Genotype, viral load and age as independent predictors of treatment outcome of interferon-alpha 2a treatment in patients with chronic hepatitis C. Construct group

H Bell, K Hellum, S Harthug, A Maeland, S Ritland, B Myrvang, B von der Lippe, N Raknerud, K Skaug, B G Gutigard, R Skjaerven, L E Prescott, P Simmonds

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

Patients with chronic hepatitis C respond differently when treated with interferon. We randomized 116 patients with chronic hepatitis C in order to compare two dosage regimens of recombinant interferon alpha 2a:3 MIU x 3 per week for 6 months (arm A) or 6 MIU x 3 per week for 3 months and then 3 MIU x 3 per week for 3 months (arm B). There were no significant differences concerning outcome between the two dose regimens: sustained clearance of HCV viremia 6 months after the end of treatment was obtained in 12/59 (20%) in group A compared with 18/57 (32%) in group B (p = 0.24). In patients with genotype 1a, 4/31 (13%), in genotype 1b, none of 9 (0%), 9/15 (60%) in genotype 2, and 17/58 (29%) in genotype 3, showed sustained clearance of HCV viremia 6 months after the end of treatment (p = 0.002). In a stepwise logistic regression analysis, only pretreatment viral load (p = 0.0001), genotype (p = 0.001) and age (p = 0.04) were identified as independent predictors of sustained clearance of HCV viremia. Liver histology as assessed by Knodell index was significantly improved in patients with sustained HCV RNA response 6 months after the end of treatment (5.2 +/- 2.2 vs 2.6 +/- 2.2, p <0.001), but not in responders with relapse or in non-responders. In conclusion, stepwise logistic regression analysis showed that viral load, HCV genotype and age were the only independent predictors for sustained HCV RNA response.
Original languageEnglish
Pages (from-to)17-22
Number of pages6
JournalScandinavian Journal of Infectious Diseases
Volume29
Issue number1
DOIs
Publication statusPublished - 1997

Keywords / Materials (for Non-textual outputs)

  • Age Factors
  • Alanine Transaminase
  • Antiviral Agents
  • Chi-Square Distribution
  • Chronic Disease
  • Female
  • Genotype
  • Hepacivirus
  • Hepatitis C
  • Humans
  • Interferon-alpha
  • Liver
  • Logistic Models
  • Male
  • Norway
  • Odds Ratio
  • Polymerase Chain Reaction
  • Polymorphism, Restriction Fragment Length
  • RNA, Viral
  • Recombinant Proteins
  • Treatment Outcome
  • Viral Load
  • Viremia

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