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ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 40 Issue 4
Apr.  2024
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Article Contents

Value of Fetuin-A, Fetuin-B, and insulin resistance index in predicting nonalcoholic fatty liver disease

DOI: 10.12449/JCH240409
Research funding:

Yunnan Provincial Joint Basic Research Project for Local Undergraduate Colleges and Universities (202001BA070001-103)

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  • Corresponding author: LI Lihua, lilihuayncn@163.com (ORCID: 0000-0003-3987-5851)
  • Received Date: 2023-07-15
  • Accepted Date: 2023-08-04
  • Published Date: 2024-04-25
  •   Objective  To investigate the value of serum Fetuin-A and Fetuin-B combined with Homeostasis Model Assessment of Insulin Resistance (HOMA-IR) in predicting nonalcoholic fatty liver disease (NAFLD).  Methods  A total of 120 patients with NAFLD who attended Department of Gastroenterology, The First Affiliated Hospital of Dali University, from June 2020 to June 2021, and 120 healthy individuals who underwent physical examination at Physical Examination Center during the same period of time were enrolled as subjects, and clinical data were collected from all subjects. The serum levels of Fetuin-A and Fetuin-B were measured. The independent-samples t test or the Mann-Whitney U test was used for comparison of continuous data between two groups, and the chi-square test was used for comparison of categorical data between two groups; the multivariate Logistic regression analysis was used to assess the risk factors for NAFLD. The receiver operating characteristic (ROC) curve was plotted to evaluate the predictive efficacy of Fetuin-A and Fetuin-B combined with HOMA-IR in NAFLD patients.  Results  Compared with the healthy control group, the NAFLD group had significantly higher levels of body mass index, systolic blood pressure, diastolic blood pressure, alanine aminotransferase, aspartate aminotransferase, fasting blood glucose, fasting insulin, triglycerides, HOMA-IR, Fetuin-A, and Fetuin-B (all P<0.05). The multivariate Logistic regression analysis showed that Fetuin-A (odds ratio [OR]=1.010, 95% confidence interval [CI]: 1.001‍‍‍ ‍‍‍—‍‍‍ ‍‍1.020, P<0.05), Fetuin-B (OR=1.113, 95%CI: 1.021‍ ‍‍—‍‍ ‍1.214, P<0.05), and HOMA-IR (OR=24.053, 95%CI: 2.624‍ ‍‍—‍‍ ‍220.470, P<0.05) were independent risk factors for NAFLD. The ROC curve analysis showed that Fetuin-A, Fetuin-B or HOMA-IR alone had an area under the ROC curve (AUC) of 0.637 (95%CI: 0.551‍ ‍—‍ ‍0.722), 0.853 (95%CI: 0.796‍ ‍—‍ ‍0.912), and 0.837 (95%CI: 0.763‍ ‍—‍ ‍0.912), respectively, and Fetuin-A combined with Fetuin-B, Fetuin-A combined with HOMA-IR, and Fetuin-B combined with HOMA-IR had an AUC of 0.853 (95%CI: 0.795‍ ‍—‍ ‍0.911), 0.843 (95%CI: 0.770‍ ‍—‍ ‍0.916), 0.922 (95%CI: 0.877‍ ‍—‍ ‍0.967), respectively, while the combination of these three indicators had an AUC of 0.922 (95%CI: 0.877‍ ‍—‍ ‍0.966).  Conclusion  Fetuin-A and Fetuin-B have a certain value in predicting NAFLD, and Fetuin-B combined with HOMA-IR tends to have a higher predictive value.

     

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  • [1]
    YOUNOSSI ZM, GOLABI P, PAIK JM, et al. The global epidemiology of nonalcoholic fatty liver disease(NAFLD) and nonalcoholic steatohepatitis(NASH): A systematic review[J]. Hepatology, 2023, 77( 4): 1335- 1347. DOI: 10.1097/HEP.0000000000000004.
    [2]
    ESTES C, ANSTEE QM, ARIAS-LOSTE MT, et al. Modeling NAFLD disease burden in China, France, Germany, Italy, Japan, Spain, United Kingdom, and United States for the period 2016-2030[J]. J Hepatol, 2018, 69( 4): 896- 904. DOI: 10.1016/j.jhep.2018.05.036.
    [3]
    WU CM, ZHANG CY, XU HL, et al. Epidemiological research and diagnosis of nonalcoholic fatty liver disease in China[J]. China Med Herald, 2023, 20( 11): 158- 161. DOI: 10.20047/j.issn1673-7210.2023.11.36.

    吴车敏, 张从玉, 徐慧丽, 等. 我国非酒精性脂肪性肝病的流行病学研究和诊断现状分析[J]. 中国医药导报, 2023, 20( 11): 158- 161. DOI: 10.20047/j.issn1673-7210.2023.11.36.
    [4]
    SARDANA O, GOYAL R, BEDI O. Molecular and pathobiological involvement of fetuin-A in the pathogenesis of NAFLD[J]. Inflammopharmacology, 2021, 29( 4): 1061- 1074. DOI: 10.1007/s10787-021-00837-4.
    [5]
    CHEKOL ABEBE E, TILAHUN MUCHE Z, BEHAILE T/MARIAM A, et al. Role of fetuin-A in the pathogenesis of psoriasis and its potential clinical applications[J]. Clin Cosmet Investig Dermatol, 2022, 15: 595- 607. DOI: 10.2147/CCID.S356801.
    [6]
    STEFAN N, FRITSCHE A, WEIKERT C, et al. Plasma fetuin-A levels and the risk of type 2 diabetes[J]. Diabetes, 2008, 57( 10): 2762- 2767. DOI: 10.2337/db08-0538.
    [7]
    SONG AY, XU M, BI YF, et al. Serum fetuin-A associates with type 2 diabetes and insulin resistance in Chinese adults[J]. PLoS One, 2011, 6( 4): e19228. DOI: 10.1371/journal.pone.0019228.
    [8]
    SUN JR, ZHANG D, XU J, et al. Circulating FABP4, nesfatin-1, and osteocalcin concentrations in women with gestational diabetes mellitus: A meta-analysis[J]. Lipids Health Dis, 2020, 19( 1): 199. DOI: 10.1186/s12944-020-01365-w.
    [9]
    XIAO Y, SHU LL, WU XP, et al. Fatty acid binding protein 4 promotes autoimmune diabetes by recruitment and activation of pancreatic islet macrophages[J]. JCI Insight, 2021, 6( 7): e141814. DOI: 10.1172/jci.insight.141814.
    [10]
    OLIVIER E, SOURY E, RUMINY P, et al. Fetuin-B, a second member of the fetuin family in mammals[J]. Biochem J, 2000, 350( Pt 2): 589- 597.
    [11]
    MUSTAFA AI, KADAH AS, FAWZY EM, et al. Serum fetuin-A: A novel potential link between post-adolescent acne and insulin resistance[J]. J Clin Aesthet Dermatol, 2022, 15( 12): 33- 37.
    [12]
    DENG WJ, GU J, ZUO LJ, et al. The level changes and influencing factors of serum fetuin-B in patients with type 2 diabetes mellitus and non-alcoholic fatty liver disease[J]. Chin J Diabetes, 2019, 27( 3): 198- 201. DOI: 10.3969/j.issn.1006-6187.2019.03.007.

    邓文娟, 谷君, 左丽娟, 等. 2型糖尿病合并非酒精性脂肪性肝病患者血清胎球蛋白B水平变化及影响因素分析[J]. 中国糖尿病杂志, 2019, 27( 3): 198- 201. DOI: 10.3969/j.issn.1006-6187.2019.03.007.
    [13]
    National Workshop on Fatty Liver and Alcoholic Liver Disease, Chinese Society of Hepatology, Chinese Medical Association; Fatty Liver Expert Committee, Chinese Medical Doctor Association. Guidelines of prevention and treatment for nonalcoholic fatty liver disease: A 2018 update[J]. J Clin Hepatol, 2018, 34( 5): 947- 957. DOI: 10.3969/j.issn.1001-5256.2018.05.007.

    中华医学会肝病学分会脂肪肝和酒精性肝病学组, 中国医师协会脂肪性肝病专家委员会. 非酒精性脂肪性肝病防治指南(2018年更新版)[J]. 临床肝胆病杂志, 2018, 34( 5): 947- 957. DOI: 10.3969/j.issn.1001-5256.2018.05.007.
    [14]
    YOUNOSSI ZM, HENRY L, BUSH H, et al. Clinical and economic burden of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis[J]. Clin Liver Dis, 2018, 22( 1): 1- 10. DOI: 10.1016/j.cld.2017.08.001.
    [15]
    STEFAN N, HENNIGE AM, STAIGER H, et al. Alpha2-heremans-schmid glycoprotein/fetuin-A is associated with insulin resistance and fat accumulation in the liver in humans[J]. Diabetes Care, 2006, 29( 4): 853- 857. DOI: 10.2337/diacare.29.04.06.dc05-1938.
    [16]
    CHEKOL ABEBE E, TILAHUN MUCHE Z, BEHAILE T/MARIAM A, et al. The structure, biosynthesis, and biological roles of fetuin-A: A review[J]. Front Cell Dev Biol, 2022, 10: 945287. DOI: 10.3389/fcell.2022.945287.
    [17]
    LI LN, SPRANGER L, STOBÄUS N, et al. Fetuin-B, a potential link of liver-adipose tissue cross talk during diet-induced weight loss-weight maintenance[J]. Nutr Diabetes, 2021, 11( 1): 31. DOI: 10.1038/s41387-021-00174-z.
    [18]
    DI MINNO A, ZANOBINI M, MYASOEDOVA VA, et al. Could circulating fetuin A be a biomarker of aortic valve stenosis?[J]. Int J Cardiol, 2017, 249: 426- 430. DOI: 10.1016/j.ijcard.2017.05.040.
    [19]
    Low serum fetuin-a as a biomarker to predict pneumococcal necrotizing pneumonia and hemolytic uremic syndrome in children: Erratum[J]. Medicine, 2018, 97( 3): e9684. DOI: 10.1097/MD.0000000000009684.
    [20]
    ZHOU ZW, SUN MZ, JIN H, et al. Fetuin-A to adiponectin ratio is a sensitive indicator for evaluating metabolic syndrome in the elderly[J]. Lipids Health Dis, 2020, 19( 1): 61. DOI: 10.1186/s12944-020-01251-5.
    [21]
    ZHAO LL, SHANG Y, LUO QZ, et al. Decreased plasma fetuin-A level as a novel bioindicator of poor prognosis in community-acquired pneumonia: A multi-center cohort study[J]. Front Med, 2022, 9: 807536. DOI: 10.3389/fmed.2022.807536.
    [22]
    DIAO WQ, SHEN N, DU YP, et al. Fetuin-B(FETUB): A plasma biomarker candidate related to the severity of lung function in COPD[J]. Sci Rep, 2016, 6: 30045. DOI: 10.1038/srep30045.
    [23]
    YURTCU N, ORAL S, CELIK S, et al. Predıctıve value of pregnancy of follıcular fluıd fetuın-A and-B levels ın infertıle women after intra-cytoplasmic sperm injection[J]. J Obstet And Gynaecol, 2022, 48( 1): 178- 187. DOI: 10.1111/jog.15070.
    [24]
    LIU SS, XIAO JH, ZHAO ZZ, et al. Systematic review and meta-analysis of circulating fetuin-a levels in nonalcoholic fatty liver disease[J]. J Clin Transl Hepatol, 2021, 9( 1): 3- 14. DOI: 10.14218/JCTH.2020.00081.
    [25]
    LU CW, LEE YC, CHIANG CH, et al. Independent dose-response associations between fetuin-A and lean nonalcoholic fatty liver disease[J]. Nutrients, 2021, 13( 9): 2928. DOI: 10.3390/nu13092928.
    [26]
    BALLESTRI S, MESCHIARI E, BALDELLI E, et al. Relationship of serum fetuin-a levels with coronary atherosclerotic burden and NAFLD in patients undergoing elective coronary angiography[J]. Metab Syndr Relat Disord, 2013, 11( 4): 289- 295. DOI: 10.1089/met.2012.0149.
    [27]
    IX JH, SHARMA K. Mechanisms linking obesity, chronic kidney disease, and fatty liver disease: The roles of fetuin-A, adiponectin, and AMPK[J]. J Am Soc Nephrol, 2010, 21( 3): 406- 412. DOI: 10.1681/ASN.2009080820.
    [28]
    LANTHIER N, LEBRUN V, MOLENDI-COSTE O, et al. Liver fetuin-A at initiation of insulin resistance[J]. Metabolites, 2022, 12( 11): 1023. DOI: 10.3390/metabo12111023.
    [29]
    PETER A, KOVAROVA M, STAIGER H, et al. The hepatokines fetuin-A and fetuin-B are upregulated in the state of hepatic steatosis and may differently impact on glucose homeostasis in humans[J]. Am J Physiol Endocrinol Metab, 2018, 314( 3): E266- E273. DOI: 10.1152/ajpendo.00262.2017.
    [30]
    CHOI JW, LIU H, MUKHERJEE R, et al. Downregulation of fetuin-B and zinc-α2-glycoprotein is linked to impaired fatty acid metabolism in liver cells[J]. Cell Physiol Biochem, 2012, 30( 2): 295- 306. DOI: 10.1159/000339065.
    [31]
    DABROWSKA AM, TARACH JS, WOJTYSIAK-DUMA B, et al. Fetuin-A(AHSG) and its usefulness in clinical practice. Review of the literature[J]. Biomed Pap Med Fac Univ Palacky Olomouc Czech Repub, 2015, 159( 3): 352- 359. DOI: 10.5507/bp.2015.018.
    [32]
    ZHAO CL, SHANG DF, ZHOU C, et al. Mechanism of lipid metabolism mediated by hepatokines and adipokines in nonalcoholic fatty liver disease[J]. J Clin Hepatol, 2023, 39( 1): 168- 174. DOI: 10.3969/j.issn.1001-5256.2023.01.026.

    赵晨露, 尚东方, 周铖, 等. 肝因子和脂肪因子介导的脂代谢在非酒精性脂肪性肝病中的作用机制[J]. 临床肝胆病杂志, 2023, 39( 1): 168- 174. DOI: 10.3969/j.issn.1001-5256.2023.01.026.
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