Evidence map›Paper›PMID 41569941›Full record

ArticleJCI insight2026

Coronary pathophysiology in idiopathic pulmonary arterial hypertension.

Erin Boland, Michael G Freeman, David S Corcoran, Thomas J Ford, Barry Hennigan, Damien Collison, Aida Llucià-Valldeperas, Frances S de Man, Kanarath P Balachandran, Martin Johnson and 2 more

Abstract read
In one paragraph

Article in JCI insight, 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

12 authors.

Erin BolandBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.
Michael G FreemanBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.
David S CorcoranBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.
Thomas J FordCentral Heart, Toukley, New South Wales, Australia.
Barry HenniganBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.
Damien CollisonBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.
Aida Llucià-ValldeperasDepartment of Pulmonary Medicine, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, PHEniX Laboratory, Amsterdam, Netherlands.
Frances S de ManDepartment of Pulmonary Medicine, Amsterdam University Medical Centre, Vrije Universiteit Amsterdam, PHEniX Laboratory, Amsterdam, Netherlands.
Kanarath P BalachandranDepartment of Cardiology, Royal Blackburn Teaching Hospital, East Lancashire Hospitals NHS Trust, Lancashire, United Kingdom.
Martin JohnsonWest of Scotland Heart and Lung Centre, Golden Jubilee National Hospital, Glasgow, Scotland, United Kingdom.
Colin ChurchWest of Scotland Heart and Lung Centre, Golden Jubilee National Hospital, Glasgow, Scotland, United Kingdom.
Colin BerryBritish Heart Foundation Glasgow Cardiovascular Research Centre, University of Glasgow, Scotland, United Kingdom.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUNDIdiopathic pulmonary arterial hypertension (IPAH) alters right ventricular size and function, curtailing life expectancy. Patients may experience angina and myocardial ischemia. However, the underlying mechanisms are poorly understood.METHODSThis study had a cross-sectional, case-control design. Patients with IPAH undergoing right heart catheterization were prospectively enrolled and underwent functional testing during coronary angiography using a dual pressure/temperature-sensitive guidewire. Cardiovascular MRI measured left and right ventricular mass and function. Right ventricular tissue from individuals with end-stage PAH and control individuals were analyzed for pathophysiology.RESULTSEleven IPAH and 15 control participants completed the protocol: 73% of IPAH patients had an elevated index of microcirculatory resistance (IMR > 25) and 55% had reduced coronary flow reserve (CFR < 2.0). Mean IMR was significantly higher in IPAH participants (39.2 ± 27.0 vs. 15.3 ± 5.0, P = 0.002), whereas mean CFR was lower (2.8 ± 2.1 vs. 4.0 ± 1.4; P = 0.077). Paired right coronary artery/ventricular measurements (n = 6) revealed IMR positively correlated with right ventricular mass (r = 0.91, P = 0.12) and negatively with CFR (r = -0.82, P = 0.046). Compared with controls (n = 5), PAH participants (n = 4) had reduced right ventricular capillary density, increased cardiomyocyte area, and increased mural area in pre-capillary arterioles.CONCLUSIONInvasive coronary function testing was feasible and safe in IPAH. Coronary microvascular dysfunction was prevalent in IPAH and correlated with increased right ventricular mass. Histopathology revealed vascular rarefaction and remodeling of pre-capillary arterioles.FUNDINGThe British Heart Foundation (BHF) (PG/18/6134217) and the Golden Jubilee Research Foundation.

Indexed as

Coronary VesselsFamilial Primary Pulmonary HypertensionAdultCardiac CatheterizationCase-Control StudiesCoronary AngiographyCoronary CirculationCross-Sectional StudiesFemaleHeart VentriclesHumansMagnetic Resonance ImagingMaleMicrocirculationMiddle AgedProspective StudiesCardiologyCardiovascular diseaseHypertensionMicrocirculationPulmonologyVascular biology

Identifiers

PMID41569941
PMCPMC13041685

What Socratic holds

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LicenceCC BY
Read underepoch 390

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.