High Prevalence of Left Ventricular Non-Compaction and Its Effect on Chemotherapy-Related Cardiac Dysfunction in Patients With Hematological Diseases.


Journal

Circulation journal : official journal of the Japanese Circulation Society
ISSN: 1347-4820
Titre abrégé: Circ J
Pays: Japan
ID NLM: 101137683

Informations de publication

Date de publication:
23 10 2020
Historique:
pubmed: 13 10 2020
medline: 15 12 2021
entrez: 12 10 2020
Statut: ppublish

Résumé

Recent progress in chemotherapy has prolonged the survival of patients with hematological diseases, but has also increased the number of patients with chemotherapy-related cardiac dysfunction (CTRCD). However, the causes of individual variations and risk factors for CTRCD have yet to be fully elucidated.Methods and Results:Consecutive echocardiograms of 371 patients were retrospectively evaluated for the presence of left ventricular (LV) non-compaction (LVNC). Individual LV ejection fraction (LVEF) outcome estimates were made using bivariate linear regression with log-transformed duration Akaike information criterion (AIC) model fitting. The prevalence of LVNC was 6-fold higher in patients with hematological diseases than in those with non-hematological diseases (12% vs. 2%; risk ratio 6.1; 95% confidence interval [CI] 2.0, 18.2). Among patients with hematological diseases, the ratio of myeloid diseases was significantly higher in the group with LVNC (P=0.031). Deterioration of LVEF was more severe in patients with than without LVNC (-14.4 percentage points/year [95% CI -21.0, -7.9] vs. -4.6 percentage points/year [95% CI -6.8, -2.4], respectively), even after multivariate adjustment for baseline LVEF, background disease distributions, cumulative anthracycline dose, and other baseline factors. LVNC is relatively prevalent in patients with hematological diseases (particularly myeloid diseases) and can be one of the major risk factors for CTRCD. Detailed cardiac evaluations including LVNC are recommended for patients undergoing chemotherapy.

Sections du résumé

BACKGROUND
Recent progress in chemotherapy has prolonged the survival of patients with hematological diseases, but has also increased the number of patients with chemotherapy-related cardiac dysfunction (CTRCD). However, the causes of individual variations and risk factors for CTRCD have yet to be fully elucidated.Methods and Results:Consecutive echocardiograms of 371 patients were retrospectively evaluated for the presence of left ventricular (LV) non-compaction (LVNC). Individual LV ejection fraction (LVEF) outcome estimates were made using bivariate linear regression with log-transformed duration Akaike information criterion (AIC) model fitting. The prevalence of LVNC was 6-fold higher in patients with hematological diseases than in those with non-hematological diseases (12% vs. 2%; risk ratio 6.1; 95% confidence interval [CI] 2.0, 18.2). Among patients with hematological diseases, the ratio of myeloid diseases was significantly higher in the group with LVNC (P=0.031). Deterioration of LVEF was more severe in patients with than without LVNC (-14.4 percentage points/year [95% CI -21.0, -7.9] vs. -4.6 percentage points/year [95% CI -6.8, -2.4], respectively), even after multivariate adjustment for baseline LVEF, background disease distributions, cumulative anthracycline dose, and other baseline factors.
CONCLUSIONS
LVNC is relatively prevalent in patients with hematological diseases (particularly myeloid diseases) and can be one of the major risk factors for CTRCD. Detailed cardiac evaluations including LVNC are recommended for patients undergoing chemotherapy.

Identifiants

pubmed: 33041289
doi: 10.1253/circj.CJ-20-0344
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1957-1964

Auteurs

Mitsuhito Hirano (M)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Koichi Kimura (K)

Department of Laboratory Medicine, The Institute of Medical Science, The University of Tokyo.
Department of General Medicine, The Institute of Medical Science, The University of Tokyo.
Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Tomohiro Ishigaki (T)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.
Department of Laboratory Medicine, The Institute of Medical Science, The University of Tokyo.

Masanori Nojima (M)

Center for Translational Research, The Institute of Medical Science, The University of Tokyo.

Masao Daimon (M)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.
Department of Laboratory Medicine, The University of Tokyo Hospital, The University of Tokyo.

Hiroyuki Morita (H)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Katsu Takenaka (K)

Department of Laboratory Medicine, The University of Tokyo Hospital, The University of Tokyo.

Boqing Xu (B)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Naoko Sawada (N)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Megumi Hirokawa (M)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Issei Komuro (I)

Department of Cardiovascular Medicine, Graduate School of Medicine, The University of Tokyo.

Takayuki Morisaki (T)

Department of General Medicine, The Institute of Medical Science, The University of Tokyo.

Hiroshi Yotsuyanagi (H)

Department of General Medicine, The Institute of Medical Science, The University of Tokyo.

Toyotaka Kawamata (T)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Kazuaki Yokoyama (K)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Takaaki Konuma (T)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Seiko Kato (S)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Hiroshi Yasui (H)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Tokiko Nagamura-Inoue (T)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.
Department of Laboratory Medicine, The Institute of Medical Science, The University of Tokyo.

Kaoru Uchimaru (K)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Satoshi Takahashi (S)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Yoichi Imai (Y)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

Arinobu Tojo (A)

Department of Hematology/Oncology, The Institute of Medical Science, The University of Tokyo.

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