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Liver fibrosis and the risk of coronary artery disease, stent thrombosis, restenosis, and adverse clinical outcomes

Liver fibrosis and the risk of coronary artery disease, stent thrombosis, restenosis, and adverse clinical outcomes
Liver fibrosis and the risk of coronary artery disease, stent thrombosis, restenosis, and adverse clinical outcomes
Background and aims: liver fibrosis may be associated with coronary artery disease (CAD) and adverse cardiovascular outcomes, but data remain limited. This study aimed to explore the relationship between liver fibrosis and the incidence of CAD, stent thrombosis (ST), in-stent restenosis (ISR) and long-term clinical outcomes.

Methods: two cohorts were analysed: the UK Biobank (UKB) cohort examined liver fibrosis and CAD incidence and clinical outcomes in the general population, while the Wenzhou cohort assessed its relationship with ST and ISR and long-term outcomes in post-PCI patients. CAD incidence was defined as coronary stenosis ≥ 50% or clinical events, such as myocardial ischaemia, myocardial infarction and acute coronary syndrome. ST was confirmed via angiography, and ISR was defined as ≥ 50% stenosis within the stent. Major adverse cardiovascular events (MACE) included all-cause mortality, myocardial infarction, heart failure and stroke. Liver fibrosis was assessed using FIB-4, categorised as ≤ 1.3, 1.3–2.67 and > 2.67.

Results: 394,625 participants were included. In the UKB cohort (n = 380,638), 7102 (1.9%) had FIB-4 > 2.67. Over 14.4 years, FIB-4 > 2.67 was associated with higher CAD incidence (aHR = 1.41, p < 0.001) and MACE (aHR = 1.69, p < 0.001). In the Wenzhou cohort (n = 13,987), 3173 (22.7%) had FIB-4 > 2.67. Over 3.0 years, FIB-4 > 2.67 was associated with increased risks of ST and ISR (aHR = 1.34, p = 0.001) and MACE (aHR = 1.97, p < 0.001).

Conclusions: liver fibrosis is common among patients with CAD and is associated with CAD incidence, stent thrombosis, restenosis and long-term cardiovascular risk.
0269-2813
Tian, Na
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Xiao, Tie
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Xia, Tianyi
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Yuan, Hai-Yang
ea825b9a-c01a-40a5-a658-8684c4c480ef
Shapiro, Michael D.
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Lip, Gregory Y.H.
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Fanren, Cheng-Han
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Lian, Li-You
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Huang, Chen-Xiao
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Wei, Yi-Xuan
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Targher, Giovanni
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Byrne, Christopher D.
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Hong, Cheng-Lv
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Ju, Shenghong
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Zheng, Ming-Hua
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Tian, Na
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Xiao, Tie
792b58a0-0ecb-42f1-9d97-28b90532a34f
Xia, Tianyi
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Yuan, Hai-Yang
ea825b9a-c01a-40a5-a658-8684c4c480ef
Shapiro, Michael D.
5968c14d-00e7-482d-b041-3c75a32d26c1
Lip, Gregory Y.H.
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Fanren, Cheng-Han
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Lian, Li-You
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Huang, Chen-Xiao
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Wei, Yi-Xuan
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Targher, Giovanni
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Byrne, Christopher D.
1370b997-cead-4229-83a7-53301ed2a43c
Hong, Cheng-Lv
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Ju, Shenghong
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Zheng, Ming-Hua
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Tian, Na, Xiao, Tie, Xia, Tianyi, Yuan, Hai-Yang, Shapiro, Michael D., Lip, Gregory Y.H., Fanren, Cheng-Han, Lian, Li-You, Huang, Chen-Xiao, Wei, Yi-Xuan, Targher, Giovanni, Byrne, Christopher D., Hong, Cheng-Lv, Ju, Shenghong and Zheng, Ming-Hua (2025) Liver fibrosis and the risk of coronary artery disease, stent thrombosis, restenosis, and adverse clinical outcomes. Alimentary pharmacology & therapeutics. (doi:10.1111/apt.70306).

Record type: Article

Abstract

Background and aims: liver fibrosis may be associated with coronary artery disease (CAD) and adverse cardiovascular outcomes, but data remain limited. This study aimed to explore the relationship between liver fibrosis and the incidence of CAD, stent thrombosis (ST), in-stent restenosis (ISR) and long-term clinical outcomes.

Methods: two cohorts were analysed: the UK Biobank (UKB) cohort examined liver fibrosis and CAD incidence and clinical outcomes in the general population, while the Wenzhou cohort assessed its relationship with ST and ISR and long-term outcomes in post-PCI patients. CAD incidence was defined as coronary stenosis ≥ 50% or clinical events, such as myocardial ischaemia, myocardial infarction and acute coronary syndrome. ST was confirmed via angiography, and ISR was defined as ≥ 50% stenosis within the stent. Major adverse cardiovascular events (MACE) included all-cause mortality, myocardial infarction, heart failure and stroke. Liver fibrosis was assessed using FIB-4, categorised as ≤ 1.3, 1.3–2.67 and > 2.67.

Results: 394,625 participants were included. In the UKB cohort (n = 380,638), 7102 (1.9%) had FIB-4 > 2.67. Over 14.4 years, FIB-4 > 2.67 was associated with higher CAD incidence (aHR = 1.41, p < 0.001) and MACE (aHR = 1.69, p < 0.001). In the Wenzhou cohort (n = 13,987), 3173 (22.7%) had FIB-4 > 2.67. Over 3.0 years, FIB-4 > 2.67 was associated with increased risks of ST and ISR (aHR = 1.34, p = 0.001) and MACE (aHR = 1.97, p < 0.001).

Conclusions: liver fibrosis is common among patients with CAD and is associated with CAD incidence, stent thrombosis, restenosis and long-term cardiovascular risk.

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More information

Accepted/In Press date: 19 July 2025
e-pub ahead of print date: 31 July 2025

Identifiers

Local EPrints ID: 504991
URI: http://eprints.soton.ac.uk/id/eprint/504991
ISSN: 0269-2813
PURE UUID: a072f8fd-075d-4ca2-b8ce-06f644b1d05e
ORCID for Christopher D. Byrne: ORCID iD orcid.org/0000-0001-6322-7753

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Date deposited: 23 Sep 2025 17:06
Last modified: 24 Sep 2025 01:37

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Contributors

Author: Na Tian
Author: Tie Xiao
Author: Tianyi Xia
Author: Hai-Yang Yuan
Author: Michael D. Shapiro
Author: Gregory Y.H. Lip
Author: Cheng-Han Fanren
Author: Li-You Lian
Author: Chen-Xiao Huang
Author: Yi-Xuan Wei
Author: Giovanni Targher
Author: Cheng-Lv Hong
Author: Shenghong Ju
Author: Ming-Hua Zheng

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