Association of coronary artery calcification with liver fibrosis in Japanese patients with non-alcoholic fatty liver disease
Aims Cardiovascular events are the leading cause of death among patients with non‐alcoholic fatty liver disease (NAFLD), but their relationship remains unclear. This study examined the association between coronary atherosclerosis and liver fibrosis, represented by the coronary artery calcification (...
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          | Published in | Hepatology research Vol. 46; no. 11; pp. 1107 - 1117 | 
|---|---|
| Main Authors | , , , , , , , , , , , , , , , , , , | 
| Format | Journal Article | 
| Language | English | 
| Published | 
        Netherlands
          Blackwell Publishing Ltd
    
        01.10.2016
     | 
| Subjects | |
| Online Access | Get full text | 
| ISSN | 1386-6346 1872-034X  | 
| DOI | 10.1111/hepr.12665 | 
Cover
| Abstract | Aims
Cardiovascular events are the leading cause of death among patients with non‐alcoholic fatty liver disease (NAFLD), but their relationship remains unclear. This study examined the association between coronary atherosclerosis and liver fibrosis, represented by the coronary artery calcification (CAC) score and non‐invasive fibrosis markers, respectively.
Methods
Among 698 patients with chest pain or electrocardiographic abnormalities who underwent coronary computed tomography (CT) between April 2006 and March 2010, those with known liver disorders or history of emergency coronary angioplasty were excluded, leaving 366 patients for this study. Diagnosis of NAFLD was based on abdominal CT and history of alcohol consumption. Subjects with CAC of 100 AU or more were categorized into the high‐risk group for cardiovascular events. Patient records were examined for clinical parameters including CAC score and non‐invasive fibrosis marker FIB‐4 index.
Results
Ninety‐four patients (25.7%) had NAFLD. In this group, univariate analysis identified old age, high diastolic blood pressure, high liver to spleen ratio and high FIB‐4 index as risk factors for cardiovascular events and multivariate analysis identified age of 66 years or older and FIB‐4 index of 2.09 or more as the significant risk factors. For the observation period until August 2014, the cumulative proportion of PCI performance was significantly higher in patients with FIB‐4 of 2.09 or more than those with FIB‐4 of less than 2.09.
Conclusion
The progression of arteriosclerosis and that of liver fibrosis may be associated in NAFLD patients. The FIB‐4 index can be easily determined and thus can be a useful marker for predicting cardiovascular events in NAFLD patients. | 
    
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| AbstractList | Aims
Cardiovascular events are the leading cause of death among patients with non‐alcoholic fatty liver disease (NAFLD), but their relationship remains unclear. This study examined the association between coronary atherosclerosis and liver fibrosis, represented by the coronary artery calcification (CAC) score and non‐invasive fibrosis markers, respectively.
Methods
Among 698 patients with chest pain or electrocardiographic abnormalities who underwent coronary computed tomography (CT) between April 2006 and March 2010, those with known liver disorders or history of emergency coronary angioplasty were excluded, leaving 366 patients for this study. Diagnosis of NAFLD was based on abdominal CT and history of alcohol consumption. Subjects with CAC of 100 AU or more were categorized into the high‐risk group for cardiovascular events. Patient records were examined for clinical parameters including CAC score and non‐invasive fibrosis marker FIB‐4 index.
Results
Ninety‐four patients (25.7%) had NAFLD. In this group, univariate analysis identified old age, high diastolic blood pressure, high liver to spleen ratio and high FIB‐4 index as risk factors for cardiovascular events and multivariate analysis identified age of 66 years or older and FIB‐4 index of 2.09 or more as the significant risk factors. For the observation period until August 2014, the cumulative proportion of PCI performance was significantly higher in patients with FIB‐4 of 2.09 or more than those with FIB‐4 of less than 2.09.
Conclusion
The progression of arteriosclerosis and that of liver fibrosis may be associated in NAFLD patients. The FIB‐4 index can be easily determined and thus can be a useful marker for predicting cardiovascular events in NAFLD patients. AIMSCardiovascular events are the leading cause of death among patients with non-alcoholic fatty liver disease (NAFLD), but their relationship remains unclear. This study examined the association between coronary atherosclerosis and liver fibrosis, represented by the coronary artery calcification (CAC) score and non-invasive fibrosis markers, respectively.METHODSAmong 698 patients with chest pain or electrocardiographic abnormalities who underwent coronary computed tomography (CT) between April 2006 and March 2010, those with known liver disorders or history of emergency coronary angioplasty were excluded, leaving 366 patients for this study. Diagnosis of NAFLD was based on abdominal CT and history of alcohol consumption. Subjects with CAC of 100 AU or more were categorized into the high-risk group for cardiovascular events. Patient records were examined for clinical parameters including CAC score and non-invasive fibrosis marker FIB-4 index.RESULTSNinety-four patients (25.7%) had NAFLD. In this group, univariate analysis identified old age, high diastolic blood pressure, high liver to spleen ratio and high FIB-4 index as risk factors for cardiovascular events and multivariate analysis identified age of 66 years or older and FIB-4 index of 2.09 or more as the significant risk factors. For the observation period until August 2014, the cumulative proportion of PCI performance was significantly higher in patients with FIB-4 of 2.09 or more than those with FIB-4 of less than 2.09.CONCLUSIONThe progression of arteriosclerosis and that of liver fibrosis may be associated in NAFLD patients. The FIB-4 index can be easily determined and thus can be a useful marker for predicting cardiovascular events in NAFLD patients. Cardiovascular events are the leading cause of death among patients with non-alcoholic fatty liver disease (NAFLD), but their relationship remains unclear. This study examined the association between coronary atherosclerosis and liver fibrosis, represented by the coronary artery calcification (CAC) score and non-invasive fibrosis markers, respectively. Among 698 patients with chest pain or electrocardiographic abnormalities who underwent coronary computed tomography (CT) between April 2006 and March 2010, those with known liver disorders or history of emergency coronary angioplasty were excluded, leaving 366 patients for this study. Diagnosis of NAFLD was based on abdominal CT and history of alcohol consumption. Subjects with CAC of 100 AU or more were categorized into the high-risk group for cardiovascular events. Patient records were examined for clinical parameters including CAC score and non-invasive fibrosis marker FIB-4 index. Ninety-four patients (25.7%) had NAFLD. In this group, univariate analysis identified old age, high diastolic blood pressure, high liver to spleen ratio and high FIB-4 index as risk factors for cardiovascular events and multivariate analysis identified age of 66 years or older and FIB-4 index of 2.09 or more as the significant risk factors. For the observation period until August 2014, the cumulative proportion of PCI performance was significantly higher in patients with FIB-4 of 2.09 or more than those with FIB-4 of less than 2.09. The progression of arteriosclerosis and that of liver fibrosis may be associated in NAFLD patients. The FIB-4 index can be easily determined and thus can be a useful marker for predicting cardiovascular events in NAFLD patients.  | 
    
| Author | Arai, Masahiro Taketani, Hiroyoshi Ishiba, Hiroshi Sumida, Yoshio Tanaka, Muhei Hara, Tasuku Akabame, Satoshi Seko, Yuya Moriguchi, Michihisa Yasui, Kohichiroh Yamaguchi, Kanji Mitsuyoshi, Hironori Nishikawa, Taichiro Kataoka, Seita Kuroda, Masaaki Tomiyasu, Kiichiro Umemura, Atsushi Okajima, Akira Itoh, Yoshito  | 
    
| Author_xml | – sequence: 1 givenname: Hiroshi surname: Ishiba fullname: Ishiba, Hiroshi organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 2 givenname: Yoshio surname: Sumida fullname: Sumida, Yoshio email: sumida@koto.kpu-m.ac.jp, sumida@koto.kpu-m.ac.jp organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 3 givenname: Seita surname: Kataoka fullname: Kataoka, Seita organization: Department of Gastroenterology, Kyoto Yamashiro General Medical Center – sequence: 4 givenname: Masaaki surname: Kuroda fullname: Kuroda, Masaaki organization: Department of Gastroenterology, Kyoto Yamashiro General Medical Center – sequence: 5 givenname: Satoshi surname: Akabame fullname: Akabame, Satoshi organization: Department of Cardiology, Kyoto Yamashiro General Medical Center – sequence: 6 givenname: Kiichiro surname: Tomiyasu fullname: Tomiyasu, Kiichiro organization: Department of Cardiology, Kyoto Yamashiro General Medical Center – sequence: 7 givenname: Muhei surname: Tanaka fullname: Tanaka, Muhei organization: Department of Endocrinology and Metabolism, Kyoto Prefectural University of Medicine, Kyoto, Japan – sequence: 8 givenname: Masahiro surname: Arai fullname: Arai, Masahiro organization: Department of Gastroenterology, Kyoto Yamashiro General Medical Center – sequence: 9 givenname: Hiroyoshi surname: Taketani fullname: Taketani, Hiroyoshi organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 10 givenname: Yuya surname: Seko fullname: Seko, Yuya organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 11 givenname: Akira surname: Okajima fullname: Okajima, Akira organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 12 givenname: Tasuku surname: Hara fullname: Hara, Tasuku organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 13 givenname: Atsushi surname: Umemura fullname: Umemura, Atsushi organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 14 givenname: Taichiro surname: Nishikawa fullname: Nishikawa, Taichiro organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 15 givenname: Kanji surname: Yamaguchi fullname: Yamaguchi, Kanji organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 16 givenname: Michihisa surname: Moriguchi fullname: Moriguchi, Michihisa organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 17 givenname: Hironori surname: Mitsuyoshi fullname: Mitsuyoshi, Hironori organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 18 givenname: Kohichiroh surname: Yasui fullname: Yasui, Kohichiroh organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine – sequence: 19 givenname: Yoshito surname: Itoh fullname: Itoh, Yoshito organization: Departments of Gastroenterology and Hepatology, Kyoto Prefectural University of Medicine  | 
    
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| Keywords | coronary artery disease liver fibrosis non-alcoholic fatty liver disease coronary artery calcification FIB-4 index  | 
    
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Expert Rev Gastroenterol Hepatol 2015; 9: 629-50. 2010; 56 1985; 28 2004; 40 2012; 2012 2012 1990; 15 2013; 88 2013; 43 2010; 17 2013; 62 2013; 61 2015; 30 2008; 19 2010; 363 2006; 130 2005; 42 2003; 38 2008; 57 2007; 191 2007; 30 2012; 35 2015; 9 2012; 56 2012; 12 2006; 114 2012; 308 2014; 20 2013; 19 2015; 45 2015; 27 1987; 40 2013; 57 2006; 43 2015; 61 2007; 132 2008; 29 2004; 78 2008; 28 2009; 7 1999; 74 2011; 25 1999; 94 1999; 116 2007; 27 2007; 49 e_1_2_6_32_1 e_1_2_6_30_1 e_1_2_6_19_1 e_1_2_6_13_1 e_1_2_6_36_1 e_1_2_6_11_1 e_1_2_6_34_1 e_1_2_6_17_1 e_1_2_6_15_1 e_1_2_6_38_1 e_1_2_6_43_1 e_1_2_6_20_1 e_1_2_6_41_1 Japan Atherosclerosis Society (JAS) (e_1_2_6_21_1) 2012 e_1_2_6_9_1 e_1_2_6_5_1 Ishiba H (e_1_2_6_46_1) e_1_2_6_7_1 e_1_2_6_24_1 e_1_2_6_49_1 e_1_2_6_3_1 e_1_2_6_22_1 e_1_2_6_28_1 e_1_2_6_45_1 e_1_2_6_26_1 e_1_2_6_47_1 e_1_2_6_10_1 e_1_2_6_31_1 e_1_2_6_50_1 e_1_2_6_14_1 e_1_2_6_35_1 e_1_2_6_12_1 e_1_2_6_33_1 e_1_2_6_18_1 e_1_2_6_39_1 e_1_2_6_16_1 e_1_2_6_37_1 e_1_2_6_42_1 e_1_2_6_40_1 e_1_2_6_8_1 e_1_2_6_4_1 e_1_2_6_6_1 e_1_2_6_25_1 e_1_2_6_48_1 e_1_2_6_23_1 e_1_2_6_2_1 e_1_2_6_29_1 e_1_2_6_44_1 e_1_2_6_27_1  | 
    
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| Snippet | Aims
Cardiovascular events are the leading cause of death among patients with non‐alcoholic fatty liver disease (NAFLD), but their relationship remains... Cardiovascular events are the leading cause of death among patients with non-alcoholic fatty liver disease (NAFLD), but their relationship remains unclear.... AIMSCardiovascular events are the leading cause of death among patients with non-alcoholic fatty liver disease (NAFLD), but their relationship remains unclear....  | 
    
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| SubjectTerms | coronary artery calcification coronary artery disease FIB-4 index liver fibrosis non-alcoholic fatty liver disease  | 
    
| Title | Association of coronary artery calcification with liver fibrosis in Japanese patients with non-alcoholic fatty liver disease | 
    
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