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Article: Association between the liver fat score (LFS) and cardiovascular diseases in the national health and nutrition examination survey 1999–2016
Title | Association between the liver fat score (LFS) and cardiovascular diseases in the national health and nutrition examination survey 1999–2016 |
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Authors | |
Keywords | Cardiovascular disease prevention Metabolic syndrome Non-alcoholic fatty liver disease score Liver fat score |
Issue Date | 2021 |
Publisher | Taylor & Francis. The Journal's web site is located at https://www.tandfonline.com/journals/iann20 |
Citation | Annals of Medicine, 2021, v. 53 n. 1, p. 1067-1075 How to Cite? |
Abstract | Background:
The liver fat score (LFS) has been proposed to be a simple non-invasive marker of non-alcoholic fatty liver disease (NAFLD), which is highly prevalent in the general population. We tested its association with cardiovascular diseases (CVDs) and prognosis.
Methods:
17,244 adult participants from the National Health and Nutrition Examination Survey 1999–2016 were included. LFS is calculated from variables including serum aspartate transaminase/alanine transaminase (AST/ALT) ratio, fasting serum aspartate transaminase (AST) level, fasting serum insulin level, presence of metabolic syndrome and diabetes mellitus. In cross-sectional analysis, logistic regression was used to examine the association of the LFS with coronary heart disease (CHD), myocardial infarction (MI), congestive heart failure (CHF), stroke and angina pectoris. Mortality during follow-up was analysed using Cox proportional hazard regression.
Results:
LFS was associated with CHD (adjusted odds ratio [OR]: 1.09 per standard deviation [SD], 95% confidence interval [95% CI]: 1.03–1.15) (p = .003), CHF (1.11, 1.04–1.18) (p = .003) and angina pectoris (1.08, 1.02–1.13) (p = .005). LFS was not associated with MI or stroke, but was associated with increased all-cause and cardiovascular mortality with hazard ratios (HRs) of 1.10 (95% CI: 1.07–1.13) (p < .001) and 1.12 (95% CI: 1.06–1.17) (p < .001), respectively.
Conclusions:
NAFLD is usually asymptomatic, but this large study of a large general population shows that LFS is associated with CHD, CHF, angina pectoris, cardiovascular and all-cause mortality. Determining the LFS is worthwhile, as it identifies people with NAFLD, who may also be at increased cardiovascular risk. |
Persistent Identifier | http://hdl.handle.net/10722/304690 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.306 |
PubMed Central ID | |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Lee, CO | - |
dc.contributor.author | Li, HL | - |
dc.contributor.author | Tsoi, MF | - |
dc.contributor.author | Cheung, CL | - |
dc.contributor.author | Cheung, BMY | - |
dc.date.accessioned | 2021-10-05T02:33:45Z | - |
dc.date.available | 2021-10-05T02:33:45Z | - |
dc.date.issued | 2021 | - |
dc.identifier.citation | Annals of Medicine, 2021, v. 53 n. 1, p. 1067-1075 | - |
dc.identifier.issn | 0785-3890 | - |
dc.identifier.uri | http://hdl.handle.net/10722/304690 | - |
dc.description.abstract | Background: The liver fat score (LFS) has been proposed to be a simple non-invasive marker of non-alcoholic fatty liver disease (NAFLD), which is highly prevalent in the general population. We tested its association with cardiovascular diseases (CVDs) and prognosis. Methods: 17,244 adult participants from the National Health and Nutrition Examination Survey 1999–2016 were included. LFS is calculated from variables including serum aspartate transaminase/alanine transaminase (AST/ALT) ratio, fasting serum aspartate transaminase (AST) level, fasting serum insulin level, presence of metabolic syndrome and diabetes mellitus. In cross-sectional analysis, logistic regression was used to examine the association of the LFS with coronary heart disease (CHD), myocardial infarction (MI), congestive heart failure (CHF), stroke and angina pectoris. Mortality during follow-up was analysed using Cox proportional hazard regression. Results: LFS was associated with CHD (adjusted odds ratio [OR]: 1.09 per standard deviation [SD], 95% confidence interval [95% CI]: 1.03–1.15) (p = .003), CHF (1.11, 1.04–1.18) (p = .003) and angina pectoris (1.08, 1.02–1.13) (p = .005). LFS was not associated with MI or stroke, but was associated with increased all-cause and cardiovascular mortality with hazard ratios (HRs) of 1.10 (95% CI: 1.07–1.13) (p < .001) and 1.12 (95% CI: 1.06–1.17) (p < .001), respectively. Conclusions: NAFLD is usually asymptomatic, but this large study of a large general population shows that LFS is associated with CHD, CHF, angina pectoris, cardiovascular and all-cause mortality. Determining the LFS is worthwhile, as it identifies people with NAFLD, who may also be at increased cardiovascular risk. | - |
dc.language | eng | - |
dc.publisher | Taylor & Francis. The Journal's web site is located at https://www.tandfonline.com/journals/iann20 | - |
dc.relation.ispartof | Annals of Medicine | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | Cardiovascular disease prevention | - |
dc.subject | Metabolic syndrome | - |
dc.subject | Non-alcoholic fatty liver disease score | - |
dc.subject | Liver fat score | - |
dc.title | Association between the liver fat score (LFS) and cardiovascular diseases in the national health and nutrition examination survey 1999–2016 | - |
dc.type | Article | - |
dc.identifier.email | Cheung, CL: lung1212@hku.hk | - |
dc.identifier.email | Cheung, BMY: mycheung@hkucc.hku.hk | - |
dc.identifier.authority | Cheung, CL=rp01749 | - |
dc.identifier.authority | Cheung, BMY=rp01321 | - |
dc.description.nature | published_or_final_version | - |
dc.identifier.doi | 10.1080/07853890.2021.1943514 | - |
dc.identifier.pmid | 34184611 | - |
dc.identifier.pmcid | PMC8245099 | - |
dc.identifier.scopus | eid_2-s2.0-85109164627 | - |
dc.identifier.hkuros | 326192 | - |
dc.identifier.volume | 53 | - |
dc.identifier.issue | 1 | - |
dc.identifier.spage | 1067 | - |
dc.identifier.epage | 1075 | - |
dc.identifier.isi | WOS:000667962000001 | - |
dc.publisher.place | Sweden | - |