Evidence map›Paper›PMID 40891072›Full record

ArticleEuropean heart journal. Cardiovascular Imaging2025

Predicting prognosis of light-chain cardiac amyloidosis by magnetic resonance imaging and deep learning.

Shuo Wang, Chengcai Liu, Yubo Guo, Haolin Sang, Xiao Li, Lu Lin, Xiaohu Li, Yi Wu, Long Jiang Zhang, Jie Tian and 2 more

Abstract read
In one paragraph

Article in European heart journal. Cardiovascular Imaging, 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. Imaging Advances in Light Chain Amyloidosis.Diagnostics (Basel, Switzerland) · 2026
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

Shuo WangBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.
Chengcai LiuBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.ORCID 0009-0006-5706-2300
Yubo GuoDepartment of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Haolin SangBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.
Xiao LiDepartment of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Lu LinDepartment of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.
Xiaohu LiDepartment of Radiology, First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.
Yi WuBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.
Long Jiang ZhangDepartment of Diagnostic Radiology, Jinling Hospital, Medical School of Nanjing University, Nanjing, Jiangsu, China.ORCID 0000-0002-6664-7224
Jie TianBeijing Advanced Innovation Center for Big Data-Based Precision Medicine, School of Engineering Medicine, Beihang University, Beijing, China.
Jian LiDepartment of Hematology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.ORCID 0000-0002-4549-0694
Yining WangDepartment of Radiology, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing 100730, China.ORCID 0000-0001-6441-2002

Funding

Beijing Natural Science Foundation L232131Fundamental Research Funds for the Central UniversitiesMinistry of Science and Technology of China 2023YFC2506502National High Level Hospital Clinical Research Funding 2022-PUMCH-B-027National High Level Hospital Clinical Research Funding 2022-PUMCH-D-002National Natural Science Foundation of China 62027901National Natural Science Foundation of China 81930053National Natural Science Foundation of China 82020108018National Natural Science Foundation of China 82325026National Natural Science Foundation of China 92259105
6 · The paper itself

Abstract

aimsLight-chain cardiac amyloidosis (AL-CA) is a progressive heart disease with high mortality rate and variable prognosis. The presently used Mayo staging method can only stratify patients into four stages, highlighting the necessity for a more individualized prognosis prediction method. We aim to develop a novel deep learning (DL) model for the whole-heart analysis of cardiovascular magnetic resonance-derived late gadolinium enhancement (LGE) images to predict individualized prognosis in AL-CA. METHODS AND

resultsThis study included 394 patients with AL-CA who underwent standardized chemotherapy and had at least 1 year of follow-up. The approach involved automated segmentation of the heart in LGE images and feature extraction using a Transformer-based DL model. To enhance feature differentiation and mitigate overfitting, a contrastive pretraining strategy was employed to accentuate distinct features between patients with different prognoses while clustering similar cases. Finally, an ensemble learning strategy was used to integrate predictions from 15 models at 15 survival time points into a comprehensive prognostic model. In the testing set of 79 patients, the DL model achieved a concordance index (C-index) of 0.91 and an area under the curve (AUC) of 0.95 in predicting 2.6-year survival (HR: 2.67), outperforming the Mayo model (C-index = 0.65; AUC = 0.71). The DL model effectively distinguished patients with the same Mayo stage but different prognoses. Visualization techniques revealed that the model captures complex, high-dimensional prognostic features across multiple cardiac regions, extending beyond the amyloid-affected areas.

conclusionThis fully automated DL model can predict individualized prognosis of AL-CA through LGE images, which complements the presently used Mayo staging method.

Indexed as

CardiomyopathiesDeep LearningImmunoglobulin Light-chain AmyloidosisMagnetic Resonance ImagingMagnetic Resonance Imaging, CineAgedFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisRetrospective Studiesartificial intelligencecardiac amyloidosiscardiac magnetic resonance (CMR)deep learninglight-chain (AL) amyloidosisprognosis

Identifiers

PMID40891072
PMCPMC12571507

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

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.