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血红素加氧酶-1基因启动子中的微卫星多态性与缅甸人群患脑型疟疾的易感性相关。

Microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with susceptibility to cerebral malaria in Myanmar.

作者信息

Takeda Masato, Kikuchi Mihoko, Ubalee Ratawan, Na-Bangchang Kesara, Ruangweerayut Ronnatrai, Shibahara Shigeki, Imai So-ichi, Hirayama Kenji

机构信息

Department of Medical Zoology, Saitama Medical School, Saitama 350-0495, Japan.

出版信息

Jpn J Infect Dis. 2005 Oct;58(5):268-71.

Abstract

Cerebral malaria (CM) is a serious complication of Plasmodium falciparum malaria, and its pathogenesis leading to coma remains unknown. Heme oxygenase-1 (HO-1) catalyzes heme breakdown, eventually generating bilirubin, iron and carbon monoxide. The HO-1 gene promoter contains a polymorphic (GT)n repeat which may influence the expression level of HO-1. To explore the correlation between this (GT)n polymorphism and susceptibility to CM, we analyzed the frequencies of the (GT)n alleles in 120 Myanmarese patients with uncomplicated malaria (UM) and 30 patients with CM. The frequency of homozygotes for the short (GT)n alleles (<28 repeats) in CM patients was significantly higher than those in UM patients (P < 0.008, OR = 3.14). Thus, short (GT)n alleles represent a genetic risk factor for CM.

摘要

脑型疟疾(CM)是恶性疟原虫疟疾的一种严重并发症,其导致昏迷的发病机制尚不清楚。血红素加氧酶-1(HO-1)催化血红素分解,最终生成胆红素、铁和一氧化碳。HO-1基因启动子包含一个多态性(GT)n重复序列,可能影响HO-1的表达水平。为了探讨这种(GT)n多态性与CM易感性之间的相关性,我们分析了120例缅甸非重症疟疾(UM)患者和30例CM患者中(GT)n等位基因的频率。CM患者中短(GT)n等位基因(<28次重复)纯合子的频率显著高于UM患者(P < 0.008,OR = 3.14)。因此,短(GT)n等位基因是CM的一个遗传危险因素。

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