Evidence map›Paper›PMID 40611480›Full record

ArticleJournal of the American Heart Association2025

Association Between Mineralocorticoid Receptor Antagonist Use With Worsening Renal Function and Prognosis in Patients With Acute Heart Failure.

Yudai Fujimoto, Yasuyuki Shiraishi, Kazutaka Nogi, Shun Kohsaka, Takashi Kohno, Mitsunobu Kitamura, Yuji Nagatomo, Tomoya Ueda, Maki Nogi, Satomi Ishihara and 12 more

Abstract readMulticenter Study
In one paragraph

Article in Journal of the American Heart Association, 2025. 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

22 authors.

Yudai FujimotoDepartment of Cardiovascular Biology and Medicine Juntendo University Graduate School of Medicine Tokyo Japan.ORCID 0009-0004-8286-3228
Yasuyuki ShiraishiDepartment of Cardiology Keio University School of Medicine Tokyo Japan.ORCID 0000-0001-8788-1186
Kazutaka NogiDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.ORCID 0000-0003-0516-8753
Shun KohsakaDepartment of Cardiology Keio University School of Medicine Tokyo Japan.ORCID 0000-0003-3779-2972
Takashi KohnoDepartment of Cardiovascular Medicine Kyorin University Faculty of Medicine Tokyo Japan.ORCID 0000-0003-2604-1284
Mitsunobu KitamuraDepartment of Cardiology Sakakibara Heart Institute Tokyo Japan.ORCID 0000-0002-7573-7176
Yuji NagatomoDepartment of Cardiology National Defense Medical College Tokorozawa Japan.ORCID 0000-0002-3430-4614
Tomoya UedaDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.ORCID 0000-0002-0656-3336
Maki NogiDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.
Satomi IshiharaDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.ORCID 0000-0002-2816-4926
Yasuki NakadaDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.ORCID 0000-0003-0510-6923
Rika KawakamiDepartment of Cardiology Saiseikai Suita Hospital Suita Suita Japan.ORCID 0000-0002-2904-4993
Takeshi KitaiDepartment of Cardiovascular Medicine National Cerebral and Cardiovascular Center Osaka Japan.ORCID 0000-0003-2416-5865
Shogo OishiDepartment of Cardiology Harima-Himeji General Medical Center Himeji Japan.
Eiichi AkiyamaDivision of Cardiology Yokohama City University Medical Center Yokohama Japan.
Satoshi SuzukiDepartment of Cardiovascular Medicine Fukushima Medical University Fukushima Japan.ORCID 0000-0002-3548-1604
Masayoshi YamamotoCardiovascular Division, Faculty of Medicine University of Tsukuba Tsukuba Japan.ORCID 0000-0002-1447-9126
Keisuke KidaDepartment of Pharmacology St. Marianna University School of Medicine Kawasaki Kanagawa Japan.ORCID 0000-0002-3464-6016
Takahiro OkumuraDepartment of Cardiology Nagoya University Graduate School of Medicine Nagoya Japan.ORCID 0000-0001-5076-2052
Tsutomu YoshikawaDepartment of Cardiology Sakakibara Heart Institute Tokyo Japan.
Yoshihiko SaitoDepartment of Cardiovascular Medicine Nara Medical University Kashihara Japan.ORCID 0000-0001-5574-3571
Yuya MatsueDepartment of Cardiovascular Biology and Medicine Juntendo University Graduate School of Medicine Tokyo Japan.ORCID 0000-0003-2456-8525

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPrognostic implications of mineralocorticoid receptor antagonist (MRA) initiation in the context of worsening renal function (WRF) in patients with acute heart failure (AHF) remain unknown.

methodsThis was a post hoc analysis using data from Japanese AHF registries (NARA-HF [Nara Registry and Analyses for Heart Failure], WET-HF [West Tokyo Heart Failure], REALITY-AHF [Registry Focused on Very Early Presentation and Treatment in Emergency Department of Acute Heart Failure]). MRA-naïve patients at baseline were included, comprising 1632 patients with HF with reduced ejection fraction (HFrEF) and 2407 with heart failure with mildly reduced or preserved ejection fraction (HFmr/pEF). They were divided into 3 groups: MRA initiated without WRF (HFrEF, n=590; HFmr/pEF, n=572), MRA initiated with WRF (HFrEF, n=74; HFmr/pEF, n=100), and no MRA initiation (HFrEF, n=968; HFmr/pEF, n=1735). WRF was defined as a 0.3 mg/dL increase from admission to discharge. The composite of death or HF hospitalization after discharge was assessed.

resultsDuring the 1-year follow-up, 369 and 593 events occurred in patients with HFrEF and HFmr/pEF, respectively. Overall, MRA initiation during hospitalization of AHF was independently associated with better prognosis (hazard ratio [HR], 0.81), mainly driven by HF hospitalization. Among patients with HFrEF, the groups with MRA with and without WRF showed a lower incidence of the outcome than the no-MRA group, even after adjusting for risk factors (HR, 0.75 and 0.49, respectively). Among patients with HFmr/pEF, MRA initiation without WRF was independently associated with better prognosis (HR, 0.78), but MRA initiation with WRF was not.

conclusionsInitiating an MRA during AHF hospitalization was associated with better postdischarge outcomes in HFrEF, irrespective of creatinine elevation, whereas no such consistent association was observed in HFmr/pEF.

Indexed as

Glomerular Filtration RateHeart FailureKidneyMineralocorticoid Receptor AntagonistsAcute DiseaseAgedAged, 80 and overDisease ProgressionFemaleHospitalizationHumansJapanMaleMiddle AgedPrognosisRegistriesMineralocorticoid Receptor Antagonistsacute heart failureMRAprognosisWRF

Identifiers

PMID40611480
PMCPMC12533620

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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.