中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 40 Issue 4
Apr.  2024
Turn off MathJax
Article Contents

Association between urinary thallium and nonalcoholic fatty liver disease

DOI: 10.12449/JCH240408
Research funding:

National Natural Science Foundation of China (81673806);

China Medical Education Association Research Project (2020KTY001)

More Information
  • Corresponding author: WANG Ruilin, wrl7905@163.com (ORCID: 0000-0002-7129-016X)
  • Received Date: 2023-08-09
  • Accepted Date: 2023-09-01
  • Published Date: 2024-04-25
  •   Objective  To investigate the association between urinary thallium (TL) and nonalcoholic fatty liver disease (NAFLD).  Methods  Related data were collected from the registered participants aged ≥18 years in National Health and Nutrition Examination Survey from 2017 to 2020, with th exclusion of the individuals with a lack of liver transient elastography data and urinary TL indicators and those with hepatitis B, hepatitis C or significant alcohol consumption. A total of individuals were divided into NAFLD group and non-NAFLD group. Urinary TL level was quantitatively measured using high-performance liquid chromatography-electrospray ionization-tandem mass spectrometry and online solid-phase extraction combined with isotope dilution. The two groups were compared in terms of age, sex, race, marital status, education, family income poverty impact ratio (FMPIR), body mass index (BMI), smoking, alcohol consumption, diabetes mellitus (DM), hypertension (HTN), hyperlipidemia (HL), and urinary TL level. The independent-samples t test or the Wilcoxon rank-sum 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. Descriptive analysis, multivariable Logistic regression, restricted cubic spline regression analysis, subgroup analysis, and interaction analysis were conducted to investigate the risk association between urinary TL and NAFLD.  Results  A total of 2 511 individuals were included, with 1 612 (64.20%) in the NAFLD group and 899 (35.80%) in the non-NAFLD group, and the NAFLD group had a significantly higher urinary TL level than the non-NAFLD group [0.18 (0.11‍ ‍— ‍0.26)μg/L vs 0.16 (0.09 — ‍0.25)μg/L, Z=-2.76, P=0.01]. After adjustment for the covariates of age, sex, race, education, marital status, FMPIR, BMI, smoking, alcohol consumption, DM, HTN, and HL, the urinary TL Q4 group had a significant increase in the risk of NAFLD (odds ratio [OR]=1.90, 95% confidence interval [CI]: 1.48‍ — ‍2.44, P<0.01). There was a positive dose-response relationship (P<0.01) and a non-linear relationship (P<0.01) between urinary TL and the risk of NAFLD. A significant interaction was observed between urinary TL and smoking/BMI (P<0.05). For individuals taking ≥100 cigarettes in their lifetime, the risk of NAFLD was increased by 50% for every quartile increase in urinary TL (OR=1.50, 95%CI: 1.24‍ — ‍1.80), and for individuals taking<100 cigarettes in their lifetime, the risk of NAFLD was increased by 20% for every quartile increase in urinary TL (OR=1.20, 95%CI: 1.03‍ — ‍1.40); for individuals with a BMI of ≥30 kg/m2, the risk of NAFLD was increased by 30% for every quartile increase in urinary TL (OR=1.30, 95%CI: 1.05‍ — ‍1.70), with a statistical significance (P<0.05).  Conclusion  Urinary TL level is significantly associated with the risk of NAFLD.

     

  • loading
  • [1]
    CHALASANI N, YOUNOSSI Z, LAVINE JE, et al. The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases[J]. Hepatology, 2018, 67( 1): 328- 357. DOI: 10.1002/hep.29367.
    [2]
    YOUNOSSI ZM, KOENIG AB, ABDELATIF D, et al. Global epidemiology of nonalcoholic fatty liver disease-Meta-analytic assessment of prevalence, incidence, and outcomes[J]. Hepatology, 2016, 64( 1): 73- 84. DOI: 10.1002/hep.28431.
    [3]
    ESTES C, RAZAVI H, LOOMBA R, et al. Modeling the epidemic of nonalcoholic fatty liver disease demonstrates an exponential increase in burden of disease[J]. Hepatology, 2018, 67( 1): 123- 133. DOI: 10.1002/hep.29466.
    [4]
    QUEK J, CHAN KE, WONG ZY, et al. Global prevalence of non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in the overweight and obese population: A systematic review and meta-analysis[J]. Lancet Gastroenterol Hepatol, 2023, 8( 1): 20- 30. DOI: 10.1016/S2468-1253(22)00317-X.
    [5]
    CALZADILLA BERTOT L, ADAMS LA. The natural course of non-alcoholic fatty liver disease[J]. Int J Mol Sci, 2016, 17( 5): 774. DOI: 10.3390/ijms17050774.
    [6]
    WANG J, WANG LL, WANG YX, et al. Emerging risks of toxic metal(loid)s in soil-vegetables influenced by steel-making activities and isotopic source apportionment[J]. Environ Int, 2021, 146: 106207. DOI: 10.1016/j.envint.2020.106207.
    [7]
    RADIĆ S, CVJETKO P, GLAVAS K, et al. Oxidative stress and DNA damage in broad bean(Vicia faba L.) seedlings induced by thallium[J]. Environ Toxicol Chem, 2009, 28( 1): 189- 196. DOI: 10.1897/08-188.1.
    [8]
    MOTA M, BANINI BA, CAZANAVE SC, et al. Molecular mechanisms of lipotoxicity and glucotoxicity in nonalcoholic fatty liver disease[J]. Metabolism, 2016, 65( 8): 1049- 1061. DOI: 10.1016/j.metabol.2016.02.014.
    [9]
    PETER AL, VIRARAGHAVAN T. Thallium: A review of public health and environmental concerns[J]. Environ Int, 2005, 31( 4): 493- 501. DOI: 10.1016/j.envint.2004.09.003.
    [10]
    SÁNCHEZ-CHAPUL L, SANTAMARÍA A, ASCHNER M, et al. Thallium-induced DNA damage, genetic, and epigenetic alterations[J]. Front Genet, 2023, 14: 1168713. DOI: 10.3389/fgene.2023.1168713.
    [11]
    SHEKA AC, ADEYI O, THOMPSON J, et al. Nonalcoholic steatohepatitis: A review[J]. JAMA, 2020, 323( 12): 1175- 1183. DOI: 10.1001/jama.2020.2298.
    [12]
    JOHNSON CL, PAULOSE-RAM R, OGDEN CL, et al. National health and nutrition examination survey: Analytic guidelines, 1999-2010[J]. Vital Health Stat 2, 2013( 161): 1- 24.
    [13]
    ZHANG KW, NULALI J, ZHANG CX, et al. The association between serum vitamin A and NAFLD among US adults varied in different BMI groups: A cross-sectional study[J]. Food Funct, 2023, 14( 2): 836- 844. DOI: 10.1039/d2fo02204d.
    [14]
    PENG HY, PAN L, RAN SM, et al. Prediction of MAFLD and NAFLD using different screening indexes: A cross-sectional study in U.S. adults[J]. Front Endocrinol, 2023, 14: 1083032. DOI: 10.3389/fendo.2023.1083032.
    [15]
    CHEN XY, TIAN F, WU JF, et al. Associations of phthalates with NAFLD and liver fibrosis: A nationally representative cross-sectional study from NHANES 2017 to 2018[J]. Front Nutr, 2022, 9: 1059675. DOI: 10.3389/fnut.2022.1059675.
    [16]
    PARK E, KIM J, KIM B, et al. Association between environmental exposure to cadmium and risk of suspected non-alcoholic fatty liver disease[J]. Chemosphere, 2021, 266: 128947. DOI: 10.1016/j.chemosphere.2020.128947.
    [17]
    CHEN C, ZHOU Q, YANG RY, et al. Copper exposure association with prevalence of non-alcoholic fatty liver disease and insulin resistance among US adults(NHANES 2011-2014)[J]. Ecotoxicol Environ Saf, 2021, 218: 112295. DOI: 10.1016/j.ecoenv.2021.112295.
    [18]
    WANG X, SEO YA, PARK SK. Serum selenium and non-alcoholic fatty liver disease(NAFLD) in U.S. adults: National Health and Nutrition Examination Survey(NHANES) 2011-2016[J]. Environ Res, 2021, 197: 111190. DOI: 10.1016/j.envres.2021.111190.
    [19]
    LIU J, TAN L, LIU ZY, et al. Blood and urine manganese exposure in non-alcoholic fatty liver disease and advanced liver fibrosis: An observational study[J]. Environ Sci Pollut Res Int, 2023, 30( 9): 22222- 22231. DOI: 10.1007/s11356-022-23630-4.
    [20]
    LI D, YAO H, DU L, et al. Thallium(I and III) exposure leads to liver damage and disorders of fatty acid metabolism in mice[J]. Chemosphere, 2022, 307( Pt 1): 135618. DOI: 10.1016/j.chemosphere.2022.135618.
    [21]
    CHEN RS, XU Y, XU C, et al. Associations between mercury exposure and the risk of nonalcoholic fatty liver disease(NAFLD) in US adolescents[J]. Environ Sci Pollut Res Int, 2019, 26( 30): 31384- 31391. DOI: 10.1007/s11356-019-06224-5.
    [22]
    ASPROULI E, KALAFATI IP, SAKELLARI A, et al. Evaluation of plasma trace elements in different stages of nonalcoholic fatty liver disease[J]. Biol Trace Elem Res, 2019, 188( 2): 326- 333. DOI: 10.1007/s12011-018-1432-9.
    [23]
    NGUYEN HD, KIM MS. Cadmium, lead, and mercury mixtures interact with non-alcoholic fatty liver diseases[J]. Environ Pollut, 2022, 309: 119780. DOI: 10.1016/j.envpol.2022.119780.
    [24]
    FREDIANI JK, NAIOTI EA, VOS MB, et al. Arsenic exposure and risk of nonalcoholic fatty liver disease(NAFLD) among U.S. adolescents and adults: An association modified by race/ethnicity, NHANES 2005-2014[J]. Environ Health, 2018, 17( 1): 6. DOI: 10.1186/s12940-017-0350-1.
    [25]
    HYDER O, CHUNG M, COSGROVE D, et al. Cadmium exposure and liver disease among US adults[J]. J Gastrointest Surg, 2013, 17( 7): 1265- 1273. DOI: 10.1007/s11605-013-2210-9.
    [26]
    HUH JH, LEE KJ, LIM JS, et al. High dietary sodium intake assessed by estimated 24-h urinary sodium excretion is associated with NAFLD and hepatic fibrosis[J]. PLoS One, 2015, 10( 11): e0143222. DOI: 10.1371/journal.pone.0143222.
    [27]
    DUAN WX, WANG YY, LI ZQ, et al. Thallium exposure at low concentration leads to early damage on multiple organs in children: A case study followed-up for four years[J]. Environ Pollut, 2020, 258: 113319. DOI: 10.1016/j.envpol.2019.113319.
    [28]
    KOROTKOV SM, LAPIN AV. Thallium induces opening of the mitochondrial permeability transition pore in the inner membrane of rat liver mitochondria[J]. Dokl Biochem Biophys, 2003, 392: 247- 252. DOI: 10.1023/a:1026182511897.
    [29]
    ESKANDARI MR, MASHAYEKHI V, ASLANI M, et al. Toxicity of thallium on isolated rat liver mitochondria: The role of oxidative stress and MPT pore opening[J]. Environ Toxicol, 2015, 30( 2): 232- 241. DOI: 10.1002/tox.21900.
    [30]
    TANG P, LIAO Q, TANG Y, et al. Independent and combined associations of urinary metals exposure with markers of liver injury: Results from the NHANES 2013-2016[J]. Chemosphere, 2023, 338: 139455. DOI: 10.1016/j.chemosphere.2023.139455.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(2)  / Tables(3)

    Article Metrics

    Article views (301) PDF downloads(56) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return