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The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking

BACKGROUND: To investigate the difference of right ventricular (RV) structural and functional alteration in patients with diabetes mellitus (DM) with preserved left ventricular ejection fraction (LVEF), and the ventricular interdependence in these patients, using cardiac MR (CMR) feature tracking. M...

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Autores principales: Shi, Rui, Yang, Zhi-Gang, Guo, Ying-Kun, Qian, Wen-Lei, Gao, Yue, Li, Xue-Ming, Jiang, Li, Xu, Hua-Yan, Li, Yuan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122304/
https://www.ncbi.nlm.nih.gov/pubmed/37085847
http://dx.doi.org/10.1186/s12933-023-01806-7
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author Shi, Rui
Yang, Zhi-Gang
Guo, Ying-Kun
Qian, Wen-Lei
Gao, Yue
Li, Xue-Ming
Jiang, Li
Xu, Hua-Yan
Li, Yuan
author_facet Shi, Rui
Yang, Zhi-Gang
Guo, Ying-Kun
Qian, Wen-Lei
Gao, Yue
Li, Xue-Ming
Jiang, Li
Xu, Hua-Yan
Li, Yuan
author_sort Shi, Rui
collection PubMed
description BACKGROUND: To investigate the difference of right ventricular (RV) structural and functional alteration in patients with diabetes mellitus (DM) with preserved left ventricular ejection fraction (LVEF), and the ventricular interdependence in these patients, using cardiac MR (CMR) feature tracking. METHODS: From December 2016 to February 2022, 148 clinically diagnosed patients with DM who underwent cardiac MR (CMR) in our hospital were consecutively recruited. Fifty-four healthy individuals were included as normal controls. Biventricular strains, including left/right ventricular global longitudinal strain (LV-/RVGLS), left/right ventricular global circumferential strain (LV-/RVGCS), left/right ventricular global radial strain (LV-/RVGRS) were evaluated, and compared between patients with DM and healthy controls. Multiple linear regression and mediation analyses were used to evaluate DM's direct and indirect effects on RV strains. RESULTS: No differences were found in age (56.98 ± 10.98 vs. 57.37 ± 8.41, p = 0.985), sex (53.4% vs. 48.1%, p = 0.715), and body surface area (BSA) (1.70 ± 0.21 vs. 1.69 ± 0.17, p = 0.472) between DM and normal controls. Patients with DM had decreased RVGLS (− 21.86 ± 4.14 vs. − 24.49 ± 4.47, p = 0.001), RVGCS (− 13.16 ± 3.86 vs. − 14.92 ± 3.08, p = 0.011), and no decrease was found in RVGRS (22.62 ± 8.11 vs. 23.15 ± 9.05, p = 0.743) in patients with DM compared with normal controls. The difference in RVGLS between normal controls and patients with DM was totally mediated by LVGLS (indirect effecting: 0.655, bootstrapped 95%CI 0.138–0.265). The difference in RVGCS between normal controls and DM was partly mediated by the LVGLS (indirect effecting: 0.336, bootstrapped 95%CI 0.002–0.820) and LVGCS (indirect effecting: 0.368, bootstrapped 95%CI 0.028–0.855). CONCLUSIONS: In the patients with DM and preserved LVEF, the difference in RVGLS between DM and normal controls was totally mediated by LVGLS. Although there were partly mediating effects of LVGLS and LVGCS, the decrease in RVGCS might be directly affected by the DM.
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spelling pubmed-101223042023-04-23 The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking Shi, Rui Yang, Zhi-Gang Guo, Ying-Kun Qian, Wen-Lei Gao, Yue Li, Xue-Ming Jiang, Li Xu, Hua-Yan Li, Yuan Cardiovasc Diabetol Research BACKGROUND: To investigate the difference of right ventricular (RV) structural and functional alteration in patients with diabetes mellitus (DM) with preserved left ventricular ejection fraction (LVEF), and the ventricular interdependence in these patients, using cardiac MR (CMR) feature tracking. METHODS: From December 2016 to February 2022, 148 clinically diagnosed patients with DM who underwent cardiac MR (CMR) in our hospital were consecutively recruited. Fifty-four healthy individuals were included as normal controls. Biventricular strains, including left/right ventricular global longitudinal strain (LV-/RVGLS), left/right ventricular global circumferential strain (LV-/RVGCS), left/right ventricular global radial strain (LV-/RVGRS) were evaluated, and compared between patients with DM and healthy controls. Multiple linear regression and mediation analyses were used to evaluate DM's direct and indirect effects on RV strains. RESULTS: No differences were found in age (56.98 ± 10.98 vs. 57.37 ± 8.41, p = 0.985), sex (53.4% vs. 48.1%, p = 0.715), and body surface area (BSA) (1.70 ± 0.21 vs. 1.69 ± 0.17, p = 0.472) between DM and normal controls. Patients with DM had decreased RVGLS (− 21.86 ± 4.14 vs. − 24.49 ± 4.47, p = 0.001), RVGCS (− 13.16 ± 3.86 vs. − 14.92 ± 3.08, p = 0.011), and no decrease was found in RVGRS (22.62 ± 8.11 vs. 23.15 ± 9.05, p = 0.743) in patients with DM compared with normal controls. The difference in RVGLS between normal controls and patients with DM was totally mediated by LVGLS (indirect effecting: 0.655, bootstrapped 95%CI 0.138–0.265). The difference in RVGCS between normal controls and DM was partly mediated by the LVGLS (indirect effecting: 0.336, bootstrapped 95%CI 0.002–0.820) and LVGCS (indirect effecting: 0.368, bootstrapped 95%CI 0.028–0.855). CONCLUSIONS: In the patients with DM and preserved LVEF, the difference in RVGLS between DM and normal controls was totally mediated by LVGLS. Although there were partly mediating effects of LVGLS and LVGCS, the decrease in RVGCS might be directly affected by the DM. BioMed Central 2023-04-21 /pmc/articles/PMC10122304/ /pubmed/37085847 http://dx.doi.org/10.1186/s12933-023-01806-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Shi, Rui
Yang, Zhi-Gang
Guo, Ying-Kun
Qian, Wen-Lei
Gao, Yue
Li, Xue-Ming
Jiang, Li
Xu, Hua-Yan
Li, Yuan
The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title_full The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title_fullStr The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title_full_unstemmed The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title_short The right ventricular dysfunction and ventricular interdependence in patients with DM: assessment using cardiac MR feature tracking
title_sort right ventricular dysfunction and ventricular interdependence in patients with dm: assessment using cardiac mr feature tracking
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10122304/
https://www.ncbi.nlm.nih.gov/pubmed/37085847
http://dx.doi.org/10.1186/s12933-023-01806-7
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