Association of insulin resistance indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome

To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. This cross-...

Full description

Saved in:
Bibliographic Details
Published inBMC gastroenterology Vol. 24; no. 1; pp. 26 - 13
Main Authors Kuo, Tzu-chia, Lu, Yang-bor, Yang, Chieh-lun, Wang, Bin, Chen, Lin-xin, Su, Ching-ping
Format Journal Article
LanguageEnglish
Published England BioMed Central Ltd 09.01.2024
BioMed Central
BMC
Subjects
Online AccessGet full text

Cover

Loading…
Abstract To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC). A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients. HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
AbstractList Abstract Background To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. Methods This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017–2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC). Results A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668–0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656–0.730), TyG (AUC = 0.627, 95%CI: 0.587–0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648–0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients. Conclusion HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC). A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients. HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC). A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients. HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
BackgroundTo investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS.MethodsThis cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017–2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC).ResultsA total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668–0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656–0.730), TyG (AUC = 0.627, 95%CI: 0.587–0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648–0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients.ConclusionHOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
Background To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS. Methods This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC). Results A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients. Conclusion HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis. Keywords: TyG-WHtR, Hepatic steatosis, Hepatic fibrosis, Metabolic syndrome, NHANES
To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS.BACKGROUNDTo investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as well as to compare the diagnostic value of these indicators in identifying hepatic steatosis and fibrosis in individuals with MetS.This cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC).METHODSThis cross-sectional study used the data from the National Health and Nutrition Examination Survey 2017-2018. IR indicators included homeostasis model assessment of IR (HOMA-IR), triglyceride/glucose (TyG) index, triglyceride glucose-waist-to-height ratio (TyG-WHtR), and metabolic score for IR (METS-IR). The main endpoints of this study were hepatic steatosis and hepatic fibrosis. Weighted univariate and multivariate logistic regression models were employed to evaluate the association between four IR indicators and both hepatic steatosis, hepatic fibrosis. The efficacy of various IR indicators in the detection of hepatic steatosis and hepatic fibrosis were assessed using receiver operating characteristics curve (ROC).A total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients.RESULTSA total of 876 participants with MetS were enrolled. Among the participants, hepatic steatosis was observed in 587 MetS individuals, while hepatic fibrosis was identified in 151 MetS individuals. In multivariate logistic regression model, HOMA-IR, TyG, TyG-WHtR, and METS-IR were related to the increased odd of hepatic steatosis. Additionally, HOMA-IR, TyG-WHtR, and METS-IR were associated with increased odd of hepatic fibrosis. According to the ROC analysis, the area under the curve (AUC) of the TyG-WHtR (AUC = 0.705, 95%CI: 0.668-0.743) was higher than HOMA-IR (AUC = 0.693, 95%CI: 0.656-0.730), TyG (AUC = 0.627, 95%CI: 0.587-0.666), and METS-IR (AUC = 0.685, 95%CI: 0.648-0.722) for identifying hepatic steatosis of MetS patients. Likewise, TyG-WHtR was also higher than HOMA-IR, TyG, and METS-IR for identifying hepatic fibrosis of MetS patients.HOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.CONCLUSIONHOMA-IR, TyG-WHtR, and METS-IR may be associated with the risk of hepatic steatosis and fibrosis among the U.S. adult population with MetS. In addition, TyG-WHtR may have a good predictive value for hepatic steatosis and hepatic fibrosis.
ArticleNumber 26
Audience Academic
Author Kuo, Tzu-chia
Su, Ching-ping
Yang, Chieh-lun
Lu, Yang-bor
Chen, Lin-xin
Wang, Bin
Author_xml – sequence: 1
  givenname: Tzu-chia
  surname: Kuo
  fullname: Kuo, Tzu-chia
– sequence: 2
  givenname: Yang-bor
  surname: Lu
  fullname: Lu, Yang-bor
– sequence: 3
  givenname: Chieh-lun
  surname: Yang
  fullname: Yang, Chieh-lun
– sequence: 4
  givenname: Bin
  surname: Wang
  fullname: Wang, Bin
– sequence: 5
  givenname: Lin-xin
  surname: Chen
  fullname: Chen, Lin-xin
– sequence: 6
  givenname: Ching-ping
  surname: Su
  fullname: Su, Ching-ping
BackLink https://www.ncbi.nlm.nih.gov/pubmed/38195414$$D View this record in MEDLINE/PubMed
BookMark eNp9kktv1DAUhSNURB_wB1igSGzYpPiR2M4KjSqglSqxAYmd5fgx41FiD7anqP-em5lp6VQIZeHk-jsnOvY5r05CDLaq3mJ0ibFgHzMmgrMGEdogivquYS-qM9xy3BCKfp48eT-tznNeI4S5IPRVdUoF7rsWt2dVWeQctVfFx1BHV_uQt6MPdbLZ56KCtjAyXqsSU65_-7KqV3YDuK5zsTAFrFbB1M4PafcB4nnfhnLgJ1vUEMdZcR9MipN9Xb10asz2zWG9qH58-fz96rq5_fb15mpx2-iOtaXRjAyCt5oj4zQ1rjXEaaad6hXtnYN0ne45Zb1QjBplLMgw7dlgOtdrSHpR3ex9TVRruUl-UuleRuXlbhDTUqoEUUYrW4uHQQhF0GDbwXaCu04wp4ehRS1DHLw-7b0222GyRkO-pMYj0-Od4FdyGe8kRpx3Hcfg8OHgkOKvrc1FTj5rO44q2LjNkvSYIkEYEYC-f4au4zYFOKuZaolAiOG_1FJBAh9chB_r2VQuOO8RwRTPh3D5DwoeYyevoVHOw_xI8O5p0seID6UBQOwBDTeek3VS-7JrEDj7ERLLuZ9y308J_ZS7fkoGUvJM-uD-H9Efw8LpmQ
CitedBy_id crossref_primary_10_1016_j_diabres_2024_111911
crossref_primary_10_1186_s12933_025_02651_6
crossref_primary_10_3389_fendo_2025_1514093
crossref_primary_10_1111_jdi_14352
crossref_primary_10_3390_diagnostics15050565
crossref_primary_10_3390_ijerph21101298
Cites_doi 10.1016/j.cgh.2020.06.048
10.1016/S0140-6736(20)32511-3
10.1155/2019/5121574
10.1097/HJH.0000000000002920
10.1089/met.2020.0092
10.47391/JPMA.22-63
10.1055/a-1341-9710
10.1155/2020/3920196
10.1016/j.dsx.2022.102581
10.1111/jgh.14595
10.1152/ajpendo.00645.2007
10.1530/EJE-17-0883
10.3390/nu14153039
10.3389/fendo.2022.951689
10.1016/j.chemosphere.2021.132953
10.1016/j.ejim.2017.03.006
10.3389/fendo.2022.851338
10.1016/j.chest.2021.03.056
10.3748/wjg.v22.i45.9880
10.1186/s12944-020-01393-6
10.3803/EnM.2022.1434
10.1007/s12020-021-02815-w
10.2174/1381612819666131206111352
10.2337/dc20-1778
10.2174/1570161114666161007164510
10.3748/wjg.v23.i47.8263
ContentType Journal Article
Copyright 2024. The Author(s).
COPYRIGHT 2024 BioMed Central Ltd.
2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
The Author(s) 2024
Copyright_xml – notice: 2024. The Author(s).
– notice: COPYRIGHT 2024 BioMed Central Ltd.
– notice: 2024. This work is licensed under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: The Author(s) 2024
DBID AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
3V.
7QP
7QR
7T5
7X7
7XB
88E
8FD
8FI
8FJ
8FK
ABUWG
AFKRA
AZQEC
BENPR
CCPQU
DWQXO
FR3
FYUFA
GHDGH
H94
K9.
M0S
M1P
P64
PHGZM
PHGZT
PIMPY
PJZUB
PKEHL
PPXIY
PQEST
PQQKQ
PQUKI
PRINS
7X8
5PM
DOA
DOI 10.1186/s12876-023-03095-6
DatabaseName CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
ProQuest Central (Corporate)
Calcium & Calcified Tissue Abstracts
Chemoreception Abstracts
Immunology Abstracts
Health & Medical Collection
ProQuest Central (purchase pre-March 2016)
Medical Database (Alumni Edition)
Technology Research Database
Hospital Premium Collection
Hospital Premium Collection (Alumni Edition)
ProQuest Central (Alumni) (purchase pre-March 2016)
ProQuest Central (Alumni)
ProQuest Central UK/Ireland
ProQuest Central Essentials
ProQuest Central
ProQuest One
ProQuest Central Korea
Engineering Research Database
Proquest Health Research Premium Collection
Health Research Premium Collection (Alumni)
AIDS and Cancer Research Abstracts
ProQuest Health & Medical Complete (Alumni)
ProQuest Health & Medical Collection
Medical Database
Biotechnology and BioEngineering Abstracts
ProQuest Central Premium
ProQuest One Academic (New)
Publicly Available Content Database
ProQuest Health & Medical Research Collection
ProQuest One Academic Middle East (New)
ProQuest One Health & Nursing
ProQuest One Academic Eastern Edition (DO NOT USE)
ProQuest One Academic
ProQuest One Academic UKI Edition
ProQuest Central China
MEDLINE - Academic
PubMed Central (Full Participant titles)
DOAJ Directory of Open Access Journals
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
Publicly Available Content Database
Technology Research Database
ProQuest One Academic Middle East (New)
ProQuest Central Essentials
ProQuest Health & Medical Complete (Alumni)
ProQuest Central (Alumni Edition)
ProQuest One Community College
ProQuest One Health & Nursing
ProQuest Central China
ProQuest Central
ProQuest Health & Medical Research Collection
Health Research Premium Collection
Health and Medicine Complete (Alumni Edition)
ProQuest Central Korea
Health & Medical Research Collection
AIDS and Cancer Research Abstracts
Chemoreception Abstracts
ProQuest Central (New)
ProQuest Medical Library (Alumni)
ProQuest One Academic Eastern Edition
ProQuest Hospital Collection
Health Research Premium Collection (Alumni)
ProQuest Hospital Collection (Alumni)
Biotechnology and BioEngineering Abstracts
ProQuest Health & Medical Complete
ProQuest Medical Library
ProQuest One Academic UKI Edition
Immunology Abstracts
Engineering Research Database
ProQuest One Academic
Calcium & Calcified Tissue Abstracts
ProQuest One Academic (New)
ProQuest Central (Alumni)
MEDLINE - Academic
DatabaseTitleList

MEDLINE
Publicly Available Content Database

MEDLINE - Academic
Database_xml – sequence: 1
  dbid: DOA
  name: DOAJ Directory of Open Access Journals
  url: https://www.doaj.org/
  sourceTypes: Open Website
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: BENPR
  name: ProQuest Central
  url: https://www.proquest.com/central
  sourceTypes: Aggregation Database
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1471-230X
EndPage 13
ExternalDocumentID oai_doaj_org_article_4e1bb88a20be4be587f586fcbb404607
PMC10775571
A779021312
38195414
10_1186_s12876_023_03095_6
Genre Journal Article
GeographicLocations Taiwan
China
GeographicLocations_xml – name: Taiwan
– name: China
GroupedDBID ---
0R~
23N
2WC
53G
5VS
6J9
6PF
7X7
88E
8FI
8FJ
AAFWJ
AAJSJ
AASML
AAWTL
AAYXX
ABDBF
ABUWG
ACGFO
ACGFS
ACIHN
ACIWK
ACPRK
ACUHS
ADBBV
ADRAZ
ADUKV
AEAQA
AENEX
AFKRA
AFPKN
AHBYD
AHMBA
AHYZX
ALIPV
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIJS
BAPOH
BAWUL
BCNDV
BENPR
BFQNJ
BMC
BPHCQ
BVXVI
C6C
CCPQU
CITATION
CS3
DIK
E3Z
EAD
EAP
EAS
EBD
EBLON
EBS
EMB
EMK
EMOBN
ESX
F5P
FYUFA
GROUPED_DOAJ
GX1
HMCUK
HYE
IAO
IHR
INH
INR
ITC
KQ8
M1P
M48
M~E
O5R
O5S
OK1
OVT
P2P
PHGZM
PHGZT
PIMPY
PQQKQ
PROAC
PSQYO
RBZ
RNS
ROL
RPM
RSV
SMD
SOJ
SV3
TR2
TUS
UKHRP
W2D
WOQ
WOW
XSB
-A0
3V.
ACRMQ
ADINQ
C24
CGR
CUY
CVF
ECM
EIF
NPM
PMFND
7QP
7QR
7T5
7XB
8FD
8FK
AZQEC
DWQXO
FR3
H94
K9.
P64
PJZUB
PKEHL
PPXIY
PQEST
PQUKI
PRINS
7X8
5PM
PUEGO
ID FETCH-LOGICAL-c564t-c62b874c70dfc3df4d2fc6cfa9a39ff1475c973698a63dadec561396bd5f9c823
IEDL.DBID M48
ISSN 1471-230X
IngestDate Wed Aug 27 01:16:17 EDT 2025
Thu Aug 21 18:41:57 EDT 2025
Thu Jul 10 17:17:13 EDT 2025
Fri Jul 25 21:08:38 EDT 2025
Tue Jun 17 22:26:24 EDT 2025
Tue Jun 10 21:14:52 EDT 2025
Wed Feb 19 02:12:50 EST 2025
Tue Jul 01 04:12:11 EDT 2025
Thu Apr 24 23:11:51 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 1
Keywords Hepatic fibrosis
NHANES
Hepatic steatosis
Metabolic syndrome
TyG-WHtR
Language English
License 2024. The Author(s).
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c564t-c62b874c70dfc3df4d2fc6cfa9a39ff1475c973698a63dadec561396bd5f9c823
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 14
content type line 23
OpenAccessLink https://doaj.org/article/4e1bb88a20be4be587f586fcbb404607
PMID 38195414
PQID 2914280061
PQPubID 44673
PageCount 13
ParticipantIDs doaj_primary_oai_doaj_org_article_4e1bb88a20be4be587f586fcbb404607
pubmedcentral_primary_oai_pubmedcentral_nih_gov_10775571
proquest_miscellaneous_2913082628
proquest_journals_2914280061
gale_infotracmisc_A779021312
gale_infotracacademiconefile_A779021312
pubmed_primary_38195414
crossref_citationtrail_10_1186_s12876_023_03095_6
crossref_primary_10_1186_s12876_023_03095_6
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 2024-01-09
PublicationDateYYYYMMDD 2024-01-09
PublicationDate_xml – month: 01
  year: 2024
  text: 2024-01-09
  day: 09
PublicationDecade 2020
PublicationPlace England
PublicationPlace_xml – name: England
– name: London
PublicationTitle BMC gastroenterology
PublicationTitleAlternate BMC Gastroenterol
PublicationYear 2024
Publisher BioMed Central Ltd
BioMed Central
BMC
Publisher_xml – name: BioMed Central Ltd
– name: BioMed Central
– name: BMC
References S Ciardullo (3095_CR3) 2021; 19
J Zhou (3095_CR18) 2022; 291
G Gutierrez-Buey (3095_CR24) 2017; 41
VK Ramdas Nayak (3095_CR9) 2022; 72
W Guo (3095_CR26) 2020; 19
Z Gluvic (3095_CR7) 2017; 15
AD Kaze (3095_CR6) 2021; 39
JH Lee (3095_CR17) 2022; 14
BJ Perumpail (3095_CR4) 2017; 23
H Fujii (3095_CR13) 2019; 34
DL Tahapary (3095_CR8) 2022; 16
AA El-Sehrawy (3095_CR15) 2021; 53
S Ciardullo (3095_CR21) 2021; 44
M Rosselli (3095_CR5) 2014; 20
R Muniyappa (3095_CR22) 2008; 294
M Malek (3095_CR25) 2021; 74
RN Karanjia (3095_CR2) 2016; 22
A Kitae (3095_CR23) 2019; 2019
OY Bello-Chavolla (3095_CR20) 2018; 178
DM Tanase (3095_CR12) 2020; 2020
EE Powell (3095_CR1) 2021; 397
Y Xue (3095_CR10) 2022; 13
KY Han (3095_CR11) 2022; 13
TH Raimi (3095_CR19) 2021; 19
TD Wu (3095_CR16) 2021; 160
JC Bae (3095_CR14) 2022; 37
References_xml – volume: 19
  start-page: 384
  year: 2021
  ident: 3095_CR3
  publication-title: Clin Gastroenterol Hepatol
  doi: 10.1016/j.cgh.2020.06.048
– volume: 397
  start-page: 2212
  year: 2021
  ident: 3095_CR1
  publication-title: Lancet.
  doi: 10.1016/S0140-6736(20)32511-3
– volume: 2019
  start-page: 5121574
  year: 2019
  ident: 3095_CR23
  publication-title: Can J Gastroenterol Hepatol
  doi: 10.1155/2019/5121574
– volume: 39
  start-page: 2200
  year: 2021
  ident: 3095_CR6
  publication-title: J Hypertens
  doi: 10.1097/HJH.0000000000002920
– volume: 19
  start-page: 76
  year: 2021
  ident: 3095_CR19
  publication-title: Metab Syndr Relat Disord
  doi: 10.1089/met.2020.0092
– volume: 72
  start-page: 986
  year: 2022
  ident: 3095_CR9
  publication-title: J Pak Med Assoc
  doi: 10.47391/JPMA.22-63
– volume: 53
  start-page: 100
  year: 2021
  ident: 3095_CR15
  publication-title: Horm Metab Res
  doi: 10.1055/a-1341-9710
– volume: 2020
  start-page: 3920196
  year: 2020
  ident: 3095_CR12
  publication-title: J Diabetes Res
  doi: 10.1155/2020/3920196
– volume: 16
  year: 2022
  ident: 3095_CR8
  publication-title: Diabetes Metab Syndr
  doi: 10.1016/j.dsx.2022.102581
– volume: 34
  start-page: 1390
  year: 2019
  ident: 3095_CR13
  publication-title: J Gastroenterol Hepatol
  doi: 10.1111/jgh.14595
– volume: 294
  start-page: E15
  year: 2008
  ident: 3095_CR22
  publication-title: Am J Physiol Endocrinol Metab
  doi: 10.1152/ajpendo.00645.2007
– volume: 178
  start-page: 533
  year: 2018
  ident: 3095_CR20
  publication-title: Eur J Endocrinol
  doi: 10.1530/EJE-17-0883
– volume: 14
  start-page: 3039
  year: 2022
  ident: 3095_CR17
  publication-title: Nutrients.
  doi: 10.3390/nu14153039
– volume: 13
  year: 2022
  ident: 3095_CR10
  publication-title: Front Endocrinol (Lausanne).
  doi: 10.3389/fendo.2022.951689
– volume: 291
  year: 2022
  ident: 3095_CR18
  publication-title: Chemosphere.
  doi: 10.1016/j.chemosphere.2021.132953
– volume: 41
  start-page: 74
  year: 2017
  ident: 3095_CR24
  publication-title: Eur J Intern Med
  doi: 10.1016/j.ejim.2017.03.006
– volume: 13
  year: 2022
  ident: 3095_CR11
  publication-title: Front Endocrinol (Lausanne)
  doi: 10.3389/fendo.2022.851338
– volume: 160
  start-page: 1026
  year: 2021
  ident: 3095_CR16
  publication-title: Chest.
  doi: 10.1016/j.chest.2021.03.056
– volume: 22
  start-page: 9880
  year: 2016
  ident: 3095_CR2
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v22.i45.9880
– volume: 19
  start-page: 218
  year: 2020
  ident: 3095_CR26
  publication-title: Lipids Health Dis
  doi: 10.1186/s12944-020-01393-6
– volume: 37
  start-page: 455
  year: 2022
  ident: 3095_CR14
  publication-title: Endocrinol Metab (Seoul)
  doi: 10.3803/EnM.2022.1434
– volume: 74
  start-page: 538
  year: 2021
  ident: 3095_CR25
  publication-title: Endocrine.
  doi: 10.1007/s12020-021-02815-w
– volume: 20
  start-page: 5010
  year: 2014
  ident: 3095_CR5
  publication-title: Curr Pharm Des
  doi: 10.2174/1381612819666131206111352
– volume: 44
  start-page: 519
  year: 2021
  ident: 3095_CR21
  publication-title: Diabetes Care
  doi: 10.2337/dc20-1778
– volume: 15
  start-page: 30
  year: 2017
  ident: 3095_CR7
  publication-title: Curr Vasc Pharmacol
  doi: 10.2174/1570161114666161007164510
– volume: 23
  start-page: 8263
  year: 2017
  ident: 3095_CR4
  publication-title: World J Gastroenterol
  doi: 10.3748/wjg.v23.i47.8263
SSID ssj0017823
Score 2.3956635
Snippet To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome (MetS), as...
Background To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome...
BackgroundTo investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome...
Abstract Background To investigate the association of four insulin resistance (IR) indicators with hepatic steatosis and fibrosis in patients with metabolic...
SourceID doaj
pubmedcentral
proquest
gale
pubmed
crossref
SourceType Open Website
Open Access Repository
Aggregation Database
Index Database
Enrichment Source
StartPage 26
SubjectTerms Adult
Blood pressure
Cardiovascular disease
Care and treatment
Cholesterol
Complications and side effects
Creatinine
Cross-Sectional Studies
Dextrose
Diabetes
Diagnosis
Fatty liver
Fatty Liver - complications
Fibrosis
Gender
Glucose
Health aspects
Health surveys
Heart failure
Hepatic fibrosis
Hepatic steatosis
Hepatitis
High density lipoprotein
Homeostasis
Humans
Hypertension
Insulin Resistance
Lipoproteins
Liver
Liver Cirrhosis
Medical research
Medicine, Experimental
Metabolic syndrome
Metabolic Syndrome - complications
Metabolic syndrome X
NHANES
Nutrition Surveys
Population
Prevention
Proteins
Regression analysis
Review boards
Risk factors
Smoking
Steatosis
Surveys
Triglycerides
TyG-WHtR
Type 2 diabetes
Womens health
SummonAdditionalLinks – databaseName: DOAJ Directory of Open Access Journals
  dbid: DOA
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwrV3NixUxDC-yB_Eifju6SgXBgwy7069pj6u4LIKeXNhbadOWFdZ54pv9_006fY83CHrxONMEpknaJpP0F8beJg02a-oBqKPolQmujxIduShdljmVJKAWyH41F5fq85W-Omj1RTVhCzzwIrgTlYcYrQ3iNGYVs7Zj0dYUiFFRTq_eI8czbxdMtfwBnntyd0XGmpMt7sIjFdvKnlIKujerY6ii9f-5Jx8cSuuCyYMT6PwBu99cR362fPJDdidPj9jdLy05_pjNB6Lmm8JbmTnHgJqcRNQupwQ1UJi95fQDll9nKqgGTqqeN0jGw5R4wRC6PiBzw11t9D_yjEZzQxwN6eAJuzz_9O3jRd-aKvSgjZp7MCLaUcF4mgrIVFQSBQyU4IJ0pQxq1OBGaZwNRqaQMlCI4UxMujhAsT5lR9Nmys8ZLwl9reIwaAyDgmTCEIo2MIbTMaZSTMeGnYw9NMRxanxx42vkYY1f9OJRL77qxSPP-z3PzwVv46_UH0h1e0rCyq4v0IJ8syD_Lwvq2DtSvKcVjZ8HoV1MwEkSNpY_I0hGMchBdOx4RYkrEdbDO9PxbSfYeuEI0448xY692Q8TJ1W3TXlzW2kINcgI27Fni6Xtp0QRNbVq75hd2eBqzuuR6ft1xQkfCN5Qj8OL_yGll-yeQH-u_n1yx-xo_nWbX6E_NsfXden9BpaHNRw
  priority: 102
  providerName: Directory of Open Access Journals
– databaseName: Health & Medical Collection
  dbid: 7X7
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3NaxUxEA9aQbyI365WiSB4kKUv38lJqliKoCcL7xbyaYV2t_Zt_38zeXnrW4QedzMDm8xkMpOZ_Q1C76MIOgnoASg87bl0pvesOHKemcRSzJGGWiD7Q56e8W9rsW4XbptWVrmzidVQxzHAHfkRNYANBifup6s_PXSNguxqa6FxF90D6DIo6VLrOeAi5fRjux9ltDzaFFusoOSW9ZBYEL1cHEYVs_9_y7x3NC3LJvfOoZNH6GFzIPHxVuKP0Z00PEH3v7cU-VM07S04HjNuxea4hNXgKhYZY0hTBwi2NxiuYfF5grLqgEHg01jIsBsiziWQrg-FuaGvNvrLNBXVuQCOhnfwDJ2dfP355bRvrRX6ICSf-iCp14oHtYo5sJh5pDnIkJ1xzORMuBLBKCaNdpJFF1OAQMNIH0U2oSzrc3QwjEN6iXCOxePKpoSOjvAQpSMuCxmUWykfc5YdIrs1tqHhjkP7iwtb4w8t7VYutsjFVrnYwvNx5rnaom7cSv0ZRDdTAmJ2fTFe_7JtA1qeiPdaO7ryifsktMpCyxy855AbVh36AIK3sK_L5wXXfk8okwSELHsMwIyUMEI7dLigLPsxLId3qmObPdjYf9rboXfzMHBCjduQxptKA9hBkuoOvdhq2jwliKuhYXuH9EIHF3Nejgy_zytaOAGQQ6HIq9u_6zV6QIu_Vm-XzCE6mK5v0pvib03-bd1UfwE03iwV
  priority: 102
  providerName: ProQuest
Title Association of insulin resistance indicators with hepatic steatosis and fibrosis in patients with metabolic syndrome
URI https://www.ncbi.nlm.nih.gov/pubmed/38195414
https://www.proquest.com/docview/2914280061
https://www.proquest.com/docview/2913082628
https://pubmed.ncbi.nlm.nih.gov/PMC10775571
https://doaj.org/article/4e1bb88a20be4be587f586fcbb404607
Volume 24
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwfV3raxNBEF_6APGL-Pa0hhUEP8hp77GvDyKNtBShRYqB4Jdln60QL5pcQf97ZzabmMPSL4FkZ8LtzszuzM7cbwh57ZmTgWEPQGbrsuVGlbYBR842KjTBR1-7VCB7zk8n7ecpm-6QdbujvIDLG0M77Cc1Wcze_f715yMY_Idk8JK_X8IeK7CUtikxYcBKvkv24WQSaKhn7b-sApyGqeAeNuQSXO_p-iWaG_9jcFAlPP__d-2tY2tYUrl1Rp3cJ_eyc0mPVtrwgOyE7iG5c5bT549IvyUMOo80F6JTCLnRjQT5U0xhOwzElxSvaOlVwJJrR1EZ-jmQUdN5GiHITl-AOSOzZvofoQe1miFHxkJ4TCYnx18_nZa57ULpGG_70vHaStE6ceija3xsfR0dd9Eo06gYYfWYU6LhShreeOODwyBEcetZVA6W-AnZ6-ZdeEZo9OCNRQVhpala57mpTGTcCXMorI-RF6Rar7F2GZMcW2PMdIpNJNcruWiQi05y0cDzdsPzc4XIcSv1GEW3oUQ07fTDfHGps3HqNlTWSmnqQxtaG5gUkUkenbUt5o1FQd6g4DVqITyeM_nVBZgkomfpIwRtrKumqgtyMKAEW3XD4bXq6LWq61oh6h36kgV5tRlGTqx_68L8OtEgrhCvZUGerjRtMyWMubGZe0HkQAcHcx6OdN-vEpJ4hQCITFTPb3_sF-RuDb5cunlSB2SvX1yHl-CL9XZEdsVUjMj--Pj8y8Uo3WiMktHB58X4219o_jWB
linkProvider Scholars Portal
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9QwELaqrQRcEG8CBYwE4oCibvyKc0CohVZb2q4QaqXejJ8UqSSlmwrxp_iNeBJn2Qiptx4Tj6U4M56HZ_wNQq8ct9Jz6AHIDcmZ0FVuaHTkDK089S44YrsC2bmYHbNPJ_xkDf0Z7sJAWeWgEztF7RoLZ-SbpAJsMLC4789_5tA1CrKrQwuNXiz2_e9fMWRbvNv7GPn7mpDdnaMPszx1FcgtF6zNrSBGlsyWUxcsdYE5EqywQVeaViEUrOS2KqmopBbUaect-NiVMI6HykoAOogqf53RGMpM0Pr2zvzzl2XeItpbOlzNkWJzEbV_CUW-NIdUBs_FyPx1XQL-twUrxnBcqLli-XbvoNvJZcVbvYzdRWu-voduHKak_H3UrrAYNwGn8nYcA3lwTqNUYUiMWwjvFxgOfvGph0Jui0HE2iaSYV07HGLo3j3EyQnvNdH_8G0U1jOYkRAWHqDja_ntD9Gkbmr_GOHgoo8Xqhis6oJZJ3ShAxe21NPSuBBEhorhHyubkM6h4caZ6iIeKVTPFxX5ojq-qDjn7XLOeY_zcSX1NrBuSQkY3d2L5uKbSlteMV8YI6UmU-OZ8VyWgUsRrDEMstFlht4A4xVokvh5VqcLEXGRgMmltgAKkhS0IBnaGFFGDWDHw4PoqKSBFurffsnQy-UwzISquto3lx0NoBUJIjP0qJe05ZIgkocW8RmSIxkcrXk8Un8_7fDJC4BV5GXx5OrveoFuzo4OD9TB3nz_KbpForfYnW1VG2jSXlz6Z9Hba83ztMUw-nrdu_ovPkRr5A
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=Association+of+insulin+resistance+indicators+with+hepatic+steatosis+and+fibrosis+in+patients+with+metabolic+syndrome&rft.jtitle=BMC+gastroenterology&rft.au=Kuo%2C+Tzu-chia&rft.au=Lu%2C+Yang-bor&rft.au=Yang%2C+Chieh-lun&rft.au=Wang%2C+Bin&rft.date=2024-01-09&rft.pub=BioMed+Central+Ltd&rft.issn=1471-230X&rft.eissn=1471-230X&rft.volume=24&rft.issue=1&rft_id=info:doi/10.1186%2Fs12876-023-03095-6&rft.externalDocID=A779021312
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1471-230X&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1471-230X&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1471-230X&client=summon