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A Protocol for Analyzing Hepatitis C Virus Replication
Published on: June 26, 2014
Hepatitis C virus infection and lymphoproliferative diseases in France: a national study. The GERMIVIC Group
P Hausfater1, P Cacoub, E Rosenthal
1Service de Médecine Interne, Secrétariat du GERMIVIC, CHU Pitié-Salpêtrière, Paris, France.
Insights
Hepatitis C virus (HCV) infection is linked to lymphoproliferative diseases (LPD), particularly B-cell non-Hodgkin lymphoma (NHL). This French study found a 2.49% LPD frequency in HCV patients, supporting the association but noting a lower rate than in Italy.
Area of Science:
- Hepatology
- Oncology
- Immunology
Background:
- Hepatitis C virus (HCV) infection is associated with lymphoproliferative diseases (LPD) in North America and Southern Europe.
- High HCV seroprevalence is reported in patients with B-cell non-Hodgkin lymphoma (NHL).
Purpose of the Study:
- To investigate the association between chronic HCV infection and LPD in France.
- To determine the frequency of LPD among HCV-infected patients in a national cohort.
Main Methods:
- Retrospective national study involving 72 Internal Medicine and Infectious Diseases departments.
- Data collection on LPD cases in relation to HCV infection status and timing.
- Analysis of HCV extrahepatic manifestations and LPD subtypes.
Main Results:
- 43 LPD cases were recorded, including 31 B-cell NHL.
- The frequency of LPD among 1,485 HCV-infected patients was approximately 2.49%.
- 14 patients exhibited HCV extrahepatic manifestations, with 9 cases of mixed cryoglobulinemia and 5 of sicca syndrome, often associated with NHL.
Conclusions:
- The study supports the hypothesis of HCV-associated LPD, especially B-cell NHL, in France.
- The observed association in France appears less frequent compared to Italy.
- Further research is required to elucidate HCV's precise role in the pathogenesis of monoclonal proliferation.
Abstract:
The putative role of hepatitis C virus (HCV) infection in the pathophysiology of lymphoproliferative diseases (LPD) is supported by North American and southern European studies reporting high HCV seroprevalence in patients with B-cell-non-Hodgkin lymphoma (NHL). In order to evaluate the situation in France, we conducted a retrospective national study about the association of chronic HCV infection and LPD. 72 Internal Medicine and Infectious Diseases departments were contacted. Response rate was 51.4%. We recorded 43 LPD (19 males, 24 females): 31 B-cell-NHL, 4 Waldenström's macroglobulinemia, 3 chronic lymphocytic leukemia, 2 multiple myeloma, 2 lymphomas of the mucosa-associated lymphoid tissue, and 1 Hodgkin's disease. Mean age at HCV diagnosis was 62 years (range 33-84). In 16 cases, LPD occurred in patients known to be HCV-infected. For 11 patients, LPD diagnosis preceded the diagnosis of HCV infection, whereas diagnosis was done simultaneously in 11 patients. For those with accurate infection date, mean interval between both events was 15.2 years. Fourteen patients had HCV extrahepatic manifestations: 9 mixed cryoglobulinemia, including 7 with NHL, 5 sicca syndrome (5 NHL), and both in one patient. Cohort of HCV-infected patients could be accurately determined for 16 departments, totaling 1,485 patients and 37 cases. Thus, from our data the frequency of LPD among HCV-infected patients approximates 2. 49%. Despite possible bias inherent to this retrospective study, our data support the hypothesis of HCV-associated LPD and particularly B-cell-NHL. In France, this association is much lower than in Italy. Further studies are needed to assess the precise role of HCV in the multistep process leading to monoclonal proliferation.
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