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Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting

OBJECTIVE: Myocardial ischemia is known to suppress fatty acid metabolism and favor glucose metabolism. However, changes in myocardial metabolism after coronary revascularization are not fully elucidated. METHODS: Thirty-eight patients with coronary artery disease were retrospectively enrolled. Thes...

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Autores principales: Morishima, Motoko, Kiriyama, Tomonari, Miyagi, Yasuo, Otsuka, Toshiaki, Fukushima, Yoshimitsu, Kumita, Shin-ichiro, Ishii, Yosuke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Singapore 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897360/
https://www.ncbi.nlm.nih.gov/pubmed/34822103
http://dx.doi.org/10.1007/s12149-021-01696-3
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author Morishima, Motoko
Kiriyama, Tomonari
Miyagi, Yasuo
Otsuka, Toshiaki
Fukushima, Yoshimitsu
Kumita, Shin-ichiro
Ishii, Yosuke
author_facet Morishima, Motoko
Kiriyama, Tomonari
Miyagi, Yasuo
Otsuka, Toshiaki
Fukushima, Yoshimitsu
Kumita, Shin-ichiro
Ishii, Yosuke
author_sort Morishima, Motoko
collection PubMed
description OBJECTIVE: Myocardial ischemia is known to suppress fatty acid metabolism and favor glucose metabolism. However, changes in myocardial metabolism after coronary revascularization are not fully elucidated. METHODS: Thirty-eight patients with coronary artery disease were retrospectively enrolled. These patients had undergone stress perfusion single photon emission computed tomography (SPECT) and (123)I-BMIPP SPECT in both the short-term (6.4 ± 4.7 months) and mid-term (29.9 ± 7.2 months) after isolated coronary artery bypass grafting. Tracer uptake was graded using a 17-segment, 5-point scoring model. Serial changes in SRS (summed rest score), SDS (summed difference score), the BMIPP score (total defect score of BMIPP), and the mismatch score (BMIPP score–SRS) were evaluated. In addition, persistent perfusion–metabolism mismatch (PM) was defined as mismatch score minus SDS of 3 or more during the mid-term postoperative period. The clinical parameters associated with PM were examined. RESULTS: From short- to mid-term postoperative period, the extent of infarcted myocardium (SRS) did not change significantly (7.8 ± 8.0 to 7.1 ± 7.0, P = 0.117). The extent of ischemic myocardium (SDS), the BMIPP score and the mismatch score, which reflects perfusion–metabolism mismatch, were significantly improved (2.0 ± 2.8 to 0.7 ± 1.0, P = 0.010; 12.2 ± 9.0 to 9.5 ± 7.9, P < 0.001; 4.4 ± 3.7 to 2.5 ± 2.6, P < 0.001; respectively). Remarkably, perfusion–metabolism mismatch persisted in 13 patients (34%) even in the mid-term postoperative period. eGFR and SYNTAX score were independent predictors of persistent perfusion–metabolic mismatch in multivariable analysis (OR = 0.951, 95% CI 0.898–0.985, P = 0.010 and OR = 1.126, 95% CI 1.011–1.254, P = 0.031, respectively). The mismatch score both in the short- and mid-term significantly correlated with SYNTAX score (r = 0.400 and r = 0.472, respectively). CONCLUSIONS: Fatty acid metabolism disturbance improved from short- to mid-term postoperative period in patients with successful reperfusion by coronary artery bypass grafting. However, in patients with severe atherosclerosis, impaired fatty acid metabolism was sustained until the mid-term postoperative period, even though ischemia had resolved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12149-021-01696-3.
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spelling pubmed-88973602022-03-08 Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting Morishima, Motoko Kiriyama, Tomonari Miyagi, Yasuo Otsuka, Toshiaki Fukushima, Yoshimitsu Kumita, Shin-ichiro Ishii, Yosuke Ann Nucl Med Original Article OBJECTIVE: Myocardial ischemia is known to suppress fatty acid metabolism and favor glucose metabolism. However, changes in myocardial metabolism after coronary revascularization are not fully elucidated. METHODS: Thirty-eight patients with coronary artery disease were retrospectively enrolled. These patients had undergone stress perfusion single photon emission computed tomography (SPECT) and (123)I-BMIPP SPECT in both the short-term (6.4 ± 4.7 months) and mid-term (29.9 ± 7.2 months) after isolated coronary artery bypass grafting. Tracer uptake was graded using a 17-segment, 5-point scoring model. Serial changes in SRS (summed rest score), SDS (summed difference score), the BMIPP score (total defect score of BMIPP), and the mismatch score (BMIPP score–SRS) were evaluated. In addition, persistent perfusion–metabolism mismatch (PM) was defined as mismatch score minus SDS of 3 or more during the mid-term postoperative period. The clinical parameters associated with PM were examined. RESULTS: From short- to mid-term postoperative period, the extent of infarcted myocardium (SRS) did not change significantly (7.8 ± 8.0 to 7.1 ± 7.0, P = 0.117). The extent of ischemic myocardium (SDS), the BMIPP score and the mismatch score, which reflects perfusion–metabolism mismatch, were significantly improved (2.0 ± 2.8 to 0.7 ± 1.0, P = 0.010; 12.2 ± 9.0 to 9.5 ± 7.9, P < 0.001; 4.4 ± 3.7 to 2.5 ± 2.6, P < 0.001; respectively). Remarkably, perfusion–metabolism mismatch persisted in 13 patients (34%) even in the mid-term postoperative period. eGFR and SYNTAX score were independent predictors of persistent perfusion–metabolic mismatch in multivariable analysis (OR = 0.951, 95% CI 0.898–0.985, P = 0.010 and OR = 1.126, 95% CI 1.011–1.254, P = 0.031, respectively). The mismatch score both in the short- and mid-term significantly correlated with SYNTAX score (r = 0.400 and r = 0.472, respectively). CONCLUSIONS: Fatty acid metabolism disturbance improved from short- to mid-term postoperative period in patients with successful reperfusion by coronary artery bypass grafting. However, in patients with severe atherosclerosis, impaired fatty acid metabolism was sustained until the mid-term postoperative period, even though ischemia had resolved. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s12149-021-01696-3. Springer Singapore 2021-11-25 2022 /pmc/articles/PMC8897360/ /pubmed/34822103 http://dx.doi.org/10.1007/s12149-021-01696-3 Text en © The Author(s) 2021, corrected publication 2021 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/) .
spellingShingle Original Article
Morishima, Motoko
Kiriyama, Tomonari
Miyagi, Yasuo
Otsuka, Toshiaki
Fukushima, Yoshimitsu
Kumita, Shin-ichiro
Ishii, Yosuke
Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title_full Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title_fullStr Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title_full_unstemmed Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title_short Serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
title_sort serial change in perfusion–metabolism mismatch after coronary artery bypass grafting
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8897360/
https://www.ncbi.nlm.nih.gov/pubmed/34822103
http://dx.doi.org/10.1007/s12149-021-01696-3
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