TY - JOUR
T1 - The Impact of the G6PD Gene Mutations in Patients with Chronic Hepatitis C Infection Treated with Direct-Acting Antivirals: A Multicenter Observational Study
AU - SMIRNE, Carlo
AU - Crobu, Maria
AU - Gerevini, Chiara
AU - Berton, Alessandro
AU - Rapetti, Rachele
AU - Pasini, Barbara
AU - Ravanini, Paolo
AU - PIRISI, Mario
PY - 2024
Y1 - 2024
N2 - Following the advent of direct-acting antivirals (DAAs), the treatment of hepatitis C virus (HCV) infection is now rarely challenging. However, data are still limited concerning DAA use in patients affected by glucose-6-phosphate dehydrogenase deficiency (G6PDd). Based on these considerations, the goal of this study was to evaluate the effectiveness and safety of DAAs in this subpopulation. A retrospective multicenter observational study (2015–2023) was conducted on all 2754 consecutive HCV-positive patients treated with first- and second-generation all-oral DAAs, and with a G6PDd diagnosis confirmed by quantitative testing (n = 38). At the treating clinician’s discretion, an enhanced clinical and laboratory follow-up was performed, generally on a monthly basis both during treatment and up to six months after the end of it. Concerning hematochemical parameters, no significant differences were found between any considered time point. In all cases, no treatment-related adverse events were reported, and virologic response rates were as expected without G6PDd. In conclusion, in a large experience which, to the best of our knowledge, is unprecedented in the literature, the treatment of HCV hepatitis with nearly all available DAAs in patients with G6PDd as a comorbidity—a common occurrence in countries such as Italy—proved to be highly effective and safe.
AB - Following the advent of direct-acting antivirals (DAAs), the treatment of hepatitis C virus (HCV) infection is now rarely challenging. However, data are still limited concerning DAA use in patients affected by glucose-6-phosphate dehydrogenase deficiency (G6PDd). Based on these considerations, the goal of this study was to evaluate the effectiveness and safety of DAAs in this subpopulation. A retrospective multicenter observational study (2015–2023) was conducted on all 2754 consecutive HCV-positive patients treated with first- and second-generation all-oral DAAs, and with a G6PDd diagnosis confirmed by quantitative testing (n = 38). At the treating clinician’s discretion, an enhanced clinical and laboratory follow-up was performed, generally on a monthly basis both during treatment and up to six months after the end of it. Concerning hematochemical parameters, no significant differences were found between any considered time point. In all cases, no treatment-related adverse events were reported, and virologic response rates were as expected without G6PDd. In conclusion, in a large experience which, to the best of our knowledge, is unprecedented in the literature, the treatment of HCV hepatitis with nearly all available DAAs in patients with G6PDd as a comorbidity—a common occurrence in countries such as Italy—proved to be highly effective and safe.
KW - glucose-6-phosphate dehydrogenase deficiency
KW - favism
KW - anemia
KW - hemolytic
KW - hepatitis C virus
KW - direct-acting antivirals agents
KW - pegylated interferon
KW - ribavirin
KW - drug-related side effects and adverse reactions
KW - liver cirrhosis
KW - sofosbuvir
KW - glucose-6-phosphate dehydrogenase deficiency
KW - favism
KW - anemia
KW - hemolytic
KW - hepatitis C virus
KW - direct-acting antivirals agents
KW - pegylated interferon
KW - ribavirin
KW - drug-related side effects and adverse reactions
KW - liver cirrhosis
KW - sofosbuvir
UR - https://iris.uniupo.it/handle/11579/201063
U2 - 10.3390/genes15091116
DO - 10.3390/genes15091116
M3 - Article
SN - 2073-4425
VL - 15
SP - 1
EP - 12
JO - Genes
JF - Genes
IS - 9
ER -