Evidence map›Paper›PMID 42618626›Full record

Observational studyHypertension research : official journal of the Japanese Society of Hypertension2026

Aldosterone-renin ratio and plasma renin activity as biomarkers for treatment response in resistant hypertension.

Kyeong-Hyeon Chun, Chan Joo Lee, Dong-Ho Shin, Jin-Ok Jeong, Ju Han Kim, JiWung Ryu, Hae-Young Lee, Seonghoon Choi, Eun Mi Lee, Jung Hyun Choi and 7 more

Abstract readObservational Study
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In one paragraph

Observational study in Hypertension research : official journal of the Japanese Society of Hypertension, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

17 authors.

Kyeong-Hyeon Chun *Division of Cardiology, Department of Internal Medicine, Gangnam Severance Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Chan Joo Lee *Division of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea.
Dong-Ho ShinDivision of General Internal Medicine, Department of Internal Medicine, Severance Hospital, Seoul, Republic of Korea.
Jin-Ok JeongDepartment of Cardiology in Internal Medicine, Chungnam National University College of Medicine, Chungnam National University Hospital, Daejeon, Republic of Korea.
Ju Han KimDepartment of Cardiology, Chonnam National University Hospital, Gwangju, Republic of Korea.
JiWung RyuDivision of Cardiology, Department of Internal Medicine, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Republic of Korea.
Hae-Young LeeDepartment of Internal Medicine, Seoul National University Hospital, Seoul, Republic of Korea.
Seonghoon ChoiDivision of Cardiology, Department of Internal Medicine, Kangnam Sacred Heart Hospital, Hallym University College of Medicine, Seoul, Republic of Korea.
Eun Mi LeeCardiovascular Center, Dongguk University Ilsan Hospital, Goyang, Republic of Korea.
Jung Hyun ChoiDivision of Cardiology, Department of Internal Medicine, Pusan National University Hospital, Pusan National University School of Medicine, Busan, Republic of Korea.
Kwang-Il KimDepartment of Internal Medicine, Seoul National University College of Medicine, Seoul National University Bundang Hospital, Seongnam, Republic of Korea.
Jinho ShinDivision of Cardiology, Department of Internal Medicine, College of Medicine, Hanyang University, Seoul, Republic of Korea.
Wook Bum PyunDivision of Cardiology, Department of Internal Medicine, Ewha Womans University Seoul Hospital, Ewha Womans University College of Medicine, Seoul, Republic of Korea.
Dae-Hee KimDivision of Cardiology, Department of Internal Medicine, Asan Medical Center, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Bryan WilliamsInstitute of Cardiovascular Science, University College London, London, UK.
Sang-Hyun IhmDivision of Cardiology, Department of Internal Medicine, Bucheon St Mary's Hospital and the Catholic Research Institute for Intractable Cardiovascular Disease, College of Medicine, Catholic University of Korea, Seoul, Republic of Korea. limsh@catholic.ac.kr.
Sungha ParkDivision of Cardiology, Severance Cardiovascular Hospital, Yonsei University College of Medicine, Seoul, Republic of Korea. shpark0530@yuhs.ac.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent randomised trial demonstrated the non-inferiority of amiloride versus spironolactone in resistant hypertension, with exploratory analyses suggesting heterogeneity in treatment response based on baseline aldosterone-renin ratio (ARR). We evaluated associations between baseline renin-aldosterone status and blood pressure-lowering responses to each agent. This post hoc subgroup analysis used data from the abovementioned trial. Among 114 patients, 113 had available ARR data and were included and stratified by median ARR into two groups. Subgroup analyses were also performed according to baseline plasma renin activity (PRA) levels. The primary endpoint was the change in home systolic blood pressure (SBP) from baseline to 12 weeks. Patients with higher ARR were older and had higher baseline SBP than those with lower ARR. Multivariate regression analysis showed that female sex, higher nighttime SBP, higher ARR, and lower PRA were associated with a greater reduction in home SBP in response to treatment. In treatment-specific analyses, the home SBP-lowering response to spironolactone was pronounced in patients with higher ARR (-18.8 ± 11.6 vs -9.8 ± 8.4 mmHg, vs. lower ARR) and lower PRA (-19.1 ± 11.8 vs. -10.1 ± 8.4 mmHg, vs. higher PRA), yielding significant ARR-by-treatment (p = 0.046) and PRA-by-treatment (p = 0.027) interactions. In contrast, the home SBP-lowering response to amiloride was not significantly different according to baseline ARR or PRA. These exploratory findings suggest that renin-aldosterone profiling may help identify biological heterogeneity in treatment and warrant prospective evaluation as a candidate tool for treatment selection in resistant hypertension. This post-hoc analysis of a randomized trial in resistant hypertension evaluated. whether renin-aldosterone status predicts differential BP responses to spironolactone versus. amiloride. Women, higher nighttime SBP, higher aldosterone-renin ratio (ARR), and lower. plasma renin activity (PRA) were associated with greater BP reduction. Spironolactone showed greater efficacy in patients with high ARR or low PRA, with significant treatment-by-ARR (p = 0.046) and treatment-by-PRA (p = 0.027) interactions. Amiloride demonstrated consistent efficacy regardless of renin-aldosterone profile. No significant between-drug difference was efficacy regardless of renin-aldosterone profile. No significant between-drug difference was observed within individual strata.

Indexed as

AldosteroneAntihypertensive AgentsHypertensionReninAgedAmilorideBiomarkersBlood PressureFemaleHumansMaleMiddle AgedRandomized Controlled Trials as TopicSpironolactoneTreatment Effect HeterogeneityTreatment OutcomeAldosteroneAmilorideAntihypertensive AgentsBiomarkersReninSpironolactoneAldosterone-renin ratioAmilorideHypertensionMorning hypertensionResistant hypertensionSpironolactone

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.