Evidence map›Paper›PMID 39841643›Full record

ArticlePloS one2025

Automated extracellular volume fraction measurement for diagnosis and prognostication in patients with light-chain cardiac amyloidosis.

In-Chang Hwang, Eun Ju Chun, Pan Ki Kim, Myeongju Kim, Jiesuck Park, Hong-Mi Choi, Yeonyee E Yoon, Goo-Yeong Cho, Byoung Wook Choi

Abstract read
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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

In-Chang HwangCardiovascular Center, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.ORCID 0000-0003-4966-3924
Eun Ju ChunDepartment of Radiology, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Pan Ki KimPhantomics, Inc., Seoul, South Korea.
Myeongju KimCenter for Artificial Intelligence in Healthcare, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Jiesuck ParkCardiovascular Center, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Hong-Mi ChoiCardiovascular Center, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Yeonyee E YoonCardiovascular Center, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Goo-Yeong ChoCardiovascular Center, Seoul National University Bundang Hospital, Seongnam, Gyeonggi, South Korea.
Byoung Wook ChoiPhantomics, Inc., Seoul, South Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsT1 mapping on cardiac magnetic resonance (CMR) imaging is useful for diagnosis and prognostication in patients with light-chain cardiac amyloidosis (AL-CA). We conducted this study to evaluate the performance of T1 mapping parameters, derived from artificial intelligence (AI)-automated segmentation, for detection of cardiac amyloidosis (CA) in patients with left ventricular hypertrophy (LVH) and their prognostic values in patients with AL-CA. METHODS AND

resultsA total of 300 consecutive patients who underwent CMR for differential diagnosis of LVH were analyzed. CA was confirmed in 50 patients (39 with AL-CA and 11 with transthyretin amyloidosis), hypertrophic cardiomyopathy in 198, hypertensive heart disease in 47, and Fabry disease in 5. A semi-automated deep learning algorithm (Myomics-Q) was used for the analysis of the CMR images. The optimal cutoff extracellular volume fraction (ECV) for the differentiation of CA from other etiologies was 33.6% (diagnostic accuracy 85.6%). The automated ECV measurement showed a significant prognostic value for a composite of cardiovascular death and heart failure hospitalization in patients with AL-CA (revised Mayo stage III or IV) (adjusted hazard ratio 4.247 for ECV ≥40%, 95% confidence interval 1.215-14.851, p-value = 0.024). Incorporation of automated ECV measurement into the revised Mayo staging system resulted in better risk stratification (integrated discrimination index 27.9%, p = 0.013; categorical net reclassification index 13.8%, p = 0.007).

conclusionsT1 mapping on CMR imaging, derived from AI-automated segmentation, not only allows for improved diagnosis of CA from other etiologies of LVH, but also provides significant prognostic value in patients with AL-CA.

Indexed as

CardiomyopathiesImmunoglobulin Light-chain AmyloidosisAgedDeep LearningDiagnosis, DifferentialFemaleHumansHypertrophy, Left VentricularMagnetic Resonance ImagingMaleMiddle AgedPrognosis

Identifiers

PMID39841643
PMCPMC11753688

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