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Hepatitis G virus infection in hemodialysis patients from urban Delhi
Deepak Kumar1, Ashu Arora, Narendera Pal Singh
1Department of Medicine, Maulana Azad Medical College, New Delhi, India.
Insights
Hepatitis G virus (HGV) infection is not significantly more prevalent in chronic renal failure patients on hemodialysis compared to healthy individuals. HGV appears to be an innocent bystander, not influencing the disease course in these patients.
Area of Science:
- Hepatology
- Virology
- Nephrology
Background:
- Chronic renal failure patients undergoing hemodialysis are at risk for various infections.
- Hepatotropic viruses, including Hepatitis G Virus (HGV), Hepatitis B Virus (HBV), and Hepatitis C Virus (HCV), are of concern in this population.
- Understanding the seroprevalence and impact of HGV in hemodialysis patients is crucial for patient management.
Purpose of the Study:
- To evaluate the seroprevalence of Hepatitis G Virus (HGV) infection in chronic renal failure patients undergoing hemodialysis.
- To assess the impact of HGV infection and its relationship with other hepatotropic viruses (HBV, HCV) in this patient group.
- To determine if HGV influences the clinical course and liver function in hemodialysis patients.
Main Methods:
- Nested reverse transcription polymerase chain reaction (RT-PCR) was used to detect HGV RNA in serum samples.
- Serological assays screened for Hepatitis B surface antigen (HbsAg) and Anti-HCV antibodies.
- A study group of 100 chronic renal failure patients on hemodialysis was compared with 100 age- and sex-matched healthy controls.
Main Results:
- HGV RNA was detected in 6% of chronic renal failure patients and 3% of healthy controls; this difference was not statistically significant.
- HCV infection was present in 27% and HBV infection in 10% of the patients.
- Mixed HGV and HCV infection occurred in 33.3% of HGV-positive patients, while HGV and HBV coinfection was not observed. ALT levels were significantly elevated in HCV-positive patients.
Conclusions:
- Hepatitis G Virus (HGV) seroprevalence is not significantly higher in chronic renal failure patients on hemodialysis compared to healthy individuals.
- HGV infection does not appear to influence the clinical course or liver function profile in hemodialysis patients.
- HGV infection in this population may represent post-transfusion exposure and is likely an innocent bystander.
Abstract:
This study was designed to evaluate the seroprevalence of hepatitis G virus (HGV) infection, its impact, and its relationship with other hepatotropic viruses among chronic renal failure patients undergoing hemodialysis at the Lok Nayak Hospital, New Delhi. The study group consisted of 100 consecutive cases of patients with chronic renal failure undergoing hemodialysis and equal healthy controls matched for age and sex. The patients were included on the basis of detailed history, clinical examination, and liver function profile. HGV RNA was detected in serum samples of all patients as well as of healthy controls using nested reverse transcription polymerase chain reaction (RT-PCR). The primers used were derived from the NS3 helicase region of the viral genome. Serological assay was used for screening the viral markers for hepatitis B and C (HbsAg and Anti HCV). A history of blood transfusion was recorded in 65% of the cases. HGV RNA was detected in only six out of 100 (6%) cases of chronic renal failure. The seroprevalence of HCV infection was detected in 27 (27%), while HBV infection was seen in 10 (10%) out of 100 cases. The mixed infection of HGV and HCV was seen in 33.3% (two out of six) of the chronic renal failure cases, while the coinfection between HGV and HBV was not observed. In the 100 cases of healthy controls, HGV RNA was detected in only three (3%) subjects. Serological markers for Anti HCV antibody and HbsAg were positive in only one (1%) and two (2%) of the subjects, respectively. The seroprevalence of HGV infection in chronic renal failure was found to be statistically nonsignificant when compared to that of healthy controls. Also, there was no difference in clinical course and liver function profile of HGV-positive and HGV-negative cases. However, alanine aminotransferase (ALT) was significantly out of range in HCV-positive patients compared with HCV-negative patients. The presence of HGV infection reflected a postparental exposure to blood and blood-contaminated products in hemodialysis patients. It is suggested that HGV infection in cases of chronic renal failure is unlikely to influence the course of the disease and may be considered an innocent bystander.
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