viernes, 10 de mayo de 2019

Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females | Biology of Sex Differences | Full Text

Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females | Biology of Sex Differences | Full Text

Biology of Sex Differences

Sex-specific responses to mineralocorticoid receptor antagonism in hypertensive African American males and females

Biology of Sex Differences201910:24
  • Received: 21 December 2018
  • Accepted: 16 April 2019
  • Published: 

Abstract

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.

Keywords

  • Sex-specific
  • Hypertension
  • Mineralocorticoid antagonist
  • African American

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