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Long-Term Persistence of Mitochondrial DNA Instability among HCV-Cured People Who Inject Drugs.
Durand, Mélusine; Nagot, Nicolas; Nhu, Quynh Bach Thi; Vizeneux, Amélie; Thuy, Linh Le Thi; Duong, Huong Thi; Thanh, Binh Nguyen; Rapoud, Delphine; Vallo, Roselyne; Quillet, Catherine; Tran, Hong Thi; Michel, Laurent; Tuyet, Thanh Nham Thi; Hai, Oanh Khuat Thi; Hai, Vinh Vu; Feelemyer, Jonathan; Vande Perre, Philippe; Des Jarlais, Don; Minh, Khue Pham; Laureillard, Didier; Molès, Jean-Pierre.
Afiliação
  • Durand M; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Nagot N; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Nhu QBT; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Vizeneux A; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Thuy LLT; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Duong HT; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Thanh BN; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Rapoud D; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Vallo R; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Quillet C; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Tran HT; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Michel L; Pierre Nicole Center, French Red Cross, 75005 Paris, France.
  • Tuyet TNT; Supporting Community Development Initiatives, Hanoi 111000, Vietnam.
  • Hai OKT; Supporting Community Development Initiatives, Hanoi 111000, Vietnam.
  • Hai VV; Infectious Diseases Department, Viet Tiep Hospital, Hai Phong 180000, Vietnam.
  • Feelemyer J; College of Global Public Health, New York University, New York, NY 10012, USA.
  • Vande Perre P; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Des Jarlais D; College of Global Public Health, New York University, New York, NY 10012, USA.
  • Minh KP; Faculty of Public Health, Hai Phong University of Medicine and Pharmacy, Hai Phong 180000, Vietnam.
  • Laureillard D; Pathogenesis and Control of Chronic and Emerging Infections, University of Montpellier, INSERM, 34000 Montpellier, France.
  • Molès JP; Infectious Diseases Department, Caremeau University Hospital, 30029 Nîmes, France.
Biomedicines ; 10(10)2022 Oct 12.
Article em En | MEDLINE | ID: mdl-36289803
People who inject drugs (PWID) are a population exposed to many genotoxicants and with a high prevalence of HCV infection. Direct-acting antiviral (DAA) regimens are now widely used to treat chronic HCV infection. Although side effects to treatment are currently rare, the long-term effects such as suspicions of de novo hepatocellular carcinoma (HCC) occurrence or HCC recurrence and cardiac defects are still up for debate. Given the structure of DAAs, the molecules have a potential mitochondrial DNA (mtDNA) genotoxicity. We have previously reported acute mtDNA toxicity of three DAA regimens among PWID with a strong impact on the rate of mtDNA deletion, less on the quantity of mtDNA copy per cell at sustained viral response at 12 weeks (SVR12). Herein, we report the mtDNA parameters nine months after drug discontinuation. We observed that the percentage of the deleted mtDNA genome increased over time. No exposure to any other genotoxicants during this period was associated with a high deletion percentage, suggesting that the replicative advantage of the deleted molecules outweighed their elimination processes. Such observation calls for longer-term follow-up and may contribute to the molecular basis of subclinical side effects of DAA treatments.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Biomedicines Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Risk_factors_studies Idioma: En Revista: Biomedicines Ano de publicação: 2022 Tipo de documento: Article País de afiliação: França