Korean J Parasitol.  2022 Feb;60(1):39-43. 10.3347/kjp.2022.60.1.39.

Four Times of Relapse of Plasmodium vivax Malaria Despite Primaquine Treatment in a Patient with Impaired Cytochrome P450 2D6 Function

Affiliations
  • 1Department of Infectious Diseases, Dongguk University Ilsan Hospital, Goyang 10326, Korea
  • 2Department of Infectious Diseases, National Health Insurance Service Ilsan Hospital, Goyang 10444, Korea
  • 3Department of Internal Medicine, Inje University Ilsan Paik Hospital, Ilsan 10380, Korea
  • 4Department of Infectious Diseases, International St. Mary’s Hospital, College of Medicine, Catholic Kwandong University, Incheon 22711, Korea
  • 5Division of Infectious Diseases, Department of Internal Medicine, Inha University School of Medicine, Incheon 22332, Korea
  • 6Division of Vectors and Parasitic Diseases, Bureau of Infectious Disease Diagnosis Control, Korea Disease Control and Prevention Agency, Chungbuk 28159, Korea
  • 7Division of Infectious Disease, Department of Internal Medicine, Armed Forces Capital Hospital, Seongnam 13574, Korea
  • 8Department of Internal Medicine, Division of Infectious Disease, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin 16995, Korea
  • 9Department of Medical Environmental Biology and Tropical Medicine, School of Medicine, Kangwon National University, Chuncheon 24341, Korea
  • 10Department of Infectious Diseases, Asan Medical Center, University of Ulsan College of Medicine, Seoul 05505, Korea

Abstract

Plasmodium vivax exhibits dormant liver-stage parasites, called hypnozoites, which can cause relapse of malaria. The only drug currently used for eliminating hypnozoites is primaquine. The antimalarial properties of primaquine are dependent on the production of oxidized metabolites by the cytochrome P450 isoenzyme 2D6 (CYP2D6). Reduced primaquine metabolism may be related to P. vivax relapses. We describe a case of 4 episodes of recurrence of vivax malaria in a patient with decreased CYP2D6 function. The patient was 52-year-old male with body weight of 52 kg. He received total gastrectomy and splenectomy 7 months before the first episode and was under chemotherapy for the gastric cancer. The first episode occurred in March 2019 and each episode had intervals of 34, 41, and 97 days, respectively. At the first and second episodes, primaquine was administered as 15 mg for 14 days. The primaquine dose was increased with 30 mg for 14 days at the third and fourth episodes. Seven gene sequences of P. vivax were analyzed and revealed totally identical for all the 4 samples. The CYP2D6 genotype was analyzed and intermediate metabolizer phenotype with decreased function was identified.

Keyword

recurrence; primaquine; CYP2D6
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