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Future of personalized pharmacotherapy in chronic heart failure patients
Nicholas B Norgard1, Gina M Prescott
1University at Buffalo, School of Pharmacy & Pharmaceutical Sciences, New York State Center of Excellence in Bioinformatics & Life Sciences, B3-322, 701 Ellicott Street, Buffalo, NY 1420, USA. nnorgard@buffalo.edu
Insights
Personalizing heart failure (HF) treatment is crucial due to patient diversity. Emerging pharmacogenetics offers a path to tailor HF therapies, predict patient responses, and reduce adverse events.
Area of Science:
- Cardiology
- Pharmacology
- Genetics
Background:
- Heart failure (HF) patient populations exhibit significant diversity.
- Current HF treatment guidelines often fail to account for individual response variations.
- Standard treatment protocols derived from limited demographics are broadly applied to diverse groups, including women and African-Americans.
Purpose of the Study:
- To highlight the need for personalized heart failure pharmacotherapy.
- To introduce pharmacogenetics as a strategy for tailoring HF treatment.
- To emphasize the role of genetic biomarkers in predicting treatment response and toxicity.
Main Methods:
- Review of subgroup analyses from randomized HF trials.
- Analysis of retrospective cohort studies on HF treatment customization.
- Exploration of emerging pharmacogenetic approaches in HF management.
Main Results:
- Existing HF treatment strategies lack personalization for diverse patient groups.
- Subgroup analyses and cohort studies provide some basis for customizing regimens.
- Pharmacogenetics presents a promising avenue for predicting individual treatment outcomes.
Conclusions:
- Personalized HF management is essential to maximize therapeutic benefits.
- Genetic biomarkers hold potential for predicting patient response and toxicity.
- Further research is needed to fully integrate pharmacogenetics into clinical HF practice to limit adverse events.
Abstract:
There is a significant amount of diversity among heart failure (HF) patients. Contemporary HF regimens often do not take into consideration many of the factors that might influence an individual's response to treatment. Clinical recommendations based on trial data derived from mainly younger Caucasian male study populations have, in most cases, been applied equally to women and African-Americans. Subgroup analyses of randomized HF trials and results of retrospective cohort studies have been used for customizing HF regimens in women and African-Americans. Pharmacogenetics is an emerging strategy for personalizing HF therapy. Genetic biomarkers may play an important role in predicting a patient's response to treatment and in predicting those at risk of toxicity. HF pharmacotherapy has improved over the last two decades; however, substantial work remains in order to personalize HF management and maximize the benefit of pharmacologic interventions, while limiting adverse events.
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