cardiovasculares
  • Neurología
  • Farmacología

Sus Antecedentes

  • La migraña está relacionada con un aumento de los riesgos cardiovasculares, incluida la hipertensión.
  • Los anticuerpos monoclonales del péptido relacionado con el gen de la calcitonina (CGRP, por sus siglas en inglés) (mAbs) son eficaces en la prevención de la migraña.
  • Existen preocupaciones con respecto a los posibles efectos hipertensivos de los mAbs anti-CGRP.

Objetivo Del Estudio

  • Para evaluar los cambios tempranos en la presión arterial (PA) durante el tratamiento con anti-CGRP mAb en pacientes con migraña.
  • Evaluar la seguridad cardiovascular de los anti-CGRP mAbs en la fase inicial del tratamiento.

Principales Métodos

  • Estudio prospectivo en el mundo real de 20 pacientes con migraña episódica (EM).
  • Monitoreo de la presión arterial Holter de 24 horas antes y 4 semanas después de la primera inyección de mAb anti-CGRP.
  • Resultados primarios: cambio en la presión arterial sistólica media (PAS); resultados secundarios: presión arterial diastólica (PAD), presión arterial diurna/nocturna, frecuencia cardíaca (RH), patrones de inmersión.

Principales Resultados

  • No hay cambios significativos en el promedio de 24 horas SBP (-2,4 mmHg) o DBP (-1,8 mmHg).
  • Reducción significativa de la PBC nocturna (-2,6 mmHg, p=0,026) y aumento del perfil fisiológico de inmersión (45,0% a 85,0%, p=0,008).
  • La HR se mantuvo sin cambios; ningún paciente experimentó eventos adversos o hipertensión clínicamente significativa.

Conclusiones

  • Los mAbs anti-CGRP no indujeron aumentos de la presión arterial clínicamente relevantes en el tratamiento temprano de EM.
  • El tratamiento se asoció con una mejora de la DBP nocturna y un cambio favorable en el perfil de inmersión.
  • Los resultados sugieren la seguridad cardiovascular a corto plazo de los mAbs anti-CGRP, lo que justifica nuevos estudios a largo plazo.

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