Volume 13 Issue 9
Sep.  2023
Turn off MathJax
Article Contents
Jiaojiao Wei, Tao Chen, Yamin Liu, Shuai Sun, Zhiqing Yuan, Yixin Zhang, Aizhen Xiong, Linnan Li, Zhengtao Wang, Li Yang. Targeted bile acids metabolomics in cholesterol gallbladder polyps and gallstones: From analytical method development towards application to clinical samples[J]. Journal of Pharmaceutical Analysis, 2023, 13(9): 1080-1087. doi: 10.1016/j.jpha.2023.06.003
Citation: Jiaojiao Wei, Tao Chen, Yamin Liu, Shuai Sun, Zhiqing Yuan, Yixin Zhang, Aizhen Xiong, Linnan Li, Zhengtao Wang, Li Yang. Targeted bile acids metabolomics in cholesterol gallbladder polyps and gallstones: From analytical method development towards application to clinical samples[J]. Journal of Pharmaceutical Analysis, 2023, 13(9): 1080-1087. doi: 10.1016/j.jpha.2023.06.003

Targeted bile acids metabolomics in cholesterol gallbladder polyps and gallstones: From analytical method development towards application to clinical samples

doi: 10.1016/j.jpha.2023.06.003
Funds:

This work is financially supported by the National Natural Science Foundation of China (Grant Nos.: 81920108033, and 82274223).

  • Received Date: Mar. 14, 2023
  • Accepted Date: Jun. 05, 2023
  • Rev Recd Date: May 30, 2023
  • Publish Date: Jun. 07, 2023
  • Bile acids (BAs) are synthesized by the liver from cholesterol through several complementary pathways and aberrant cholesterol metabolism plays pivotal roles in the pathogeneses of cholesterol gallbladder polyps (CGP) and cholesterol gallstones (CGS). To date, there is neither systematic study on BAs profile of CGP or CGS, nor the relationship between them. To explore the metabolomics profile of plasma BAs in healthy volunteers, CGP and CGS patients, an ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method was developed and validated for simultaneous determination of 42 free and conjugated BAs in human plasma. The developed method was sensitive and reproducible to be applied for the quantification of BAs in the investigation of plasma samples. The results show that, compared to healthy volunteers, CGP and CGS were both characterized by the significant decrease in plasma BAs pool size, furthermore CGP and CGS shared aberrant BAs metabolic characteristics. Chenodeoxycholic acid, glycochenodeoxycholic acid, λ-muricholic acid, deoxycholic acid, and 7-ketolithocholic acid were shared potential markers of these two cholesterol gallbladder diseases. Subsequent analysis showed that clinical characteristics including cysteine, ornithine and body mass index might be closely related to metabolisms of certain BA modules. This work provides metabolomic information for the study of gallbladder diseases and analytical methodologies for clinical target analysis and efficacy evaluation related to BAs in medical institutions.
  • loading
  • E.-H. Yoo, S.-Y. Lee. The prevalence and risk factors for gallstone disease, Clin. Chem. Lab. Med. 47 (2009) 795-807.
    N.R. Bhatt, A. Gillis, C.O. Smoothey, et al., Evidence based management of polyps of the gall bladder: A systematic review of the risk factors of malignancy, Surg. 14 (2016) 278-286.
    S. Ryu, Y. Chang, K.E. Yun, et al., Gallstones and the risk of gallbladder cancer mortality: A cohort study, Am. J. Gastroenterol. 111 (2016) 1476-1487.
    A.W. Hsing, Y.T. Gao, T.Q. Han, et al., Gallstones and the risk of biliary tract cancer: A population-based study in China, Br. J. Cancer 97 (2007) 1577-1582
    J.C. Roa, P. Garcia, V.K. Kapoor, et al., Gallbladder cancer, Nat. Rev. Dis. Primers. 8 (2022), 69.
    C. Valibouze, M. El Amrani, S. Truant, et al., The management of gallbladder polyps, J. Visc. Surg. 157 (2020) 410-417.
    F. Lammert, K. Gurusamy, C.W. Ko, et al., Gallstones, Nat. Rev. Dis. Primers. 2 (2016), 16024.
    M.H. Yu, Y.J. Kim, H.S. Park, et al., Benign gallbladder diseases: Imaging techniques and tips for differentiating with malignant gallbladder diseases, World. J. Gastroenterol. 26 (2020) 2967-2986.
    Z.C. Riddell, C. Corallo, R. Albazaz, et al., Gallbladder polyps and adenomyomatosis, Br. J. Radiol. 96 (2022), 20220115.
    M.J. Monte, J.J.G. Marin, A. Antelo, et al., Bile acids: Chemistry, physiology, and pathophysiology, World. J. Gastroenterol. 15 (2009) 804-816
    A.F. Hofmann, L.R. Hagey. Bile acids: chemistry, pathochemistry, biology, pathobiology, and therapeutics, Cell. Mol. Life. Sci. 65 (2008) 2461-2483.
    C. Rajani, W. Jia. Bile acids and their effects on diabetes, Front. Med. 12 (2018) 608-623.
    T.R. Ahmad, R.A. Haeusler. Bile acids in glucose metabolism and insulin signalling-mechanisms and research needs, Nat. Rev. Endocrinol. 15 (2019) 701-712.
    B.I. Babu, A.R. Dennison, G. Garcea. Management and diagnosis of gallbladder polyps: A systematic review, Langenbecks. Arch. Surg. 400 (2015) 455-462.
    A. Cariati, E. Piromalli. Limits and perspective of oral therapy with statins and aspirin for the prevention of symptomatic cholesterol gallstone disease, Expert. Opin. Pharmacother. 13 (2012) 1223-1227.
    R. Lam, A. Zakko, J.C. Petrov, et al., Gallbladder disorders: A comprehensive review, Dis. Mon. 67 (2021), 101130.
    S. Leng, A. Zhao, Q. Li, et al., Metabolic status and lifestyle factors associated with gallbladder polyps: A covariance structure analysis, BMC. Gastroenterol. 18 (2018), 159.
    G. Salen, G. Nicolau, S. Shefer, et al., Hepatic cholesterol metabolism in patients with gallstones, Gastroenterology. 69 (1975) 676-684.
    Z.R. Vlahcevic, C.C. Bell, I. Buhac, et al., Diminished bile acid pool size in patients with gallstones, Gastroenterology. 59 (1970) 165-173.
    K. Nilsell, B. Angelin, L. Liljeqvist, et al., Biliary lipid output and bile acid kinetics in cholesterol gallstone disease: Evidence for an increased hepatic secretion of cholesterol in swedish patients, Gastroenterology. 89 (1985) 287-293.
    M. Rudling, A. Laskar, S. Straniero. Gallbladder bile supersaturated with cholesterol in gallstone patients preferentially develops from shortage of bile acids, J. Lipid. Res. 60 (2019) 498-505.
    X. Fu, Y. Xiao, J. Golden, et al., Serum bile acids profiling by liquid chromatography-tandem mass spectrometry (LC-MS/MS) and its application on pediatric liver and intestinal diseases, Clin. Chem. Lab. Med. 58 (2020) 787-797.
    K. Habler, B. Koeppl, F. Bracher, et al., Targeted profiling of 24 sulfated and non-sulfated bile acids in urine using two-dimensional isotope dilution UHPLC-MS/MS, Clin. Chem. Lab. Med. 60 (2022) 220-228.
    X. Robin, N. Turck, A. Hainard, et al., pROC: An open-source package for R and S+ to analyze and compare ROC curves, BMC Bioinformatics. 12 (2011), 77.
    G. Xie, Y. Wang, X. Wang, et al., Profiling of serum bile acids in a healthy Chinese population using UPLC-MS/MS, J. Proteome. Res. 14 (2015) 850-859.
    J. Jahnel, E. Zohrer, H. Scharnagl, et al., Reference ranges of serum bile acids in children and adolescents, Clin. Chem. Lab. Med. 53 (2015) 1807-1813.
    J.P. Dusserre, A.M. Montet, J.C. Montet. Effect of hyocholic acid on the prevention and dissolution of biliary cholesterol crystals in mice, Can. J. Physiol. Pharmacol. 66 (1988) 1028-1034.
    J. Shoda, B.F. He, N. Tanaka, et al., Increase of deoxycholate in supersaturated bile of patients with cholesterol gallstone disease and its correlation with de novo syntheses of cholesterol and bile acids in liver, gallbladder emptying, and small intestinal transit, Hepatology. 21 (1995) 1291-1302.
    U. Gustafsson, S. Sahlin, C. Einarsson. High level of deoxycholic acid in human bile does not promote cholesterol gallstone formation, World. J. Gastroenterol. 9 (2003) 1576-1579.
    K. Jin, Y. Yan, S. Wang, et al., iERM: An interpretable deep learning system to classify epiretinal membrane for different optical coherence tomography devices: A multi-center analysis, J. Clin. Med. 12 (2023), 400.
    Z. Gao, X. Pan, J. Shao, et al., Automatic interpretation and clinical evaluation for fundus fluorescein angiography images of diabetic retinopathy patients by deep learning, Br. J. Ophthalmol. (2022).10.1136/bjo-2022-321472
    X. Zhang, Y.Y. Qu, L. Liu, et al. Homocysteine inhibits pro-insulin receptor cleavage and causes insulin resistance via protein cysteine-homocysteinylation, Cell Rep. 37 (2021) 109821.10.1016/j.celrep.2021.109821
    H. Xu, K. Van der Jeught, Z. Zhou, et al. Atractylenolide I enhances responsiveness to immune checkpoint blockade therapy by activating tumor antigen presentation, J. Clin. Invest. 131 (2021).10.1172/JCI146832.
    Y. Wang, W. Zhai, S. Cheng, et al., Surface-functionalized design of blood-contacting biomaterials for preventing coagulation and promoting hemostasis, Friction. (2023).10.1007/s40544-022-0710-x.
    Y. Tian, H. Xiao, Y. Yang, et al., Crosstalk between 5-methylcytosine and N(6)-methyladenosine machinery defines disease progression, therapeutic response and pharmacogenomic landscape in hepatocellular carcinoma, Mol. Cancer 22 (2023), 5.
    J. Li, D. Zhou, W. Qiu, et al., Application of weighted gene co-expression network analysis for data from paired design, Sci. Rep. 8 (2018), 622.
    Y. Wang, J. Li, D. Matye, et al., Bile acids regulate cysteine catabolism and glutathione regeneration to modulate hepatic sensitivity to oxidative injury, JCI. Insight. 3 (2018), e99676.
    L. Peric-Golia, R.S. Jones. Ornithocholanic acids and cholelithiasis in man, Science. 142 (1963) 245-246.
  • 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(1)

    Article Metrics

    Article views (1183) PDF downloads(56) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return