Evidence map›Paper›PMID 42516681›Full record

ArticlePulmonary circulation2026

Phenotypic Clustering of Idiopathic Pulmonary Arterial Hypertension: Insights Into Pulmonary Vascular and Cardiometabolic Co-Morbidity Trajectories.

Cihangir Kaymaz, Barkin Kultursay, Hacer Ceren Tokgoz, Seda Tanyeri, Cagdas Bulus, Berhan Keskin, Caglar Emre Cagliyan, Metehan Kibar, Can Erdem, Aziz Vezir and 5 more

Abstract read
In one paragraph

Article in Pulmonary circulation, 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

15 authors.

Cihangir KaymazDepartment of Cardiology, İstanbul Hospital Başkent University Istanbul Turkey.ORCID https://orcid.org/0000-0003-2627-9081
Barkin KultursayDepartment of Cardiology Tunceli State Hospital Tunceli Turkey.ORCID https://orcid.org/0000-0002-1424-2209
Hacer Ceren TokgozKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0000-0001-8187-7290
Seda TanyeriKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0000-0002-0933-9233
Cagdas BulusKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0000-0002-2433-3593
Berhan KeskinDepartment of Cardiology, Faculty of Medicine Medipol University Istanbul Turkey.ORCID https://orcid.org/0000-0002-5879-2245
Caglar Emre CagliyanDepartment of Cardiology, Faculty of Medicine Cukurova University Adana Turkey.ORCID https://orcid.org/0000-0002-2529-4995
Metehan KibarKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0009-0004-2577-6355
Can ErdemKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0009-0000-6571-8118
Aziz VezirKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0009-0005-1072-1084
Ipek AkkusKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0009-0006-4207-1669
Muhammet BulutKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0009-0009-5069-7874
Aykun HakgorDepartment of Cardiology, Faculty of Medicine Medipol University Istanbul Turkey.ORCID https://orcid.org/0000-0001-8252-0373
Ibrahim Halil TanbogaDepartment of Cardiology, Hisar Intercontinental Hospital Nisantasi University Istanbul Turkey.ORCID https://orcid.org/0000-0003-4546-9227
Nihal OzdemirKartal Koşuyolu Heart Education and Training Hospital Istanbul Turkey.ORCID https://orcid.org/0000-0002-6337-7716

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Idiopathic pulmonary arterial hypertension (IPAH) exhibits significant clinical heterogeneity, necessitating a precision medicine approach. This study aimed to identify distinct IPAH phenotypes using machine learning-based clustering and to evaluate their longitudinal therapeutic responses and long-term survival. We analyzed 297 IPAH patients using hierarchical agglomerative clustering based on baseline demographics, hemodynamics, and comorbidities. The cohort was characterized by two distinctive yet overlapping phenotypic patterns: Cluster 1 (

Indexed as

clusteringcomorbidityEUPHRATESphenotypepulmonary arterial hypertension

Identifiers

PMID42516681
PMCPMC13404791

What OpenQuestion holds

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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 OpenQuestion graph.