Impact of liver fibrosis score on prognosis in patients with previous myocardial infarction: A prospective cohort study

BACKGROUND & AIMS Liver fibrosis score (LFS) has been used for predicting the cardiovascular outcomes (CVOs) in diverse populations. However, the association of LFS with CVOs in patients with previous myocardial infarction (MI) remains undetermined. We aimed to examine the prognostic value of LF...

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Veröffentlicht in:Liver international 2021-06, Vol.41 (6), p.1294-1304
Hauptverfasser: Cao, Ye‐Xuan, Zhang, Meng, Zhang, Hui‐Wen, Jin, Jing‐Lu, Liu, Hui‐Hui, Zhang, Yan, Guo, Yuan‐Lin, Wu, Na‐Qiong, Zhu, Cheng‐Gang, Xu, Rui‐Xia, Gao, Ying, Dong, Qian, Sun, Jing, Li, Jian‐Jun
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container_end_page 1304
container_issue 6
container_start_page 1294
container_title Liver international
container_volume 41
creator Cao, Ye‐Xuan
Zhang, Meng
Zhang, Hui‐Wen
Jin, Jing‐Lu
Liu, Hui‐Hui
Zhang, Yan
Guo, Yuan‐Lin
Wu, Na‐Qiong
Zhu, Cheng‐Gang
Xu, Rui‐Xia
Gao, Ying
Dong, Qian
Sun, Jing
Li, Jian‐Jun
description BACKGROUND & AIMS Liver fibrosis score (LFS) has been used for predicting the cardiovascular outcomes (CVOs) in diverse populations. However, the association of LFS with CVOs in patients with previous myocardial infarction (MI) remains undetermined. We aimed to examine the prognostic value of LFS in patients with prior MI in a prospective cohort. METHODS A total of 3718 patients with previous MI were consecutively enrolled from March 2009 to January 2019. Five LFSs including the fibrosis‐4 (FIB‐4) score, non‐alcohol fatty liver disease fibrosis score (NFS), Forns score, HUI score and BARD score were used. The CVOs covered major adverse cardiac event (MACEs), cardiovascular mortality and all‐cause mortality. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence intervals (CIs). RESULTS During a mean follow‐up of 47.4 ± 24.8 months, 431 (11.6%) MACEs occurred. Kaplan‐Meier analysis demonstrated that higher LFSs resulted in a significantly higher probability of CVOs. Compared to the lowest score group, multivariable‐adjusted HRs (95% CIs) of the highest group of FIB‐4, NFS, Forns score, HUI score and BARD score were 1.75 (1.32‐2.33), 2.37 (1.70‐3.33), 2.44 (1.61‐3.73), 1.58 (1.16‐2.14) and 1.27 (1.03‐1.57) respectively. These LFSs were also independent predictors of cardiovascular mortality and all‐cause mortality. Similar results were observed across subgroups analysis. The addition of LFSs to a prediction model significantly increased the C‐statistic for CVOs. CONCLUSIONS The present study firstly demonstrated that LFS could be used as a risk stratification tool for predicting CVOs in patients with previous MI, which should be evaluated further.
doi_str_mv 10.1111/liv.14780
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However, the association of LFS with CVOs in patients with previous myocardial infarction (MI) remains undetermined. We aimed to examine the prognostic value of LFS in patients with prior MI in a prospective cohort. METHODS A total of 3718 patients with previous MI were consecutively enrolled from March 2009 to January 2019. Five LFSs including the fibrosis‐4 (FIB‐4) score, non‐alcohol fatty liver disease fibrosis score (NFS), Forns score, HUI score and BARD score were used. The CVOs covered major adverse cardiac event (MACEs), cardiovascular mortality and all‐cause mortality. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence intervals (CIs). RESULTS During a mean follow‐up of 47.4 ± 24.8 months, 431 (11.6%) MACEs occurred. Kaplan‐Meier analysis demonstrated that higher LFSs resulted in a significantly higher probability of CVOs. Compared to the lowest score group, multivariable‐adjusted HRs (95% CIs) of the highest group of FIB‐4, NFS, Forns score, HUI score and BARD score were 1.75 (1.32‐2.33), 2.37 (1.70‐3.33), 2.44 (1.61‐3.73), 1.58 (1.16‐2.14) and 1.27 (1.03‐1.57) respectively. These LFSs were also independent predictors of cardiovascular mortality and all‐cause mortality. Similar results were observed across subgroups analysis. The addition of LFSs to a prediction model significantly increased the C‐statistic for CVOs. CONCLUSIONS The present study firstly demonstrated that LFS could be used as a risk stratification tool for predicting CVOs in patients with previous MI, which should be evaluated further.</description><identifier>ISSN: 1478-3223</identifier><identifier>EISSN: 1478-3231</identifier><identifier>DOI: 10.1111/liv.14780</identifier><identifier>PMID: 33389804</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>all‐cause mortality ; Cardiovascular diseases ; cardiovascular mortality ; Cohort analysis ; Confidence intervals ; Fatty liver ; Fibrosis ; Health hazards ; Heart attacks ; Liver ; Liver diseases ; liver fibrosis score ; major adverse cardiac event ; Mortality ; Myocardial infarction ; Prediction models ; Statistical analysis ; Statistical models ; Subgroups</subject><ispartof>Liver international, 2021-06, Vol.41 (6), p.1294-1304</ispartof><rights>2021 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd</rights><rights>2021 John Wiley &amp; Sons A/S. Published by John Wiley &amp; Sons Ltd.</rights><rights>2021 John Wiley &amp; Sons A/S</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3530-a7660dbe9493b719453b38aeca3504f7d839a020b52ce08ad498f527ec859a0e3</citedby><cites>FETCH-LOGICAL-c3530-a7660dbe9493b719453b38aeca3504f7d839a020b52ce08ad498f527ec859a0e3</cites><orcidid>0000-0003-2536-4364</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fliv.14780$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fliv.14780$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33389804$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cao, Ye‐Xuan</creatorcontrib><creatorcontrib>Zhang, Meng</creatorcontrib><creatorcontrib>Zhang, Hui‐Wen</creatorcontrib><creatorcontrib>Jin, Jing‐Lu</creatorcontrib><creatorcontrib>Liu, Hui‐Hui</creatorcontrib><creatorcontrib>Zhang, Yan</creatorcontrib><creatorcontrib>Guo, Yuan‐Lin</creatorcontrib><creatorcontrib>Wu, Na‐Qiong</creatorcontrib><creatorcontrib>Zhu, Cheng‐Gang</creatorcontrib><creatorcontrib>Xu, Rui‐Xia</creatorcontrib><creatorcontrib>Gao, Ying</creatorcontrib><creatorcontrib>Dong, Qian</creatorcontrib><creatorcontrib>Sun, Jing</creatorcontrib><creatorcontrib>Li, Jian‐Jun</creatorcontrib><title>Impact of liver fibrosis score on prognosis in patients with previous myocardial infarction: A prospective cohort study</title><title>Liver international</title><addtitle>Liver Int</addtitle><description>BACKGROUND &amp; AIMS Liver fibrosis score (LFS) has been used for predicting the cardiovascular outcomes (CVOs) in diverse populations. However, the association of LFS with CVOs in patients with previous myocardial infarction (MI) remains undetermined. We aimed to examine the prognostic value of LFS in patients with prior MI in a prospective cohort. METHODS A total of 3718 patients with previous MI were consecutively enrolled from March 2009 to January 2019. Five LFSs including the fibrosis‐4 (FIB‐4) score, non‐alcohol fatty liver disease fibrosis score (NFS), Forns score, HUI score and BARD score were used. The CVOs covered major adverse cardiac event (MACEs), cardiovascular mortality and all‐cause mortality. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence intervals (CIs). RESULTS During a mean follow‐up of 47.4 ± 24.8 months, 431 (11.6%) MACEs occurred. Kaplan‐Meier analysis demonstrated that higher LFSs resulted in a significantly higher probability of CVOs. Compared to the lowest score group, multivariable‐adjusted HRs (95% CIs) of the highest group of FIB‐4, NFS, Forns score, HUI score and BARD score were 1.75 (1.32‐2.33), 2.37 (1.70‐3.33), 2.44 (1.61‐3.73), 1.58 (1.16‐2.14) and 1.27 (1.03‐1.57) respectively. These LFSs were also independent predictors of cardiovascular mortality and all‐cause mortality. Similar results were observed across subgroups analysis. The addition of LFSs to a prediction model significantly increased the C‐statistic for CVOs. 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AIMS Liver fibrosis score (LFS) has been used for predicting the cardiovascular outcomes (CVOs) in diverse populations. However, the association of LFS with CVOs in patients with previous myocardial infarction (MI) remains undetermined. We aimed to examine the prognostic value of LFS in patients with prior MI in a prospective cohort. METHODS A total of 3718 patients with previous MI were consecutively enrolled from March 2009 to January 2019. Five LFSs including the fibrosis‐4 (FIB‐4) score, non‐alcohol fatty liver disease fibrosis score (NFS), Forns score, HUI score and BARD score were used. The CVOs covered major adverse cardiac event (MACEs), cardiovascular mortality and all‐cause mortality. Cox proportional hazards model was used to calculate hazard ratios (HRs) with 95% confidence intervals (CIs). RESULTS During a mean follow‐up of 47.4 ± 24.8 months, 431 (11.6%) MACEs occurred. Kaplan‐Meier analysis demonstrated that higher LFSs resulted in a significantly higher probability of CVOs. Compared to the lowest score group, multivariable‐adjusted HRs (95% CIs) of the highest group of FIB‐4, NFS, Forns score, HUI score and BARD score were 1.75 (1.32‐2.33), 2.37 (1.70‐3.33), 2.44 (1.61‐3.73), 1.58 (1.16‐2.14) and 1.27 (1.03‐1.57) respectively. These LFSs were also independent predictors of cardiovascular mortality and all‐cause mortality. Similar results were observed across subgroups analysis. The addition of LFSs to a prediction model significantly increased the C‐statistic for CVOs. CONCLUSIONS The present study firstly demonstrated that LFS could be used as a risk stratification tool for predicting CVOs in patients with previous MI, which should be evaluated further.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>33389804</pmid><doi>10.1111/liv.14780</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2536-4364</orcidid></addata></record>
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subjects all‐cause mortality
Cardiovascular diseases
cardiovascular mortality
Cohort analysis
Confidence intervals
Fatty liver
Fibrosis
Health hazards
Heart attacks
Liver
Liver diseases
liver fibrosis score
major adverse cardiac event
Mortality
Myocardial infarction
Prediction models
Statistical analysis
Statistical models
Subgroups
title Impact of liver fibrosis score on prognosis in patients with previous myocardial infarction: A prospective cohort study
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