Evidence map›Paper›PMID 41116329›Full record

ArticleESC heart failure2025

Role of NPPB for recovery post ventricular assist device in paediatric dilated cardiomyopathy: Single-cell multiomics.

Yosuke Kugo, Takuji Kawamura, Akima Harada, Yuji Tominaga, Kenji Miki, Hidekazu Ishida, Takayoshi Ueno, Shigeru Miyagawa

Abstract read
In one paragraph

Article in ESC heart failure, 2025. 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

8 authors.

Yosuke KugoDepartment of Cardiovascular Surgery, Graduate School of Medicine Faculty of Medicine, The University of Osaka, Suita, Japan.
Takuji KawamuraDepartment of Cardiovascular Surgery, Graduate School of Medicine Faculty of Medicine, The University of Osaka, Suita, Japan.
Akima HaradaDepartment of Cardiovascular Surgery, Graduate School of Medicine Faculty of Medicine, The University of Osaka, Suita, Japan.
Yuji TominagaDepartment of Pediatric Cardiovascular Surgery, National Cerebral and Cardiovascular Center, Suita, Japan.
Kenji MikiPremium Research Institute for Human Metaverse Medicine, The University of Osaka, Suita, Japan.
Hidekazu IshidaDepartment of Pediatrics, Graduate School of Medicine Faculty of Medicine, The University of Osaka, Suita, Japan.
Takayoshi UenoDivision of Health Sciences, Graduate School of Medicine, The University of Osaka, Suita, Japan.
Shigeru MiyagawaDepartment of Cardiovascular Surgery, Graduate School of Medicine Faculty of Medicine, The University of Osaka, Suita, Japan.ORCID https://orcid.org/0000-0003-0015-6569

Funding

JSPS KAKENHI JP20H00542JSPS KAKENHI JP22K08919
6 · The paper itself

Abstract

aimsPaediatric heart transplantation requires lifelong immunosuppression, highlighting the need for recovery-oriented strategies. A subset of children with dilated cardiomyopathy (DCM) recovers left ventricular (LV) function after LV assist device (LVAD) implantation, allowing for device explantation. We aimed to identify factors associated with LV functional recovery using single-nucleus multiomics analysis of LV tissue collected at LVAD implantation.

methodsWe included children with idiopathic DCM who underwent LVAD implantation between 2013 and 2023. Patients who achieved device explantation and medical stabilization were classified as the recovery group while those who required transplantation or died were classified as the non-recovery group. Single-nucleus RNA and ATAC sequencing were performed in six representative cases. Differential gene expression, chromatin accessibility and gene ontology (GO) enrichment analyses were conducted. Candidate markers were validated histologically and serologically in the full cohort.

resultsTwenty-five cases were included (non-recovery, n = 15; recovery, n = 10). Age at LVAD implantation [median (range)] was 0.9 (0.1-4.6) versus 0.8 (0.3-5.6) years (P = 0.8), sex 27% versus 30% male (P > 0.9) and body weight 5.9 (3.8-14.0) versus 7.5 (5.0-26.0) kg (P = 0.049). LV ejection fraction at implantation was similar (24 (10-44) % vs. 15 (10-25) %, P = 0.2). RNA sequencing showed elevated NPPB, MYL7 and PCDH9 in recovery-group cardiomyocytes, with NPPB highest expression [baseMean = 16 305; log

conclusionsElevated NPPB expression and BNP levels at LVAD implantation are associated with LV recovery in paediatric DCM. These findings support an anti-apoptotic role of BNP in successful bridge-to-recovery outcomes.

Indexed as

Cardiomyopathy, DilatedHeart-Assist DevicesRecovery of FunctionVentricular Function, LeftChildChild, PreschoolFemaleFollow-Up StudiesHumansInfantMaleMultiomicsRetrospective StudiesSingle-Cell Analysisapoptosisbridge to recoverydilated cardiomyopathyleft ventricular assist devicenatriuretic peptidespaediatricsingle‐cell multiomics

Identifiers

PMID41116329
PMCPMC12719843

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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.