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Automated extracellular volume fraction measurement for diagnosis and prognostication in patients with light-chain cardiac amyloidosis
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Hwang, In-Chang | - |
| dc.contributor.author | Chun, Eun Ju | - |
| dc.contributor.author | Kim, Pan Ki | - |
| dc.contributor.author | Kim, Myeongju | - |
| dc.contributor.author | Park, Jiesuck | - |
| dc.contributor.author | Choi, Hong-Mi | - |
| dc.contributor.author | Yoon, Yeonyee E. | - |
| dc.contributor.author | Cho, Goo-Yeong | - |
| dc.contributor.author | Choi, Byoung Wook | - |
| dc.date.accessioned | 2025-11-10T07:37:40Z | - |
| dc.date.available | 2025-11-10T07:37:40Z | - |
| dc.date.created | 2025-08-19 | - |
| dc.date.issued | 2025-01 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/208581 | - |
| dc.description.abstract | Aims T1 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 results A 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). Conclusions T1 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. | - |
| dc.language | English | - |
| dc.publisher | Public Library of Science | - |
| dc.relation.isPartOf | PLOS ONE | - |
| dc.relation.isPartOf | PLOS ONE | - |
| dc.subject.MESH | Aged | - |
| dc.subject.MESH | Cardiomyopathies* / diagnosis | - |
| dc.subject.MESH | Cardiomyopathies* / diagnostic imaging | - |
| dc.subject.MESH | Deep Learning | - |
| dc.subject.MESH | Diagnosis, Differential | - |
| dc.subject.MESH | Female | - |
| dc.subject.MESH | Humans | - |
| dc.subject.MESH | Hypertrophy, Left Ventricular / diagnostic imaging | - |
| dc.subject.MESH | Immunoglobulin Light-chain Amyloidosis* / diagnosis | - |
| dc.subject.MESH | Immunoglobulin Light-chain Amyloidosis* / diagnostic imaging | - |
| dc.subject.MESH | Immunoglobulin Light-chain Amyloidosis* / pathology | - |
| dc.subject.MESH | Magnetic Resonance Imaging / methods | - |
| dc.subject.MESH | Male | - |
| dc.subject.MESH | Middle Aged | - |
| dc.subject.MESH | Prognosis | - |
| dc.title | Automated extracellular volume fraction measurement for diagnosis and prognostication in patients with light-chain cardiac amyloidosis | - |
| dc.type | Article | - |
| dc.contributor.googleauthor | Hwang, In-Chang | - |
| dc.contributor.googleauthor | Chun, Eun Ju | - |
| dc.contributor.googleauthor | Kim, Pan Ki | - |
| dc.contributor.googleauthor | Kim, Myeongju | - |
| dc.contributor.googleauthor | Park, Jiesuck | - |
| dc.contributor.googleauthor | Choi, Hong-Mi | - |
| dc.contributor.googleauthor | Yoon, Yeonyee E. | - |
| dc.contributor.googleauthor | Cho, Goo-Yeong | - |
| dc.contributor.googleauthor | Choi, Byoung Wook | - |
| dc.identifier.doi | 10.1371/journal.pone.0317741 | - |
| dc.relation.journalcode | J02540 | - |
| dc.identifier.eissn | 1932-6203 | - |
| dc.identifier.pmid | 39841643 | - |
| dc.contributor.affiliatedAuthor | Choi, Byoung Wook | - |
| dc.identifier.scopusid | 2-s2.0-85216298024 | - |
| dc.identifier.wosid | 001492214200063 | - |
| dc.citation.volume | 20 | - |
| dc.citation.number | 1 | - |
| dc.identifier.bibliographicCitation | PLOS ONE, Vol.20(1), 2025-01 | - |
| dc.identifier.rimsid | 88691 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordPlus | HYPERTROPHIC CARDIOMYOPATHY | - |
| dc.subject.keywordPlus | QUANTIFICATION | - |
| dc.subject.keywordPlus | ASSOCIATION | - |
| dc.subject.keywordPlus | BIOMARKERS | - |
| dc.subject.keywordPlus | SOCIETY | - |
| dc.subject.keywordPlus | ESC | - |
| dc.subject.keywordPlus | T1 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | Y | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Multidisciplinary Sciences | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.identifier.articleno | e0317741 | - |
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