Evidence map›Paper›PMID 41859897›Full record

ArticleJournal of the American Heart Association2026

Prognostic Impact of Elevated Pulmonary Vascular Resistance in Group 2 Pulmonary Hypertension: Insights From a Japanese Multicenter Registry.

Taijyu Satoh, Koichiro Sugimura, Yoshihiro Fukumoto, Kohtaro Abe, Yoshihiro Dohi, Kaoru Dohi, Yu Taniguchi, Akiyoshi Hashimoto, Shigehiko Kato, Kazuto Nakamura and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

23 authors.

Taijyu SatohDepartment of Cardiovascular Medicine Tohoku University Graduate School of Medicine Sendai Japan.ORCID 0000-0002-1795-6872
Koichiro SugimuraDepartment of Cardiology International University of Health and Welfare Narita Hospital Narita Japan.ORCID 0000-0001-5354-9687
Yoshihiro FukumotoDivision of Cardiovascular Medicine, Department of Internal Medicine Kurume University School of Medicine Kurume Japan.ORCID 0000-0002-8947-109X
Kohtaro AbeDepartment of Cardiovascular Medicine, Faculty of Medical Sciences Kyushu University Fukuoka Japan.ORCID 0000-0003-4131-5423
Yoshihiro DohiDepartment of Cardiovascular Medicine Kure Kyosai Hospital Hiroshima Japan.ORCID 0000-0002-4240-2097
Kaoru DohiDepartment of Cardiology and Nephrology Mie University Graduate School of Medicine Tsu Japan.
Yu TaniguchiDivision of Cardiovascular Medicine, Department of Internal Medicine Kobe University Graduate School of Medicine Kobe Japan.ORCID 0000-0002-8430-2123
Akiyoshi HashimotoDepartment of Patient Safety and Hospital Administration Sapporo Medical University School of Medicine Sapporo Japan.ORCID 0000-0002-9485-8635
Shigehiko KatoDepartment of Cardiology, Pulmonology, and Nephrology Yamagata University School of Medicine Yamagata Japan.ORCID 0000-0003-3308-6392
Kazuto NakamuraDepartment of Cardiovascular Medicine University of Yamanashi Yamanshi Japan.ORCID 0000-0002-2313-017X
Noriaki TakamaDepartment of Cardiovascular Medicine Gunma University Graduate School of Medicine Maebashi Japan.
Toru HashimotoDepartment of Cardiovascular Medicine, Faculty of Medical Sciences Kyushu University Fukuoka Japan.ORCID 0000-0001-9607-0852
Yusuke YamadaDepartment of Cardiovascular Medicine Tohoku University Graduate School of Medicine Sendai Japan.ORCID 0009-0008-7108-7306
Yosuke TeruiDepartment of Cardiovascular Medicine Iwate Prefectural Isawa Hospital Sendai Japan.
Yutaka MiuraDepartment of Cardiovascular Medicine Ishinomaki City Hospital Sendai Japan.
Masaki IshiyamaDepartment of Cardiology and Nephrology Mie University Graduate School of Medicine Tsu Japan.ORCID 0000-0001-8051-8982
Masayuki KoyamaDepartment of Cardiovascular, Renal and Metabolic Medicine Sapporo Medical University School of Medicine Sapporo Japan.ORCID 0000-0002-8165-5855
Fusako SeraDepartment of Cardiovascular Medicine The University of Osaka Graduate School of Medicine Osaka Japan.ORCID 0000-0002-9260-6901
Yuichi TamuraDepartment of Cardiology International University of Health and Welfare Mita Hospital Tokyo Japan.
Yasushi SakataDepartment of Cardiovascular Medicine The University of Osaka Graduate School of Medicine Osaka Japan.ORCID 0000-0002-5618-4721
Masaru HatanoDepartment of Cardiovascular Medicine, Graduate School of Medicine The University of Tokyo Tokyo Japan.ORCID 0000-0003-2135-3625
Satoshi YasudaDepartment of Cardiovascular Medicine Tohoku University Graduate School of Medicine Sendai Japan.
Japan PH Registry Network Group 2 PH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundGroup 2 pulmonary hypertension (PH), defined as PH caused due to left heart disease, remains a challenging condition. However, its prognostic impact and implications for emerging therapies are unclear. We aimed to evaluate the real-world relationship between pulmonary vascular resistance (PVR) and prognosis in Group 2 PH and assess the efficacy of emerging therapies.

methodsTwo prospective registries supported by Japanese PH societies were analyzed: a current (2018-2024; n=563) and a previous (2012-2016; n=425) registry. The composite end points were hospitalization for heart failure, all-cause death, ventricular assist device implantation, or cardiac transplantation.

resultsStratified analyses using propensity score-matched data demonstrated a significant association between PVR >3 Wood units and prognosis in patients with Group 2 PH (6-year event-free rates, PVR >3 Wood units versus PVR ≦3 Wood units, previous registry: 72.9% versus 61.4%; current registry: 75.2% versus 55.4%). Consistent patterns were observed in both heart failure with reduced ejection fraction and heart failure with preserved ejection fraction subgroups. The use of SGLT2 (sodium-glucose cotransporter-2) inhibitors in the current registry was associated with improved outcomes in patients with elevated PVR, showing event-free rates of 73.8% versus 35.5% in those without treatment. Among multivariate analyses including major treatment options, SGLT2 inhibitor treatment exhibited significant associations with improvement of composite end points.

conclusionsElevated PVR (>3 Wood units) identified a high-risk subset of patients with Group 2 PH. The association between the use of SGLT2 inhibitors and better outcomes suggests a potential therapeutic role that warrants further investigation through controlled studies.

Indexed as

Hypertension, PulmonaryVascular ResistanceAgedEast Asian PeopleFemaleHeart FailureHumansJapanMaleMiddle AgedPrognosisProspective StudiesRegistriesejection fractionpulmonary hypertensionpulmonary vascular remodelingpulmonary vascular resistanceSGLT2 inhibitors

Identifiers

PMID41859897
PMCPMC13279068

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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.