Paper Details 
Original Abstract of the Article :
Direct-acting antivirals have revolutionized the treatment of chronic hepatitis C. Sofosbuvir and simeprevir are prescribed worldwide. However, there is a scarcity of information regarding their genotoxicity. Therefore, the present study assessed the cytotoxic and genotoxic effects of sofosbuvir and...See full text at original site
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引用元:
https://doi.org/10.1590/0001-3765202120200632

データ提供:米国国立医学図書館(NLM)

Investigating the Genotoxicity of Sofosbuvir and Simeprevir: A Safety Assessment

Direct-acting antivirals (DAAs) have revolutionized the treatment of hepatitis C. Sofosbuvir and simeprevir are two commonly prescribed DAAs, but limited information exists about their potential genotoxicity. This research investigates the cytotoxic and genotoxic effects of these drugs, both alone and in combination with ribavirin, using a human-derived liver cell line.

Simeprevir Shows Genotoxic Potential While Sofosbuvir Does Not

The results of this study indicate that simeprevir, but not sofosbuvir, has genotoxic effects in HepG2 cells. Simeprevir was found to increase the frequency of micronuclei, a marker of chromosomal damage, at higher concentrations. The combination of sofosbuvir and ribavirin showed antagonistic effects, meaning they reduced the genotoxic effects of ribavirin.

Navigating the Safety of Antiviral Medications: A Need for Vigilance

This research highlights the importance of carefully evaluating the safety of antiviral medications. While DAAs have been transformative in the treatment of hepatitis C, ongoing research is crucial to ensure that these medications are safe for long-term use.

Dr. Camel's Conclusion

Just as a camel navigates a desert landscape, we need to navigate the complex world of antiviral medications with a keen eye for safety. This research underscores the importance of ongoing safety assessments to ensure that these medications are providing effective treatment without compromising patient health.

Date :
  1. Date Completed 2021-10-01
  2. Date Revised 2021-10-01
Further Info :

Pubmed ID

34586319

DOI: Digital Object Identifier

10.1590/0001-3765202120200632

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English

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