Predictors of cirrhosis in chronic hepatitis C: Findings from a 24-month follow-up study in Almaty, Kazakhstan
Keywords:
chronic hepatitis C, cirrhosis, predictors, diabetes mellitus, sustained virological response, glycemic control, risk factors, Kazakhstan, follow-up study, liver disease progressionAbstract
Background and aim: Hepatitis C virus (HCV) infection remains a significant global health challenge, affecting an estimated 50 million people worldwide and causing approximately 1 million new cases annually. The presence of cirrhosis and diabetes mellitus appear to amplify the clinical and economic impact of HCV related disease. This study aims to evaluate the incidence of liver cirrhosis within a 24‑month follow‑up period after HCV diagnosis, as well as its association with diabetes and other prognostic factors.
Methods: We performed a retrospective analysis of adults with chronic HCV in Almaty, Kazakhstan, using surveillance and medical record data through December 2024. Eligible patients (ICD‑10 B18.2) had ≥24 months of follow‑up and were assessed for cirrhosis (FibroScan F4) in relation to demographic, clinical, and laboratory factors, including diabetes. Group comparisons and logistic regression identified independent predictors, with statistical significance set at p < 0.05.
Results: We performed a retrospective analysis of adults with chronic HCV in Almaty, Kazakhstan, using surveillance and medical record data through December 2024. Eligible patients (ICD‑10 B18.2) had ≥24 months of follow‑up and were assessed for cirrhosis (FibroScan F4) in relation to demographic, clinical, and laboratory factors, including diabetes. Group comparisons and logistic regression identified independent predictors, with statistical significance set at p < 0.05.
Conclusions: In patients with chronic HCV in Almaty, Kazakhstan, diabetes, poor glycemic control, elevated GGT, and low platelet count were independent predictors of cirrhosis, while sustained virological response was protective. These findings highlight the need for integrated antiviral and metabolic management, with tailored monitoring for high‑risk patients to reduce disease progression beyond existing dispanserization measures (www.actabiomedica.it)
References
1. Soliman AT, De Sanctis V, Yassin M, Wagdy M, Soliman N. Chronic anemia and thyroid function. Acta Biomed. 2017;88(1):119–27. doi:10.23750/abm.v88i1.6048
2. Narsule CK, Sridhar P, Nair D, et al. Percutaneous thermal ablation for stage IA non-small cell lung cancer: long-term follow-up. J Thorac Dis. 2017;9(10):4039–45. doi:10.21037/jtd.2017.08.142
3. World Health Organization (WHO). Hepatitis C. Key facts. 2025. https://www.who.int/news-room/fact-sheets/detail/hepatitis-c (accessed 2025 Aug 28)
4. Scott N, Kuschel C, Pedrana A, et al. A model of the economic benefits of global hepatitis C elimination: an investment case. Lancet Gastroenterol Hepatol. 2020;5(10):940–7. doi:10.1016/S2468-1253(20)30008-X
5. Asselah T, Marcellin P, Schinazi RF. Treatment of hepatitis C virus infection with direct-acting antiviral agents: 100% cure? Liver Int. 2018;38(Suppl 1):7. doi:10.1111/liv.13673
6. Negro F, Forton D, Craxì A, Sulkowski MS, Feld JJ, Manns MP. Extrahepatic morbidity and mortality of chronic hepatitis C. Gastroenterology. 2015;149(6):1345–60. doi:10.1053/j.gastro.2015.08.035
7. Angel M, Petrosyan Y, Doyle MA, Cooper C. HCV infection characteristics, treatment uptake and outcomes in patients with diabetes mellitus. BMC Endocr Disord. 2022;22(1):1–9. doi:10.1186/s12902-022-01198-x
8. Shoji I, Deng L, Hotta H. Molecular mechanism of hepatitis C virus-induced glucose metabolic disorders. Front Microbiol. 2012;2:20229. doi:10.3389/fmicb.2011.00278
9. Parvaiz F, Manzoor S, Tariq H, Javed F, Fatima K, Qadri I. Hepatitis C virus infection: molecular pathways to insulin resistance. Virol J. 2011;8(1):474. doi:10.1186/1743-422x-8-474
10. Li Z, Ye Y, Zhang Y, Xu W, Liu Y. Metabolic dysfunction, cirrhosis, and HCV genotype 3a drive type 2 diabetes risk in chronic hepatitis C: a Southern Chinese cohort study. BMC Gastroenterol. 2025;25(1):1–9. doi:10.1186/s12876-025-04109-1
11. Yamana H, Imai S, Yamasaki K, et al. Prognosis of patients with liver cirrhosis: a multi-center retrospective observational study. Hepatol Res. 2021;51(12):1196–206. doi:10.1111/hepr.13711
12. Order of the Minister of Health of the Republic of Kazakhstan. On approval of the list of socially significant diseases, No. KR DSM-108/2020. Registered with the Ministry of Justice of the Republic of Kazakhstan on September 24, 2020 No. 21263. 2020. https://adilet.zan.kz/rus/docs/V2000021263 (accessed 2025 Aug 28)
13. EGOV: Government services and information online. Guaranteed amount of free medical care. Who can get a guaranteed amount of free medical care and how? 2023. https://egov.kz/cms/ru/articles/health_care/2Fgarant_obyiom_med_pomoshi (accessed 2025 Aug 28)
14. Baimukhanova M, Nurgaliyeva B. Dynamics of viral hepatitis C incidence in Almaty for the period from 2021–2023. Pharmacy of Kazakhstan. 2025;4(261):31–40. doi:10.53511/pharmkaz.2025.4.3
15. Posit team. RStudio: Integrated development environment for R. Posit Software, PBC. 2023. http://www.posit.co/ (accessed 2024 Jan 22)
16. Zein NN, Abdulkarim AS, Wiesner RH, Egan KS, Persing DH. Prevalence of diabetes mellitus in patients with end-stage liver cirrhosis due to hepatitis C, alcohol, or cholestatic disease. J Hepatol. 2000;32(2):209–17. doi:10.1016/s0168-8278(00)80065-3
17. Li X, Gao Y, Xu H, Hou J, Gao P. Diabetes mellitus is a significant risk factor for the development of liver cirrhosis in chronic hepatitis C patients. Sci Rep. 2017;7(1):1–6. doi:10.1038/s41598-017-09825-7
18. Elkrief L, Chouinard P, Bendersky N, et al. Diabetes mellitus is an independent prognostic factor for major liver-related outcomes in patients with cirrhosis and chronic hepatitis C. Hepatology. 2014;60(3):823–31. doi:10.1002/hep.27228
19. Fabiani S, Fallahi P, Ferrari SM, Miccoli M, Antonelli A. Hepatitis C virus infection and development of type 2 diabetes mellitus: systematic review and meta-analysis of the literature. Rev Endocr Metab Disord. 2018;19(4):405–20. doi:10.1007/s11154-017-9440-1
20. Pan CQ, Park AJ, Park JS. New perspectives in hepatocellular carcinoma surveillance after hepatitis C virus eradication. Gastroenterol Rep (Oxf). 2024;12:goae085. doi:10.1093/gastro/goae085
21. Velosa J, Serejo F, Marinho R, Nunes J, Glória H. Eradication of hepatitis C virus reduces the risk of hepatocellular carcinoma in patients with compensated cirrhosis. Dig Dis Sci. 2011;56(6):1853–61. doi:10.1007/s10620-011-1621-2
22. Akhtar E, Manne V, Saab S. Cirrhosis regression in hepatitis C patients with sustained virological response after antiviral therapy: a meta-analysis. Liver Int. 2015;35(1):30–6. doi:10.1111/liv.12576
23. Kazbekova A, Akanov Z, Abseitova D, et al. The prevalence of diabetes mellitus in Kazakhstan: a systematic review and meta-analysis. Acta Biomed. 2024;95(6):e2024130. doi:10.23750/abm.v95i6.15905
24. Baimukhanova M, Sadykova S, Kurmanova G, et al. Pandemic and policy effects on hepatitis C and diabetes: insights from Kazakhstan using interrupted time series analysis. Acta Biomed. 2025;96(1):16445. doi:10.23750/abm.v96i1.16445
25. Shaki D, Aimbetova G, Baysugurova V, et al. Level of patient satisfaction with quality of primary healthcare in Almaty during COVID-19 pandemic. Int J Environ Res Public Health. 2025;22(5):804. doi:10.3390/ijerph22050804
26. Moiynbayeva S, Akhmetov V, Narymbayeva N, et al. Health policy implications for cardiovascular disease, type 2 diabetes mellitus, and stroke in Central Asia: a decadal forecast of their impact on women of reproductive age. Front Public Health. 2024;12:1456187. doi:10.3389/fpubh.2024.1456187
27. Kaidar E, Turgambayeva A, Zhussupov B, Stukas R, Sultangaziyev T, Yessenbayev B. The effects of COVID-19 severity on health status in Kazakhstan: a prospective cohort study. Clin Epidemiol Glob Health. 2024;29:101761. doi:10.1016/j.cegh.2024.101761
28. Hiebert-Suwondo L, Manning J, Tohme RA, et al. A 2024 global report on national policies, programmes, and progress towards hepatitis C elimination: findings from 33 hepatitis elimination profiles. Lancet Gastroenterol Hepatol. 2025;10(7):685–700. doi:10.1016/s2468-1253(25)00068-8
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Copyright (c) 2025 Manzura Baimukhanova, Gaukhar Kurmanova, Gulzhan Trimova, Zhanar Serikbayeva, Nazgul Aliftenova, Bayan Nurgaliyeva, Assem Kazbekova, Shugyla Amirtayeva, Daniyar Sultankulov, Sholpan Sadykova

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