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一名细胞色素P450 2D6功能受损患者在接受伯氨喹治疗后间日疟四次复发

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

作者信息

Choi Sungim, Choi Heun, Park Seong Yeon, Kwak Yee Gyung, Song Je Eun, Shin So Youn, Baek Ji Hyeon, Shin Hyun-Il, Oh Hong Sang, Kim Yong Chan, Yeom Joon-Sup, Han Jin-Hee, Kim Min Jae

机构信息

Department of Infectious Diseases, Dongguk University Ilsan Hospital, Goyang 10326, Korea.

Department of Infectious Diseases, National Health Insurance Service Ilsan Hospital, Goyang 10444, Korea.

出版信息

Korean J Parasitol. 2022 Feb;60(1):39-43. doi: 10.3347/kjp.2022.60.1.39. Epub 2022 Feb 23.

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.

摘要

间日疟原虫存在休眠的肝期寄生虫,称为休眠子,可导致疟疾复发。目前唯一用于消除休眠子的药物是伯氨喹。伯氨喹的抗疟特性取决于细胞色素P450同工酶2D6(CYP2D6)产生的氧化代谢产物。伯氨喹代谢降低可能与间日疟复发有关。我们描述了1例CYP2D6功能降低的患者出现4次间日疟复发的病例。该患者为52岁男性,体重52kg。他在首次发作前7个月接受了全胃切除术和脾切除术,当时正在接受胃癌化疗。首次发作于2019年3月,每次发作间隔分别为34天、41天和97天。在首次和第二次发作时,给予伯氨喹15mg,共14天。在第三次和第四次发作时,伯氨喹剂量增加至30mg,共14天。对4份间日疟原虫样本的7个基因序列进行分析,结果显示完全相同。对CYP2D6基因型进行分析,确定为功能降低的中间代谢型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6edd/8898651/9a4db74e4da0/kjp-60-1-39f1.jpg

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