Startseite Routine blood test markers for predicting liver disease post HBV infection: precision pathology and pattern recognition
Artikel
Lizenziert
Nicht lizenziert Erfordert eine Authentifizierung

Routine blood test markers for predicting liver disease post HBV infection: precision pathology and pattern recognition

  • Busayo I. Ajuwon EMAIL logo , Katrina Roper , Alice Richardson und Brett A. Lidbury
Veröffentlicht/Copyright: 20. September 2023
Diagnosis
Aus der Zeitschrift Diagnosis Band 10 Heft 4

Abstract

Background

Early stages of hepatitis B virus (HBV) infection usually involve inflammation of the liver. Patients with chronic infection have an increased risk of progressive liver fibrosis, cirrhosis, and life-threatening clinical complications of end-stage hepatocellular carcinoma (HCC).

Content

Early diagnosis of hepatic fibrosis and timely clinical management are critical to controlling disease progression and decreasing the burden of end-stage liver cancer. Fibrosis staging, through its current gold standard, liver biopsy, improves patient outcomes, but the clinical procedure is invasive with unpleasant post-procedural complications. Routine blood test markers offer promising diagnostic potential for early detection of liver disease without biopsy. There is a plethora of candidate routine blood test markers that have gone through phases of biomarker validation and have shown great promise, but their current limitations include a predictive ability that is limited to only a few stages of fibrosis. However, the advent of machine learning, notably pattern recognition, presents an opportunity to refine blood-based non-invasive models of hepatic fibrosis in the future.

Summary

In this review, we highlight the current landscape of routine blood-based non-invasive models of hepatic fibrosis, and appraise the potential application of machine learning (pattern recognition) algorithms to refining these models and optimising clinical predictions of HBV-associated liver disease.

Outlook

Machine learning via pattern recognition algorithms takes data analytics to a new realm, and offers the opportunity for enhanced multi-marker fibrosis stage prediction using pathology profile that leverages information across patient routine blood tests.


Corresponding author: Busayo I. Ajuwon, National Centre for Epidemiology and Population Health, ANU College of Health and Medicine, The Australian National University, Acton, Australian Capital Territory 2601, Australia; and Department of Microbiology, Faculty of Pure and Applied Sciences, Kwara State University, Malete, Nigeria, E-mail:

Funding source: Australian National Health and Medical Research Ideas Grant

Award Identifier / Grant number: 1184720

Funding source: Australian Commonwealth Department of Health Quality Use of Pathology Programme

Award Identifier / Grant number: 4-2UJWED1

Funding source: RSTMH Early Career Grants Programme

  1. Research ethics: Not applicable.

  2. Informed consent: Not applicable.

  3. Author contributions: The authors have accepted responsibility for the entire content of this manuscript and approved its submission.

  4. Competing interests: The authors state no conflict of interest.

  5. Research funding: BIA was supported by funding from the National Institute for Health Research (NIHR, UK) through the RSTMH Early Career Grants Programme. AR was partly funded by the Australian National Health and Medical Research Ideas Grant (1184720). BAL was supported by funding from the Australian Commonwealth Department of Health Quality Use of Pathology Programme (QUPP) funding (4-2UJWED1).

  6. Data availability: Not applicable.

References

1. World Health Organization. Hepatitis B key facts; 2021. https://www.who.int/newsroom/factsheets/detail/hepatitis-b.Suche in Google Scholar

2. Friedman, SL. Mechanisms of hepatic fibrogenesis. Gastroenterology 2008;134:1655–69. https://doi.org/10.1053/j.gastro.2008.03.003.Suche in Google Scholar PubMed PubMed Central

3. Yang, L, Kwon, J, Popov, Y, Gajdos, GB, Ordog, T, Brekken, RA, et al.. Vascular endothelial growth factor promotes fibrosis resolution and repair in mice. Gastroenterology 2014;146:1339–50.e1. https://doi.org/10.1053/j.gastro.2014.01.061.Suche in Google Scholar PubMed PubMed Central

4. Golabi, P, Fazel, S, Otgonsuren, M, Sayiner, M, Locklear, CT, Younossi, ZM. Mortality assessment of patients with hepatocellular carcinoma according to underlying disease and treatment modalities. Medicine 2017;96:e5904. https://doi.org/10.1097/md.0000000000005904.Suche in Google Scholar PubMed PubMed Central

5. Heimbach, JK, Kulik, LM, Finn, RS, Sirlin, CB, Abecassis, MM, Roberts, LR, et al.. AASLD guidelines for the treatment of hepatocellular carcinoma. Hepatology 2018;67:358–80. https://doi.org/10.1002/hep.29086.Suche in Google Scholar PubMed

6. Rockey, DC, Caldwell, SH, Goodman, ZD, Nelson, RC, Smith, AD. Liver biopsy. Hepatology 2009;49:1017–44. https://doi.org/10.1002/hep.22742.Suche in Google Scholar PubMed

7. Pasha, T, Gabriel, S, Therneau, T, Dickson, ER, Lindor, KD. Cost-effectiveness of ultrasound-guided liver biopsy. Hepatology 1998;27:1220–6. https://doi.org/10.1002/hep.510270506.Suche in Google Scholar PubMed

8. Guido, M, Rugge, M. Liver biopsy sampling in chronic viral hepatitis. Semin Liver Dis 2004;24:89–97. https://doi.org/10.1055/s-2004-823103.Suche in Google Scholar PubMed

9. Jin, SY. Role of liver biopsy in the assessment of hepatic fibrosis--its utility and limitations. Korean J Hepatol 2007;13:138–45.Suche in Google Scholar

10. Lim, JK, Flamm, SL, Singh, S, Falck-Ytter, YT, Gerson, L, Hirano, I, et al.. American gastroenterological association institute guideline on the role of elastography in the evaluation of liver fibrosis. Gastroenterology 2017;152:1536–43. https://doi.org/10.1053/j.gastro.2017.03.017.Suche in Google Scholar PubMed

11. Castera, L. Noninvasive methods to assess liver disease in patients with hepatitis B or C. Gastroenterology 2012;142:1293–302. https://doi.org/10.1053/j.gastro.2012.02.017.Suche in Google Scholar PubMed

12. Marcellin, P, Ziol, M, Bedossa, P, Douvin, C, Poupon, R, de Lédinghen, V, et al.. Non-invasive assessment of liver fibrosis by stiffness measurement in patients with chronic hepatitis B. Liver Int 2009;29:242–7. https://doi.org/10.1111/j.1478-3231.2008.01802.x.Suche in Google Scholar PubMed

13. Degos, F, Perez, P, Roche, B, Mahmoudi, A, Asselineau, J, Voitot, H, et al.. Diagnostic accuracy of FibroScan and comparison to liver fibrosis biomarkers in chronic viral hepatitis: a multicenter prospective study (the FIBROSTIC study). J Hepatol 2010;53:1013–21. https://doi.org/10.1016/j.jhep.2010.05.035.Suche in Google Scholar PubMed

14. Chan, HL, Wong, GL, Choi, PC, Chan, AW, Chim, AM, Yiu, KK, et al.. Alanine aminotransferase-based algorithms of liver stiffness measurement by transient elastography (Fibroscan) for liver fibrosis in chronic hepatitis B. J Viral Hepat 2009;16:36–44. https://doi.org/10.1111/j.1365-2893.2008.01037.x.Suche in Google Scholar PubMed

15. Kim, DY, Kim, SU, Ahn, SH, Park, JY, Lee, JM, Park, YN, et al.. Usefulness of FibroScan for detection of early compensated liver cirrhosis in chronic hepatitis B. Dig Dis Sci 2009;54:1758–63. https://doi.org/10.1007/s10620-008-0541-2.Suche in Google Scholar PubMed

16. Millonig, G, Reimann, FM, Friedrich, S, Fonouni, H, Mehrabi, A, Büchler, MW, et al.. Extrahepatic cholestasis increases liver stiffness (FibroScan) irrespective of fibrosis. Hepatology 2008;48:1718–23. https://doi.org/10.1002/hep.22577.Suche in Google Scholar PubMed

17. Kim, SU, Han, KH, Park, JY, Ahn, SH, Chung, MJ, Chon, CY, et al.. Liver stiffness measurement using FibroScan is influenced by serum total bilirubin in acute hepatitis. Liver Int 2009;29:810–5. https://doi.org/10.1111/j.1478-3231.2008.01894.x.Suche in Google Scholar PubMed

18. Fung, J, Lai, CL, Cheng, C, Wu, R, Wong, DK, Yuen, MF. Mild-to-moderate elevation of alanine aminotransferase increases liver stiffness measurement by transient elastography in patients with chronic hepatitis B. Am J Gastroenterol 2011;106:492–6. https://doi.org/10.1038/ajg.2010.463.Suche in Google Scholar PubMed

19. World Health Organization. Guidelines for the prevention, care and treatment of persons with chronic hepatitis B infection; 2015. Availabe from https://apps.who.int/iris/bitstream/handle/10665/154590/9789241549059_eng.pdf?sequence=1.Suche in Google Scholar

20. Martínez, SM, Crespo, G, Navasa, M, Forns, X. Noninvasive assessment of liver fibrosis. Hepatology 2011;53:325–35. https://doi.org/10.1002/hep.24013.Suche in Google Scholar PubMed

21. Wells, RG, Schwabe, RF. Origin and function of myofibroblasts in the liver. Semin Liver Dis 2015;35:97–106. https://doi.org/10.1055/s-0035-1550061.Suche in Google Scholar PubMed

22. Xu, J, Kisseleva, T. Bone marrow-derived fibrocytes contribute to liver fibrosis. Exp Biol Med 2015;240:691–700. https://doi.org/10.1177/1535370215584933.Suche in Google Scholar PubMed PubMed Central

23. Rajakannu, M, Cherqui, D, Ciacio, O, Golse, N, Pittau, G, Allard, MA, et al.. Liver stiffness measurement by transient elastography predicts late posthepatectomy outcomes in patients undergoing resection for hepatocellular carcinoma. Surgery 2017;162:766–74. https://doi.org/10.1016/j.surg.2017.06.006.Suche in Google Scholar PubMed

24. Singh, S, Muir, AJ, Dieterich, DT, Falck-Ytter, YT. American gastroenterological association institute technical review on the role of elastography in chronic liver diseases. Gastroenterology 2017;152:1544–77. https://doi.org/10.1053/j.gastro.2017.03.016.Suche in Google Scholar PubMed

25. Kamath, PS, Shah, VH. Overview of cirrhosis. In: Feldman, M, Friedman, LS, Brandt, LJ, editors. Sleisenger and Fordtran’s gastrointestinal and liver disease, 11th ed. Philadelphia, PA: Elsevier, Inc.; 2021.Suche in Google Scholar

26. Dionigi, E, Garcovich, M, Borzio, M, Leandro, G, Majumdar, A, Tsami, A, et al.. Bacterial infections change natural history of cirrhosis irrespective of liver disease severity. Am J Gastroenterol 2017;112:588–96. https://doi.org/10.1038/ajg.2017.19.Suche in Google Scholar PubMed

27. Yee, HF, Davern, TJ. 3 – molecular and cellular basis of hepatic failure. In: Busuttil, RW, Klintmalm, GK, editors Transplantation of the liver, 2nd ed. Philadelphia: W.B. Saunders; 2005. pp. 43–56.10.1016/B978-0-7216-0118-2.50008-2Suche in Google Scholar

28. Holmes, JA, Chung, RT. Sleisenger and fordtran’s gastrointestinal and liver disease: hepatitis C. Elsevier, Inc.; 2021.Suche in Google Scholar

29. Sasso, FC, Carbonara, O, Torella, R, Mezzogiorno, A, Esposito, V, Demagistris, L, et al.. Ultrastructural changes in enterocytes in subjects with Hashimoto’s thyroiditis. Gut 2004;53:1878–80. https://doi.org/10.1136/gut.2004.047498.Suche in Google Scholar PubMed PubMed Central

30. Layden, TJ. Percutaneous needle biopsy specimens: sampling variability in patients with chronic hepatitis and cirrhosis. Arch Intern Med 1979;139:856. https://doi.org/10.1001/archinte.139.8.856.Suche in Google Scholar PubMed

31. Bedossa, P. Intraobserver and interobserver variations in liver biopsy interpretation in patients with chronic hepatitis C. The French METAVIR Cooperative Study Group. Hepatology 1994;20:15–20. https://doi.org/10.1002/hep.1840200104.Suche in Google Scholar

32. Bedossa, P, Dargère, D, Paradis, V. Sampling variability of liver fibrosis in chronic hepatitis C. Hepatology 2003;38:1449–57. https://doi.org/10.1016/j.hep.2003.09.022.Suche in Google Scholar PubMed

33. Scheuer, PJ. Liver biopsy size matters in chronic hepatitis: bigger is better. Hepatology 2003;38:1356–8. https://doi.org/10.1016/j.hep.2003.10.010.Suche in Google Scholar PubMed

34. Colloredo, G, Guido, M, Sonzogni, A, Leandro, G. Impact of liver biopsy size on histological evaluation of chronic viral hepatitis: the smaller the sample, the milder the disease. J Hepatol 2003;39:239–44. https://doi.org/10.1016/s0168-8278(03)00191-0.Suche in Google Scholar PubMed

35. Bedossa, P. Utility and appropriateness of the fatty liver inhibition of progression (FLIP) algorithm and steatosis, activity, and fibrosis (SAF) score in the evaluation of biopsies of nonalcoholic fatty liver disease. Hepatology 2014;60:565–75. https://doi.org/10.1002/hep.27173.Suche in Google Scholar PubMed

36. Rousselet, MC, Michalak, S, Dupré, F, Croué, A, Bedossa, P, Saint-André, JP, et al.. Sources of variability in histological scoring of chronic viral hepatitis. Hepatology 2005;41:257–64. https://doi.org/10.1002/hep.20535.Suche in Google Scholar PubMed

37. Chou, R, Wasson, N. Blood tests to diagnose fibrosis or cirrhosis in patients with chronic hepatitis C virus infection: a systematic review. Ann Intern Med 2013;158:807–20. https://doi.org/10.7326/0003-4819-158-11-201306040-00005.Suche in Google Scholar PubMed

38. Ding, D, Li, H, Liu, P, Chen, L, Kang, J, Zhang, Y, et al.. FibroScan, aspartate aminotransferase and alanine aminotransferase ratio (AAR), aspartate aminotransferase to platelet ratio index (APRI), fibrosis index based on the 4 factor (FIB-4), and their combinations in the assessment of liver fibrosis in patients with hepatitis B. Int J Clin Exp Med 2015;8:20876–82.Suche in Google Scholar

39. Huang, R, Wang, G, Tian, C, Liu, Y, Jia, B, Wang, J, et al.. Gamma-glutamyl-transpeptidase to platelet ratio is not superior to APRI,FIB-4 and RPR for diagnosing liver fibrosis in CHB patients in China. Sci Rep 2017;7:8543. https://doi.org/10.1038/s41598-017-09234-w.Suche in Google Scholar PubMed PubMed Central

40. Xiao, G, Yang, J, Yan, L. Comparison of diagnostic accuracy of aspartate aminotransferase to platelet ratio index and fibrosis-4 index for detecting liver fibrosis in adult patients with chronic hepatitis B virus infection: a systemic review and meta-analysis. Hepatology 2015;61:292–302. https://doi.org/10.1002/hep.27382.Suche in Google Scholar PubMed

41. Kim, WR, Berg, T, Asselah, T, Flisiak, R, Fung, S, Gordon, SC, et al.. Evaluation of APRI and FIB-4 scoring systems for non-invasive assessment of hepatic fibrosis in chronic hepatitis B patients. J Hepatol 2016;64:773–80. https://doi.org/10.1016/j.jhep.2015.11.012.Suche in Google Scholar PubMed

42. Chen, B, Ye, B, Zhang, J, Ying, L, Chen, Y. RDW to platelet ratio: a novel noninvasive index for predicting hepatic fibrosis and cirrhosis in chronic hepatitis B. PLoS One 2013;8:e68780. https://doi.org/10.1371/journal.pone.0068780.Suche in Google Scholar PubMed PubMed Central

43. Lemoine, M, Shimakawa, Y, Nayagam, S, Khalil, M, Suso, P, Lloyd, J, et al.. The gamma-glutamyl transpeptidase to platelet ratio (GPR) predicts significant liver fibrosis and cirrhosis in patients with chronic HBV infection in West Africa. Gut 2016;65:1369–76. https://doi.org/10.1136/gutjnl-2015-309260.Suche in Google Scholar PubMed PubMed Central

44. Bonnard, P, Sombié, R, Lescure, FX, Bougouma, A, Guiard-Schmid, JB, Poynard, T, et al.. Comparison of elastography, serum marker scores, and histology for the assessment of liver fibrosis in hepatitis B virus (HBV)-infected patients in Burkina Faso. Am J Trop Med Hyg 2010;82:454–8. https://doi.org/10.4269/ajtmh.2010.09-0088.Suche in Google Scholar PubMed PubMed Central

45. Ren, T, Wang, H, Wu, R, Niu, J. Gamma-glutamyl transpeptidase-to-platelet ratio predicts significant liver fibrosis of chronic hepatitis B patients in China. Gastroenterol Res Pract 2017;2017:7089702. https://doi.org/10.1155/2017/7089702.Suche in Google Scholar PubMed PubMed Central

46. Zhang, Z, Wang, G, Kang, K, Wu, G, Wang, P. The diagnostic accuracy and clinical utility of three noninvasive models for predicting liver fibrosis in patients with HBV infection. PLoS One 2016;11:e0152757. https://doi.org/10.1371/journal.pone.0152757.Suche in Google Scholar PubMed PubMed Central

47. Chin, JL, Pavlides, M, Moolla, A, Ryan, JD. Non-invasive markers of liver fibrosis: adjuncts or alternatives to liver biopsy? Front Pharmacol 2016;7. https://doi.org/10.3389/fphar.2016.00159.Suche in Google Scholar PubMed PubMed Central

48. Chen, YP, Hu, XM, Liang, XE, Huang, LW, Zhu, YF, Hou, JL. Stepwise application of fibrosis index based on four factors, red cell distribution width-platelet ratio, and aspartate aminotransferase-platelet ratio for compensated hepatitis B fibrosis detection. J Gastroenterol Hepatol 2018;33:256–63. https://doi.org/10.1111/jgh.13811.Suche in Google Scholar PubMed

49. Li, Q, Ren, X, Lu, C, Li, W, Huang, Y, Chen, L. Evaluation of APRI and FIB-4 for noninvasive assessment of significant fibrosis and cirrhosis in HBeAg-negative CHB patients with ALT ≤2 ULN: a retrospective cohort study. Medicine 2017;96:e6336. https://doi.org/10.1097/md.0000000000006336.Suche in Google Scholar PubMed PubMed Central

50. Li, Q, Lu, C, Li, W, Huang, Y, Chen, L. The gamma-glutamyl transpeptidase to platelet ratio for non-invasive assessment of liver fibrosis in patients with chronic hepatitis B and non-alcoholic fatty liver disease. Oncotarget 2017;8:28641–9. https://doi.org/10.18632/oncotarget.16162.Suche in Google Scholar PubMed PubMed Central

51. Wang, RQ, Zhang, QS, Zhao, SX, Niu, XM, Du, JH, Du, HJ, et al.. Gamma-glutamyl transpeptidase to platelet ratio index is a good noninvasive biomarker for predicting liver fibrosis in Chinese chronic hepatitis B patients. J Int Med Res 2016;44:1302–13. https://doi.org/10.1177/0300060516664638.Suche in Google Scholar PubMed PubMed Central

52. Williams, AL, Hoofnagle, JH. Ratio of serum aspartate to alanine aminotransferase in chronic hepatitis. Relationship to cirrhosis. Gastroenterology 1988;95:734–9. https://doi.org/10.1016/s0016-5085(88)80022-2.Suche in Google Scholar PubMed

53. Diehl, AM, Potter, J, Boitnott, J, Van Duyn, MA, Herlong, HF, Mezey, E. Relationship between pyridoxal 5′-phosphate deficiency and aminotransferase levels in alcoholic hepatitis. Gastroenterology 1984;86:632–6. https://doi.org/10.1016/s0016-5085(84)80110-9.Suche in Google Scholar

54. Cohen, JA, Kaplan, MM. The SGOT/SGPT ratio--an indicator of alcoholic liver disease. Dig Dis Sci 1979;24:835–8. https://doi.org/10.1007/bf01324898.Suche in Google Scholar PubMed

55. Kamimoto, Y, Horiuchi, S, Tanase, S, Morino, Y. Plasma clearance of intravenously injected aspartate aminotransferase isozymes: evidence for preferential uptake by sinusoidal liver cells. Hepatology 1985;5:367–75. https://doi.org/10.1002/hep.1840050305.Suche in Google Scholar PubMed

56. Ganaway, JR, Allen, AM, Moore, TD. Tyzzer’s disease. Am J Pathol 1971;64:717–30.Suche in Google Scholar

57. Dufour, DR, Lott, JA, Nolte, FS, Gretch, DR, Koff, RS, Seeff, LB. Diagnosis and monitoring of hepatic injury. I. Performance characteristics of laboratory tests. Clin Chem 2000;46:2027–49. https://doi.org/10.1093/clinchem/46.12.2027.Suche in Google Scholar

58. Eminler, AT, Ayyildiz, T, Irak, K, Kiyici, M, Gurel, S, Dolar, E, et al.. AST/ALT ratio is not useful in predicting the degree of fibrosis in chronic viral hepatitis patients. Eur J Gastroenterol Hepatol 2015;27:1361–6. https://doi.org/10.1097/meg.0000000000000468.Suche in Google Scholar

59. Teshale, E, Lu, M, Rupp, LB, Holmberg, SD, Moorman, AC, Spradling, P, et al.. APRI and FIB-4 are good predictors of the stage of liver fibrosis in chronic hepatitis B: the Chronic Hepatitis Cohort Study (CHeCS). J Viral Hepat 2014;21:917–20. https://doi.org/10.1111/jvh.12279.Suche in Google Scholar PubMed

60. Desalegn, H, Aberra, H, Berhe, N, Gundersen, SG, Johannessen, A. Are non-invasive fibrosis markers for chronic hepatitis B reliable in sub-Saharan Africa? Liver Int 2017;37:1461–7. https://doi.org/10.1111/liv.13393.Suche in Google Scholar PubMed PubMed Central

61. Shin, WG, Park, SH, Jang, MK, Hahn, TH, Kim, JB, Lee, MS, et al.. Aspartate aminotransferase to platelet ratio index (APRI) can predict liver fibrosis in chronic hepatitis B. Dig Liver Dis 2008;40:267–74. https://doi.org/10.1016/j.dld.2007.10.011.Suche in Google Scholar PubMed

62. Udell, JA, Wang, CS, Tinmouth, J, FitzGerald, JM, Ayas, NT, Simel, DL, et al.. Does this patient with liver disease have cirrhosis? JAMA 2012;307:832–42. https://doi.org/10.1001/jama.2012.186.Suche in Google Scholar PubMed

63. Afdhal, NH, Giannini, EG, Tayyab, G, Mohsin, A, Lee, JW, Andriulli, A, et al.. Eltrombopag before procedures in patients with cirrhosis and thrombocytopenia. N Engl J Med 2012;367:716–24. https://doi.org/10.1056/nejmoa1110709.Suche in Google Scholar

64. Tapper, EB, Robson, SC, Malik, R. Coagulopathy in cirrhosis – the role of the platelet in hemostasis. J Hepatol 2013;59:889–90. https://doi.org/10.1016/j.jhep.2013.03.040.Suche in Google Scholar PubMed

65. Sterling, RK, Lissen, E, Clumeck, N, Sola, R, Correa, MC, Montaner, J, et al.. Development of a simple noninvasive index to predict significant fibrosis in patients with HIV/HCV coinfection. Hepatology 2006;43:1317–25. https://doi.org/10.1002/hep.21178.Suche in Google Scholar PubMed

66. Torriani, FJ, Rodriguez-Torres, M, Rockstroh, JK, Lissen, E, Gonzalez-García, J, Lazzarin, A, et al.. Peginterferon Alfa-2a plus ribavirin for chronic hepatitis C virus infection in HIV-infected patients. N Engl J Med 2004;351:438–50. https://doi.org/10.1056/nejmoa040842.Suche in Google Scholar PubMed

67. Erdogan, S, Dogan, HO, Sezer, S, Uysal, S, Ozhamam, E, Kayacetin, S, et al.. The diagnostic value of non-invasive tests for the evaluation of liver fibrosis in chronic hepatitis B patients. Scand J Clin Lab Invest 2013;73:300–8. https://doi.org/10.3109/00365513.2013.773592.Suche in Google Scholar PubMed

68. Kim, BK, Kim, DY, Park, JY, Ahn, SH, Chon, CY, Kim, JK, et al.. Validation of FIB-4 and comparison with other simple noninvasive indices for predicting liver fibrosis and cirrhosis in hepatitis B virus-infected patients. Liver Int 2010;30:546–53. https://doi.org/10.1111/j.1478-3231.2009.02192.x.Suche in Google Scholar PubMed

69. Mallet, V, Dhalluin-Venier, V, Roussin, C, Bourliere, M, Pettinelli, ME, Giry, C, et al.. The accuracy of the FIB-4 index for the diagnosis of mild fibrosis in chronic hepatitis B. Aliment Pharmacol Ther 2009;29:409–15. https://doi.org/10.1111/j.1365-2036.2008.03895.x.Suche in Google Scholar PubMed

70. Ucar, F, Sezer, S, Ginis, Z, Ozturk, G, Albayrak, A, Basar, O, et al.. APRI, the FIB-4 score, and Forn’s index have noninvasive diagnostic value for liver fibrosis in patients with chronic hepatitis B. Eur J Gastroenterol Hepatol 2013;25:1076–81. https://doi.org/10.1097/meg.0b013e32835fd699.Suche in Google Scholar PubMed

71. Wang, H, Xue, L, Yan, R, Zhou, Y, Wang, MS, Cheng, MJ, et al.. Comparison of FIB-4 and APRI in Chinese HBV-infected patients with persistently normal ALT and mildly elevated ALT. J Viral Hepat 2013;20:e3–10. https://doi.org/10.1111/jvh.12010.Suche in Google Scholar PubMed

72. Wang, Y, Xu, MY, Zheng, RD, Xian, JC, Xu, HT, Shi, JP, et al.. Prediction of significant fibrosis and cirrhosis in hepatitis B e-antigen negative patients with chronic hepatitis B using routine parameters. Hepatol Res 2013;43:441–51. https://doi.org/10.1111/j.1872-034x.2012.01094.x.Suche in Google Scholar

73. Ma, J, Jiang, Y, Gong, G. Evaluation of seven noninvasive models in staging liver fibrosis in patients with chronic hepatitis B virus infection. Eur J Gastroenterol Hepatol 2013;25:428–34. https://doi.org/10.1097/meg.0b013e32835cb5dd.Suche in Google Scholar

74. Kassaye, S, Li, Y, Huhn, G, Peters, MG, French, AL, Tien, PC, et al.. Direct and indirect serum markers of liver fibrosis compared with transient elastography among women in the women’s interagency HIV study. J AIDS Clin Res 2015;6:446. https://doi.org/10.4172/2155-6113.1000446.Suche in Google Scholar PubMed PubMed Central

75. Goldberg, DM, Martin, JV. Role of gamma-glutamyl transpeptidase activity in the diagnosis of hepatobiliary disease. Digestion 1975;12:232–46. https://doi.org/10.1159/000197682.Suche in Google Scholar PubMed

76. Lemoine, M, Thursz, M, Mallet, V, Shimakawa, Y. Diagnostic accuracy of the gamma-glutamyl transpeptidase to platelet ratio (GPR) using transient elastography as a reference. Gut 2017;66:195–6. https://doi.org/10.1136/gutjnl-2016-311554.Suche in Google Scholar PubMed

77. Schiavon, LL, Narciso-Schiavon, JL, Ferraz, MLG, Silva, AEB, Carvalho-Filho, RJ. The γ-glutamyl transpeptidase to platelet ratio (GPR) in HBV patients: just adding up? Gut 2017;66:1169–70. https://doi.org/10.1136/gutjnl-2016-312658.Suche in Google Scholar PubMed

78. Tian, T, Wang, J, Huang, P, Li, J, Yu, R, Fan, H, et al.. Genetic variations in NF-κB were associated with the susceptibility to hepatitis C virus infection among Chinese high-risk population. Sci Rep 2018;8:104. https://doi.org/10.1038/s41598-017-18463-y.Suche in Google Scholar PubMed PubMed Central

79. Kingsford, C, Salzberg, SL. What are decision trees? Nat Biotechnol 2008;26:1011–3. https://doi.org/10.1038/nbt0908-1011.Suche in Google Scholar PubMed PubMed Central

80. Zhou, ZH. Ensemble methods: foundations and algorithms. London: Taylor & Francis Group; 2012.10.1201/b12207Suche in Google Scholar

81. Shang, G, Richardson, A, Gahan, ME, Easteal, S, Ohms, S, Lidbury, BA. Predicting the presence of hepatitis B virus surface antigen in Chinese patients by pathology data mining. J Med Virol 2013;85:1334–9. https://doi.org/10.1002/jmv.23609.Suche in Google Scholar PubMed

82. Wei, R, Wang, J, Wang, X, Xie, G, Wang, Y, Zhang, H, et al.. Clinical prediction of HBV and HCV related hepatic fibrosis using machine learning. EBioMedicine 2018;35:124–32. https://doi.org/10.1016/j.ebiom.2018.07.041.Suche in Google Scholar PubMed PubMed Central

83. Canbay, A, Bechmann, L, Gerken, G. Lipid metabolism in the liver. Z Gastroenterol 2007;45:35–41. https://doi.org/10.1055/s-2006-927368.Suche in Google Scholar PubMed

84. Roberts, MS, Magnusson, BM, Burczynski, FJ, Weiss, M. Enterohepatic circulation: physiological, pharmacokinetic and clinical implications. Clin Pharmacokinet 2002;41:751–90. https://doi.org/10.2165/00003088-200241100-00005.Suche in Google Scholar PubMed

85. Campollo, O, Sprengers, D, McIntyre, N. The BCAA/AAA ratio of plasma amino acids in three different groups of cirrhotics. Rev Invest Clin 1992;44:513–8.Suche in Google Scholar

86. Zhang, Q, Takahashi, M, Noguchi, Y, Sugimoto, T, Kimura, T, Okumura, A, et al.. Plasma amino acid profiles applied for diagnosis of advanced liver fibrosis in patients with chronic hepatitis C infection. Hepatol Res 2006;34:170–7. https://doi.org/10.1016/j.hepres.2005.12.006.Suche in Google Scholar PubMed

87. Zhang, J, Zhao, Y, Xu, C, Hong, Y, Lu, H, Wu, J, et al.. Association between serum free fatty acid levels and nonalcoholic fatty liver disease: a cross-sectional study. Sci Rep 2014;4:5832. https://doi.org/10.1038/srep05832.Suche in Google Scholar PubMed PubMed Central

88. Chen, T, Xie, G, Wang, X, Fan, J, Qiu, Y, Zheng, X, et al.. Serum and urine metabolite profiling reveals potential biomarkers of human hepatocellular carcinoma. Mol Cell Proteomics 2011;10:M110:004945. https://doi.org/10.1074/mcp.a110.004945.Suche in Google Scholar

89. Wang, X, Wang, X, Xie, G, Zhou, M, Yu, H, Lin, Y, et al.. Urinary metabolite variation is associated with pathological progression of the post-hepatitis B cirrhosis patients. J Proteome Res 2012;11:3838–47. https://doi.org/10.1021/pr300337s.Suche in Google Scholar PubMed

90. Xie, G, Wang, X, Wei, R, Wang, J, Zhao, A, Chen, T, et al.. Serum metabolite profiles are associated with the presence of advanced liver fibrosis in Chinese patients with chronic hepatitis B viral infection. BMC Med 2020;18:144. https://doi.org/10.1186/s12916-020-01595-w.Suche in Google Scholar PubMed PubMed Central

Received: 2023-06-28
Accepted: 2023-08-25
Published Online: 2023-09-20

© 2023 Walter de Gruyter GmbH, Berlin/Boston

Artikel in diesem Heft

  1. Frontmatter
  2. Reviews
  3. Diagnostic errors in uncommon conditions: a systematic review of case reports of diagnostic errors
  4. Routine blood test markers for predicting liver disease post HBV infection: precision pathology and pattern recognition
  5. Opinion Papers
  6. The challenge of clinical reasoning in chronic multimorbidity: time and interactions in the Health Issues Network model
  7. The first diagnostic excellence conference in Japan
  8. Clouds across the new dawn for clinical, diagnostic and biological data: accelerating the development, delivery and uptake of personalized medicine
  9. Original Articles
  10. Towards diagnostic excellence on academic ward teams: building a conceptual model of team dynamics in the diagnostic process
  11. Error codes at autopsy to study potential biases in diagnostic error
  12. Multicenter evaluation of a method to identify delayed diagnosis of diabetic ketoacidosis and sepsis in administrative data
  13. Detection of fake papers in the era of artificial intelligence
  14. Is language an issue? Accuracy of the German computerized diagnostic decision support system ISABEL and cross-validation with the English counterpart
  15. The feasibility of a mystery case curriculum to enhance diagnostic reasoning skills among medical students: a process evaluation
  16. Internal medicine intern performance on the gastrointestinal physical exam
  17. Scaling up a diagnostic pause at the ICU-to-ward transition: an exploration of barriers and facilitators to implementation of the ICU-PAUSE handoff tool
  18. Learned cautions regarding antibody testing in mast cell activation syndrome
  19. Diagnostic properties of natriuretic peptides and opportunities for personalized thresholds for detecting heart failure in primary care
  20. Incomplete filling of spray-dried K2EDTA evacuated blood tubes: impact on measuring routine hematological parameters on Sysmex XN-10
  21. Letters to the Editor
  22. The diagnostic accuracy of AI-based predatory journal detectors: an analogy to diagnosis
  23. Explainable AI for gut microbiome-based diagnostics: colorectal cancer as a case study
  24. Restless X syndrome: a new diagnostic family of nocturnal, restless, abnormal sensations of various body parts
  25. Erratum
  26. Retraction of: Establishing a stable platform for the measurement of blood endotoxin levels in the dialysis population
Heruntergeladen am 27.9.2025 von https://www.degruyterbrill.com/document/doi/10.1515/dx-2023-0078/html
Button zum nach oben scrollen