Ethnicity in Pulmonary Arterial Hypertension
| Autor: | Sandeep Sahay, Sarah K. Medrek |
|---|---|
| Rok vydání: | 2018 |
| Předmět: |
Pulmonary and Respiratory Medicine
Portopulmonary hypertension medicine.medical_specialty business.industry Ethnic group 030204 cardiovascular system & hematology Critical Care and Intensive Care Medicine medicine.disease Precision medicine Pulmonary hypertension Clinical trial 03 medical and health sciences Race (biology) 0302 clinical medicine 030228 respiratory system Heart failure Physical therapy Medicine Personalized medicine Cardiology and Cardiovascular Medicine business Intensive care medicine |
| Zdroj: | Chest. 153:310-320 |
| ISSN: | 0012-3692 |
| DOI: | 10.1016/j.chest.2017.08.1159 |
| Popis: | In the past decade and a half, the introduction of new therapeutic agents has revolutionized the management of pulmonary arterial hypertension (PAH). These new treatment options have improved the quality of life and survival in PAH. With an armamentarium of options available, the identification of unique phenotypes can help practitioners choose tailored treatment regimens. Experts in other cardiovascular diseases, such as congestive heart failure and hypertension, have recommended race-specific treatments in their fields based on data highlighting variations in response to therapies. With this perspective, we review evidence supporting the hypothesis that ethnicity or race plays an important role in the management of PAH. Preliminary research suggests that races/ethnicities have differences in the presentation and outcome of PAH and could respond to PAH-specific medications with varying efficacy. Genetic, physiological, and anatomic differences exist between races, particularly regarding the structure and function of the right ventricle. Unfortunately, clinical trials have not adequately included minorities, and registry data often omit inclusion of this demographic information. Further studies are needed to characterize the role that ethnicity plays in the prevalence, presentation, outcomes, and optimal treatment of PAH. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
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