Charles Antoine Béguelin
University of Bern
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Featured researches published by Charles Antoine Béguelin.
Journal of Hepatology | 2017
Charles Antoine Béguelin; Darius Moradpour; Roland Sahli; Franziska Suter-Riniker; Alexander Lüthi; Matthias Cavassini; Huldrych F. Günthard; Manuel Battegay; Enos Bernasconi; Patrick Schmid; Alexandra Calmy; Dominique L. Braun; Hansjakob Furrer; Andri Rauch; Gilles Wandeler
BACKGROUND & AIMS Hepatitis delta virus (HDV) infection accelerates the progression of hepatitis B virus (HBV)-related liver disease. We assessed the epidemiological characteristics of HDV infection in the nationwide Swiss HIV Cohort Study and evaluated its impact on clinical outcomes. METHODS All HIV-infected patients with a positive hepatitis B surface antigen test were considered and tested for anti-HDV antibodies. HDV amplification and sequencing were performed in anti-HDV-positive patients. Demographic and clinical characteristics at initiation of antiretroviral therapy, as well as causes of death were compared between HDV-positive and HDV-negative individuals using descriptive statistics. Kaplan-Meier and multivariable Cox regression analyses were used to evaluate the association between HDV infection and overall mortality, liver-related mortality as well as incidence of hepatocellular carcinoma (HCC). RESULTS Of 818 patients with a positive hepatitis B surface antigen tests, 771 (94%) had a stored serum sample available and were included. The prevalence of HDV infection was 15.4% (119/771, 95% CI: 12.9-18.0) and the proportion of HDV-positive patients with HDV replication 62.9% (73/116). HDV-infected patients were more likely to be persons who inject drugs (60.6% vs. 9.1%) and to have a positive hepatitis C virus (HCV) serology (73.1% vs. 17.8%) compared to HDV-uninfected ones. HDV infection was strongly associated with overall death (adjusted hazard ratio 2.33, 95% CI 1.41-3.84), liver-related death (7.71, 3.13-18.97) and with the occurrence of HCC (9.30, 3.03-28.61). Results were similar when persons who inject drugs or HCV-coinfected patients were excluded from the analyses. CONCLUSIONS The prevalence of HDV in hepatitis B surface antigen-positive patients in the Swiss HIV Cohort Study (SHCS) is high and HDV infection is independently associated with mortality and liver-related events, including HCC. LAY SUMMARY Hepatitis delta virus (HDV) infection accelerates the progression of hepatitis B virus (HBV)-related liver disease. In a nationwide cohort of HIV-infected individuals in Switzerland, 15% of HBV-coinfected patients had antibodies to HDV infection, of which a majority had active HDV replication. HDV-infected individuals were 2.5 times more likely to die, eight times more likely to die from a liver-related cause and nine times more likely to develop liver cancer compared to HDV-uninfected ones. Our results emphasize the need for prevention programs (including HBV vaccination), the systematic screening of at risk populations as well as close monitoring, and underline the importance of developing new treatments for chronic HDV infection.
Journal of Hepatology | 2017
Daniëla K. van Santen; Jannie J. van der Helm; Julia del Amo; Laurence Meyer; Antonella d'Arminio Monforte; Matthew Price; Charles Antoine Béguelin; Robert Zangerle; Mette Sannes; Kholoud Porter; Ronald B. Geskus; Maria Prins
BACKGROUND & AIMS Hepatitis C virus (HCV) incidence among HIV-positive men who have sex with men (MSM) has increased since 2000, although there are regional differences. We aimed to 1) estimate trends in HCV incidence among HIV-positive MSM, 2) assess the association between incidence and geographical region, age and HIV-related measurements and, 3) assess temporal changes from HIV seroconversion to HCV infection. METHODS Data was used from MSM with well-estimated dates of HIV seroconversion from the CASCADE Collaboration (1990-2014). Smoothly varying trends in HCV incidence over time were allowed, using restricted cubic splines. The association of calendar year, age, CD4 count (lagged), HIV RNA (lagged), geographical region and HIV infection stage (recent vs. chronic) with HCV incidence were assessed using Poisson regression. RESULTS Of 5,941 MSM, 337 acquired HCV during follow-up. HCV incidence significantly increased from 0.7/1,000 person-years in 1990 to 18/1,000 person-years in 2014. Recent calendar years, younger age, recent HIV infection and higher HIV RNA levels were significantly associated with HCV incidence, while CD4 count was not. Trends differed by geographical region; while incidence appeared to have stabilized in Western Europe and remained stable in Southern Europe, it continued to increase in Northern Europe in recent years. Time from HIV to HCV infection significantly decreased over time (p<0.001). CONCLUSIONS HCV has continued to spread among HIV-positive MSM in recent years, but trends differ by geographical region. Interventions to decrease the risk of HCV acquisition and increase early diagnosis are warranted. LAY SUMMARY Hepatitis C virus infection continues to spread among HIV-positive men who have sex with men, especially among younger individuals. However, trends seem to differ by European region in recent years. Furthermore, men who have sex with men with a higher HIV RNA load were more likely to get infected with the hepatitis C virus. During recent HIV infection, MSM appear to be at higher risk of acquiring hepatitis C.
Journal of the International AIDS Society | 2014
Charles Antoine Béguelin; Miriam Vázquez; Manuel Bertschi; Sabine Yerly; Denise de Jong; Andri Rauch; Alexia Cusini
HIV‐1 viral escape in the cerebrospinal fluid (CSF) despite viral suppression in plasma is rare [ 1 , 2 ]. We describe the case of a 50‐year‐old HIV‐1 infected patient who was diagnosed with HIV‐1 in 1995. Antiretroviral therapy (ART) was started in 1998 with a CD4 T cell count of 71 cells/ìL and HIV‐viremia of 46,000 copies/mL. ART with zidovudine (AZT), lamivudine (3TC) and efavirenz achieved full viral suppression. After the patient had interrupted ART for two years, treatment was re‐introduced with tenofovir (TDF), emtricitabin (FTC) and ritonavir boosted atazanavir (ATVr). This regimen suppressed HIV‐1 in plasma for nine years and CD4 cells stabilized around 600 cells/ìL. Since July 2013, the patient complained about severe gait ataxia and decreased concentration.
Clinical Infectious Diseases | 2017
Charles Antoine Béguelin; Nicole Friolet; Darius Moradpour; Roland Sahli; Franziska Marta Suter; Alexander Lüthi; Matthias Cavassini; Huldrych F. Günthard; Manuel Battegay; Enos Bernasconi; Patrick Schmid; Alexandra Calmy; Andrew Atkinson; Andri Rauch; Gilles Wandeler
We analyzed changes in hepatitis B virus and hepatitis delta virus (HDV) viral loads (VL) during tenofovir-containing antiretroviral therapy among patients with a replicating HDV infection in the Swiss HIV Cohort Study. Only 28.6% experienced a ≥2.0 log reduction in HDV RNA, and 14.3% had undetectable HDV VL within 5 years.
Clinical Infectious Diseases | 2017
Charles Antoine Béguelin; Nicole Friolet; Darius Moradpour; Roland Sahli; Franziska Suter-Riniker; Alexander Lüthi; Matthias Cavassini; Huldrych F. Günthard; Manuel Battegay; Enos Bernasconi; Patrick Schmid; Alexandra Calmy; Andrew Atkinson; Andri Rauch; Gilles Wandeler
We analyzed changes in hepatitis B virus and hepatitis delta virus (HDV) viral loads (VL) during tenofovir-containing antiretroviral therapy among patients with a replicating HDV infection in the Swiss HIV Cohort Study. Only 28.6% experienced a ≥2.0 log reduction in HDV RNA, and 14.3% had undetectable HDV VL within 5 years.
Open Forum Infectious Diseases | 2016
Charles Antoine Béguelin; Miriam Vázquez; Manuel Bertschi; Sabine Yerly; Denise de Jong; Klemens Gutbrod; Andri Rauch; Alexia Cusini
In this study, we report the case of a patient infected with human immunodeficiency virus (HIV)-1 who developed ataxia and neurocognitive impairment due to viral escape within the central nervous system (CNS) with a multidrug-resistant HIV-1 despite long-term viral suppression in plasma. Antiretroviral therapy optimization with drugs with high CNS penetration led to viral suppression in the CSF, regression of ataxia, and improvement of neurocognitive symptoms.
Liver International | 2018
Charles Antoine Béguelin; Annatina Suter; Enos Bernasconi; Jan Fehr; Helen Kovari; Heiner C. Bucher; Marcel Stoeckle; Mathias Cavassini; Mathieu Rougemont; Patrick Schmid; Gilles Wandeler; Andri Rauch
Hepatitis C virus (HCV) therapies with interferon‐free second‐generation direct‐acting antivirals (DAAs) are highly effective and well tolerated. They have the potential to increase treatment eligibility and efficacy in HIV‐infected patients. We assessed the impact of DAAs on treatment uptake and efficacy, as well as its impact on the burden of liver disease in the Swiss HIV Cohort Study (SHCS).
Journal of the International AIDS Society | 2018
Rachel Sacks-Davis; Joseph S. Doyle; Andri Rauch; Charles Antoine Béguelin; Alisa Pedrana; Gail V. Matthews; Maria Prins; Marc van der Valk; Marina B. Klein; Sahar Saeed; Karine Lacombe; Nikoloz Chkhartishvili; Frederick L. Altice; Margaret Hellard
There is currently no published data on the effectiveness of DAA treatment for elimination of HCV infection in HIV‐infected populations at a population level. However, a number of relevant studies and initiatives are emerging. This research aims to report cascade of care data for emerging HCV elimination initiatives and studies that are currently being evaluated in HIV/HCV co‐infected populations in the context of implementation science theory.
Open Forum Infectious Diseases | 2018
Luisa Salazar-Vizcaya; Gilles Wandeler; Jan Fehr; Dominique L. Braun; Matthias Cavassini; Marcel Stoeckle; Enos Bernasconi; Matthias Hoffmann; Mathieu Rougemont; Charles Antoine Béguelin; Andri Rauch; Vincent Aubert; Manuel Battegay; E Bernasconi; Jürg Böni; D L Braun; H C Bucher; A Calmy; Angela Ciuffi; G Dollenmaier; Matthias Egger; L Elzi; J. Fehr; Jacques Fellay; Hansjakob Furrer; Christoph A. Fux; Huldrych F. Günthard; D Haerry; Barbara Hasse; Hans H. Hirsch
Abstract In the Swiss HIV Cohort Study, the number of people who inject drugs with replicating hepatitis C virus (HCV) infection decreased substantially after the introduction of direct-acting antivirals (DAAs). Among men who have sex with men, the increase in DAA uptake and efficacy was counterbalanced by frequent incident HCV infections.
Archive | 2018
Dominique L. Braun; Benjamin Hampel; Eileen Martin; Roger D. Kouyos; Katharina Kusejko; Christina Grube; Markus Flepp; Marcel Stöckle; Anna Conen; Charles Antoine Béguelin; Patrick Schmid; Julie Delaloye; Mathieu Rougemont; Enos Bernasconi; Andri Rauch; Huldrych F. Günthard; Jürg Böni; Jan Fehr
Background The proportion of undiagnosed hepatitis C virus (HCV) infections in high-risk populations, such as human immunodeficiency virus (HIV)-infected men who have sex with men (MSM) is unclear. Identification of potential HCV transmitters is important to reach World Health Organization HCV elimination targets. Methods Between October 2015 and May 2016, we performed a systematic HCV RNA-based screening among HIV-infected MSM participating in the Swiss HIV Cohort Study (SHCS). HCV antibodies were measured from all HCV RNA-positive samples. Results Of 4257 MSM recorded in the SHCS database, we screened 3722 (87%) by HCV polymerase chain reaction, and 177 (4.8%) harbored a replicating HCV infection. We identified 24 individuals (14%) with incident HCV infection; one-third of them had a negative HCV antibody result at the time of HCV RNA positivity. In a multivariable model, elevated liver enzyme values (odds ratio, 14.52; 95% confidence interval, 9.92-21.26), unprotected sex with occasional partners (2.01; 1.36-2.98), intravenous drug use (7.13; 4.36-11.64), noninjectable drug use (1.94; 1.3-2.88), and previous syphilis diagnosis (2.56; 1.74-3.76) were associated with HCV RNA positivity. Conclusions A systematic HCV RNA-based screening among HIV-infected MSM revealed a high number of potential transmitters. A substantial subpopulation of MSM had incident infection, one-third of whom had a negative HCV antibody test result at the time of the HCV RNA positivity. These data reveal that one-time RNA testing of a high-risk population for HCV RNA might identify more infected persons than routine testing for HCV antibodies and liver enzymes. Clinical Trials Registration NCT02785666.