Evidence map›Paper›PMID 42364940›Full record

ArticleEuropean journal of internal medicine2026

Low-renin hypertension in incidental adrenal adenomas and response to aldosterone-targeted therapy: a prospective study.

Thomas Uslar, Benjamín Sanfuentes, Roberto Olmos, Alberth Burnier, Pauline Böhm, Francisco J Guarda, Álvaro Huete, Nicolás Mertens, Cecilia Besa, Marcelo Andía and 9 more

Abstract read
In one paragraph

Article in European journal of internal medicine, 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

19 authors.

Thomas UslarDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile; Program for Adrenal Disorders CETREN-UC, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Benjamín SanfuentesDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile; Program for Adrenal Disorders CETREN-UC, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Roberto OlmosFundación Arturo Lopez Perez, Santiago, 7601003, Chile.
Alberth BurnierDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Pauline BöhmDepartment of Internal Medicine, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Francisco J GuardaDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Álvaro HueteDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Nicolás MertensDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Cecilia BesaDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Marcelo AndíaDepartment of Radiology, School of Medicine Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Alejandro MajersonDepartment of Urology, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Jaime CartesDepartment of Urology, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Alejandra TapiaDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Cristian A CarvajalDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Carlos E FardellaDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Fidel AllendeDepartment of Clinical Laboratory, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Sandra SolariDepartment of Clinical Laboratory, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile.
Anand VaidyaCenter for Adrenal Disorders, Division of Endocrinology, Diabetes and Hypertension, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, 02115, USA.
Rene BaudrandDepartment of Endocrinology, School of Medicine, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile; Program for Adrenal Disorders CETREN-UC, Red Salud UC-CHRISTUS, Pontificia Universidad Católica de Chile, Santiago, 8330077, Chile. Electronic address: rbaudran@uc.cl.

Funding

Unrecognized Primary Aldosteronism as a Pathogenic Mechanism for Chronic Kidney Disease in DiabetesR01DK115392 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI Anand Vaidya · 2018 to 2026
$6.0M
Aldosterone, the Mineralocorticoid Receptor, and Cardiovascular Disease in ObesityR01HL153004 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI VAIDYA, ANAND · 2020 to 2024
$4.4M
Primary Aldosteronism Subtypes: Pathophysiology and Steroid SignaturesR01HL155834 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI TURCU, ADINA F · 2021 to 2025
$3.5M
NHLBI NIH HHS R01 HL153004NHLBI NIH HHS R01 HL155834NIDDK NIH HHS R01 DK115392
6 · The paper itself

Abstract

backgroundIncidental adrenal adenomas are common, yet renin status is infrequently assessed in hypertensive patients. Emerging evidence supports a spectrum of renin-independent aldosterone excess associated with adverse cardiovascular risk. OBJECTIVE AND

methodsTo determine the frequency of a low-renin phenotype in a prospective cohort of hypertensive patients with adrenal adenomas and to evaluate the clinical response to aldosterone-targeted therapy across baseline aldosterone categories. Low-renin phenotype was defined as suppressed renin (PRA <1.0 ng/mL/h or DRC <10 µIU/mL). Among these patients, plasma aldosterone concentration (PAC) was categorized as 5-10 ng/dL (Group 1), 10-15 ng/dL (Group 2), and >15 ng/dL (Group 3). Patients with suppressed renin were treated with MR antagonists or adrenalectomy and followed longitudinally using PAMO/PASO criteria.

resultsLow renin was present in 47% (138/290) of hypertensive patients. Increasing aldosterone levels were associated with higher systolic blood pressure (SBP), resistant hypertension, higher antihypertensive treatment burden, lower potassium, and reduced eGFR (p-trend <0.001). After a mean follow-up of 24±18 months (n = 121), aldosterone-targeted therapy (75% medical, 25% surgical) led to significant reductions in SBP (-18, -26, and -30 mmHg across Groups 1-3; all p < 0.001), decreased medication and significant increases in renin (all p < 0.001), irrespective of aldosterone category.

conclusionsNearly half of hypertensive patients with adrenal incidentalomas exhibit suppressed renin levels associated with greater blood pressure burden and favorable response to aldosterone-targeted therapy, even in lower aldosterone levels categories. These findings support systematic renin assessment in hypertensive patients with incidental adrenal adenomas and provide a rationale for testing aldosterone-targeted therapy in broader hypertensive populations beyond adrenal adenomas.

Indexed as

Adrenal adenomasAdrenal incidentalomaAldosterone dysregulationHypertensionLow renin hypertensionMineralocorticoid receptorPrimary aldosteronism

Identifiers

PMID42364940
PMCPMC13491542

What Socratic holds

Textmetadata
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Registered trials

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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 Socratic graph.