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Neonatal Hyperbilirubinemia in Japanese Neonates: Analysis of the Heme Oxygenase-1 Gene and Fetal Hemoglobin Composition in Cord Blood

机译:日本新生儿新生儿高胆红素血症:脐血中血红素加氧酶-1基因和胎儿血红蛋白组成的分析

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Neonatal hyperbilirubinemia is frequent and severe in Japanese infants. Although the G71R mutation of the bilirubin uridine diphosphate-glucuronosyltransferase gene is associated with severe neonatal hyperbilirubinemia in this population, it accounts for only half of the neonates with severe hyperbilirubinemia. It was suggested that increased bilirubin production would also be associated with severe neonatal hyperbilirubinemia in Japanese infants. To elucidate the genetic factors causing severe hyperbilirubinemia in these patients, we studied two notable factors associated with bilirubin production: heme oxygenase-1, a key enzyme of heme metabolism, and fetal Hb composition, a factor possibly associated with heme load in neonates. We first determined the sequences of promoter and all coding regions of the heme oxygenase-1 gene in Japanese neonates who had undergone phototherapy, but found no mutation except for the polymorphic (GT)n repeats in the promoter region. These repeats modulate the transcription of the heme oxygenase-1 gene, and the longer repeat sequences are known to reduce the transcription. We detected a significant difference in the allele frequencies of each number of (GT)n repeats between Japanese and German populations. However, we could not find a relation between those polymorphisms and neonatal hyperbilirubinemia. We next analyzed the state of Hb switching of the γ- to β-globin chain and the phenotype of γ-globin chain isoforms in cord blood. We found no relation between fetal Hb composition and neonatal hyperbilirubinemia. Further studies are required to elucidate genetic or environmental factors in neonatal hyperbilirubinemia in Japanese infants.Abbreviations: B-UGT, bilirubin uridine diphosphate-glucuronosyltransferase (EC 2.4.1.17); HO-1, heme oxygenase-1 (EC 1.14.99.3); CO, carbon monoxide; HbF, fetal hemoglobin; TCBR, transcutaneous bilirubinometer reading
机译:在日本婴儿中,新生儿高胆红素血症频繁且严重。尽管该人群中胆红素尿苷二磷酸-葡萄糖醛酸转移酶基因的G71R突变与严重的新生儿高胆红素血症有关,但仅占严重的高胆红素血症新生儿的一半。有人提出,日本婴儿的胆红素生成增加也与严重的新生儿高胆红素血症有关。为了阐明导致这些患者严重高胆红素血症的遗传因素,我们研究了与胆红素产生相关的两个值得注意的因素:血红素加氧酶-1(血红素代谢的关键酶)和胎儿血红蛋白组成,这可能与新生儿血红素负荷有关。我们首先确定了接受光疗的日本新生儿的血红素加氧酶-1基因的启动子序列和所有编码区,但除了启动子区的多态性(GT)n重复序列外,没有发现任何突变。这些重复调节血红素加氧酶-1基因的转录,已知较长的重复序列可减少转录。我们发现日本人和德国人之间每个(GT)n重复序列的等位基因频率存在显着差异。但是,我们找不到这些多态性与新生儿高胆红素血症之间的关系。接下来,我们分析了脐带血中γ-球蛋白链的Hb转换状态和γ-球蛋白链亚型的表型。我们发现胎儿血红蛋白组成与新生儿高胆红素血症之间没有关系。需要进一步研究阐明日本婴儿新生儿高胆红素血症的遗传或环境因素。缩写:B-UGT,胆红素尿苷二磷酸-葡萄糖醛酸转移酶(EC 2.4.1.17); HO-1,血红素加氧酶-1(EC 1.14.99.3); CO,一氧化碳; HbF,胎儿血红蛋白; TCBR,经皮胆红素计读数

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