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Severe thrombocytopenia in a patient with inosine triphosphatase (ITPA)-CC genotype caused by pegylated interferon (IFN)-α-2a with ribavirin therapy: a case report.

AbstractBACKGROUND:
Pegylated interferon combined with ribavirin treatment is an effective therapy for chronic hepatitis C viral infection. However, pegylated interferon combined with ribavirin is associated with various adverse reactions. Severe thrombocytopenia is a life-threatening side effect of interferon therapy that can lead to bleeding. It is generally understood that the inosine triphosphatase-CC genotype does not have a significantly lower reduction by pegylated interferon combined with ribavirin in the mean platelet counts compared with the AA/CA genotype. We report a case of severe thrombocytopenia that developed in a patient with chronic hepatitis C treated with pegylated interferon combined with ribavirin in spite of having the inosine triphosphatase-CC genotype.
CASE PRESENTATION:
A 57-year-old female had been diagnosed as having HCV infection in 2008. The inosine triphosphatase gene showed one single nucleotide polymorphism (rs1127354) C/C (major homozygous) and the IL28B gene showed single nucleotide polymorphism (rs8099917 T/T, rs11881222 T/T) (major homozygous). The patient was treated with pegylated interferon 180 μg once a week combined with ribavirin 600 mg per day from April 2011. The hepatitis c virus ribonucleic acid turned negative 9 weeks after treatment with pegylated interferon combined with ribavirin. During the therapy, the platelet count remained above 8.0 × 10(4)/μl for about 9 months. In January 2012, the platelet count was 6.8 × 10(4)/μl. In February 2012, the 44th week from the beginning of the treatment, a sudden decrease in the platelet count to 0.8 × 10(4)/μl was observed. After prednisolone was administered, the platelet count increased. Finally the platelet count had risen above normal range.
CONCLUSION:
We should pay careful attention in the differential diagnosis for patients with the inosine triphosphatase-CC genotype because, although rare, severe thrombocytopenia could occur.
AuthorsWeimin Jiang, Hisashi Hidaka, Takahide Nakazawa, Hiroyuki Kitagawa, Wasaburo Koizumi
JournalBMC research notes (BMC Res Notes) Vol. 7 Pg. 141 (Mar 12 2014) ISSN: 1756-0500 [Electronic] England
PMID24621321 (Publication Type: Case Reports, Journal Article)
Chemical References
  • Antiviral Agents
  • Glucocorticoids
  • Interferon-alpha
  • Recombinant Proteins
  • Polyethylene Glycols
  • Ribavirin
  • Prednisolone
  • Pyrophosphatases
  • inosine triphosphatase
  • peginterferon alfa-2a
Topics
  • Antiviral Agents (adverse effects)
  • Drug Therapy, Combination
  • Female
  • Genotype
  • Glucocorticoids (therapeutic use)
  • Hepatitis C, Chronic (drug therapy)
  • Humans
  • Interferon-alpha (adverse effects)
  • Middle Aged
  • Platelet Count
  • Polyethylene Glycols (adverse effects)
  • Prednisolone (therapeutic use)
  • Pyrophosphatases (genetics)
  • Recombinant Proteins (adverse effects)
  • Ribavirin (adverse effects)
  • Thrombocytopenia (chemically induced, drug therapy)
  • Treatment Outcome

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