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Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females
BACKGROUND: African Americans (AA) develop hypertension (HTN) at an earlier age, have a greater frequency and severity of HTN, and greater prevalence of uncontrolled HTN as compared to the white population. Mineralocorticoid antagonists have been shown to be very effective in treating uncontrolled H...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507140/ https://www.ncbi.nlm.nih.gov/pubmed/31072402 http://dx.doi.org/10.1186/s13293-019-0238-6 |
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author | Clemmer, John S. Faulkner, Jessica L. Mullen, Alex J. Butler, Kenneth R. Hester, Robert L. |
author_facet | Clemmer, John S. Faulkner, Jessica L. Mullen, Alex J. Butler, Kenneth R. Hester, Robert L. |
author_sort | Clemmer, John S. |
collection | PubMed |
description | BACKGROUND: African Americans (AA) develop hypertension (HTN) at an earlier age, have a greater frequency and severity of HTN, and greater prevalence of uncontrolled HTN as compared to the white population. Mineralocorticoid antagonists have been shown to be very effective in treating uncontrolled HTN in both AA and white patients, but sex-specific responses are unclear. METHODS: We evaluated the sex-specific impact of mineralocorticoid antagonism in an AA population. An AA cohort (n = 1483) from the Genetic Epidemiology Network of Arteriopathy study was stratified based on sex and whether they were taking spironolactone, a mineralocorticoid antagonist, in their antihypertensive regimen. RESULTS: As compared to AA women not prescribed a mineralocorticoid antagonist, AA women taking spironolactone (n = 9) had lower systolic and diastolic blood pressure despite having a similar number of antihypertensive medications. The proportion of AA women with uncontrolled HTN was significantly less for patients taking spironolactone than for patients not prescribed spironolactone. Interestingly, none of these associations were found in the AA males or in white females. CONCLUSIONS: Our data suggests that spironolactone is particularly effective in reducing blood pressure and controlling HTN in AA women. Further research into the impact of this therapy in this underserved and understudied minority is warranted. |
format | Online Article Text |
id | pubmed-6507140 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-65071402019-05-13 Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females Clemmer, John S. Faulkner, Jessica L. Mullen, Alex J. Butler, Kenneth R. Hester, Robert L. Biol Sex Differ Research BACKGROUND: African Americans (AA) develop hypertension (HTN) at an earlier age, have a greater frequency and severity of HTN, and greater prevalence of uncontrolled HTN as compared to the white population. Mineralocorticoid antagonists have been shown to be very effective in treating uncontrolled HTN in both AA and white patients, but sex-specific responses are unclear. METHODS: We evaluated the sex-specific impact of mineralocorticoid antagonism in an AA population. An AA cohort (n = 1483) from the Genetic Epidemiology Network of Arteriopathy study was stratified based on sex and whether they were taking spironolactone, a mineralocorticoid antagonist, in their antihypertensive regimen. RESULTS: As compared to AA women not prescribed a mineralocorticoid antagonist, AA women taking spironolactone (n = 9) had lower systolic and diastolic blood pressure despite having a similar number of antihypertensive medications. The proportion of AA women with uncontrolled HTN was significantly less for patients taking spironolactone than for patients not prescribed spironolactone. Interestingly, none of these associations were found in the AA males or in white females. CONCLUSIONS: Our data suggests that spironolactone is particularly effective in reducing blood pressure and controlling HTN in AA women. Further research into the impact of this therapy in this underserved and understudied minority is warranted. BioMed Central 2019-05-09 /pmc/articles/PMC6507140/ /pubmed/31072402 http://dx.doi.org/10.1186/s13293-019-0238-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Clemmer, John S. Faulkner, Jessica L. Mullen, Alex J. Butler, Kenneth R. Hester, Robert L. Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title | Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title_full | Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title_fullStr | Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title_full_unstemmed | Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title_short | Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females |
title_sort | sex-specific responses to mineralocorticoid receptor antagonism in hypertensive african american males and females |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507140/ https://www.ncbi.nlm.nih.gov/pubmed/31072402 http://dx.doi.org/10.1186/s13293-019-0238-6 |
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