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Longitudinal change in cardiac structure and function following acute coronary syndrome according to culprit coronary artery lesion

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Abstract

Acute coronary syndrome (ACS) may lead to adverse remodelling and impaired cardiac function. Limited data exists on the effect of culprit coronary artery lesion site and impact on longitudinal cardiac remodelling. The present study included a total of 299 patients suffering from ACS treated with percutaneous coronary intervention (PCI). All patients had two echocardiographic examinations. The first echocardiography was median 2(IQR: 1;3) days following PCI, while the follow-up echocardiography (FUE) was median 257(IQR: 96;942) days following the first. Patients were grouped based on coronary artery PCI location; left anterior descending artery (LAD), right coronary artery (RCA) or circumflex artery (Cx). Patients with multiple lesions were excluded. Mean age was 63 ± 11 years and 77% were male. At FUE, mean left ventricular ejection fraction was 42 ± 9% and global longitudinal strain (GLS) was − 13 ± 4%. PCI treatment was allocated as 168 LAD lesions, 95 RCA lesions, and 36 Cx lesions. Linear regression analysis showed that patients with a LAD lesion displayed worsening in E/A (mean ∆ = 0.05, β = − 0.196, p = 0.001) and a larger increase in LVEDV (mean ∆ = 33.18 mL, β = 0.135, p = 0.012). Meanwhile patients with Cx lesion were significantly associated with a larger decrease in E/e′ (mean ∆ = 2.6, β = − 0.120, p = 0.028). Patients with Cx lesion were observed to have elevated E/e′ at baseline, which normalized at FUE. The present study suggests that culprit coronary artery lesion has a differential impact on myocardial remodelling. This information may potentially aid in understanding the pathophysiological differences in cardiac structure and function amongst patients with ACS.

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Funding

KR was funded by a research grant from the Novo Nordic Foundation. The sponsors had no role in the study concept, design, conduction, or interpretation of the data.

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Correspondence to Kirstine Ravnkilde.

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KR has nothing to disclose. TBS is a steering committee member of the Amgen financed GALACTIC-HF trial. TBS is a member of an advisory board in Sanofi Pasteur and Amgen and has received speaker honorarium from Sanofi Pasteur and Novartis.

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Ravnkilde, K., Skaarup, K.G., Grove, G.L. et al. Longitudinal change in cardiac structure and function following acute coronary syndrome according to culprit coronary artery lesion. Int J Cardiovasc Imaging 38, 1029–1036 (2022). https://doi.org/10.1007/s10554-021-02478-8

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  • DOI: https://doi.org/10.1007/s10554-021-02478-8

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