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Natural history of hepatitis C in HIV-negative patients with congenital coagulation disorders
1Division of Haemostasis, Thrombosis and Rheology, University Hospital Groningen, The Netherlands. k.meijer@int.azg.nl
Insights
Hepatitis C (HCV) infection in HIV-negative patients with clotting disorders shows slow progression. After 19 years, most patients remained asymptomatic, but advanced age was a key risk factor for liver disease progression.
Area of Science:
- Hepatology
- Virology
- Internal Medicine
Background:
- Understanding hepatitis C natural history is crucial for patient counseling and treatment planning.
- Data from unselected patient groups without comorbidities are needed.
- This study focuses on HIV-negative patients with congenital coagulation defects, a homogeneous group without specific hepatitis C therapy.
Purpose of the Study:
- To describe the natural history of hepatitis C infection.
- To evaluate liver disease progression two decades post-infection.
- To identify risk factors for advanced disease in a specific patient cohort.
Main Methods:
- A cohort of 45 HCV-RNA positive, HIV-negative patients (primarily hemophiliacs) was studied.
- Methods included medical history, physical examination, laboratory tests, and abdominal ultrasonography.
- Patients were classified based on ultrasonography findings to assess liver disease severity.
Main Results:
- After a median of 19 years, 58% showed only elevated transaminases, while 16% had cirrhosis on ultrasonography.
- Only two patients experienced variceal bleeding; none had ascites.
- Higher present age was identified as the primary independent risk factor for advanced liver disease.
Conclusions:
- Hepatitis C progression is slow in this cohort, with most patients asymptomatic.
- Liver cirrhosis was present in 16% of patients after two decades.
- Increasing age is the main predictor of advanced liver disease in this population.
Background/Aims:
Knowledge of the natural history of hepatitis C is useful for counselling patients and planning treatment. More data are needed from unselected patient groups without concomitant disease. The aim of this study was to describe the natural history of hepatitis C, two decades after infection, in a homogeneous and well-defined group of HIV-negative patients with congenital coagulation defects who had not received specific therapy for chronic hepatitis C.
Methods:
Medical history, physical examination, laboratory tests and abdominal ultrasonography were performed in 45 HCV-RNA positive, HIV-negative patients, mainly haemophiliacs, from a single centre. Patients were classified according to results of ultrasonography.
Results:
Two patients had experienced an episode of variceal bleeding; all others were asymptomatic. None had ascites. HCV-RNA titres were >500000 copies/ml in 23 patients, genotype was 1 in 31 patients. Forty (89%) had elevated transaminases, liver synthesis function was diminished in 7 (16%), and platelet count in 8 (18%). Ultrasonography was normal in 26 (58%) patients, 12 (27%) had isolated splenomegaly, and 7 (16%) had liver nodularity compatible with cirrhosis. Univariate analysis disclosed higher transaminases and gammaGT, higher age at acquisition of infection and higher present age as risk factors for more advanced disease. Of these, only higher present age was an independent predictor in multivariate analysis.
Conclusions:
Median 19 years after infection, 58% of patients had no other signs of liver disease than raised transaminases, 16% had cirrhosis on ultrasonography. Only 2/45 patients had symptomatic disease. Higher present age is the main risk factor for advanced disease in this group.
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