Evidence map›Paper›PMID 41804894›Full record

ArticleJournal of the American Heart Association2026

Aldosterone and Impaired Nocturnal Blood Pressure Decline in Primary Aldosteronism.

Ning-Peng Liang, Ning Li, Hao Wu, Zi-Xin Lin, Zai-Jia Wang, Chen-Guang Wu, Hong-Liang Xiong, Jiao Yang, Yi-Fei Dong

Abstract read
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Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

4 citing papers in PubMed.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors.

Ning-Peng LiangDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Ning LiDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Hao WuDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Zi-Xin LinDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Zai-Jia WangDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Chen-Guang WuDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.ORCID 0009-0004-4682-7107
Hong-Liang XiongDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.ORCID 0000-0002-2799-5031
Jiao YangDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.
Yi-Fei DongDepartment of Cardiovascular Medicine, The Second Affiliated Hospital, Jiangxi Medical College Nanchang University Jiangxi China.ORCID 0000-0002-6290-1491

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe loss of physiological nocturnal blood pressure (BP) decline is a major contributor to cardiovascular risk, yet its endocrine underpinnings in primary aldosteronism (PA) remain underexplored. This study aimed to elucidate the dose-dependent relationship between aldosterone excess and circadian BP rhythm disruption and assess whether targeted aldosterone suppression could ameliorate nocturnal dipping.

methodsWe prospectively analyzed 24-hour ambulatory BP data from 681 patients with confirmed PA, stratified by plasma aldosterone concentration. A subset of 99 patients with adrenal vein sampling-confirmed unilateral PA received targeted, minimally invasive vascular intervention for aldosterone suppression and were evaluated for changes in BP rhythm on the basis of treatment response.

resultsIn multivariable-adjusted models, both log-transformed plasma aldosterone concentration and aldosterone-to-renin ratio were inversely associated with the proportion of nocturnal systolic BP decline (log plasma aldosterone concentration: β=-0.054 [95% CI, -0.087 to -0.020];

conclusionsAldosterone excess contributes directly to circadian BP rhythm disruption in PA. Selective hormonal suppression can ameliorate physiological BP dipping in responsive patients. These findings highlight the value of rhythm-based end points and support aldosterone-targeted modulation as a strategic goal in PA management. Registration: URL: https://www.chictr.org.cn/; Unique Identifier: ChiCTR2200057297.

Indexed as

AldosteroneBlood PressureCircadian RhythmHyperaldosteronismHypertensionAdultAgedBiomarkersBlood Pressure Monitoring, AmbulatoryFemaleHumansMaleMiddle AgedMineralocorticoid Receptor AntagonistsProspective StudiesReninAldosteroneBiomarkersMineralocorticoid Receptor AntagonistsReninaldosteronehypertensionnocturnal blood pressure declineprimary aldosteronismselective adrenal arterial embolization

Identifiers

PMID41804894
PMCPMC13055784

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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.