Ultrasound imaging techniques for the evaluation of cardiovascular therapies

John J P Kastelein1, Eric de Groot

  • 1Department of Vascular Medicine, Academic Medical Center, Meibergdreef 9, 1105 AZ Amsterdam, The Netherlands. j.j.kastelein@amc.uva.nl

European Heart Journal
|March 13, 2008
PubMed

Insights

New therapies for cardiovascular disease are needed to reduce residual risk. Vascular ultrasound imaging techniques, like carotid intima-media thickness (CIMT) and intravascular ultrasound (IVUS), can accelerate drug development using surrogate endpoints.

Area of Science:

  • Cardiology
  • Medical Imaging
  • Pharmacology

Background:

  • Cardiovascular disease (CVD) is a leading cause of death globally, with significant residual risk despite current treatments.
  • Developing novel therapies to mitigate this residual risk is a critical healthcare objective.
  • Traditional clinical trials for new CVD therapies are lengthy due to the need for statistically significant clinical event data.

Purpose of the Study:

  • To review the rationale and evidence for using vascular ultrasound imaging techniques as surrogate endpoints in cardiovascular drug development.
  • To highlight the potential of surrogate endpoints to expedite the assessment of novel cardiovascular therapies.
  • To discuss the application of carotid intima-media thickness (CIMT) and intravascular ultrasound (IVUS) in clinical trials.

Main Methods:

  • Review of historical and recent clinical trials utilizing vascular ultrasound imaging.
  • Analysis of the role of carotid intima-media thickness (CIMT) measurements.
  • Evaluation of intravascular ultrasound (IVUS) data from coronary artery assessments.

Main Results:

  • Vascular ultrasound techniques (CIMT and IVUS) are increasingly employed in surrogate endpoint trials for cardiovascular therapies.
  • These surrogate endpoints offer a means to assess therapeutic efficacy earlier than traditional clinical endpoints.
  • The use of CIMT and IVUS can potentially shorten the drug development timeline for new cardiovascular treatments.

Conclusions:

  • Carotid intima-media thickness (CIMT) and intravascular ultrasound (IVUS) serve as valuable surrogate endpoints in cardiovascular research.
  • These imaging biomarkers can significantly accelerate the evaluation of novel cardiovascular therapies.
  • Utilizing surrogate endpoints in drug development is crucial for addressing the unmet need for effective treatments for residual cardiovascular risk.

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