Evidence map›Paper›PMID 37334561›Full record

ReviewJournal of clinical hypertension (Greenwich, Conn.)2023

Aprocitentan: A new development of resistant hypertension.

Yao Yao, Bin Fan, Bin Yang, Zixuan Jia, Bao Li

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of clinical hypertension (Greenwich, Conn.), 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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

5 citing papers in PubMed, 9 citations in OpenAlex.

  1. Article
  2. Current Knowledge About Aprocitentan in Hypertension.International journal of molecular sciences · 2025
    Review
  3. Review
  4. Review
  5. Aprocitentan: A new development of resistant hypertension.Journal of clinical hypertension (Greenwich, Conn.) · 2023
    Review
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

5 authors at 1 institution in 1 country.

Yao YaoDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.ORCID 0000-0002-0774-3822
Bin FanShanxi Medical University, Taiyuan, Shanxi, China.
Bin YangDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Zixuan JiaShanxi Medical University, Taiyuan, Shanxi, China.
Bao LiDepartment of Cardiology, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi, China.
Shanxi Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

As the blood pressure threshold for commencing antihypertensive treatment diminishes, the cohort suffering from resistant hypertension (RH) correspondingly expands. Notwithstanding the availability of known antihypertensive medications, there exists a conspicuous lacuna in therapeutic options specifically intended for the management of RH. Currently, aprocitentan is the sole endothelin receptor antagonist (ERA) under development for addressing this pressing clinical challenge. Aprocitentan (ACT-132577), deriving its active form as a metabolite of macitentan, demonstrates oral potency as a dual endothelin (ET) receptor antagonist. This compound effectively obstructs the binding of endothelin-1 (ET-1) to both ETA and ETB receptors, exhibiting an inhibitory potency ratio of 1:16. Clinical investigation of aprocitentan has advanced to phase 3 trials, yielding promising preliminary outcomes.

Indexed as

HypertensionAntihypertensive AgentsBlood PressureEndothelin-1Endothelin Receptor AntagonistsHumansPyrimidinesSulfonamidesAntihypertensive AgentsaprocitentanEndothelin-1Endothelin Receptor AntagonistsPyrimidinesSulfonamidesACT-132577aprocitentanphase 3 clinical trialsPRECISIONresistant hypertension

Identifiers

PMID37334561
PMCPMC10339369
OpenAlexW4381140713

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.