Evidence map›Paper›PMID 41206816›Full record

ReviewInnere Medizin (Heidelberg, Germany)2026

[Aldosterone synthase inhibitors: a new group of drugs for influencing blood pressure in the renin-angiotensin-aldosterone system].

Markus van der Giet

Abstract readEnglish AbstractReview
PubMed Publisher
In one paragraph

Review in Innere Medizin (Heidelberg, Germany), 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

1 author.

Markus van der GietMedizinische Klinik für Nephrologie und Internistische Intensivtherapie, Charité - Universitätsmedizin Berlin, Charitéplatz 1, 10117, Berlin, Deutschland. Markus.vandergiet@charite.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Despite the development of numerous drugs for the treatment of high blood pressure, there are still many difficulties in achieving successful treatment of patients with high blood pressure in routine clinical practice. The renin-angiotensin-aldosterone system plays a central role in blood pressure regulation and drugs such as angiotensin-converting enzyme (ACE) inhibitors, angiotensin receptor blockers and mineralocorticoid receptor antagonists are used in routine treatment. For decades it was not possible to specifically inhibit the formation of aldosterone, a key hormone in blood pressure regulation but in recent years this has been very successfully achieved pharmacologically. Several so-called aldosterone synthase inhibitors are currently being tested in clinical trials, primarily in patients with uncontrolled or treatment-resistant hypertension. Of the active ingredients two (baxdrostat and lorundrostat) have already been shown to be very successful in phase 3 trials, demonstrating that the use of both drugs can further reduce systolic blood pressure by approximately 10 mm Hg in complicated blood pressure situations. The safety profile of the drugs has been unremarkable so far. As expected, blocking the formation of aldosterone increases potassium levels but this has not caused any clinically unmanageable problems. This is a promising group of drugs for the treatment of complicated blood pressure but also perhaps for early treatment.

Indexed as

Antihypertensive AgentsBlood PressureCytochrome P-450 CYP11B2HypertensionRenin-Angiotensin SystemAndrostenesAngiotensin-Converting Enzyme InhibitorsHumansMineralocorticoid Receptor AntagonistsAndrostenesAngiotensin-Converting Enzyme InhibitorsAntihypertensive AgentsCytochrome P-450 CYP11B2Mineralocorticoid Receptor AntagonistsBaxdrostatHigh blood pressureLorundrostatSafety profileTreatment-resistant hypertension

Identifiers

What OpenQuestion holds

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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 OpenQuestion graph.