Fred Stephen Sarfo, Priscilla Abrafi Opare-Addo, Manolo Agbenorku, Vida Obese, Sheila Adamu, Rexford Adu Gyamfi, John Akassi, Hanson Ababio, Michael Ampofo, Nathaniel Adusei Mensah, Gideon Acheampong, Bruce Ovbiagele
{"title":"Physiologic profiling using plasma renin activity and aldosterone on blood pressure control among Ghanaian stroke survivors: A pilot trial.","authors":"Fred Stephen Sarfo, Priscilla Abrafi Opare-Addo, Manolo Agbenorku, Vida Obese, Sheila Adamu, Rexford Adu Gyamfi, John Akassi, Hanson Ababio, Michael Ampofo, Nathaniel Adusei Mensah, Gideon Acheampong, Bruce Ovbiagele","doi":"10.1016/j.neuros.2025.100013","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and purpose: </strong>Resistant hypertension (RH) is mechanistically driven largely by perturbations in renin-aldosterone, rife among stroke survivors, and portends a poorer prognosis in this population. We sought to evaluate the feasibility of a physiological profiling strategy using plasma renin and aldosterone to tailor medical therapy to control BP among stroke survivors with uncontrolled RH.</p><p><strong>Methods: </strong>This was a pilot randomized clinical trial. We enrolled stroke survivors aged ≥18 years with uncontrolled blood pressure on at least 3 antihypertensive medications at full doses at a tertiary hospital in Ghana. Participants were enrolled between June 16, 2023, and April 19, 2024, and the last participant completed follow-up on October 30, 2024. Participants randomized to the physiologic profiling arm had plasma renin activity and aldosterone levels measured and eplerenone, a mineralocorticoid receptor antagonist, or amiloride was added to their existing BP medications depending on renin-aldosterone profile. Those assigned to the control arm received usual care where physicians added antihypertensive agents as indicated. The primary clinical outcome was proportions with blood pressure < 140/90 mmHg at month 6, by intention-to-treat.</p><p><strong>Results: </strong>Among 60 eligible participants, 30 each were randomized to either the intervention or control arms, 53 % were female, mean (SD) age of 58.4 (10.3) years. The trial was feasible to implement. Primary outcome was achieved in 19 (63.3 %) in the intervention arm vs. 11 (36.7 %) in the usual care arm, p = 0.04. There were 3 major adverse cardiovascular events during follow-up, 1 (3.3 %) non-fatal recurrent stroke in the intervention arm vs 2 (6.7 %) cardiovascular deaths in the usual care arm, p = 0.55. No medication-related adverse events were reported.</p><p><strong>Conclusions: </strong>Among Ghanaian stroke survivors with RH, the addition of eplerenone to background antihypertensive medications based on plasma renin-aldosterone profile demonstrated a signal of efficacy compared with usual care. A larger study with longer follow-up powered to assess hard cardiovascular outcomes among stroke survivors with uncontrolled resistant hypertension is warranted.</p>","PeriodicalId":520832,"journal":{"name":"Equity neuroscience","volume":"1 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2025-12-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12803734/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Equity neuroscience","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1016/j.neuros.2025.100013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/10/16 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Background and purpose: Resistant hypertension (RH) is mechanistically driven largely by perturbations in renin-aldosterone, rife among stroke survivors, and portends a poorer prognosis in this population. We sought to evaluate the feasibility of a physiological profiling strategy using plasma renin and aldosterone to tailor medical therapy to control BP among stroke survivors with uncontrolled RH.
Methods: This was a pilot randomized clinical trial. We enrolled stroke survivors aged ≥18 years with uncontrolled blood pressure on at least 3 antihypertensive medications at full doses at a tertiary hospital in Ghana. Participants were enrolled between June 16, 2023, and April 19, 2024, and the last participant completed follow-up on October 30, 2024. Participants randomized to the physiologic profiling arm had plasma renin activity and aldosterone levels measured and eplerenone, a mineralocorticoid receptor antagonist, or amiloride was added to their existing BP medications depending on renin-aldosterone profile. Those assigned to the control arm received usual care where physicians added antihypertensive agents as indicated. The primary clinical outcome was proportions with blood pressure < 140/90 mmHg at month 6, by intention-to-treat.
Results: Among 60 eligible participants, 30 each were randomized to either the intervention or control arms, 53 % were female, mean (SD) age of 58.4 (10.3) years. The trial was feasible to implement. Primary outcome was achieved in 19 (63.3 %) in the intervention arm vs. 11 (36.7 %) in the usual care arm, p = 0.04. There were 3 major adverse cardiovascular events during follow-up, 1 (3.3 %) non-fatal recurrent stroke in the intervention arm vs 2 (6.7 %) cardiovascular deaths in the usual care arm, p = 0.55. No medication-related adverse events were reported.
Conclusions: Among Ghanaian stroke survivors with RH, the addition of eplerenone to background antihypertensive medications based on plasma renin-aldosterone profile demonstrated a signal of efficacy compared with usual care. A larger study with longer follow-up powered to assess hard cardiovascular outcomes among stroke survivors with uncontrolled resistant hypertension is warranted.